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    <title>Everything You Know About Disability Is Wrong</title>
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    <description>Everything You Know About Disability is Wrong is a podcast for the disability community by the disability community, hosted by two disabled women. But if you’re not disabled, listen in to learn about real issues, celebrations, and conversations disabled people are having in their communities. Powered by Easterseals.</description>
    <copyright>© 2024 Everything You Know About Disability Is Wrong Erin and Lily</copyright>
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    <podcast:locked owner="brandteam@easterseals.com">no</podcast:locked>
    <language>en-us</language>
    <pubDate>Thu, 16 Apr 2026 04:00:08 -0400</pubDate>
    <lastBuildDate>Thu, 16 Apr 2026 04:01:22 -0400</lastBuildDate>
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      <title>Everything You Know About Disability Is Wrong</title>
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    <itunes:type>episodic</itunes:type>
    <itunes:author>Easterseals</itunes:author>
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    <itunes:summary>Everything You Know About Disability is Wrong is a podcast for the disability community by the disability community, hosted by two disabled women. But if you’re not disabled, listen in to learn about real issues, celebrations, and conversations disabled people are having in their communities. Powered by Easterseals.</itunes:summary>
    <itunes:subtitle>Everything You Know About Disability is Wrong is a podcast for the disability community by the disability community, hosted by two disabled women.</itunes:subtitle>
    <itunes:keywords></itunes:keywords>
    <itunes:owner>
      <itunes:name>Erin and Lily</itunes:name>
    </itunes:owner>
    <itunes:complete>No</itunes:complete>
    <itunes:explicit>No</itunes:explicit>
    <item>
      <title>Free to Be Me: Ron Funches on Autism and Meeting Yourself Where You Are</title>
      <itunes:episode>52</itunes:episode>
      <podcast:episode>52</podcast:episode>
      <itunes:title>Free to Be Me: Ron Funches on Autism and Meeting Yourself Where You Are</itunes:title>
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      <description>
        <![CDATA[<p>On this episode of Everything You Know About Disability Is Wrong, we’re joined by <a href="https://ronfunches.com/2025/">Ron Funches</a>, a stand-up comedian, actor, and recent cast member on The Traitors. Ron shares his perspective as both an autistic adult and a parent of an autistic son, reflecting on how his recent diagnosis has deepened his understanding of himself, his family, and the power of self-acceptance. </p><p>Through humor and honesty, Ron discusses what autism acceptance looks like in real life—from recognizing shared traits with his son to navigating the transition to adulthood, caregiving challenges, and the importance of meeting people where they are. This conversation reinforces the importance of acceptance, accessible support, and empowering people with disabilities to thrive on their own terms.</p><p>Easterseals is committed to supporting autistic individuals and caregivers with <a href="https://www.easterseals.com/explore-resources/understanding-disability">resources, services, and community</a>. </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>On this episode of Everything You Know About Disability Is Wrong, we’re joined by <a href="https://ronfunches.com/2025/">Ron Funches</a>, a stand-up comedian, actor, and recent cast member on The Traitors. Ron shares his perspective as both an autistic adult and a parent of an autistic son, reflecting on how his recent diagnosis has deepened his understanding of himself, his family, and the power of self-acceptance. </p><p>Through humor and honesty, Ron discusses what autism acceptance looks like in real life—from recognizing shared traits with his son to navigating the transition to adulthood, caregiving challenges, and the importance of meeting people where they are. This conversation reinforces the importance of acceptance, accessible support, and empowering people with disabilities to thrive on their own terms.</p><p>Easterseals is committed to supporting autistic individuals and caregivers with <a href="https://www.easterseals.com/explore-resources/understanding-disability">resources, services, and community</a>. </p>]]>
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      <pubDate>Thu, 16 Apr 2026 04:00:00 -0400</pubDate>
      <author>Easterseals</author>
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      <itunes:duration>3254</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>On this episode of Everything You Know About Disability Is Wrong, we’re joined by <a href="https://ronfunches.com/2025/">Ron Funches</a>, a stand-up comedian, actor, and recent cast member on The Traitors. Ron shares his perspective as both an autistic adult and a parent of an autistic son, reflecting on how his recent diagnosis has deepened his understanding of himself, his family, and the power of self-acceptance. </p><p>Through humor and honesty, Ron discusses what autism acceptance looks like in real life—from recognizing shared traits with his son to navigating the transition to adulthood, caregiving challenges, and the importance of meeting people where they are. This conversation reinforces the importance of acceptance, accessible support, and empowering people with disabilities to thrive on their own terms.</p><p>Easterseals is committed to supporting autistic individuals and caregivers with <a href="https://www.easterseals.com/explore-resources/understanding-disability">resources, services, and community</a>. </p>]]>
      </itunes:summary>
      <itunes:keywords>Ron Funches, autism acceptance, autistic adults, parenting an autistic child, neurodiversity, disability podcast, self-acceptance, caregivers, autism support, Easterseals</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
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    <item>
      <title>Meeting People Where They Are: Dani Bowman on Autism Acceptance</title>
      <itunes:episode>51</itunes:episode>
      <podcast:episode>51</podcast:episode>
      <itunes:title>Meeting People Where They Are: Dani Bowman on Autism Acceptance</itunes:title>
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      <description>
        <![CDATA[<p>Dani Bowman is an autistic animator, entrepreneur, and educator who founded <a href="https://danimation.us/">DaniMation Entertainment</a> to help people on the autism spectrum develop creative and professional skills. Through her work and advocacy, she empowers neurodivergent individuals to pursue their passions and build meaningful careers.</p><p>In this episode, Dani reflects on her journey in animation and business, her experience on Netflix’s Love on the Spectrum, and her company DaniMation. The episode highlights the many ways Dani creates learning and employment opportunities for neurodivergent adults. The conversation also explores relationships, self-advocacy, and what authentic autism acceptance looks like in everyday life.</p><p>This episode is a kick-off to Autism Acceptance Month and our <a href="https://www.easterseals.com/explore-resources/understanding-disability">Understanding Disability</a> campaign. At Easterseals, we know that disability looks different for every person, and support should be tailored to individual strengths, goals, and needs.</p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Dani Bowman is an autistic animator, entrepreneur, and educator who founded <a href="https://danimation.us/">DaniMation Entertainment</a> to help people on the autism spectrum develop creative and professional skills. Through her work and advocacy, she empowers neurodivergent individuals to pursue their passions and build meaningful careers.</p><p>In this episode, Dani reflects on her journey in animation and business, her experience on Netflix’s Love on the Spectrum, and her company DaniMation. The episode highlights the many ways Dani creates learning and employment opportunities for neurodivergent adults. The conversation also explores relationships, self-advocacy, and what authentic autism acceptance looks like in everyday life.</p><p>This episode is a kick-off to Autism Acceptance Month and our <a href="https://www.easterseals.com/explore-resources/understanding-disability">Understanding Disability</a> campaign. At Easterseals, we know that disability looks different for every person, and support should be tailored to individual strengths, goals, and needs.</p>]]>
      </content:encoded>
      <pubDate>Wed, 01 Apr 2026 04:00:00 -0400</pubDate>
      <author>Easterseals</author>
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      <itunes:author>Easterseals</itunes:author>
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      <itunes:duration>2807</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Dani Bowman is an autistic animator, entrepreneur, and educator who founded <a href="https://danimation.us/">DaniMation Entertainment</a> to help people on the autism spectrum develop creative and professional skills. Through her work and advocacy, she empowers neurodivergent individuals to pursue their passions and build meaningful careers.</p><p>In this episode, Dani reflects on her journey in animation and business, her experience on Netflix’s Love on the Spectrum, and her company DaniMation. The episode highlights the many ways Dani creates learning and employment opportunities for neurodivergent adults. The conversation also explores relationships, self-advocacy, and what authentic autism acceptance looks like in everyday life.</p><p>This episode is a kick-off to Autism Acceptance Month and our <a href="https://www.easterseals.com/explore-resources/understanding-disability">Understanding Disability</a> campaign. At Easterseals, we know that disability looks different for every person, and support should be tailored to individual strengths, goals, and needs.</p>]]>
      </itunes:summary>
      <itunes:keywords>Autism Acceptance Month, autism acceptance, autism, autistic, disability</itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Love, Humor, and Real Life: Shane &amp; Hannah Burcaw on Relationships and Disability</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>38</itunes:episode>
      <podcast:episode>38</podcast:episode>
      <itunes:title>Love, Humor, and Real Life: Shane &amp; Hannah Burcaw on Relationships and Disability</itunes:title>
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        <![CDATA[<p><br>Shane and Hannah Burcaw, creators of the YouTube channel <em>Squirmy and Grubs</em>, join Lily and Erin for a wide-ranging conversation about relationships, content creation, and what people consistently misunderstand about disability. As a married couple whose lives are highly visible online, Shane and Hannah share how public assumptions, especially about love, worth, and caregiving, show up in comment sections far more than in real life.</p><p><br>They reflect on how a viral interview shifted their channel from casual vlogs to a platform that sparks deeper conversations, and how they learned to balance humor with heavier topics without losing their audience. From navigating internet cruelty to deciding how much of their lived experience to share on camera, Shane and Hannah speak candidly about pressure, boundaries, and staying grounded.</p><p><br>The episode also explores how caregiving fits naturally into their relationship, why long-form storytelling still matters, and how shared routines, sarcasm, and trust keep their partnership strong. Throughout the conversation, Shane and Hannah emphasize curiosity, patience, and showing up honestly, online and offline.</p><p><strong>Key Moments</strong></p><p><br>03:34 What’s wrong about disability, worth, and relationships</p><p><br>05:39 Why cruelty shows up online but never in real life</p><p><br>07:58 Going viral and suddenly becoming public educators</p><p><br>10:45 Shifting from fun vlogs to purpose-driven storytelling</p><p><br>13:40 Mixing humor with hard conversations so people keep listening</p><p><br>16:01 The pressure to always create disability-focused content</p><p><br>19:20 Why “normal” couple trends never stay neutral online</p><p><br>22:51 Long-form content as a space for nuance and depth</p><p><br>25:57 Caregiving, autonomy, and public misunderstanding</p><p><br>30:04 Writing books to show the range of disabled relationships</p><p><br>39:36 Rituals, routines, and what actually keeps their relationship strong</p><p><strong>Connect with Shane &amp; Hannah</strong></p><ul><li>Shane's Instagram: <a href="https://www.instagram.com/shaneburcaw/#">https://www.instagram.com/shaneburcaw/#</a> </li><li>Hannah's Instagram: <a href="https://www.instagram.com/hannahayl/#">https://www.instagram.com/hannahayl/#</a> </li><li>YouTube: <a href="https://www.youtube.com/c/squirmyandgrubs">https://www.youtube.com/c/squirmyandgrubs</a> </li><li>Squirmy and Grubs Website: <a href="https://www.squirmyandgrubs.com/">https://www.squirmyandgrubs.com/</a> </li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p><br>Shane and Hannah Burcaw, creators of the YouTube channel <em>Squirmy and Grubs</em>, join Lily and Erin for a wide-ranging conversation about relationships, content creation, and what people consistently misunderstand about disability. As a married couple whose lives are highly visible online, Shane and Hannah share how public assumptions, especially about love, worth, and caregiving, show up in comment sections far more than in real life.</p><p><br>They reflect on how a viral interview shifted their channel from casual vlogs to a platform that sparks deeper conversations, and how they learned to balance humor with heavier topics without losing their audience. From navigating internet cruelty to deciding how much of their lived experience to share on camera, Shane and Hannah speak candidly about pressure, boundaries, and staying grounded.</p><p><br>The episode also explores how caregiving fits naturally into their relationship, why long-form storytelling still matters, and how shared routines, sarcasm, and trust keep their partnership strong. Throughout the conversation, Shane and Hannah emphasize curiosity, patience, and showing up honestly, online and offline.</p><p><strong>Key Moments</strong></p><p><br>03:34 What’s wrong about disability, worth, and relationships</p><p><br>05:39 Why cruelty shows up online but never in real life</p><p><br>07:58 Going viral and suddenly becoming public educators</p><p><br>10:45 Shifting from fun vlogs to purpose-driven storytelling</p><p><br>13:40 Mixing humor with hard conversations so people keep listening</p><p><br>16:01 The pressure to always create disability-focused content</p><p><br>19:20 Why “normal” couple trends never stay neutral online</p><p><br>22:51 Long-form content as a space for nuance and depth</p><p><br>25:57 Caregiving, autonomy, and public misunderstanding</p><p><br>30:04 Writing books to show the range of disabled relationships</p><p><br>39:36 Rituals, routines, and what actually keeps their relationship strong</p><p><strong>Connect with Shane &amp; Hannah</strong></p><ul><li>Shane's Instagram: <a href="https://www.instagram.com/shaneburcaw/#">https://www.instagram.com/shaneburcaw/#</a> </li><li>Hannah's Instagram: <a href="https://www.instagram.com/hannahayl/#">https://www.instagram.com/hannahayl/#</a> </li><li>YouTube: <a href="https://www.youtube.com/c/squirmyandgrubs">https://www.youtube.com/c/squirmyandgrubs</a> </li><li>Squirmy and Grubs Website: <a href="https://www.squirmyandgrubs.com/">https://www.squirmyandgrubs.com/</a> </li></ul>]]>
      </content:encoded>
      <pubDate>Thu, 08 Jan 2026 09:00:00 -0500</pubDate>
      <author>Easterseals</author>
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      <itunes:author>Easterseals</itunes:author>
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      <itunes:duration>3672</itunes:duration>
      <itunes:summary>
        <![CDATA[<p><br>Shane and Hannah Burcaw, creators of the YouTube channel <em>Squirmy and Grubs</em>, join Lily and Erin for a wide-ranging conversation about relationships, content creation, and what people consistently misunderstand about disability. As a married couple whose lives are highly visible online, Shane and Hannah share how public assumptions, especially about love, worth, and caregiving, show up in comment sections far more than in real life.</p><p><br>They reflect on how a viral interview shifted their channel from casual vlogs to a platform that sparks deeper conversations, and how they learned to balance humor with heavier topics without losing their audience. From navigating internet cruelty to deciding how much of their lived experience to share on camera, Shane and Hannah speak candidly about pressure, boundaries, and staying grounded.</p><p><br>The episode also explores how caregiving fits naturally into their relationship, why long-form storytelling still matters, and how shared routines, sarcasm, and trust keep their partnership strong. Throughout the conversation, Shane and Hannah emphasize curiosity, patience, and showing up honestly, online and offline.</p><p><strong>Key Moments</strong></p><p><br>03:34 What’s wrong about disability, worth, and relationships</p><p><br>05:39 Why cruelty shows up online but never in real life</p><p><br>07:58 Going viral and suddenly becoming public educators</p><p><br>10:45 Shifting from fun vlogs to purpose-driven storytelling</p><p><br>13:40 Mixing humor with hard conversations so people keep listening</p><p><br>16:01 The pressure to always create disability-focused content</p><p><br>19:20 Why “normal” couple trends never stay neutral online</p><p><br>22:51 Long-form content as a space for nuance and depth</p><p><br>25:57 Caregiving, autonomy, and public misunderstanding</p><p><br>30:04 Writing books to show the range of disabled relationships</p><p><br>39:36 Rituals, routines, and what actually keeps their relationship strong</p><p><strong>Connect with Shane &amp; Hannah</strong></p><ul><li>Shane's Instagram: <a href="https://www.instagram.com/shaneburcaw/#">https://www.instagram.com/shaneburcaw/#</a> </li><li>Hannah's Instagram: <a href="https://www.instagram.com/hannahayl/#">https://www.instagram.com/hannahayl/#</a> </li><li>YouTube: <a href="https://www.youtube.com/c/squirmyandgrubs">https://www.youtube.com/c/squirmyandgrubs</a> </li><li>Squirmy and Grubs Website: <a href="https://www.squirmyandgrubs.com/">https://www.squirmyandgrubs.com/</a> </li></ul>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
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    <item>
      <title>The Power of Purpose: Heather Mills on Business, Courage, and Kindness</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>37</itunes:episode>
      <podcast:episode>37</podcast:episode>
      <itunes:title>The Power of Purpose: Heather Mills on Business, Courage, and Kindness</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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        <![CDATA[<p>Heather Mills, world-record-breaking Paralympic skier and founder of VBites Foods, joins Lily and Erin for a conversation that spans business, resilience, and the power of purpose. From surviving a life-changing accident to building one of the largest plant-based food companies in the world, Heather shares how every setback became a reason to innovate.</p><p><br></p><p>She recalls turning personal tragedy into global advocacy, developing new prosthetics, founding support networks for amputees, and creating opportunities for others to regain independence. With humor and insight, Heather reflects on what true confidence looks like, the importance of empathy in leadership, and why helping others is the most rewarding kind of “selfishness.”</p><p><br></p><p>Heather also discusses entrepreneurship through a values-driven lens, balancing profit with purpose, leading with compassion, and using success to make a difference. Her message is bold yet simple: face challenges head-on, stay curious, and use your energy to build solutions instead of problems.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>03:22 Airport misassumptions and using humor to reset the moment</p><p><br></p><p>05:48 Why comfort with yourself helps others feel at ease</p><p><br></p><p>07:51 How confidence and comedy reshape public reactions</p><p><br></p><p>11:33 Switching from “the problem is” to “the solution is”</p><p><br></p><p>13:26 Building better prosthetics when the market failed to deliver</p><p><br></p><p>15:42 Creating the Amputee Forum and a global peer-support network</p><p><br></p><p>19:20 Healing after injury and the path to launching VBites</p><p><br></p><p>22:50 Turning setbacks into purpose across sport and business</p><p><br></p><p>25:39 Becoming a world-record Paralympic skier at 42</p><p><br></p><p>30:27 The power of boundaries and choosing who gets your energy</p><p><br></p><p><strong>Connect with Heather Mills</strong></p><ul><li>LinkedIn: <a href="https://uk.linkedin.com/in/msheathermills">https://uk.linkedin.com/in/msheathermills</a> </li><li>Heather Mills Official Site: <a href="https://heathermills.org/">https://heathermills.org/</a> </li><li>VBites: <a href="https://www.vbites.com/">https://www.vbites.com/</a> </li><li>Facebook: <a href="https://www.facebook.com/heather.mills.official/">https://www.facebook.com/heather.mills.official/</a> </li><li>Twitter: <a href="https://twitter.com/heatherofficial/status/1755615616638341264">https://twitter.com/heatherofficial/status/1755615616638341264</a> </li><li>Instagram: <a href="https://www.instagram.com/heathermillsofficial/?hl=en">https://www.instagram.com/heathermillsofficial/?hl=en</a> <br><strong><p></p></strong><br></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Heather Mills, world-record-breaking Paralympic skier and founder of VBites Foods, joins Lily and Erin for a conversation that spans business, resilience, and the power of purpose. From surviving a life-changing accident to building one of the largest plant-based food companies in the world, Heather shares how every setback became a reason to innovate.</p><p><br></p><p>She recalls turning personal tragedy into global advocacy, developing new prosthetics, founding support networks for amputees, and creating opportunities for others to regain independence. With humor and insight, Heather reflects on what true confidence looks like, the importance of empathy in leadership, and why helping others is the most rewarding kind of “selfishness.”</p><p><br></p><p>Heather also discusses entrepreneurship through a values-driven lens, balancing profit with purpose, leading with compassion, and using success to make a difference. Her message is bold yet simple: face challenges head-on, stay curious, and use your energy to build solutions instead of problems.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>03:22 Airport misassumptions and using humor to reset the moment</p><p><br></p><p>05:48 Why comfort with yourself helps others feel at ease</p><p><br></p><p>07:51 How confidence and comedy reshape public reactions</p><p><br></p><p>11:33 Switching from “the problem is” to “the solution is”</p><p><br></p><p>13:26 Building better prosthetics when the market failed to deliver</p><p><br></p><p>15:42 Creating the Amputee Forum and a global peer-support network</p><p><br></p><p>19:20 Healing after injury and the path to launching VBites</p><p><br></p><p>22:50 Turning setbacks into purpose across sport and business</p><p><br></p><p>25:39 Becoming a world-record Paralympic skier at 42</p><p><br></p><p>30:27 The power of boundaries and choosing who gets your energy</p><p><br></p><p><strong>Connect with Heather Mills</strong></p><ul><li>LinkedIn: <a href="https://uk.linkedin.com/in/msheathermills">https://uk.linkedin.com/in/msheathermills</a> </li><li>Heather Mills Official Site: <a href="https://heathermills.org/">https://heathermills.org/</a> </li><li>VBites: <a href="https://www.vbites.com/">https://www.vbites.com/</a> </li><li>Facebook: <a href="https://www.facebook.com/heather.mills.official/">https://www.facebook.com/heather.mills.official/</a> </li><li>Twitter: <a href="https://twitter.com/heatherofficial/status/1755615616638341264">https://twitter.com/heatherofficial/status/1755615616638341264</a> </li><li>Instagram: <a href="https://www.instagram.com/heathermillsofficial/?hl=en">https://www.instagram.com/heathermillsofficial/?hl=en</a> <br><strong><p></p></strong><br></li></ul>]]>
      </content:encoded>
      <pubDate>Mon, 22 Dec 2025 09:00:00 -0500</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/bc24cad3/ebf11126.mp3" length="62147940" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/9P9AsGdZ_62onLHP3dw8xaznsQaKlqeugOSWUEXhdgc/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS83ZmU4/MzgxMzFjMWFkOGQ3/MTJmN2YyOTAzMWEy/ODFlYy5wbmc.jpg"/>
      <itunes:duration>3879</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Heather Mills, world-record-breaking Paralympic skier and founder of VBites Foods, joins Lily and Erin for a conversation that spans business, resilience, and the power of purpose. From surviving a life-changing accident to building one of the largest plant-based food companies in the world, Heather shares how every setback became a reason to innovate.</p><p><br></p><p>She recalls turning personal tragedy into global advocacy, developing new prosthetics, founding support networks for amputees, and creating opportunities for others to regain independence. With humor and insight, Heather reflects on what true confidence looks like, the importance of empathy in leadership, and why helping others is the most rewarding kind of “selfishness.”</p><p><br></p><p>Heather also discusses entrepreneurship through a values-driven lens, balancing profit with purpose, leading with compassion, and using success to make a difference. Her message is bold yet simple: face challenges head-on, stay curious, and use your energy to build solutions instead of problems.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>03:22 Airport misassumptions and using humor to reset the moment</p><p><br></p><p>05:48 Why comfort with yourself helps others feel at ease</p><p><br></p><p>07:51 How confidence and comedy reshape public reactions</p><p><br></p><p>11:33 Switching from “the problem is” to “the solution is”</p><p><br></p><p>13:26 Building better prosthetics when the market failed to deliver</p><p><br></p><p>15:42 Creating the Amputee Forum and a global peer-support network</p><p><br></p><p>19:20 Healing after injury and the path to launching VBites</p><p><br></p><p>22:50 Turning setbacks into purpose across sport and business</p><p><br></p><p>25:39 Becoming a world-record Paralympic skier at 42</p><p><br></p><p>30:27 The power of boundaries and choosing who gets your energy</p><p><br></p><p><strong>Connect with Heather Mills</strong></p><ul><li>LinkedIn: <a href="https://uk.linkedin.com/in/msheathermills">https://uk.linkedin.com/in/msheathermills</a> </li><li>Heather Mills Official Site: <a href="https://heathermills.org/">https://heathermills.org/</a> </li><li>VBites: <a href="https://www.vbites.com/">https://www.vbites.com/</a> </li><li>Facebook: <a href="https://www.facebook.com/heather.mills.official/">https://www.facebook.com/heather.mills.official/</a> </li><li>Twitter: <a href="https://twitter.com/heatherofficial/status/1755615616638341264">https://twitter.com/heatherofficial/status/1755615616638341264</a> </li><li>Instagram: <a href="https://www.instagram.com/heathermillsofficial/?hl=en">https://www.instagram.com/heathermillsofficial/?hl=en</a> <br><strong><p></p></strong><br></li></ul>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Rewriting the System: Dr. Destiny Huff on Parenting, Practice, and Advocacy</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>36</itunes:episode>
      <podcast:episode>36</podcast:episode>
      <itunes:title>Rewriting the System: Dr. Destiny Huff on Parenting, Practice, and Advocacy</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/5bae7970</link>
      <description>
        <![CDATA[<p>Dr. Destiny Huff, a late-diagnosed autistic and ADHD military spouse, therapist, and special education advocate, joins Lily and Erin for a powerful conversation on parenthood, identity, and reimagining advocacy. As the founder of Destiny Huff Consulting, she works with families across the U.S. to make education systems more responsive, compassionate, and effective for neurodivergent learners.</p><p><br>In this episode, Destiny shares how her own diagnosis transformed the way she supports families and children. She explains what it means to build <em>neuroaffirming practices</em>, from presuming competence and honoring autonomy to designing goals that match real learner needs.</p><p><br>Destiny also breaks down what an IEP really is; a <em>program</em>, not a plan, and how parents can ask for meetings, request changes, and find collaboration instead of conflict. The discussion explores bias in diagnosis, barriers faced by Black and Brown families, and how educators can check their assumptions to better support every student.</p><p><strong><br>Key Moments</strong></p><p><br></p><p><br>00:00 Tribute to Alice Wong</p><p>08:13 "Advocacy and Neurodivergence Insights"</p><p>15:24 "Neuroaffirming Special Education Handbook"</p><p>19:17 Centering Voices in Autism Advocacy</p><p>22:37 "Advocating for Diverse Learners"</p><p>30:17 "Focus, Educate, and Understand Intentions"</p><p>34:06 "Parenting Autism: Struggles and Strengths"</p><p>41:46 "Building Bridges, Not Burning Them"</p><p>48:30 Hesitation in Disclosing Diagnoses</p><p>50:43 "Embracing Accurate Labels and Support"</p><p>55:36 Bias in Disability Labels Explained</p><p>01:02:21 "Lessons on Rest and Renewal"<br></p><p><strong>Connect with Dr. Destiny Huff</strong></p><ul><li>LinkedIn: <a href="https://www.linkedin.com/in/destiny-huff-lpc-iep/">https://www.linkedin.com/in/destiny-huff-lpc-iep/</a> </li><li>Destiny Huff Consulting: <a href="https://www.destinyhuffconsulting.com/">https://www.destinyhuffconsulting.com/</a> </li><li>Instagram: <a href="https://www.instagram.com/destinyhuff_iep_advocate/">https://www.instagram.com/destinyhuff_iep_advocate/</a> </li><li>Facebook: <a href="https://www.facebook.com/destinyhuffconsulting/">https://www.facebook.com/destinyhuffconsulting/</a> <p></p></li></ul><p>HRG Counseling: <a href="https://www.hrgcounseling.com/">https://www.hrgcounseling.com/</a> </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Dr. Destiny Huff, a late-diagnosed autistic and ADHD military spouse, therapist, and special education advocate, joins Lily and Erin for a powerful conversation on parenthood, identity, and reimagining advocacy. As the founder of Destiny Huff Consulting, she works with families across the U.S. to make education systems more responsive, compassionate, and effective for neurodivergent learners.</p><p><br>In this episode, Destiny shares how her own diagnosis transformed the way she supports families and children. She explains what it means to build <em>neuroaffirming practices</em>, from presuming competence and honoring autonomy to designing goals that match real learner needs.</p><p><br>Destiny also breaks down what an IEP really is; a <em>program</em>, not a plan, and how parents can ask for meetings, request changes, and find collaboration instead of conflict. The discussion explores bias in diagnosis, barriers faced by Black and Brown families, and how educators can check their assumptions to better support every student.</p><p><strong><br>Key Moments</strong></p><p><br></p><p><br>00:00 Tribute to Alice Wong</p><p>08:13 "Advocacy and Neurodivergence Insights"</p><p>15:24 "Neuroaffirming Special Education Handbook"</p><p>19:17 Centering Voices in Autism Advocacy</p><p>22:37 "Advocating for Diverse Learners"</p><p>30:17 "Focus, Educate, and Understand Intentions"</p><p>34:06 "Parenting Autism: Struggles and Strengths"</p><p>41:46 "Building Bridges, Not Burning Them"</p><p>48:30 Hesitation in Disclosing Diagnoses</p><p>50:43 "Embracing Accurate Labels and Support"</p><p>55:36 Bias in Disability Labels Explained</p><p>01:02:21 "Lessons on Rest and Renewal"<br></p><p><strong>Connect with Dr. Destiny Huff</strong></p><ul><li>LinkedIn: <a href="https://www.linkedin.com/in/destiny-huff-lpc-iep/">https://www.linkedin.com/in/destiny-huff-lpc-iep/</a> </li><li>Destiny Huff Consulting: <a href="https://www.destinyhuffconsulting.com/">https://www.destinyhuffconsulting.com/</a> </li><li>Instagram: <a href="https://www.instagram.com/destinyhuff_iep_advocate/">https://www.instagram.com/destinyhuff_iep_advocate/</a> </li><li>Facebook: <a href="https://www.facebook.com/destinyhuffconsulting/">https://www.facebook.com/destinyhuffconsulting/</a> <p></p></li></ul><p>HRG Counseling: <a href="https://www.hrgcounseling.com/">https://www.hrgcounseling.com/</a> </p>]]>
      </content:encoded>
      <pubDate>Thu, 11 Dec 2025 09:00:00 -0500</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/5bae7970/98dcaf79.mp3" length="56974710" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/tumx15SHbBtkSFTiKzRyRAGYAi-ZecSW-6tjt9sJgd4/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS81Yzdi/OWFkZDNiNDBiZDFi/ZjY4NzY2MjFlZDNl/YzZlYS5wbmc.jpg"/>
      <itunes:duration>3556</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Dr. Destiny Huff, a late-diagnosed autistic and ADHD military spouse, therapist, and special education advocate, joins Lily and Erin for a powerful conversation on parenthood, identity, and reimagining advocacy. As the founder of Destiny Huff Consulting, she works with families across the U.S. to make education systems more responsive, compassionate, and effective for neurodivergent learners.</p><p><br>In this episode, Destiny shares how her own diagnosis transformed the way she supports families and children. She explains what it means to build <em>neuroaffirming practices</em>, from presuming competence and honoring autonomy to designing goals that match real learner needs.</p><p><br>Destiny also breaks down what an IEP really is; a <em>program</em>, not a plan, and how parents can ask for meetings, request changes, and find collaboration instead of conflict. The discussion explores bias in diagnosis, barriers faced by Black and Brown families, and how educators can check their assumptions to better support every student.</p><p><strong><br>Key Moments</strong></p><p><br></p><p><br>00:00 Tribute to Alice Wong</p><p>08:13 "Advocacy and Neurodivergence Insights"</p><p>15:24 "Neuroaffirming Special Education Handbook"</p><p>19:17 Centering Voices in Autism Advocacy</p><p>22:37 "Advocating for Diverse Learners"</p><p>30:17 "Focus, Educate, and Understand Intentions"</p><p>34:06 "Parenting Autism: Struggles and Strengths"</p><p>41:46 "Building Bridges, Not Burning Them"</p><p>48:30 Hesitation in Disclosing Diagnoses</p><p>50:43 "Embracing Accurate Labels and Support"</p><p>55:36 Bias in Disability Labels Explained</p><p>01:02:21 "Lessons on Rest and Renewal"<br></p><p><strong>Connect with Dr. Destiny Huff</strong></p><ul><li>LinkedIn: <a href="https://www.linkedin.com/in/destiny-huff-lpc-iep/">https://www.linkedin.com/in/destiny-huff-lpc-iep/</a> </li><li>Destiny Huff Consulting: <a href="https://www.destinyhuffconsulting.com/">https://www.destinyhuffconsulting.com/</a> </li><li>Instagram: <a href="https://www.instagram.com/destinyhuff_iep_advocate/">https://www.instagram.com/destinyhuff_iep_advocate/</a> </li><li>Facebook: <a href="https://www.facebook.com/destinyhuffconsulting/">https://www.facebook.com/destinyhuffconsulting/</a> <p></p></li></ul><p>HRG Counseling: <a href="https://www.hrgcounseling.com/">https://www.hrgcounseling.com/</a> </p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Gaming with Purpose: ChiChi White on Soft Content, Mental Health, and Connection</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>35</itunes:episode>
      <podcast:episode>35</podcast:episode>
      <itunes:title>Gaming with Purpose: ChiChi White on Soft Content, Mental Health, and Connection</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/62a62b30</link>
      <description>
        <![CDATA[<p>ChiChi White, a content creator, therapist, and social advocate, joins Lily and Erin to explore the world of cozy gaming, mindful streaming, and collective care. Known online as HummingMints, ChiChi plays games like Stardew Valley and Animal Crossing, combining sensory-friendly gameplay with open conversations about neurodiversity, mental health, and authentic connection.</p><p><br></p><p>In this episode, ChiChi breaks down the meaning of soft content from creating relaxing, sensory-friendly gaming experiences that prioritize comfort, accessibility, and community over competition. They share how mindfulness shows up in gaming, how cozy spaces allow for meaningful conversation, and why it’s okay to play for joy rather than mastery.</p><p><br></p><p>ChiChi also opens up about founding the Disabled Content Creators Collective (DC3), a growing hub for disabled streamers and creators. Through DC3, he organizes raid trains, charity events, and collaborative streams that help disabled creators connect, share resources, and grow their audiences.</p><p><br></p><p>From discussions on masking and authenticity to harm reduction and self-acceptance, this conversation offers a grounded look at how online spaces can become real sources of healing, joy, and purpose.<strong></strong></p><p><br></p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>03:05 What people get wrong about direct communication and tone<br></p><p>04:46 Balancing authenticity and “masking” in streaming<br></p><p>10:05 What soft content means and why sensory-friendly gaming matters<br></p><p>11:55 How cozy games create calm for both players and viewers<br></p><p>19:24 Creating safe spaces for teens in streaming and mental health<br></p><p>24:17 Founding the Disabled Content Creators Collective (DC3)<br></p><p>28:26 What a raid train is and why it matters for disabled creators<br></p><p>41:57 Understanding harm reduction in therapy and daily life<br></p><p>44:01 Why self-acceptance is a lifelong cycle, not a finish line<br></p><p>49:51 Collective wellness: how community helps us thrive</p><p><br><strong>Connect with ChiChi White</strong></p><ul><li>LinkedIn: <a href="https://www.linkedin.com/in/chichi-white-929350297">https://www.linkedin.com/in/chichi-white-929350297</a> </li><li>Twitch: <a href="http://twitch.tv/HummingMints">twitch.tv/HummingMints</a> </li><li>YouTube: <a href="https://www.youtube.com/@hummingmints">https://www.youtube.com/@hummingmints</a> </li><li>TikTok: <a href="http://tiktok.com/@HummingMints">tiktok.com/@HummingMints</a> </li><li>Instagram: <a href="http://instagram.com/HummingMints">instagram.com/HummingMints</a> <p></p></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>ChiChi White, a content creator, therapist, and social advocate, joins Lily and Erin to explore the world of cozy gaming, mindful streaming, and collective care. Known online as HummingMints, ChiChi plays games like Stardew Valley and Animal Crossing, combining sensory-friendly gameplay with open conversations about neurodiversity, mental health, and authentic connection.</p><p><br></p><p>In this episode, ChiChi breaks down the meaning of soft content from creating relaxing, sensory-friendly gaming experiences that prioritize comfort, accessibility, and community over competition. They share how mindfulness shows up in gaming, how cozy spaces allow for meaningful conversation, and why it’s okay to play for joy rather than mastery.</p><p><br></p><p>ChiChi also opens up about founding the Disabled Content Creators Collective (DC3), a growing hub for disabled streamers and creators. Through DC3, he organizes raid trains, charity events, and collaborative streams that help disabled creators connect, share resources, and grow their audiences.</p><p><br></p><p>From discussions on masking and authenticity to harm reduction and self-acceptance, this conversation offers a grounded look at how online spaces can become real sources of healing, joy, and purpose.<strong></strong></p><p><br></p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>03:05 What people get wrong about direct communication and tone<br></p><p>04:46 Balancing authenticity and “masking” in streaming<br></p><p>10:05 What soft content means and why sensory-friendly gaming matters<br></p><p>11:55 How cozy games create calm for both players and viewers<br></p><p>19:24 Creating safe spaces for teens in streaming and mental health<br></p><p>24:17 Founding the Disabled Content Creators Collective (DC3)<br></p><p>28:26 What a raid train is and why it matters for disabled creators<br></p><p>41:57 Understanding harm reduction in therapy and daily life<br></p><p>44:01 Why self-acceptance is a lifelong cycle, not a finish line<br></p><p>49:51 Collective wellness: how community helps us thrive</p><p><br><strong>Connect with ChiChi White</strong></p><ul><li>LinkedIn: <a href="https://www.linkedin.com/in/chichi-white-929350297">https://www.linkedin.com/in/chichi-white-929350297</a> </li><li>Twitch: <a href="http://twitch.tv/HummingMints">twitch.tv/HummingMints</a> </li><li>YouTube: <a href="https://www.youtube.com/@hummingmints">https://www.youtube.com/@hummingmints</a> </li><li>TikTok: <a href="http://tiktok.com/@HummingMints">tiktok.com/@HummingMints</a> </li><li>Instagram: <a href="http://instagram.com/HummingMints">instagram.com/HummingMints</a> <p></p></li></ul>]]>
      </content:encoded>
      <pubDate>Fri, 28 Nov 2025 09:00:00 -0500</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/62a62b30/277a9970.mp3" length="54793790" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/CijyZCNyL073-FL4JuUCcGu_bcdPB3cvJ6anKGgIqEQ/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS8yNGFh/ZmMzMWVlODgzYzEy/MGIyYmY5MDliMDI0/YWI1NC5wbmc.jpg"/>
      <itunes:duration>3420</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>ChiChi White, a content creator, therapist, and social advocate, joins Lily and Erin to explore the world of cozy gaming, mindful streaming, and collective care. Known online as HummingMints, ChiChi plays games like Stardew Valley and Animal Crossing, combining sensory-friendly gameplay with open conversations about neurodiversity, mental health, and authentic connection.</p><p><br></p><p>In this episode, ChiChi breaks down the meaning of soft content from creating relaxing, sensory-friendly gaming experiences that prioritize comfort, accessibility, and community over competition. They share how mindfulness shows up in gaming, how cozy spaces allow for meaningful conversation, and why it’s okay to play for joy rather than mastery.</p><p><br></p><p>ChiChi also opens up about founding the Disabled Content Creators Collective (DC3), a growing hub for disabled streamers and creators. Through DC3, he organizes raid trains, charity events, and collaborative streams that help disabled creators connect, share resources, and grow their audiences.</p><p><br></p><p>From discussions on masking and authenticity to harm reduction and self-acceptance, this conversation offers a grounded look at how online spaces can become real sources of healing, joy, and purpose.<strong></strong></p><p><br></p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>03:05 What people get wrong about direct communication and tone<br></p><p>04:46 Balancing authenticity and “masking” in streaming<br></p><p>10:05 What soft content means and why sensory-friendly gaming matters<br></p><p>11:55 How cozy games create calm for both players and viewers<br></p><p>19:24 Creating safe spaces for teens in streaming and mental health<br></p><p>24:17 Founding the Disabled Content Creators Collective (DC3)<br></p><p>28:26 What a raid train is and why it matters for disabled creators<br></p><p>41:57 Understanding harm reduction in therapy and daily life<br></p><p>44:01 Why self-acceptance is a lifelong cycle, not a finish line<br></p><p>49:51 Collective wellness: how community helps us thrive</p><p><br><strong>Connect with ChiChi White</strong></p><ul><li>LinkedIn: <a href="https://www.linkedin.com/in/chichi-white-929350297">https://www.linkedin.com/in/chichi-white-929350297</a> </li><li>Twitch: <a href="http://twitch.tv/HummingMints">twitch.tv/HummingMints</a> </li><li>YouTube: <a href="https://www.youtube.com/@hummingmints">https://www.youtube.com/@hummingmints</a> </li><li>TikTok: <a href="http://tiktok.com/@HummingMints">tiktok.com/@HummingMints</a> </li><li>Instagram: <a href="http://instagram.com/HummingMints">instagram.com/HummingMints</a> <p></p></li></ul>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Dance Through It: The Story Behind “Disabled” and a New Era of Disabled Joy</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>34</itunes:episode>
      <podcast:episode>34</podcast:episode>
      <itunes:title>Dance Through It: The Story Behind “Disabled” and a New Era of Disabled Joy</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">826d3dd9-142f-4076-a0e7-7dfcd72fbd6d</guid>
      <link>https://share.transistor.fm/s/4fed1be8</link>
      <description>
        <![CDATA[<p>Pop artist and model Austin Halls joins Lily and Erin for a funny, candid conversation about music, face difference, and building a career that actually works. Born with Möbius syndrome (complete facial paralysis at birth), Austin talks about growing up with media that coded face differences as villainy, and how that shaped first impressions, assumptions, and everyday interactions.</p><p><br></p><p>Austin’s answer is art and access. His dance-pop track “Disabled” flips the script with a hook that invites everyone onto the floor, shifting from pity narratives to unapologetic confidence. He shares how fashion and stagecraft became tools of self-expression, why “success ≠ cured,” and how to handle lateral ableism when visibility rises.</p><p><br></p><p>From Runway of Dreams and New York Fashion Week to mentorship with RAMPD and a seat at the GRAMMYs (now a Recording Academy voting member), Austin shows what practical pathways look like: make the room workable, choose teams who get it, and insist on authentic casting rather than performances of disability. </p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>02:20 Audio descriptions and why on-mic context matters</p><p><br></p><p>03:11 Writing “Disabled”: reclaiming a word with a dance-pop hook</p><p><br></p><p>08:39 Breaking the villain trope for face difference in media</p><p><br></p><p>11:47 “Command the room”: reframing visibility as an advantage</p><p><br></p><p>18:01 Beyond pity narratives: success for talent, not sympathy clicks</p><p><br></p><p>27:46 Runway of Dreams to NYFW: firsts and why fashion became a tool</p><p><br></p><p>31:08 Success doesn’t cancel disability: on lateral ableism</p><p><br></p><p>40:46 RAMPD mentorship to the GRAMMYs: from guest to voting member</p><p><br></p><p>45:45 Why empathy and perspective shape the work (and the wins)</p><p><br></p><p>49:51 Finding community: from resisting it to the Möbius Conference pivot</p><p><br></p><p>55:53 Real-world friendship and the lift of being in the same room</p><p><br></p><p><strong><br>Connect with Austin Halls</strong></p><p>Website: <a href="https://austinhalls.com/">https://austinhalls.com/</a> <br>LinkedIn: <a href="https://www.linkedin.com/in/austinhalls">https://www.linkedin.com/in/austinhalls</a> <br>Instagram: <a href="https://www.instagram.com/theaustinhalls/">https://www.instagram.com/theaustinhalls/</a> <br>TikTok: <a href="https://www.tiktok.com/@austinhalls?lang=en">https://www.tiktok.com/@austinhalls?lang=en</a> <br>YouTube: <a href="https://www.youtube.com/@AustinHalls">https://www.youtube.com/@AustinHalls</a> <br>Spotify: <a href="https://open.spotify.com/artist/1wuAlAwVjnnmeNJ1NiaMSF?autoplay=true">https://open.spotify.com/artist/1wuAlAwVjnnmeNJ1NiaMSF?autoplay=true</a> <strong><br></strong>RAMPD: <a href="https://rampd.org/profile/austin-halls">https://rampd.org/profile/austin-halls</a> </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Pop artist and model Austin Halls joins Lily and Erin for a funny, candid conversation about music, face difference, and building a career that actually works. Born with Möbius syndrome (complete facial paralysis at birth), Austin talks about growing up with media that coded face differences as villainy, and how that shaped first impressions, assumptions, and everyday interactions.</p><p><br></p><p>Austin’s answer is art and access. His dance-pop track “Disabled” flips the script with a hook that invites everyone onto the floor, shifting from pity narratives to unapologetic confidence. He shares how fashion and stagecraft became tools of self-expression, why “success ≠ cured,” and how to handle lateral ableism when visibility rises.</p><p><br></p><p>From Runway of Dreams and New York Fashion Week to mentorship with RAMPD and a seat at the GRAMMYs (now a Recording Academy voting member), Austin shows what practical pathways look like: make the room workable, choose teams who get it, and insist on authentic casting rather than performances of disability. </p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>02:20 Audio descriptions and why on-mic context matters</p><p><br></p><p>03:11 Writing “Disabled”: reclaiming a word with a dance-pop hook</p><p><br></p><p>08:39 Breaking the villain trope for face difference in media</p><p><br></p><p>11:47 “Command the room”: reframing visibility as an advantage</p><p><br></p><p>18:01 Beyond pity narratives: success for talent, not sympathy clicks</p><p><br></p><p>27:46 Runway of Dreams to NYFW: firsts and why fashion became a tool</p><p><br></p><p>31:08 Success doesn’t cancel disability: on lateral ableism</p><p><br></p><p>40:46 RAMPD mentorship to the GRAMMYs: from guest to voting member</p><p><br></p><p>45:45 Why empathy and perspective shape the work (and the wins)</p><p><br></p><p>49:51 Finding community: from resisting it to the Möbius Conference pivot</p><p><br></p><p>55:53 Real-world friendship and the lift of being in the same room</p><p><br></p><p><strong><br>Connect with Austin Halls</strong></p><p>Website: <a href="https://austinhalls.com/">https://austinhalls.com/</a> <br>LinkedIn: <a href="https://www.linkedin.com/in/austinhalls">https://www.linkedin.com/in/austinhalls</a> <br>Instagram: <a href="https://www.instagram.com/theaustinhalls/">https://www.instagram.com/theaustinhalls/</a> <br>TikTok: <a href="https://www.tiktok.com/@austinhalls?lang=en">https://www.tiktok.com/@austinhalls?lang=en</a> <br>YouTube: <a href="https://www.youtube.com/@AustinHalls">https://www.youtube.com/@AustinHalls</a> <br>Spotify: <a href="https://open.spotify.com/artist/1wuAlAwVjnnmeNJ1NiaMSF?autoplay=true">https://open.spotify.com/artist/1wuAlAwVjnnmeNJ1NiaMSF?autoplay=true</a> <strong><br></strong>RAMPD: <a href="https://rampd.org/profile/austin-halls">https://rampd.org/profile/austin-halls</a> </p>]]>
      </content:encoded>
      <pubDate>Thu, 13 Nov 2025 09:00:00 -0500</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/4fed1be8/67da31db.mp3" length="58174493" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/SVaTVD_orkAQvknuYWunj_z2uj7GkTkX0i2I-GV8seg/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS84OWJh/NGJlNzU5YTkwZGIw/NDNhMGQ5MTcxMzcy/NTk3MS5wbmc.jpg"/>
      <itunes:duration>3631</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Pop artist and model Austin Halls joins Lily and Erin for a funny, candid conversation about music, face difference, and building a career that actually works. Born with Möbius syndrome (complete facial paralysis at birth), Austin talks about growing up with media that coded face differences as villainy, and how that shaped first impressions, assumptions, and everyday interactions.</p><p><br></p><p>Austin’s answer is art and access. His dance-pop track “Disabled” flips the script with a hook that invites everyone onto the floor, shifting from pity narratives to unapologetic confidence. He shares how fashion and stagecraft became tools of self-expression, why “success ≠ cured,” and how to handle lateral ableism when visibility rises.</p><p><br></p><p>From Runway of Dreams and New York Fashion Week to mentorship with RAMPD and a seat at the GRAMMYs (now a Recording Academy voting member), Austin shows what practical pathways look like: make the room workable, choose teams who get it, and insist on authentic casting rather than performances of disability. </p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>02:20 Audio descriptions and why on-mic context matters</p><p><br></p><p>03:11 Writing “Disabled”: reclaiming a word with a dance-pop hook</p><p><br></p><p>08:39 Breaking the villain trope for face difference in media</p><p><br></p><p>11:47 “Command the room”: reframing visibility as an advantage</p><p><br></p><p>18:01 Beyond pity narratives: success for talent, not sympathy clicks</p><p><br></p><p>27:46 Runway of Dreams to NYFW: firsts and why fashion became a tool</p><p><br></p><p>31:08 Success doesn’t cancel disability: on lateral ableism</p><p><br></p><p>40:46 RAMPD mentorship to the GRAMMYs: from guest to voting member</p><p><br></p><p>45:45 Why empathy and perspective shape the work (and the wins)</p><p><br></p><p>49:51 Finding community: from resisting it to the Möbius Conference pivot</p><p><br></p><p>55:53 Real-world friendship and the lift of being in the same room</p><p><br></p><p><strong><br>Connect with Austin Halls</strong></p><p>Website: <a href="https://austinhalls.com/">https://austinhalls.com/</a> <br>LinkedIn: <a href="https://www.linkedin.com/in/austinhalls">https://www.linkedin.com/in/austinhalls</a> <br>Instagram: <a href="https://www.instagram.com/theaustinhalls/">https://www.instagram.com/theaustinhalls/</a> <br>TikTok: <a href="https://www.tiktok.com/@austinhalls?lang=en">https://www.tiktok.com/@austinhalls?lang=en</a> <br>YouTube: <a href="https://www.youtube.com/@AustinHalls">https://www.youtube.com/@AustinHalls</a> <br>Spotify: <a href="https://open.spotify.com/artist/1wuAlAwVjnnmeNJ1NiaMSF?autoplay=true">https://open.spotify.com/artist/1wuAlAwVjnnmeNJ1NiaMSF?autoplay=true</a> <strong><br></strong>RAMPD: <a href="https://rampd.org/profile/austin-halls">https://rampd.org/profile/austin-halls</a> </p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Beyond the Binary: Maria Pendolino on Disability, Fat Liberation, and Voiceover</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>33</itunes:episode>
      <podcast:episode>33</podcast:episode>
      <itunes:title>Beyond the Binary: Maria Pendolino on Disability, Fat Liberation, and Voiceover</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/53f09a02</link>
      <description>
        <![CDATA[<p><br>Voice actor Maria Pendolino joins Lily for an episode that challenges the narrow way society views disability. Maria shares her experiences as an ambulatory mobility-aid user, explaining how fluctuating conditions are often misunderstood or erased in media and medicine. With candid honesty, she connects her journey of psoriatic arthritis, knee replacements, and self-advocacy to building a career that truly works for her body, through voiceover and a fully accessible home studio.</p><p><br>The conversation also takes on fat bias in healthcare, how outdated tools like BMI continue to be used to deny or delay care, and the scripts Maria uses to set boundaries in appointments. Her message: you deserve to be treated as a whole person, not reduced to a number or assumption.</p><p><br>Maria details the creation of the Disabled Voice Actors Directory, now housed under the National Association of Voice Actors, which helps casting directors find authentic talent. It’s a resource born out of a belief that disabled people don’t just deserve representation on-screen, they should be hired behind the microphone, too.</p><p><br></p><p><strong>Key Moments<br></strong><br></p><p>02:50 Breaking the myth of disability as “all or nothing”</p><p>06:02 What fluctuating disability really looks like in practice</p><p>14:16 Age bias in surgery: when doctors refuse joint replacements under 50</p><p>21:31 Why BMI is flawed and how it blocks real care</p><p>29:46 Self-advocacy scripts: “I will not be weighed”</p><p>42:34 The audition turning point: “Are you limping?”</p><p>46:54 Building an accessible home studio and thriving as a voice actor</p><p>54:11 Founding the Disabled Voice Actors Directory</p><p>1:04:11 Know the Facts: fat phobia and systemic barriers</p><p><br></p><p><strong>Connect with Maria Pendolino</strong></p><p>Website: <a href="https://www.voicebymaria.com/">https://www.voicebymaria.com/</a> </p><p>YouTube: <a href="https://www.youtube.com/channel/UCGkmvgiBP89fHUl9-8awQRA/videos">https://www.youtube.com/channel/UCGkmvgiBP89fHUl9-8awQRA/videos</a> </p><p>Maria Pendolino - London Voice Over: <a href="https://www.londonvoiceover.com/artists/maria-pendolino/">https://www.londonvoiceover.com/artists/maria-pendolino/</a> </p><p>Maria Pendolino - London Voice Over: <a href="https://voice123.com/voice-actor/voicebymaria">https://voice123.com/voice-actor/voicebymaria</a> </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p><br>Voice actor Maria Pendolino joins Lily for an episode that challenges the narrow way society views disability. Maria shares her experiences as an ambulatory mobility-aid user, explaining how fluctuating conditions are often misunderstood or erased in media and medicine. With candid honesty, she connects her journey of psoriatic arthritis, knee replacements, and self-advocacy to building a career that truly works for her body, through voiceover and a fully accessible home studio.</p><p><br>The conversation also takes on fat bias in healthcare, how outdated tools like BMI continue to be used to deny or delay care, and the scripts Maria uses to set boundaries in appointments. Her message: you deserve to be treated as a whole person, not reduced to a number or assumption.</p><p><br>Maria details the creation of the Disabled Voice Actors Directory, now housed under the National Association of Voice Actors, which helps casting directors find authentic talent. It’s a resource born out of a belief that disabled people don’t just deserve representation on-screen, they should be hired behind the microphone, too.</p><p><br></p><p><strong>Key Moments<br></strong><br></p><p>02:50 Breaking the myth of disability as “all or nothing”</p><p>06:02 What fluctuating disability really looks like in practice</p><p>14:16 Age bias in surgery: when doctors refuse joint replacements under 50</p><p>21:31 Why BMI is flawed and how it blocks real care</p><p>29:46 Self-advocacy scripts: “I will not be weighed”</p><p>42:34 The audition turning point: “Are you limping?”</p><p>46:54 Building an accessible home studio and thriving as a voice actor</p><p>54:11 Founding the Disabled Voice Actors Directory</p><p>1:04:11 Know the Facts: fat phobia and systemic barriers</p><p><br></p><p><strong>Connect with Maria Pendolino</strong></p><p>Website: <a href="https://www.voicebymaria.com/">https://www.voicebymaria.com/</a> </p><p>YouTube: <a href="https://www.youtube.com/channel/UCGkmvgiBP89fHUl9-8awQRA/videos">https://www.youtube.com/channel/UCGkmvgiBP89fHUl9-8awQRA/videos</a> </p><p>Maria Pendolino - London Voice Over: <a href="https://www.londonvoiceover.com/artists/maria-pendolino/">https://www.londonvoiceover.com/artists/maria-pendolino/</a> </p><p>Maria Pendolino - London Voice Over: <a href="https://voice123.com/voice-actor/voicebymaria">https://voice123.com/voice-actor/voicebymaria</a> </p>]]>
      </content:encoded>
      <pubDate>Thu, 30 Oct 2025 10:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/53f09a02/ecba4146.mp3" length="97591320" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/LPS81Ng6Xqf9VHKOByKJiGJl7t714zlX4Bmv5vRkjZc/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS82YjIz/ODE1YmJjYjJmZDMz/ZGExMjljZDAzMjRm/MmY4Zi5wbmc.jpg"/>
      <itunes:duration>4059</itunes:duration>
      <itunes:summary>
        <![CDATA[<p><br>Voice actor Maria Pendolino joins Lily for an episode that challenges the narrow way society views disability. Maria shares her experiences as an ambulatory mobility-aid user, explaining how fluctuating conditions are often misunderstood or erased in media and medicine. With candid honesty, she connects her journey of psoriatic arthritis, knee replacements, and self-advocacy to building a career that truly works for her body, through voiceover and a fully accessible home studio.</p><p><br>The conversation also takes on fat bias in healthcare, how outdated tools like BMI continue to be used to deny or delay care, and the scripts Maria uses to set boundaries in appointments. Her message: you deserve to be treated as a whole person, not reduced to a number or assumption.</p><p><br>Maria details the creation of the Disabled Voice Actors Directory, now housed under the National Association of Voice Actors, which helps casting directors find authentic talent. It’s a resource born out of a belief that disabled people don’t just deserve representation on-screen, they should be hired behind the microphone, too.</p><p><br></p><p><strong>Key Moments<br></strong><br></p><p>02:50 Breaking the myth of disability as “all or nothing”</p><p>06:02 What fluctuating disability really looks like in practice</p><p>14:16 Age bias in surgery: when doctors refuse joint replacements under 50</p><p>21:31 Why BMI is flawed and how it blocks real care</p><p>29:46 Self-advocacy scripts: “I will not be weighed”</p><p>42:34 The audition turning point: “Are you limping?”</p><p>46:54 Building an accessible home studio and thriving as a voice actor</p><p>54:11 Founding the Disabled Voice Actors Directory</p><p>1:04:11 Know the Facts: fat phobia and systemic barriers</p><p><br></p><p><strong>Connect with Maria Pendolino</strong></p><p>Website: <a href="https://www.voicebymaria.com/">https://www.voicebymaria.com/</a> </p><p>YouTube: <a href="https://www.youtube.com/channel/UCGkmvgiBP89fHUl9-8awQRA/videos">https://www.youtube.com/channel/UCGkmvgiBP89fHUl9-8awQRA/videos</a> </p><p>Maria Pendolino - London Voice Over: <a href="https://www.londonvoiceover.com/artists/maria-pendolino/">https://www.londonvoiceover.com/artists/maria-pendolino/</a> </p><p>Maria Pendolino - London Voice Over: <a href="https://voice123.com/voice-actor/voicebymaria">https://voice123.com/voice-actor/voicebymaria</a> </p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Start Now: Matthew Shapiro on Advocacy &amp; Workplace Accessibility</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>32</itunes:episode>
      <podcast:episode>32</podcast:episode>
      <itunes:title>Start Now: Matthew Shapiro on Advocacy &amp; Workplace Accessibility</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/5c9d7cd3</link>
      <description>
        <![CDATA[<p><br>Matthew Shapiro, founder and CEO of Six Wheels Consulting, joins hosts Lily Newton and Erin Hawley for a candid conversation about language, work culture, and the everyday practice of access. Matthew unpacks how assumptions show up in daily life, why “disabled” is a valuable identifier, and what it means to balance personal energy with public advocacy.</p><p><br>The conversation moves from nuance in calling out ableism to concrete advice for workplaces. Matthew shares practical examples that help everyone, like standing desks and curb cuts, and invites leaders to start with simple changes that reduce friction. He challenges listeners to rethink design from the ground up and to see access as standard, not a special add-on.</p><p><br>Across the episode, Lily and Erin connect language to outcomes. They underline that asking for what you need benefits teams, and that many improvements cost more thought than money. The result is a grounded roadmap for anyone ready to begin, learn, and keep going.</p><p><strong><br>Key Moments<br></strong><br></p><ul><li>03:36 Assumptions and the myth of “needing to be fixed”<p></p></li><li>07:18 The push-pull of advocacy and fatigue<p></p></li><li>13:31 “Own the word”: why Matthew identifies as a disabled person<p></p></li><li>17:08 Ableism on social media and finding useful nuance<p></p></li><li>31:15 Standing desks, curb cuts and designing spaces that work for all<p></p></li><li>41:42 How to begin: start, listen, and make a plan you will actually use<p></p></li><li>45:19 It is not as daunting as people think<p></p></li></ul><p><strong>Connect with Matthew Shapiro<br></strong><br></p><p><strong>LinkedIn</strong>:<a href="https://www.linkedin.com/in/dylanrafaty"> </a><a href="https://www.linkedin.com/in/matthew-shapiro-16abb932">https://www.linkedin.com/in/matthew-shapiro-16abb932</a> </p><p><strong>Instagram</strong>: <a href="https://www.instagram.com/6wheelsconsulting/">https://www.instagram.com/6wheelsconsulting/</a> </p><p><strong>Six Wheels Consulting website</strong>: <a href="https://www.6wheelsconsulting.com/">https://www.6wheelsconsulting.com/</a> <br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p><br>Matthew Shapiro, founder and CEO of Six Wheels Consulting, joins hosts Lily Newton and Erin Hawley for a candid conversation about language, work culture, and the everyday practice of access. Matthew unpacks how assumptions show up in daily life, why “disabled” is a valuable identifier, and what it means to balance personal energy with public advocacy.</p><p><br>The conversation moves from nuance in calling out ableism to concrete advice for workplaces. Matthew shares practical examples that help everyone, like standing desks and curb cuts, and invites leaders to start with simple changes that reduce friction. He challenges listeners to rethink design from the ground up and to see access as standard, not a special add-on.</p><p><br>Across the episode, Lily and Erin connect language to outcomes. They underline that asking for what you need benefits teams, and that many improvements cost more thought than money. The result is a grounded roadmap for anyone ready to begin, learn, and keep going.</p><p><strong><br>Key Moments<br></strong><br></p><ul><li>03:36 Assumptions and the myth of “needing to be fixed”<p></p></li><li>07:18 The push-pull of advocacy and fatigue<p></p></li><li>13:31 “Own the word”: why Matthew identifies as a disabled person<p></p></li><li>17:08 Ableism on social media and finding useful nuance<p></p></li><li>31:15 Standing desks, curb cuts and designing spaces that work for all<p></p></li><li>41:42 How to begin: start, listen, and make a plan you will actually use<p></p></li><li>45:19 It is not as daunting as people think<p></p></li></ul><p><strong>Connect with Matthew Shapiro<br></strong><br></p><p><strong>LinkedIn</strong>:<a href="https://www.linkedin.com/in/dylanrafaty"> </a><a href="https://www.linkedin.com/in/matthew-shapiro-16abb932">https://www.linkedin.com/in/matthew-shapiro-16abb932</a> </p><p><strong>Instagram</strong>: <a href="https://www.instagram.com/6wheelsconsulting/">https://www.instagram.com/6wheelsconsulting/</a> </p><p><strong>Six Wheels Consulting website</strong>: <a href="https://www.6wheelsconsulting.com/">https://www.6wheelsconsulting.com/</a> <br></p>]]>
      </content:encoded>
      <pubDate>Thu, 16 Oct 2025 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
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      <itunes:author>Easterseals</itunes:author>
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      <itunes:duration>3126</itunes:duration>
      <itunes:summary>
        <![CDATA[<p><br>Matthew Shapiro, founder and CEO of Six Wheels Consulting, joins hosts Lily Newton and Erin Hawley for a candid conversation about language, work culture, and the everyday practice of access. Matthew unpacks how assumptions show up in daily life, why “disabled” is a valuable identifier, and what it means to balance personal energy with public advocacy.</p><p><br>The conversation moves from nuance in calling out ableism to concrete advice for workplaces. Matthew shares practical examples that help everyone, like standing desks and curb cuts, and invites leaders to start with simple changes that reduce friction. He challenges listeners to rethink design from the ground up and to see access as standard, not a special add-on.</p><p><br>Across the episode, Lily and Erin connect language to outcomes. They underline that asking for what you need benefits teams, and that many improvements cost more thought than money. The result is a grounded roadmap for anyone ready to begin, learn, and keep going.</p><p><strong><br>Key Moments<br></strong><br></p><ul><li>03:36 Assumptions and the myth of “needing to be fixed”<p></p></li><li>07:18 The push-pull of advocacy and fatigue<p></p></li><li>13:31 “Own the word”: why Matthew identifies as a disabled person<p></p></li><li>17:08 Ableism on social media and finding useful nuance<p></p></li><li>31:15 Standing desks, curb cuts and designing spaces that work for all<p></p></li><li>41:42 How to begin: start, listen, and make a plan you will actually use<p></p></li><li>45:19 It is not as daunting as people think<p></p></li></ul><p><strong>Connect with Matthew Shapiro<br></strong><br></p><p><strong>LinkedIn</strong>:<a href="https://www.linkedin.com/in/dylanrafaty"> </a><a href="https://www.linkedin.com/in/matthew-shapiro-16abb932">https://www.linkedin.com/in/matthew-shapiro-16abb932</a> </p><p><strong>Instagram</strong>: <a href="https://www.instagram.com/6wheelsconsulting/">https://www.instagram.com/6wheelsconsulting/</a> </p><p><strong>Six Wheels Consulting website</strong>: <a href="https://www.6wheelsconsulting.com/">https://www.6wheelsconsulting.com/</a> <br></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Just Between Us: Disability Language, Pride &amp; Power</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>31</itunes:episode>
      <podcast:episode>31</podcast:episode>
      <itunes:title>Just Between Us: Disability Language, Pride &amp; Power</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">416906e2-a0e4-4925-9ea9-4d842fa2f2d5</guid>
      <link>https://share.transistor.fm/s/8296ffb6</link>
      <description>
        <![CDATA[<p>Your co-hosts Erin &amp; Lily bring another “Just Between Us” conversation to <em>Everything You Know About Disability Is Wrong</em>. This time, they’re diving into disability language: why euphemisms like “differently abled” miss the mark, how identity-first vs. person-first language is used, and why words matter.</p><p><br>They share stories from their own journeys—how language has shaped their identities, how it can affirm or erase, and why offering grace and education is often the most powerful tool. With humor, honesty, and a few reframes, Erin and Lily show how shared vocabulary can build connection and strengthen advocacy.</p><p><br></p><p><strong>Timestamps</strong></p><p>00:38 Just Between Us: why language matters</p><p>01:40 Creating a disability language guide for Easterseals</p><p>02:40 Why euphemisms like “differently abled” don’t work</p><p>03:09 Identity-first vs. person-first explained</p><p>04:25 The importance of respecting personal preference</p><p>05:41 Autistic identity and self-definition</p><p>07:12 Erin’s shift from person-first to identity-first</p><p>08:55 Why treatment matters more than terminology</p><p>10:15 Writing and marketing with respectful language</p><p><br></p><p><strong>Connect with Lily Newton</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/lily-newton-3b0b5b229">https://www.linkedin.com/in/lily-newton-3b0b5b229</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p><p><strong>Connect with Erin Hawley</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/erinhawley2">https://www.linkedin.com/in/erinhawley2</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Your co-hosts Erin &amp; Lily bring another “Just Between Us” conversation to <em>Everything You Know About Disability Is Wrong</em>. This time, they’re diving into disability language: why euphemisms like “differently abled” miss the mark, how identity-first vs. person-first language is used, and why words matter.</p><p><br>They share stories from their own journeys—how language has shaped their identities, how it can affirm or erase, and why offering grace and education is often the most powerful tool. With humor, honesty, and a few reframes, Erin and Lily show how shared vocabulary can build connection and strengthen advocacy.</p><p><br></p><p><strong>Timestamps</strong></p><p>00:38 Just Between Us: why language matters</p><p>01:40 Creating a disability language guide for Easterseals</p><p>02:40 Why euphemisms like “differently abled” don’t work</p><p>03:09 Identity-first vs. person-first explained</p><p>04:25 The importance of respecting personal preference</p><p>05:41 Autistic identity and self-definition</p><p>07:12 Erin’s shift from person-first to identity-first</p><p>08:55 Why treatment matters more than terminology</p><p>10:15 Writing and marketing with respectful language</p><p><br></p><p><strong>Connect with Lily Newton</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/lily-newton-3b0b5b229">https://www.linkedin.com/in/lily-newton-3b0b5b229</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p><p><strong>Connect with Erin Hawley</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/erinhawley2">https://www.linkedin.com/in/erinhawley2</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p>]]>
      </content:encoded>
      <pubDate>Thu, 09 Oct 2025 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/8296ffb6/59b19d59.mp3" length="34492177" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/VxZfTxJdIZ5j4kvmx-vv8j0zgeCyz0lXlLR1zkssFcA/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS82NzE5/NTAzOTc5YTM4ZjRi/Y2E4ZDVlYTg3MmM2/NjI5NC5wbmc.jpg"/>
      <itunes:duration>1429</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Your co-hosts Erin &amp; Lily bring another “Just Between Us” conversation to <em>Everything You Know About Disability Is Wrong</em>. This time, they’re diving into disability language: why euphemisms like “differently abled” miss the mark, how identity-first vs. person-first language is used, and why words matter.</p><p><br>They share stories from their own journeys—how language has shaped their identities, how it can affirm or erase, and why offering grace and education is often the most powerful tool. With humor, honesty, and a few reframes, Erin and Lily show how shared vocabulary can build connection and strengthen advocacy.</p><p><br></p><p><strong>Timestamps</strong></p><p>00:38 Just Between Us: why language matters</p><p>01:40 Creating a disability language guide for Easterseals</p><p>02:40 Why euphemisms like “differently abled” don’t work</p><p>03:09 Identity-first vs. person-first explained</p><p>04:25 The importance of respecting personal preference</p><p>05:41 Autistic identity and self-definition</p><p>07:12 Erin’s shift from person-first to identity-first</p><p>08:55 Why treatment matters more than terminology</p><p>10:15 Writing and marketing with respectful language</p><p><br></p><p><strong>Connect with Lily Newton</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/lily-newton-3b0b5b229">https://www.linkedin.com/in/lily-newton-3b0b5b229</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p><p><strong>Connect with Erin Hawley</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/erinhawley2">https://www.linkedin.com/in/erinhawley2</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Disability as Strategy: Dylan M. Rafaty on Leadership, Access and Impact</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>30</itunes:episode>
      <podcast:episode>30</podcast:episode>
      <itunes:title>Disability as Strategy: Dylan M. Rafaty on Leadership, Access and Impact</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">578f5279-9422-4a78-89fc-ee7bd74da585</guid>
      <link>https://share.transistor.fm/s/201da7bf</link>
      <description>
        <![CDATA[<p>Dylan M. Rafaty, President and CEO of the North Texas Disability Chamber, joins Lily Newton and Erin Hawley to talk about disability acceptance and advocacy. With clarity and conviction, Dylan outlines why disability should never be treated as an act of charity. Instead, he frames it as a strategic investment that drives innovation, empowers communities and strengthens organizations from within.</p><p><br></p><p>Dylan reflects on his personal experience navigating the world as someone who is deaf and hard of hearing.. He explains that advocacy is often misunderstood as self-promotion, when in reality it is rooted in service to the broader disability community. His message is clear: individual success stories matter, but collective action is where lasting change begins. </p><p><br></p><p>Through storytelling, policy engagement and local civic work, Dylan models what authentic opportunity can look like in practice.This episode is a deeper understanding of how to move beyond performative allyship and into meaningful participation for all policymakers, business leaders or members of the public.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>05:47 “Disability is not a charity”: why it must be built into planning from the start</p><p>08:16 The business case for investing in accessibility and representation</p><p>12:38 Understanding the emotional labor behind self-advocacy</p><p>23:07 Why access means freedom of choice</p><p>28:58 Policy and personal experience: how one drives the other</p><p><br></p><p><strong>Connect with Dylan M. Rafaty</strong></p><p><br></p><p><strong>Website</strong>: <a href="http://northtexasdisabilitychamber.com">northtexasdisabilitychamber.com</a> <br><strong>LinkedIn</strong>:<a href="https://www.linkedin.com/in/dylanrafaty"> https://www.linkedin.com/in/dylanrafaty</a></p><p><strong>Instagram</strong>: <a href="https://www.instagram.com/dylan_rafaty">https://www.instagram.com/dylan_rafaty</a> </p><p><strong>Dylan M. Rafaty website</strong>:<a href="https://dylanrafaty.com/">https://dylanrafaty.com/</a> <br><strong>Podcast</strong>: <em>Let’s Work Inclusively</em></p><ul><li><a href="https://podcasts.apple.com/us/podcast/lets-work-inclusively-with-dylan-m-rafaty/id1834510566">Listen on Spotify</a></li></ul>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Dylan M. Rafaty, President and CEO of the North Texas Disability Chamber, joins Lily Newton and Erin Hawley to talk about disability acceptance and advocacy. With clarity and conviction, Dylan outlines why disability should never be treated as an act of charity. Instead, he frames it as a strategic investment that drives innovation, empowers communities and strengthens organizations from within.</p><p><br></p><p>Dylan reflects on his personal experience navigating the world as someone who is deaf and hard of hearing.. He explains that advocacy is often misunderstood as self-promotion, when in reality it is rooted in service to the broader disability community. His message is clear: individual success stories matter, but collective action is where lasting change begins. </p><p><br></p><p>Through storytelling, policy engagement and local civic work, Dylan models what authentic opportunity can look like in practice.This episode is a deeper understanding of how to move beyond performative allyship and into meaningful participation for all policymakers, business leaders or members of the public.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>05:47 “Disability is not a charity”: why it must be built into planning from the start</p><p>08:16 The business case for investing in accessibility and representation</p><p>12:38 Understanding the emotional labor behind self-advocacy</p><p>23:07 Why access means freedom of choice</p><p>28:58 Policy and personal experience: how one drives the other</p><p><br></p><p><strong>Connect with Dylan M. Rafaty</strong></p><p><br></p><p><strong>Website</strong>: <a href="http://northtexasdisabilitychamber.com">northtexasdisabilitychamber.com</a> <br><strong>LinkedIn</strong>:<a href="https://www.linkedin.com/in/dylanrafaty"> https://www.linkedin.com/in/dylanrafaty</a></p><p><strong>Instagram</strong>: <a href="https://www.instagram.com/dylan_rafaty">https://www.instagram.com/dylan_rafaty</a> </p><p><strong>Dylan M. Rafaty website</strong>:<a href="https://dylanrafaty.com/">https://dylanrafaty.com/</a> <br><strong>Podcast</strong>: <em>Let’s Work Inclusively</em></p><ul><li><a href="https://podcasts.apple.com/us/podcast/lets-work-inclusively-with-dylan-m-rafaty/id1834510566">Listen on Spotify</a></li></ul>]]>
      </content:encoded>
      <pubDate>Tue, 23 Sep 2025 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/201da7bf/7d3c1d5b.mp3" length="79844175" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/-mvjbOpqxwwV_HmMy1wx1F7NJLo4yFgRgUEPUQC83kg/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9kNjE5/MzUzZTNhODdhODlk/MWNiZmZjZDNlZmUz/OWU1ZS5wbmc.jpg"/>
      <itunes:duration>3319</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Dylan M. Rafaty, President and CEO of the North Texas Disability Chamber, joins Lily Newton and Erin Hawley to talk about disability acceptance and advocacy. With clarity and conviction, Dylan outlines why disability should never be treated as an act of charity. Instead, he frames it as a strategic investment that drives innovation, empowers communities and strengthens organizations from within.</p><p><br></p><p>Dylan reflects on his personal experience navigating the world as someone who is deaf and hard of hearing.. He explains that advocacy is often misunderstood as self-promotion, when in reality it is rooted in service to the broader disability community. His message is clear: individual success stories matter, but collective action is where lasting change begins. </p><p><br></p><p>Through storytelling, policy engagement and local civic work, Dylan models what authentic opportunity can look like in practice.This episode is a deeper understanding of how to move beyond performative allyship and into meaningful participation for all policymakers, business leaders or members of the public.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>05:47 “Disability is not a charity”: why it must be built into planning from the start</p><p>08:16 The business case for investing in accessibility and representation</p><p>12:38 Understanding the emotional labor behind self-advocacy</p><p>23:07 Why access means freedom of choice</p><p>28:58 Policy and personal experience: how one drives the other</p><p><br></p><p><strong>Connect with Dylan M. Rafaty</strong></p><p><br></p><p><strong>Website</strong>: <a href="http://northtexasdisabilitychamber.com">northtexasdisabilitychamber.com</a> <br><strong>LinkedIn</strong>:<a href="https://www.linkedin.com/in/dylanrafaty"> https://www.linkedin.com/in/dylanrafaty</a></p><p><strong>Instagram</strong>: <a href="https://www.instagram.com/dylan_rafaty">https://www.instagram.com/dylan_rafaty</a> </p><p><strong>Dylan M. Rafaty website</strong>:<a href="https://dylanrafaty.com/">https://dylanrafaty.com/</a> <br><strong>Podcast</strong>: <em>Let’s Work Inclusively</em></p><ul><li><a href="https://podcasts.apple.com/us/podcast/lets-work-inclusively-with-dylan-m-rafaty/id1834510566">Listen on Spotify</a></li></ul>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Showing Up Authentically: Amanda Steijlen on Confidence, Connection &amp; Care</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>29</itunes:episode>
      <podcast:episode>29</podcast:episode>
      <itunes:title>Showing Up Authentically: Amanda Steijlen on Confidence, Connection &amp; Care</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d4219c95-7a67-405b-8ba2-cdd784bdfbf9</guid>
      <link>https://share.transistor.fm/s/0dd7e400</link>
      <description>
        <![CDATA[<p><br>Amanda Steijlen is a therapist, lifestyle creator, and founder of <em>Wheelie Big Dreams</em>, a nonprofit that helps people with disabilities pursue their goals. She also leads <em>True Bloom Therapy</em>, supporting clients through life transitions with strategies that are both practical and grounded.</p><p>In this episode, Amanda shares her path to mental health work, the ways we misunderstand independence, and how caregiving can be reciprocal. She speaks candidly about online self-image, burnout, and the importance of showing up as your real self especially when people expect you to hide what you’re going through.</p><p>Amanda also reflects on Disability Pride Month and how it intersects with mental health, personal growth, and finding purpose. Whether she's guiding clients through the five core human needs or cultivating supportive friendships, Amanda emphasizes the power of real connection and redefining what success looks like.</p><p><strong><br>Key Moments<br></strong><br></p><p>02:46 Redefining independence and interdependence</p><p>10:48 Becoming a therapist after anxiety and loss</p><p>16:18 Balancing Disability Pride with grief</p><p><br>25:39 Managing self-image as a content creator</p><p><br>33:00 Finding community with other disabled creators</p><p>41:36 Rethinking mental health care in schools</p><p><br>47:43 Know the facts: 1 in 4 people are disabled</p><p><strong><br>Connect with Amanda Steijlen<br></strong><br></p><p>Instagram:<a href="https://www.instagram.com/amandasteijlen"> @amandasteijlen<br></a>Website:<a href="https://www.truebloomtherapy.com"> https://www.truebloomtherapy.com<br></a>Nonprofit:<a href="https://www.wheeliebigdreams.org"> https://www.wheeliebigdreams.org<br></a><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p><br>Amanda Steijlen is a therapist, lifestyle creator, and founder of <em>Wheelie Big Dreams</em>, a nonprofit that helps people with disabilities pursue their goals. She also leads <em>True Bloom Therapy</em>, supporting clients through life transitions with strategies that are both practical and grounded.</p><p>In this episode, Amanda shares her path to mental health work, the ways we misunderstand independence, and how caregiving can be reciprocal. She speaks candidly about online self-image, burnout, and the importance of showing up as your real self especially when people expect you to hide what you’re going through.</p><p>Amanda also reflects on Disability Pride Month and how it intersects with mental health, personal growth, and finding purpose. Whether she's guiding clients through the five core human needs or cultivating supportive friendships, Amanda emphasizes the power of real connection and redefining what success looks like.</p><p><strong><br>Key Moments<br></strong><br></p><p>02:46 Redefining independence and interdependence</p><p>10:48 Becoming a therapist after anxiety and loss</p><p>16:18 Balancing Disability Pride with grief</p><p><br>25:39 Managing self-image as a content creator</p><p><br>33:00 Finding community with other disabled creators</p><p>41:36 Rethinking mental health care in schools</p><p><br>47:43 Know the facts: 1 in 4 people are disabled</p><p><strong><br>Connect with Amanda Steijlen<br></strong><br></p><p>Instagram:<a href="https://www.instagram.com/amandasteijlen"> @amandasteijlen<br></a>Website:<a href="https://www.truebloomtherapy.com"> https://www.truebloomtherapy.com<br></a>Nonprofit:<a href="https://www.wheeliebigdreams.org"> https://www.wheeliebigdreams.org<br></a><br></p>]]>
      </content:encoded>
      <pubDate>Thu, 31 Jul 2025 12:00:04 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/0dd7e400/2029f124.mp3" length="80752430" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/PBiCsRAPM8nSpRCb5Et2OFhsyXMfQqahQgRb6YLN-Pg/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9mNmRi/YjFiYTYyNGYwZDZm/ZjJkNjg4YjNjOWM5/Mzk5NC5wbmc.jpg"/>
      <itunes:duration>3358</itunes:duration>
      <itunes:summary>
        <![CDATA[<p><br>Amanda Steijlen is a therapist, lifestyle creator, and founder of <em>Wheelie Big Dreams</em>, a nonprofit that helps people with disabilities pursue their goals. She also leads <em>True Bloom Therapy</em>, supporting clients through life transitions with strategies that are both practical and grounded.</p><p>In this episode, Amanda shares her path to mental health work, the ways we misunderstand independence, and how caregiving can be reciprocal. She speaks candidly about online self-image, burnout, and the importance of showing up as your real self especially when people expect you to hide what you’re going through.</p><p>Amanda also reflects on Disability Pride Month and how it intersects with mental health, personal growth, and finding purpose. Whether she's guiding clients through the five core human needs or cultivating supportive friendships, Amanda emphasizes the power of real connection and redefining what success looks like.</p><p><strong><br>Key Moments<br></strong><br></p><p>02:46 Redefining independence and interdependence</p><p>10:48 Becoming a therapist after anxiety and loss</p><p>16:18 Balancing Disability Pride with grief</p><p><br>25:39 Managing self-image as a content creator</p><p><br>33:00 Finding community with other disabled creators</p><p>41:36 Rethinking mental health care in schools</p><p><br>47:43 Know the facts: 1 in 4 people are disabled</p><p><strong><br>Connect with Amanda Steijlen<br></strong><br></p><p>Instagram:<a href="https://www.instagram.com/amandasteijlen"> @amandasteijlen<br></a>Website:<a href="https://www.truebloomtherapy.com"> https://www.truebloomtherapy.com<br></a>Nonprofit:<a href="https://www.wheeliebigdreams.org"> https://www.wheeliebigdreams.org<br></a><br></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Confidence Takes Time: Courn Ahn on Disability, Identity, and Belonging</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>28</itunes:episode>
      <podcast:episode>28</podcast:episode>
      <itunes:title>Confidence Takes Time: Courn Ahn on Disability, Identity, and Belonging</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">fe25b381-9684-45c3-a02a-231a0a7e2a3b</guid>
      <link>https://share.transistor.fm/s/3224baf3</link>
      <description>
        <![CDATA[<p>Courn Ahn is a designer, content creator, and advocate who cares deeply about accessibility and social justice. Their work focuses on helping people see disability, identity, and community support in a new way, especially through the lens of queerness, race, and being neurodivergent.</p><p><br>As a Queer, nonbinary, mixed-race Korean creative, Courn shares from personal experience and speaks honestly about the challenges that come with being disabled in a world full of assumptions. Courn's journey has been about unlearning shame, accepting who they are, and understanding that using visible accommodations isn’t something to hide, it’s a powerful way to take care of yourself.</p><p><br>Courn also talks about how people often assume you don’t need help if you look like you’re doing well, and how sharing online as a disabled person can be both meaningful and exhausting. Through their design work and presence on social media, Courn is not just creating content, Courn Ahn is also  creating space for real conversations, celebrating differences, and reminding us that accessibility should matter to everyone</p><p><strong>Key Moments<br></strong> 00:00  What people get wrong about autistic people<br> 06:43  Struggling with what to share online<br> 14:18  Tools that make life easier<br> 20:42  How style helps show who I am<br> 27:01  Feeling free to be myself<br> 33:13  How different parts of my identity connect<br> 52:57  Finding confidence through disability</p><p><br></p><p><strong>Connect with Courn Ahn<br></strong>Linkedin: <a href="https://www.linkedin.com/in/courtneyahndesign">https://www.linkedin.com/in/courtneyahndesign</a> </p><p>Website: <a href="https://www.courtneyahndesign.com/">https://www.courtneyahndesign.com/</a></p><p>Instagram: <a href="https://www.instagram.com/candy.courn/">https://www.instagram.com/candy.courn/</a></p><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Courn Ahn is a designer, content creator, and advocate who cares deeply about accessibility and social justice. Their work focuses on helping people see disability, identity, and community support in a new way, especially through the lens of queerness, race, and being neurodivergent.</p><p><br>As a Queer, nonbinary, mixed-race Korean creative, Courn shares from personal experience and speaks honestly about the challenges that come with being disabled in a world full of assumptions. Courn's journey has been about unlearning shame, accepting who they are, and understanding that using visible accommodations isn’t something to hide, it’s a powerful way to take care of yourself.</p><p><br>Courn also talks about how people often assume you don’t need help if you look like you’re doing well, and how sharing online as a disabled person can be both meaningful and exhausting. Through their design work and presence on social media, Courn is not just creating content, Courn Ahn is also  creating space for real conversations, celebrating differences, and reminding us that accessibility should matter to everyone</p><p><strong>Key Moments<br></strong> 00:00  What people get wrong about autistic people<br> 06:43  Struggling with what to share online<br> 14:18  Tools that make life easier<br> 20:42  How style helps show who I am<br> 27:01  Feeling free to be myself<br> 33:13  How different parts of my identity connect<br> 52:57  Finding confidence through disability</p><p><br></p><p><strong>Connect with Courn Ahn<br></strong>Linkedin: <a href="https://www.linkedin.com/in/courtneyahndesign">https://www.linkedin.com/in/courtneyahndesign</a> </p><p>Website: <a href="https://www.courtneyahndesign.com/">https://www.courtneyahndesign.com/</a></p><p>Instagram: <a href="https://www.instagram.com/candy.courn/">https://www.instagram.com/candy.courn/</a></p><p><br></p>]]>
      </content:encoded>
      <pubDate>Tue, 10 Jun 2025 12:48:54 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/3224baf3/f1537ed0.mp3" length="82973760" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/HsOddjSj1BJ3JqkGuSvCXPm2vI3k5g_C3MXy1r9yKmg/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS8wZDcx/N2ViZDI3YjViNDZl/Mzc1MjUxNGQwYjk4/MDM5NS5wbmc.jpg"/>
      <itunes:duration>3450</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Courn Ahn is a designer, content creator, and advocate who cares deeply about accessibility and social justice. Their work focuses on helping people see disability, identity, and community support in a new way, especially through the lens of queerness, race, and being neurodivergent.</p><p><br>As a Queer, nonbinary, mixed-race Korean creative, Courn shares from personal experience and speaks honestly about the challenges that come with being disabled in a world full of assumptions. Courn's journey has been about unlearning shame, accepting who they are, and understanding that using visible accommodations isn’t something to hide, it’s a powerful way to take care of yourself.</p><p><br>Courn also talks about how people often assume you don’t need help if you look like you’re doing well, and how sharing online as a disabled person can be both meaningful and exhausting. Through their design work and presence on social media, Courn is not just creating content, Courn Ahn is also  creating space for real conversations, celebrating differences, and reminding us that accessibility should matter to everyone</p><p><strong>Key Moments<br></strong> 00:00  What people get wrong about autistic people<br> 06:43  Struggling with what to share online<br> 14:18  Tools that make life easier<br> 20:42  How style helps show who I am<br> 27:01  Feeling free to be myself<br> 33:13  How different parts of my identity connect<br> 52:57  Finding confidence through disability</p><p><br></p><p><strong>Connect with Courn Ahn<br></strong>Linkedin: <a href="https://www.linkedin.com/in/courtneyahndesign">https://www.linkedin.com/in/courtneyahndesign</a> </p><p>Website: <a href="https://www.courtneyahndesign.com/">https://www.courtneyahndesign.com/</a></p><p>Instagram: <a href="https://www.instagram.com/candy.courn/">https://www.instagram.com/candy.courn/</a></p><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>From Runway to Real Life: Jillian Curwin on Fashion, Identity, and Disability</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>27</itunes:episode>
      <podcast:episode>27</podcast:episode>
      <itunes:title>From Runway to Real Life: Jillian Curwin on Fashion, Identity, and Disability</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/8c824da4</link>
      <description>
        <![CDATA[<p>Jillian Curwin, Director of Communications for the Mascots Matter Campaign, is an advocate, storyteller, and content creator reshaping the conversation around disability, access, and representation. In this episode of Everything You Know About Disability Is Wrong, she joins hosts Lily Newton and Erin Hawley for an insightful discussion.</p><p>Jillian shares her experience as a little person navigating an often inaccessible world, particularly in the fashion industry. She reflects on what sparked her advocacy, how misperceptions about disability motivated her, and why authentic representation matters. Jillian also talks about embracing a disabled identity, the value of lived experience, and the role of community in fostering self-acceptance and empowerment.</p><p>Her story offers fresh perspectives on adaptive fashion, confidence, and finding one’s voice, both in the disability community and beyond. Listeners will gain valuable insights that challenge perceptions of disability and redefine what it means to be seen and heard.</p><p><strong>Key Moments</strong></p><p><br></p><p>06:01 Awakening to Advocacy</p><p>07:11 Diverse Representation in Fashion</p><p>19:02 My Disability Advocacy Journey</p><p>23:44 Redefining Disability Through Experience</p><p>34:37 Issues in Disability Fashion Inclusion</p><p>45:00 Empowering Disability Representation</p><p><br></p><p><strong>Connect with Jillian Curwin</strong></p><p><br></p><p>LinkedIn: <a href="https://www.linkedin.com/in/jillian-curwin-04827056">https://www.linkedin.com/in/jillian-curwin-04827056</a> </p><p>Website: <a href="https://mascotsmatter.net/about-page/">https://mascotsmatter.net/about-page/</a>  </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Jillian Curwin, Director of Communications for the Mascots Matter Campaign, is an advocate, storyteller, and content creator reshaping the conversation around disability, access, and representation. In this episode of Everything You Know About Disability Is Wrong, she joins hosts Lily Newton and Erin Hawley for an insightful discussion.</p><p>Jillian shares her experience as a little person navigating an often inaccessible world, particularly in the fashion industry. She reflects on what sparked her advocacy, how misperceptions about disability motivated her, and why authentic representation matters. Jillian also talks about embracing a disabled identity, the value of lived experience, and the role of community in fostering self-acceptance and empowerment.</p><p>Her story offers fresh perspectives on adaptive fashion, confidence, and finding one’s voice, both in the disability community and beyond. Listeners will gain valuable insights that challenge perceptions of disability and redefine what it means to be seen and heard.</p><p><strong>Key Moments</strong></p><p><br></p><p>06:01 Awakening to Advocacy</p><p>07:11 Diverse Representation in Fashion</p><p>19:02 My Disability Advocacy Journey</p><p>23:44 Redefining Disability Through Experience</p><p>34:37 Issues in Disability Fashion Inclusion</p><p>45:00 Empowering Disability Representation</p><p><br></p><p><strong>Connect with Jillian Curwin</strong></p><p><br></p><p>LinkedIn: <a href="https://www.linkedin.com/in/jillian-curwin-04827056">https://www.linkedin.com/in/jillian-curwin-04827056</a> </p><p>Website: <a href="https://mascotsmatter.net/about-page/">https://mascotsmatter.net/about-page/</a>  </p>]]>
      </content:encoded>
      <pubDate>Thu, 15 May 2025 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
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      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/Gs1stYqy2Zcqzl8CEwzG57JljAgeS_0Kz1Y64xQMrDQ/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS85ODhj/ZjU1YTg3MzEyM2Ey/NTBjODUwMzAzNjc3/YjRjNy5wbmc.jpg"/>
      <itunes:duration>3586</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Jillian Curwin, Director of Communications for the Mascots Matter Campaign, is an advocate, storyteller, and content creator reshaping the conversation around disability, access, and representation. In this episode of Everything You Know About Disability Is Wrong, she joins hosts Lily Newton and Erin Hawley for an insightful discussion.</p><p>Jillian shares her experience as a little person navigating an often inaccessible world, particularly in the fashion industry. She reflects on what sparked her advocacy, how misperceptions about disability motivated her, and why authentic representation matters. Jillian also talks about embracing a disabled identity, the value of lived experience, and the role of community in fostering self-acceptance and empowerment.</p><p>Her story offers fresh perspectives on adaptive fashion, confidence, and finding one’s voice, both in the disability community and beyond. Listeners will gain valuable insights that challenge perceptions of disability and redefine what it means to be seen and heard.</p><p><strong>Key Moments</strong></p><p><br></p><p>06:01 Awakening to Advocacy</p><p>07:11 Diverse Representation in Fashion</p><p>19:02 My Disability Advocacy Journey</p><p>23:44 Redefining Disability Through Experience</p><p>34:37 Issues in Disability Fashion Inclusion</p><p>45:00 Empowering Disability Representation</p><p><br></p><p><strong>Connect with Jillian Curwin</strong></p><p><br></p><p>LinkedIn: <a href="https://www.linkedin.com/in/jillian-curwin-04827056">https://www.linkedin.com/in/jillian-curwin-04827056</a> </p><p>Website: <a href="https://mascotsmatter.net/about-page/">https://mascotsmatter.net/about-page/</a>  </p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Kids Need Neurodivergent Characters: Kyla and Jedidiah Mora on Acceptance &amp; Understanding</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>26</itunes:episode>
      <podcast:episode>26</podcast:episode>
      <itunes:title>Kids Need Neurodivergent Characters: Kyla and Jedidiah Mora on Acceptance &amp; Understanding</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/487a750a</link>
      <description>
        <![CDATA[<p>Kyla and Jedidiah Mora are a neurodivergent couple, writers, and advocates. They are the authors of “Today My Brain Is a Dinosaur,” a popular children’s book that helps kids understand autism, ADHD, and different ways of thinking.  Their journey started with their own diagnoses of autism and ADHD as adults. After years of confusion and challenges, they found clarity, self-acceptance, and a desire to help others feel less alone.  </p><p>Kyla is a high school teacher and journalist who is passionate about education and storytelling. Jedidiah works in the water industry and has a strong interest in mechanical engineering. Together, they combine their skills and personal experiences to create stories that celebrate neurodivergent kids and families. Through their writing, they aim to break down stigma and spark conversations. </p><p><strong>Key Moments</strong></p><p><br></p><p>00:00 Intro and Audio Descriptions</p><p>06:53 Own Voices, Own Stories Award for Disabled Authors</p><p>12:33 Internalizing Blame; Autism, ADHD, and Trauma</p><p>21:50 Autism and Learning to Be Your True Self</p><p>26:49 Embracing Hyperfocus in a Positive Way</p><p>28:21 Job Challenges and Personal Struggles</p><p>44:44 Unique Traits of Autistic Girls</p><p>59:09 Understanding and Accepting </p><p><br></p><p><strong>Connect with Kyla Mora </strong></p><p><br></p><p>Twitter: <a href="https://x.com/kylapmora">https://x.com/kylapmora</a> </p><p>Website: <a href="https://cherrylakepublishing.com/shop/show/54094">https://cherrylakepublishing.com/shop/show/54094</a> </p><p><br></p><p><strong>Jedidiah Mora</strong></p><p>Website: <a href="https://cherrylakepublishing.com/shop/show/54094">https://cherrylakepublishing.com/shop/show/54094</a> </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Kyla and Jedidiah Mora are a neurodivergent couple, writers, and advocates. They are the authors of “Today My Brain Is a Dinosaur,” a popular children’s book that helps kids understand autism, ADHD, and different ways of thinking.  Their journey started with their own diagnoses of autism and ADHD as adults. After years of confusion and challenges, they found clarity, self-acceptance, and a desire to help others feel less alone.  </p><p>Kyla is a high school teacher and journalist who is passionate about education and storytelling. Jedidiah works in the water industry and has a strong interest in mechanical engineering. Together, they combine their skills and personal experiences to create stories that celebrate neurodivergent kids and families. Through their writing, they aim to break down stigma and spark conversations. </p><p><strong>Key Moments</strong></p><p><br></p><p>00:00 Intro and Audio Descriptions</p><p>06:53 Own Voices, Own Stories Award for Disabled Authors</p><p>12:33 Internalizing Blame; Autism, ADHD, and Trauma</p><p>21:50 Autism and Learning to Be Your True Self</p><p>26:49 Embracing Hyperfocus in a Positive Way</p><p>28:21 Job Challenges and Personal Struggles</p><p>44:44 Unique Traits of Autistic Girls</p><p>59:09 Understanding and Accepting </p><p><br></p><p><strong>Connect with Kyla Mora </strong></p><p><br></p><p>Twitter: <a href="https://x.com/kylapmora">https://x.com/kylapmora</a> </p><p>Website: <a href="https://cherrylakepublishing.com/shop/show/54094">https://cherrylakepublishing.com/shop/show/54094</a> </p><p><br></p><p><strong>Jedidiah Mora</strong></p><p>Website: <a href="https://cherrylakepublishing.com/shop/show/54094">https://cherrylakepublishing.com/shop/show/54094</a> </p>]]>
      </content:encoded>
      <pubDate>Tue, 22 Apr 2025 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/487a750a/1203bddd.mp3" length="94966036" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/hhwmPhWw9tz9yB070X0zvTGYKArgRMdvlAKVPIJOlAs/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS82N2Y0/N2I5YjYyMDRkZWEw/ZDJhZDg1NTkzYTUy/YTRhNy5wbmc.jpg"/>
      <itunes:duration>3949</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Kyla and Jedidiah Mora are a neurodivergent couple, writers, and advocates. They are the authors of “Today My Brain Is a Dinosaur,” a popular children’s book that helps kids understand autism, ADHD, and different ways of thinking.  Their journey started with their own diagnoses of autism and ADHD as adults. After years of confusion and challenges, they found clarity, self-acceptance, and a desire to help others feel less alone.  </p><p>Kyla is a high school teacher and journalist who is passionate about education and storytelling. Jedidiah works in the water industry and has a strong interest in mechanical engineering. Together, they combine their skills and personal experiences to create stories that celebrate neurodivergent kids and families. Through their writing, they aim to break down stigma and spark conversations. </p><p><strong>Key Moments</strong></p><p><br></p><p>00:00 Intro and Audio Descriptions</p><p>06:53 Own Voices, Own Stories Award for Disabled Authors</p><p>12:33 Internalizing Blame; Autism, ADHD, and Trauma</p><p>21:50 Autism and Learning to Be Your True Self</p><p>26:49 Embracing Hyperfocus in a Positive Way</p><p>28:21 Job Challenges and Personal Struggles</p><p>44:44 Unique Traits of Autistic Girls</p><p>59:09 Understanding and Accepting </p><p><br></p><p><strong>Connect with Kyla Mora </strong></p><p><br></p><p>Twitter: <a href="https://x.com/kylapmora">https://x.com/kylapmora</a> </p><p>Website: <a href="https://cherrylakepublishing.com/shop/show/54094">https://cherrylakepublishing.com/shop/show/54094</a> </p><p><br></p><p><strong>Jedidiah Mora</strong></p><p>Website: <a href="https://cherrylakepublishing.com/shop/show/54094">https://cherrylakepublishing.com/shop/show/54094</a> </p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>From Wall Street to Changemaker: Tiffany Yu’s Story of Purpose and Possibility</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>25</itunes:episode>
      <podcast:episode>25</podcast:episode>
      <itunes:title>From Wall Street to Changemaker: Tiffany Yu’s Story of Purpose and Possibility</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">122694d4-682a-4a42-9ca0-3fb1c64134f1</guid>
      <link>https://share.transistor.fm/s/736eed80</link>
      <description>
        <![CDATA[<p>Tiffany Yu is a disability advocate, entrepreneur, and author of <em>The Anti-Ableist Manifesto</em>. She started her career at Goldman Sachs before becoming a leader in disability inclusion.  </p><p><br></p><p>After acquiring a disability as a child, she struggled with loneliness and self-doubt. Over time, she turned her experiences into advocacy and founded Diversability, a community that celebrates disability pride and fights stigma.  </p><p><br></p><p>She works to break barriers, share personal stories, and create more inclusive spaces. Through her efforts, she shows that disability is diverse and that working together can create real change.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>7:00 Overcoming Isolation and Disability</p><p>14:13 Collective Advocacy in Action</p><p>22:00 Disability Language Made Simple</p><p>23:25 Safe Spaces </p><p>35:34 Beyond Assumptions: Tiffany’s Story</p><p>49:16 Mental Health </p><p>01:02:22 Reaching Young Readers</p><p><br></p><p><strong>Connect with Tiffany Yu</strong></p><p>Twitter: <a href="https://x.com/imtiffanyyu">https://x.com/imtiffanyyu</a> </p><p>Website:<a href="http://tiffanyyu.com/">http://tiffanyyu.com/</a> </p><p>The Anti-Ableist Manifesto: <a href="https://www.tiffanyyu.com/book">https://www.tiffanyyu.com/book</a> </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Tiffany Yu is a disability advocate, entrepreneur, and author of <em>The Anti-Ableist Manifesto</em>. She started her career at Goldman Sachs before becoming a leader in disability inclusion.  </p><p><br></p><p>After acquiring a disability as a child, she struggled with loneliness and self-doubt. Over time, she turned her experiences into advocacy and founded Diversability, a community that celebrates disability pride and fights stigma.  </p><p><br></p><p>She works to break barriers, share personal stories, and create more inclusive spaces. Through her efforts, she shows that disability is diverse and that working together can create real change.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>7:00 Overcoming Isolation and Disability</p><p>14:13 Collective Advocacy in Action</p><p>22:00 Disability Language Made Simple</p><p>23:25 Safe Spaces </p><p>35:34 Beyond Assumptions: Tiffany’s Story</p><p>49:16 Mental Health </p><p>01:02:22 Reaching Young Readers</p><p><br></p><p><strong>Connect with Tiffany Yu</strong></p><p>Twitter: <a href="https://x.com/imtiffanyyu">https://x.com/imtiffanyyu</a> </p><p>Website:<a href="http://tiffanyyu.com/">http://tiffanyyu.com/</a> </p><p>The Anti-Ableist Manifesto: <a href="https://www.tiffanyyu.com/book">https://www.tiffanyyu.com/book</a> </p>]]>
      </content:encoded>
      <pubDate>Tue, 01 Apr 2025 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
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      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/POzH9fYG8KyEkNAEjJCqdYNbWU_XACMkblRv7YNdWfw/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS83NWVj/ZjBjZDBmOWQ3Y2Rk/ZDJhZjA3ZmE1MDk4/MDYzYy5wbmc.jpg"/>
      <itunes:duration>4102</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Tiffany Yu is a disability advocate, entrepreneur, and author of <em>The Anti-Ableist Manifesto</em>. She started her career at Goldman Sachs before becoming a leader in disability inclusion.  </p><p><br></p><p>After acquiring a disability as a child, she struggled with loneliness and self-doubt. Over time, she turned her experiences into advocacy and founded Diversability, a community that celebrates disability pride and fights stigma.  </p><p><br></p><p>She works to break barriers, share personal stories, and create more inclusive spaces. Through her efforts, she shows that disability is diverse and that working together can create real change.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>7:00 Overcoming Isolation and Disability</p><p>14:13 Collective Advocacy in Action</p><p>22:00 Disability Language Made Simple</p><p>23:25 Safe Spaces </p><p>35:34 Beyond Assumptions: Tiffany’s Story</p><p>49:16 Mental Health </p><p>01:02:22 Reaching Young Readers</p><p><br></p><p><strong>Connect with Tiffany Yu</strong></p><p>Twitter: <a href="https://x.com/imtiffanyyu">https://x.com/imtiffanyyu</a> </p><p>Website:<a href="http://tiffanyyu.com/">http://tiffanyyu.com/</a> </p><p>The Anti-Ableist Manifesto: <a href="https://www.tiffanyyu.com/book">https://www.tiffanyyu.com/book</a> </p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Exploring the World Through Sensory Experiences with Dr. Hoby Wedler </title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>24</itunes:episode>
      <podcast:episode>24</podcast:episode>
      <itunes:title>Exploring the World Through Sensory Experiences with Dr. Hoby Wedler </itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">243584f7-37e7-4136-bfbc-1928f0488d2f</guid>
      <link>https://share.transistor.fm/s/c2d1732f</link>
      <description>
        <![CDATA[<p>Experiencing the world isn’t just about sight, it's about tasting, touching, hearing, and smelling, too. Using all our senses helps us connect more deeply to the world around us.</p><p><br></p><p>Dr. Hoby Wedler is a chemist, entrepreneur, and advocate for inclusivity. He holds a Ph.D. in physical organic chemistry from UC Davis and founded the Wedland Group to explore how our senses shape emotions and connections. He creates unique food and drink experiences that help people appreciate the little things in life. He also works to break stereotypes about disability, inspiring others to reach their full potential.</p><p><br></p><p>Dr. Wedler is also the founder and CEO of Hobie and Company (Hobie and Co online), part of Wedland Group. His company offers amazing blindfolded tasting experiences that help people explore their nonvisual senses. He shares his passion for sensory experiences on TikTok, where he has around 200,000 followers. Lastly, he runs Emotitec (emotitec.com), a company based in Italy.</p><p><strong>Key Moments</strong></p><p><br></p><p>09:14 Embracing Unseen Experiences  </p><p>16:17 Empowerment Through Disability  </p><p>19:19 Redefining Independence  </p><p>28:24 Diversity Fuels Success  </p><p>34:43 Supporting Blind Children  </p><p>39:47 Parents Presuming Competence</p><p>52:36 Sensory Experiences Founder</p><p><strong>Connect with Dr. Hoby Wedler</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/hobywedler">https://www.linkedin.com/in/hobywedler</a> </p><p>CEO at Wedland Group: <a href="https://wendland.efsadvisors.com/">https://wendland.efsadvisors.com/</a> </p><p>President at EMOTITECH: <a href="https://emotitech.com/">https://emotitech.com/</a> </p><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Experiencing the world isn’t just about sight, it's about tasting, touching, hearing, and smelling, too. Using all our senses helps us connect more deeply to the world around us.</p><p><br></p><p>Dr. Hoby Wedler is a chemist, entrepreneur, and advocate for inclusivity. He holds a Ph.D. in physical organic chemistry from UC Davis and founded the Wedland Group to explore how our senses shape emotions and connections. He creates unique food and drink experiences that help people appreciate the little things in life. He also works to break stereotypes about disability, inspiring others to reach their full potential.</p><p><br></p><p>Dr. Wedler is also the founder and CEO of Hobie and Company (Hobie and Co online), part of Wedland Group. His company offers amazing blindfolded tasting experiences that help people explore their nonvisual senses. He shares his passion for sensory experiences on TikTok, where he has around 200,000 followers. Lastly, he runs Emotitec (emotitec.com), a company based in Italy.</p><p><strong>Key Moments</strong></p><p><br></p><p>09:14 Embracing Unseen Experiences  </p><p>16:17 Empowerment Through Disability  </p><p>19:19 Redefining Independence  </p><p>28:24 Diversity Fuels Success  </p><p>34:43 Supporting Blind Children  </p><p>39:47 Parents Presuming Competence</p><p>52:36 Sensory Experiences Founder</p><p><strong>Connect with Dr. Hoby Wedler</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/hobywedler">https://www.linkedin.com/in/hobywedler</a> </p><p>CEO at Wedland Group: <a href="https://wendland.efsadvisors.com/">https://wendland.efsadvisors.com/</a> </p><p>President at EMOTITECH: <a href="https://emotitech.com/">https://emotitech.com/</a> </p><p><br></p>]]>
      </content:encoded>
      <pubDate>Tue, 18 Mar 2025 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/c2d1732f/5bb26159.mp3" length="84820128" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/SYyUtDBz2sQzOjVjvazMjNU_BIJPFf1478mbs2ZnGXc/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS82YjBi/Mjg3YTcyNWQyOGZk/MWY0MmEwNzE3YmY2/YzQ5Zi5wbmc.jpg"/>
      <itunes:duration>3523</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Experiencing the world isn’t just about sight, it's about tasting, touching, hearing, and smelling, too. Using all our senses helps us connect more deeply to the world around us.</p><p><br></p><p>Dr. Hoby Wedler is a chemist, entrepreneur, and advocate for inclusivity. He holds a Ph.D. in physical organic chemistry from UC Davis and founded the Wedland Group to explore how our senses shape emotions and connections. He creates unique food and drink experiences that help people appreciate the little things in life. He also works to break stereotypes about disability, inspiring others to reach their full potential.</p><p><br></p><p>Dr. Wedler is also the founder and CEO of Hobie and Company (Hobie and Co online), part of Wedland Group. His company offers amazing blindfolded tasting experiences that help people explore their nonvisual senses. He shares his passion for sensory experiences on TikTok, where he has around 200,000 followers. Lastly, he runs Emotitec (emotitec.com), a company based in Italy.</p><p><strong>Key Moments</strong></p><p><br></p><p>09:14 Embracing Unseen Experiences  </p><p>16:17 Empowerment Through Disability  </p><p>19:19 Redefining Independence  </p><p>28:24 Diversity Fuels Success  </p><p>34:43 Supporting Blind Children  </p><p>39:47 Parents Presuming Competence</p><p>52:36 Sensory Experiences Founder</p><p><strong>Connect with Dr. Hoby Wedler</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/hobywedler">https://www.linkedin.com/in/hobywedler</a> </p><p>CEO at Wedland Group: <a href="https://wendland.efsadvisors.com/">https://wendland.efsadvisors.com/</a> </p><p>President at EMOTITECH: <a href="https://emotitech.com/">https://emotitech.com/</a> </p><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Entrepreneurship, Education, and Knowing Your Value with Onyinye Udokporo</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>23</itunes:episode>
      <podcast:episode>23</podcast:episode>
      <itunes:title>Entrepreneurship, Education, and Knowing Your Value with Onyinye Udokporo</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">df12a8d3-e6e1-40cc-aa30-564a85ae1ce7</guid>
      <link>https://share.transistor.fm/s/567a3de5</link>
      <description>
        <![CDATA[<p>"Just because you can’t see it, doesn’t mean it’s not real."</p><p><br>Onyinye Udokporo, CEO and founder of Enrich Learning, dives into a conversation that’s both eye-opening and deeply personal, exploring the differences between UK and US disability cultures. From how each country approaches accessibility and support to the ways people talk about neurodivergence, it’s clear that culture shapes the disability experience in ways we don’t always realize.</p><p><br>A big theme in this discussion is the power of language—how the words we use can either create understanding or reinforce barriers. Onyinye shares why being intentional with language isn’t just about being polite; it’s about making the world more inclusive and accessible for everyone. This conversation is a reminder that small shifts in how we speak and think about disability can make a huge difference.</p><p><br></p><p><strong>Key Moments</strong></p><p><br>00:37:03  Initial Rejection</p><p><br>00:38:53 Mother’s Screening</p><p><br>00:44:50  Shared Experience</p><p><br>00:45:30 Cultural &amp; Generational Factors</p><p><br>10:15 Neurodivergence vs. Mental Health</p><p><br>30:00 Empowering Language</p><p><br>45:15 Authentic Conversations</p><p><br>55:00 Cultural Pressures</p><p><br>1:05:00 Dyslexia Advocacy</p><p><br>1:30:00 Access Through Tutoring</p><p><br>1:35:00 Reclaiming “Inspiring”</p><p><br></p><p><strong>Connect with Onyinye Udokporo</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/onyinyeudokporo">linkedin.com/in/onyinyeudokporo</a></p><p>Personal Website: <a href="http://www.onyinyeudokporo.com/">onyinyeudokporo.com<br></a>Company Website: <a href="http://www.enrichlearning.co.uk/">enrichlearning.co.uk</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>"Just because you can’t see it, doesn’t mean it’s not real."</p><p><br>Onyinye Udokporo, CEO and founder of Enrich Learning, dives into a conversation that’s both eye-opening and deeply personal, exploring the differences between UK and US disability cultures. From how each country approaches accessibility and support to the ways people talk about neurodivergence, it’s clear that culture shapes the disability experience in ways we don’t always realize.</p><p><br>A big theme in this discussion is the power of language—how the words we use can either create understanding or reinforce barriers. Onyinye shares why being intentional with language isn’t just about being polite; it’s about making the world more inclusive and accessible for everyone. This conversation is a reminder that small shifts in how we speak and think about disability can make a huge difference.</p><p><br></p><p><strong>Key Moments</strong></p><p><br>00:37:03  Initial Rejection</p><p><br>00:38:53 Mother’s Screening</p><p><br>00:44:50  Shared Experience</p><p><br>00:45:30 Cultural &amp; Generational Factors</p><p><br>10:15 Neurodivergence vs. Mental Health</p><p><br>30:00 Empowering Language</p><p><br>45:15 Authentic Conversations</p><p><br>55:00 Cultural Pressures</p><p><br>1:05:00 Dyslexia Advocacy</p><p><br>1:30:00 Access Through Tutoring</p><p><br>1:35:00 Reclaiming “Inspiring”</p><p><br></p><p><strong>Connect with Onyinye Udokporo</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/onyinyeudokporo">linkedin.com/in/onyinyeudokporo</a></p><p>Personal Website: <a href="http://www.onyinyeudokporo.com/">onyinyeudokporo.com<br></a>Company Website: <a href="http://www.enrichlearning.co.uk/">enrichlearning.co.uk</a></p>]]>
      </content:encoded>
      <pubDate>Tue, 25 Feb 2025 09:00:00 -0500</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/567a3de5/07017081.mp3" length="93312914" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/ZrkEnh5G2k4d1QL0PSatJv9cZsfStrAK_8t4PDDGOnw/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS8xNjFi/N2VhZmZiZDRiMzYy/YmQxZmFjMDQ1MjJh/M2E3OS5wbmc.jpg"/>
      <itunes:duration>3878</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>"Just because you can’t see it, doesn’t mean it’s not real."</p><p><br>Onyinye Udokporo, CEO and founder of Enrich Learning, dives into a conversation that’s both eye-opening and deeply personal, exploring the differences between UK and US disability cultures. From how each country approaches accessibility and support to the ways people talk about neurodivergence, it’s clear that culture shapes the disability experience in ways we don’t always realize.</p><p><br>A big theme in this discussion is the power of language—how the words we use can either create understanding or reinforce barriers. Onyinye shares why being intentional with language isn’t just about being polite; it’s about making the world more inclusive and accessible for everyone. This conversation is a reminder that small shifts in how we speak and think about disability can make a huge difference.</p><p><br></p><p><strong>Key Moments</strong></p><p><br>00:37:03  Initial Rejection</p><p><br>00:38:53 Mother’s Screening</p><p><br>00:44:50  Shared Experience</p><p><br>00:45:30 Cultural &amp; Generational Factors</p><p><br>10:15 Neurodivergence vs. Mental Health</p><p><br>30:00 Empowering Language</p><p><br>45:15 Authentic Conversations</p><p><br>55:00 Cultural Pressures</p><p><br>1:05:00 Dyslexia Advocacy</p><p><br>1:30:00 Access Through Tutoring</p><p><br>1:35:00 Reclaiming “Inspiring”</p><p><br></p><p><strong>Connect with Onyinye Udokporo</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/onyinyeudokporo">linkedin.com/in/onyinyeudokporo</a></p><p>Personal Website: <a href="http://www.onyinyeudokporo.com/">onyinyeudokporo.com<br></a>Company Website: <a href="http://www.enrichlearning.co.uk/">enrichlearning.co.uk</a></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>The Power of Gaming: Richard Jacobs on Community, Competition, and Personal Empowerment</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>22</itunes:episode>
      <podcast:episode>22</podcast:episode>
      <itunes:title>The Power of Gaming: Richard Jacobs on Community, Competition, and Personal Empowerment</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">cd539a94-5af6-4a75-9365-ce31953b285c</guid>
      <link>https://share.transistor.fm/s/a9c76d7e</link>
      <description>
        <![CDATA[<p>Richard Jacobs is a dedicated gamer and member of the esports team QuadGods. He discusses his journey of resilience, the pivotal role gaming plays in his life, and the misconceptions he faces as a disabled individual.</p><p><br></p><p>Richard shares about the power of community and how his streaming “family” has allowed him to harness his competitive spirit and embrace his emotions. </p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>13:32 - Inspiration and belonging.</p><p>21:57 - Supports family through streaming.</p><p>31:24 - Prefers controller over keyboard/mouse.</p><p>43:23 - Handles losses calmly; focuses on perseverance.</p><p>59:44 - Builds deep community connection.</p><p><br></p><p><strong>Connect with Richard Jacobs<br></strong>Instagram: <a href="https://www.instagram.com/breadwinner1007/">https://www.instagram.com/breadwinner1007/</a></p><p>Website: <a href="https://quadgods.com/the-players">https://quadgods.com/the-players</a></p><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Richard Jacobs is a dedicated gamer and member of the esports team QuadGods. He discusses his journey of resilience, the pivotal role gaming plays in his life, and the misconceptions he faces as a disabled individual.</p><p><br></p><p>Richard shares about the power of community and how his streaming “family” has allowed him to harness his competitive spirit and embrace his emotions. </p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>13:32 - Inspiration and belonging.</p><p>21:57 - Supports family through streaming.</p><p>31:24 - Prefers controller over keyboard/mouse.</p><p>43:23 - Handles losses calmly; focuses on perseverance.</p><p>59:44 - Builds deep community connection.</p><p><br></p><p><strong>Connect with Richard Jacobs<br></strong>Instagram: <a href="https://www.instagram.com/breadwinner1007/">https://www.instagram.com/breadwinner1007/</a></p><p>Website: <a href="https://quadgods.com/the-players">https://quadgods.com/the-players</a></p><p><br></p>]]>
      </content:encoded>
      <pubDate>Tue, 14 Jan 2025 09:00:00 -0500</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/a9c76d7e/714be0ca.mp3" length="91511050" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/eVcWPbCQdIjk4OegOSCZiaaG_3KNzJE8Z6t-KM5n2I8/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9lOTZk/YTNmMTk3ODQ3YWIw/ODk4MjRhN2IzZjZi/YzMzYi5wbmc.jpg"/>
      <itunes:duration>3802</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Richard Jacobs is a dedicated gamer and member of the esports team QuadGods. He discusses his journey of resilience, the pivotal role gaming plays in his life, and the misconceptions he faces as a disabled individual.</p><p><br></p><p>Richard shares about the power of community and how his streaming “family” has allowed him to harness his competitive spirit and embrace his emotions. </p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>13:32 - Inspiration and belonging.</p><p>21:57 - Supports family through streaming.</p><p>31:24 - Prefers controller over keyboard/mouse.</p><p>43:23 - Handles losses calmly; focuses on perseverance.</p><p>59:44 - Builds deep community connection.</p><p><br></p><p><strong>Connect with Richard Jacobs<br></strong>Instagram: <a href="https://www.instagram.com/breadwinner1007/">https://www.instagram.com/breadwinner1007/</a></p><p>Website: <a href="https://quadgods.com/the-players">https://quadgods.com/the-players</a></p><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>The Advocacy Power of Humor: Steven Verdile and The Squeaky Wheel</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>21</itunes:episode>
      <podcast:episode>21</podcast:episode>
      <itunes:title>The Advocacy Power of Humor: Steven Verdile and The Squeaky Wheel</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">cf2a9a6c-04cc-4ba9-a3b5-05ae00ec8787</guid>
      <link>https://share.transistor.fm/s/f88c25fd</link>
      <description>
        <![CDATA[<p>Humor can educate and challenge, but it must highlight issues without mocking the disability community. In this episode, we explore how satire can play into advocacy and ask, “What exactly makes good satire?”. </p><p>Steven Verdile, Founder of Squeaky Wheel Media, shares his insights on the critical intersection of disability and content creation. Steven discusses the significance of focusing on specific issues, particularly those impacting the disabled community, and the protective measures taken to ensure writers' safety. </p><p><strong>Key Moments</strong></p><p><br></p><p>06:27 Humor exposes accessibility challenges.</p><p>08:41 Accessible platforms empower disabled writers.</p><p>23:11 Disability experiences and representation vary.</p><p>38:13 Humor addresses disability policy.</p><p>49:07 Steven’s school experience.</p><p><strong>Connect with Steven Verdile<br></strong>LinkedIn: <a href="https://www.linkedin.com/in/steven-verdile">https://www.linkedin.com/in/steven-verdile</a> </p><p>Website: <a href="https://thesqueakywheel.org/">https://thesqueakywheel.org/</a> </p><p>Squeaky Wheel Instagram: <a href="https://www.instagram.com/thesqkywheel/?hl=en">https://www.instagram.com/thesqkywheel/?hl=en</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Humor can educate and challenge, but it must highlight issues without mocking the disability community. In this episode, we explore how satire can play into advocacy and ask, “What exactly makes good satire?”. </p><p>Steven Verdile, Founder of Squeaky Wheel Media, shares his insights on the critical intersection of disability and content creation. Steven discusses the significance of focusing on specific issues, particularly those impacting the disabled community, and the protective measures taken to ensure writers' safety. </p><p><strong>Key Moments</strong></p><p><br></p><p>06:27 Humor exposes accessibility challenges.</p><p>08:41 Accessible platforms empower disabled writers.</p><p>23:11 Disability experiences and representation vary.</p><p>38:13 Humor addresses disability policy.</p><p>49:07 Steven’s school experience.</p><p><strong>Connect with Steven Verdile<br></strong>LinkedIn: <a href="https://www.linkedin.com/in/steven-verdile">https://www.linkedin.com/in/steven-verdile</a> </p><p>Website: <a href="https://thesqueakywheel.org/">https://thesqueakywheel.org/</a> </p><p>Squeaky Wheel Instagram: <a href="https://www.instagram.com/thesqkywheel/?hl=en">https://www.instagram.com/thesqkywheel/?hl=en</a></p>]]>
      </content:encoded>
      <pubDate>Fri, 20 Dec 2024 09:00:00 -0500</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/f88c25fd/13fe9381.mp3" length="80711049" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/flU-KJEjxGZBk4_SLlurFhxKiPCZ9PuQ9dlEh7L3k7I/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS8zMWEy/ZTllOTFiY2E0ZWJk/ZmY1MGY0MGJkZWE4/NTY3OS5wbmc.jpg"/>
      <itunes:duration>3355</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Humor can educate and challenge, but it must highlight issues without mocking the disability community. In this episode, we explore how satire can play into advocacy and ask, “What exactly makes good satire?”. </p><p>Steven Verdile, Founder of Squeaky Wheel Media, shares his insights on the critical intersection of disability and content creation. Steven discusses the significance of focusing on specific issues, particularly those impacting the disabled community, and the protective measures taken to ensure writers' safety. </p><p><strong>Key Moments</strong></p><p><br></p><p>06:27 Humor exposes accessibility challenges.</p><p>08:41 Accessible platforms empower disabled writers.</p><p>23:11 Disability experiences and representation vary.</p><p>38:13 Humor addresses disability policy.</p><p>49:07 Steven’s school experience.</p><p><strong>Connect with Steven Verdile<br></strong>LinkedIn: <a href="https://www.linkedin.com/in/steven-verdile">https://www.linkedin.com/in/steven-verdile</a> </p><p>Website: <a href="https://thesqueakywheel.org/">https://thesqueakywheel.org/</a> </p><p>Squeaky Wheel Instagram: <a href="https://www.instagram.com/thesqkywheel/?hl=en">https://www.instagram.com/thesqkywheel/?hl=en</a></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Annie Segarra on Medical Gaslighting and EDS: Her Fight for Change</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>20</itunes:episode>
      <podcast:episode>20</podcast:episode>
      <itunes:title>Annie Segarra on Medical Gaslighting and EDS: Her Fight for Change</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">566411d9-f808-489f-a5b5-5629d3ba0ae8</guid>
      <link>https://share.transistor.fm/s/e489c178</link>
      <description>
        <![CDATA[<p>Navigating a medical system that dismisses your pain ignites a fire to advocate for others who are overlooked.</p><p>Annie Segarra is an activist and content creator dedicated to disability rights, body positivity, and social justice. Annie opens up about her deeply personal experience living with Ehlers-Danlos Syndrome (EDS), discussing the emotional and physical toll of navigating a medical system that often dismisses or misdiagnoses those with chronic illnesses. She shares her frustrations with being gaslit by medical professionals and the resilience it has taken to continue advocating for herself.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>2:54Accessibility in spaces</p><p>18:27 Living with EDS</p><p>31:28 Experiencing medical gaslighting</p><p>52:45 Advocating for inclusive training and support</p><p><br></p><p><strong>Connect with  Annie Segarra<br></strong>LinkedIn:<a href="https://www.linkedin.com/in/anniesegarra">https://www.linkedin.com/in/anniesegarra</a> </p><p>Website:<a href="https://invisibleproject.org/annie-segarra/">https://invisibleproject.org/annie-segarra/</a> </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Navigating a medical system that dismisses your pain ignites a fire to advocate for others who are overlooked.</p><p>Annie Segarra is an activist and content creator dedicated to disability rights, body positivity, and social justice. Annie opens up about her deeply personal experience living with Ehlers-Danlos Syndrome (EDS), discussing the emotional and physical toll of navigating a medical system that often dismisses or misdiagnoses those with chronic illnesses. She shares her frustrations with being gaslit by medical professionals and the resilience it has taken to continue advocating for herself.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>2:54Accessibility in spaces</p><p>18:27 Living with EDS</p><p>31:28 Experiencing medical gaslighting</p><p>52:45 Advocating for inclusive training and support</p><p><br></p><p><strong>Connect with  Annie Segarra<br></strong>LinkedIn:<a href="https://www.linkedin.com/in/anniesegarra">https://www.linkedin.com/in/anniesegarra</a> </p><p>Website:<a href="https://invisibleproject.org/annie-segarra/">https://invisibleproject.org/annie-segarra/</a> </p>]]>
      </content:encoded>
      <pubDate>Thu, 12 Dec 2024 09:00:00 -0500</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/e489c178/3dbfaa8e.mp3" length="93536248" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/qUnOhpEAr9DGM1MUUNqSbVq3y5g_yxiBcZvpcsve6jA/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS84NTM5/ZmFhYmUwYWI4ZDBk/Yjg5MzU1MGJjYjA2/NGQyOC5wbmc.jpg"/>
      <itunes:duration>3888</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Navigating a medical system that dismisses your pain ignites a fire to advocate for others who are overlooked.</p><p>Annie Segarra is an activist and content creator dedicated to disability rights, body positivity, and social justice. Annie opens up about her deeply personal experience living with Ehlers-Danlos Syndrome (EDS), discussing the emotional and physical toll of navigating a medical system that often dismisses or misdiagnoses those with chronic illnesses. She shares her frustrations with being gaslit by medical professionals and the resilience it has taken to continue advocating for herself.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>2:54Accessibility in spaces</p><p>18:27 Living with EDS</p><p>31:28 Experiencing medical gaslighting</p><p>52:45 Advocating for inclusive training and support</p><p><br></p><p><strong>Connect with  Annie Segarra<br></strong>LinkedIn:<a href="https://www.linkedin.com/in/anniesegarra">https://www.linkedin.com/in/anniesegarra</a> </p><p>Website:<a href="https://invisibleproject.org/annie-segarra/">https://invisibleproject.org/annie-segarra/</a> </p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Just Between Us: All I Want is Real Portrayals in Film</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>19</itunes:episode>
      <podcast:episode>19</podcast:episode>
      <itunes:title>Just Between Us: All I Want is Real Portrayals in Film</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">aa79f017-d10a-4966-bdcf-29a98ae72499</guid>
      <link>https://share.transistor.fm/s/cd0ef5b0</link>
      <description>
        <![CDATA[<p>Your co-hosts Lily Newton and Erin Hawley return with a candid "Just Between Us" segment on this episode of Everything You Know. They discuss the importance of authentic storytelling in media, using recent casting choices in "Wicked" and Disney adaptations as a jumping-off point. The hosts explore why representation isn’t enough without real inclusion and the need for self-accommodation to destigmatize accessibility. Lily and Erin also reflect on highlights from the past year, sharing their "All I Want" asks for better support.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>00:00 Authentic casting matters</p><p>03:44 Frustration with film clichés</p><p>11:38 Tart cherry juice helps sleep</p><p>14:20 Joining Easterseals' campaign</p><p>17:14 Destigmatize accessibility</p><p><br></p><p><strong>Connect with Lily Newton</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/lily-newton-3b0b5b229">https://www.linkedin.com/in/lily-newton-3b0b5b229</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p><p><br></p><p><strong>Connect with Erin Hawley</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/erinhawley2">https://www.linkedin.com/in/erinhawley2</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Your co-hosts Lily Newton and Erin Hawley return with a candid "Just Between Us" segment on this episode of Everything You Know. They discuss the importance of authentic storytelling in media, using recent casting choices in "Wicked" and Disney adaptations as a jumping-off point. The hosts explore why representation isn’t enough without real inclusion and the need for self-accommodation to destigmatize accessibility. Lily and Erin also reflect on highlights from the past year, sharing their "All I Want" asks for better support.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>00:00 Authentic casting matters</p><p>03:44 Frustration with film clichés</p><p>11:38 Tart cherry juice helps sleep</p><p>14:20 Joining Easterseals' campaign</p><p>17:14 Destigmatize accessibility</p><p><br></p><p><strong>Connect with Lily Newton</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/lily-newton-3b0b5b229">https://www.linkedin.com/in/lily-newton-3b0b5b229</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p><p><br></p><p><strong>Connect with Erin Hawley</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/erinhawley2">https://www.linkedin.com/in/erinhawley2</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p>]]>
      </content:encoded>
      <pubDate>Mon, 09 Dec 2024 09:00:00 -0500</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/cd0ef5b0/258c50e5.mp3" length="37587821" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/-XWdYDnRfl1EtjsHlQb4xf2B36m_COC3Aay50a3KklI/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS82ZGMz/MGEyNDFmOTY2Yjg3/MGU1YTZhYTUwZTRj/ZDZhZS5wbmc.jpg"/>
      <itunes:duration>1558</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Your co-hosts Lily Newton and Erin Hawley return with a candid "Just Between Us" segment on this episode of Everything You Know. They discuss the importance of authentic storytelling in media, using recent casting choices in "Wicked" and Disney adaptations as a jumping-off point. The hosts explore why representation isn’t enough without real inclusion and the need for self-accommodation to destigmatize accessibility. Lily and Erin also reflect on highlights from the past year, sharing their "All I Want" asks for better support.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>00:00 Authentic casting matters</p><p>03:44 Frustration with film clichés</p><p>11:38 Tart cherry juice helps sleep</p><p>14:20 Joining Easterseals' campaign</p><p>17:14 Destigmatize accessibility</p><p><br></p><p><strong>Connect with Lily Newton</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/lily-newton-3b0b5b229">https://www.linkedin.com/in/lily-newton-3b0b5b229</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p><p><br></p><p><strong>Connect with Erin Hawley</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/erinhawley2">https://www.linkedin.com/in/erinhawley2</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Advocacy and Identity: Madison Tevlin’s Creative Journey</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>18</itunes:episode>
      <podcast:episode>18</podcast:episode>
      <itunes:title>Advocacy and Identity: Madison Tevlin’s Creative Journey</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">622693f9-cd80-4bdd-abf0-60e56ed6f5f1</guid>
      <link>https://share.transistor.fm/s/51078827</link>
      <description>
        <![CDATA[<p>Advocacy is not just about raising awareness; it’s about creating real change.</p><p><br>Madison Tevlin is an actor, Host, Model, and Advocate. She is known for her impactful work in the "Assume That I Can" campaign for World Down Syndrome Day and her role in "Champions" alongside Woody Harrelson. Madison shares her wonderful journey and passion for music and storytelling.</p><p><br>Madison talks about her upcoming podcast, "21 Questions," featuring stars like Paris Hilton and Nelly Furtado. Madison opens up about the challenges of breaking stereotypes associated with Down syndrome and emphasizes the importance of community support in her life.</p><p><strong>Key Moments</strong></p><p><br></p><p>00:00 Multi-faceted journey</p><p>06:24 Music and family enhance wellness</p><p>17:53 Opening up about Down syndrome</p><p>22:19 Perfect fit for the roles</p><p>27:26 Redefining Stereotypes Through Storytelling</p><p>45:25 Education integration fosters community</p><p><br></p><p><strong>Connect with Madison Tevlin<br></strong>Instagram:<a href="https://www.instagram.com/madisontevlin/?hl=en">https://www.instagram.com/madisontevlin/?hl=en</a> </p><p>Website: <a href="https://www.madisontevlin.com/">https://www.madisontevlin.com/</a> </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Advocacy is not just about raising awareness; it’s about creating real change.</p><p><br>Madison Tevlin is an actor, Host, Model, and Advocate. She is known for her impactful work in the "Assume That I Can" campaign for World Down Syndrome Day and her role in "Champions" alongside Woody Harrelson. Madison shares her wonderful journey and passion for music and storytelling.</p><p><br>Madison talks about her upcoming podcast, "21 Questions," featuring stars like Paris Hilton and Nelly Furtado. Madison opens up about the challenges of breaking stereotypes associated with Down syndrome and emphasizes the importance of community support in her life.</p><p><strong>Key Moments</strong></p><p><br></p><p>00:00 Multi-faceted journey</p><p>06:24 Music and family enhance wellness</p><p>17:53 Opening up about Down syndrome</p><p>22:19 Perfect fit for the roles</p><p>27:26 Redefining Stereotypes Through Storytelling</p><p>45:25 Education integration fosters community</p><p><br></p><p><strong>Connect with Madison Tevlin<br></strong>Instagram:<a href="https://www.instagram.com/madisontevlin/?hl=en">https://www.instagram.com/madisontevlin/?hl=en</a> </p><p>Website: <a href="https://www.madisontevlin.com/">https://www.madisontevlin.com/</a> </p>]]>
      </content:encoded>
      <pubDate>Tue, 26 Nov 2024 09:00:00 -0500</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/51078827/18f802ee.mp3" length="75648891" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/hTzKTwpLGktKwaDf8xHbOMUV4-5BrJpfMUKSzyD9cuc/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS8xZDMx/ZDZkNDE2MDE4OTk2/YjcxZTBjMWZjY2Iy/YjcyMC5wbmc.jpg"/>
      <itunes:duration>3140</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Advocacy is not just about raising awareness; it’s about creating real change.</p><p><br>Madison Tevlin is an actor, Host, Model, and Advocate. She is known for her impactful work in the "Assume That I Can" campaign for World Down Syndrome Day and her role in "Champions" alongside Woody Harrelson. Madison shares her wonderful journey and passion for music and storytelling.</p><p><br>Madison talks about her upcoming podcast, "21 Questions," featuring stars like Paris Hilton and Nelly Furtado. Madison opens up about the challenges of breaking stereotypes associated with Down syndrome and emphasizes the importance of community support in her life.</p><p><strong>Key Moments</strong></p><p><br></p><p>00:00 Multi-faceted journey</p><p>06:24 Music and family enhance wellness</p><p>17:53 Opening up about Down syndrome</p><p>22:19 Perfect fit for the roles</p><p>27:26 Redefining Stereotypes Through Storytelling</p><p>45:25 Education integration fosters community</p><p><br></p><p><strong>Connect with Madison Tevlin<br></strong>Instagram:<a href="https://www.instagram.com/madisontevlin/?hl=en">https://www.instagram.com/madisontevlin/?hl=en</a> </p><p>Website: <a href="https://www.madisontevlin.com/">https://www.madisontevlin.com/</a> </p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Pamela Schuller on Mastering the Balance between Vulnerability, Comedy, and Advocacy | Episode 15</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>17</itunes:episode>
      <podcast:episode>17</podcast:episode>
      <itunes:title>Pamela Schuller on Mastering the Balance between Vulnerability, Comedy, and Advocacy | Episode 15</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">ef8b0325-67e8-4d65-bb35-f0eee4cebc7e</guid>
      <link>https://share.transistor.fm/s/7ca8ba20</link>
      <description>
        <![CDATA[<p>Humor is a bridge to understanding; it transforms conversations about disability into moments of connection.</p><p><br></p><p>Pamela Schuller is a passionate disability advocate and stand-up comedian. Pamela shares her journey with Tourette syndrome and how humor has helped her tackle tough conversations about disabilities.</p><p><br>Pamela opens up about finding the right balance between vulnerability and oversharing, the challenges of accommodating disabilities in public spaces, and her unexpected shift from stand-up to storytelling. Pamela discusses the impact of her experiences on her mission to create more inclusive environments.</p><p><strong>Key Moments</strong></p><p><br></p><p>08:05 Challenging stereotypes.</p><p>14:27 Humor fosters resilience.</p><p>17:37 Goals: laughter and inclusivity.</p><p>30:53 Accepting emotions reduces judgment.</p><p>43:45 Tourette's and performance.</p><p><br></p><p><strong>Connect with Pamela Schuller<br></strong>LinkedIn: <a href="https://www.linkedin.com/in/pamelaschuller">https://www.linkedin.com/in/pamelaschuller</a> </p><p>Website: <a href="https://pamelacomedy.com/">https://pamelacomedy.com/</a> </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Humor is a bridge to understanding; it transforms conversations about disability into moments of connection.</p><p><br></p><p>Pamela Schuller is a passionate disability advocate and stand-up comedian. Pamela shares her journey with Tourette syndrome and how humor has helped her tackle tough conversations about disabilities.</p><p><br>Pamela opens up about finding the right balance between vulnerability and oversharing, the challenges of accommodating disabilities in public spaces, and her unexpected shift from stand-up to storytelling. Pamela discusses the impact of her experiences on her mission to create more inclusive environments.</p><p><strong>Key Moments</strong></p><p><br></p><p>08:05 Challenging stereotypes.</p><p>14:27 Humor fosters resilience.</p><p>17:37 Goals: laughter and inclusivity.</p><p>30:53 Accepting emotions reduces judgment.</p><p>43:45 Tourette's and performance.</p><p><br></p><p><strong>Connect with Pamela Schuller<br></strong>LinkedIn: <a href="https://www.linkedin.com/in/pamelaschuller">https://www.linkedin.com/in/pamelaschuller</a> </p><p>Website: <a href="https://pamelacomedy.com/">https://pamelacomedy.com/</a> </p>]]>
      </content:encoded>
      <pubDate>Tue, 12 Nov 2024 09:00:00 -0500</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/7ca8ba20/7a11aef4.mp3" length="90814018" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/Ld8zvTdpO-rC8TFM0H-rU9AKLKKeBKq4XaGs5c59dqQ/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9iMmFi/YTE4MWYxNDA2Mzdm/MmQ4ZGFlZGJhMTQ4/MTY5Yi5wbmc.jpg"/>
      <itunes:duration>3775</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Humor is a bridge to understanding; it transforms conversations about disability into moments of connection.</p><p><br></p><p>Pamela Schuller is a passionate disability advocate and stand-up comedian. Pamela shares her journey with Tourette syndrome and how humor has helped her tackle tough conversations about disabilities.</p><p><br>Pamela opens up about finding the right balance between vulnerability and oversharing, the challenges of accommodating disabilities in public spaces, and her unexpected shift from stand-up to storytelling. Pamela discusses the impact of her experiences on her mission to create more inclusive environments.</p><p><strong>Key Moments</strong></p><p><br></p><p>08:05 Challenging stereotypes.</p><p>14:27 Humor fosters resilience.</p><p>17:37 Goals: laughter and inclusivity.</p><p>30:53 Accepting emotions reduces judgment.</p><p>43:45 Tourette's and performance.</p><p><br></p><p><strong>Connect with Pamela Schuller<br></strong>LinkedIn: <a href="https://www.linkedin.com/in/pamelaschuller">https://www.linkedin.com/in/pamelaschuller</a> </p><p>Website: <a href="https://pamelacomedy.com/">https://pamelacomedy.com/</a> </p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Creative Ideas, Personal Brands, and the Workplace with Rachel Lowenstein | Episode 14</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>16</itunes:episode>
      <podcast:episode>16</podcast:episode>
      <itunes:title>Creative Ideas, Personal Brands, and the Workplace with Rachel Lowenstein | Episode 14</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">91cecf73-9896-4060-93ba-e3cc0092b9b3</guid>
      <link>https://share.transistor.fm/s/694b506f</link>
      <description>
        <![CDATA[<p>Rachel Lowenstein, Founder and Culture Expert at Rachel Lowenstein Consulting and Divergent Convergent, joins Lily Newton and Erin Hawley on the show. Rachel talks about why neuro-inclusion is a crucial part of workplace accessibility and how her work with Divergent Convergent is making a difference. </p><p><br>Rachel also opens up about her own experiences with finding her true identity, avoiding burnout, and shifting from a corporate job to running her own business. In this episode, Rachel shares her thoughts on creating inclusive work environments, the challenges of traditional corporate settings, and the importance of community support.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>13:41 Impact of Inclusive Marketing</p><p>26:34  Building Authentic Friendships</p><p>35:47 Mentor’s Advice: Pay It Forward</p><p>47:35 Remote Work and Inclusion</p><p><strong>Connect with Rachel Lowenstein<br></strong>LinkedIn: <a href="https://www.linkedin.com/in/rachel-lowenstein-49431a38">https://www.linkedin.com/in/rachel-lowenstein-49431a38</a></p><p>Instagram: <a href="https://www.instagram.com/rachelissan/?hl=en">https://www.instagram.com/rachelissan/?hl=en</a> </p><p>Divergent Convergent: <a href="https://parsnip-tetra-f2ny.squarespace.com/">https://parsnip-tetra-f2ny.squarespace.com/</a> </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Rachel Lowenstein, Founder and Culture Expert at Rachel Lowenstein Consulting and Divergent Convergent, joins Lily Newton and Erin Hawley on the show. Rachel talks about why neuro-inclusion is a crucial part of workplace accessibility and how her work with Divergent Convergent is making a difference. </p><p><br>Rachel also opens up about her own experiences with finding her true identity, avoiding burnout, and shifting from a corporate job to running her own business. In this episode, Rachel shares her thoughts on creating inclusive work environments, the challenges of traditional corporate settings, and the importance of community support.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>13:41 Impact of Inclusive Marketing</p><p>26:34  Building Authentic Friendships</p><p>35:47 Mentor’s Advice: Pay It Forward</p><p>47:35 Remote Work and Inclusion</p><p><strong>Connect with Rachel Lowenstein<br></strong>LinkedIn: <a href="https://www.linkedin.com/in/rachel-lowenstein-49431a38">https://www.linkedin.com/in/rachel-lowenstein-49431a38</a></p><p>Instagram: <a href="https://www.instagram.com/rachelissan/?hl=en">https://www.instagram.com/rachelissan/?hl=en</a> </p><p>Divergent Convergent: <a href="https://parsnip-tetra-f2ny.squarespace.com/">https://parsnip-tetra-f2ny.squarespace.com/</a> </p>]]>
      </content:encoded>
      <pubDate>Tue, 15 Oct 2024 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/694b506f/e6e175fa.mp3" length="109007794" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/OxHeNF0ympkQnw5jcpwmD_O_d93NrnGWZLRNilbEf-o/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS82OTRj/ZjkxOTI5NTRiMjlk/MjdjODMwOWYzMDFh/Nzc2Ni5wbmc.jpg"/>
      <itunes:duration>4534</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Rachel Lowenstein, Founder and Culture Expert at Rachel Lowenstein Consulting and Divergent Convergent, joins Lily Newton and Erin Hawley on the show. Rachel talks about why neuro-inclusion is a crucial part of workplace accessibility and how her work with Divergent Convergent is making a difference. </p><p><br>Rachel also opens up about her own experiences with finding her true identity, avoiding burnout, and shifting from a corporate job to running her own business. In this episode, Rachel shares her thoughts on creating inclusive work environments, the challenges of traditional corporate settings, and the importance of community support.</p><p><br></p><p><strong>Key Moments</strong></p><p><br></p><p>13:41 Impact of Inclusive Marketing</p><p>26:34  Building Authentic Friendships</p><p>35:47 Mentor’s Advice: Pay It Forward</p><p>47:35 Remote Work and Inclusion</p><p><strong>Connect with Rachel Lowenstein<br></strong>LinkedIn: <a href="https://www.linkedin.com/in/rachel-lowenstein-49431a38">https://www.linkedin.com/in/rachel-lowenstein-49431a38</a></p><p>Instagram: <a href="https://www.instagram.com/rachelissan/?hl=en">https://www.instagram.com/rachelissan/?hl=en</a> </p><p>Divergent Convergent: <a href="https://parsnip-tetra-f2ny.squarespace.com/">https://parsnip-tetra-f2ny.squarespace.com/</a> </p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Finding Balance and Owning Your Story with Jennifer Gasner | Episode 13</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>15</itunes:episode>
      <podcast:episode>15</podcast:episode>
      <itunes:title>Finding Balance and Owning Your Story with Jennifer Gasner | Episode 13</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1933e567-b197-4d36-b143-bfdf18afa373</guid>
      <link>https://share.transistor.fm/s/0ae78269</link>
      <description>
        <![CDATA[<p>"The journey of self-acceptance is ongoing and deeply personal."</p><p><br></p><p>Jennifer Gasner, author of *My Unexpected Life: Finding Balance Beyond My Diagnosis*,</p><p>shares her journey of self-acceptance and understanding of her own identity. She explores the importance of supportive workplaces, the power of tell your own story, and addressing misconceptions about disability.</p><p><br>Jennifer also highlights her personal growth in accepting help and fostering inclusivity. Her story is a powerful testament to self-acceptance, resilience, and the push for a more inclusive world, providing guidance for anyone navigating their own journey.</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>0:00 Jennifer Gasner’s Story </p><p>10:45 Finding Balance</p><p>20:30 Embracing Change</p><p>30:00 Breaking Barriers</p><p>45:15 Everyday Triumphs</p><p>55:00 Redefining Strength</p><p>1:05:00 Looking Forward</p><p><br></p><p><strong>Connect with Jennifer Gasner</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/jennifer-gasner-4b1aaa50/">https://www.linkedin.com/in/jennifer-gasner-4b1aaa50/</a> </p><p>Website:<a href="https://jennifergasner.com/">https://jennifergasner.com/</a> </p><p>My Unexpected Life by Jennifer Gasner: <a href="https://www.amazon.com/My-Unexpected-Life-Finding-Diagnosis/dp/B0CCCPG1ZJ">https://www.amazon.com/My-Unexpected-Life-Finding-Diagnosis/dp/B0CCCPG1ZJ</a> </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>"The journey of self-acceptance is ongoing and deeply personal."</p><p><br></p><p>Jennifer Gasner, author of *My Unexpected Life: Finding Balance Beyond My Diagnosis*,</p><p>shares her journey of self-acceptance and understanding of her own identity. She explores the importance of supportive workplaces, the power of tell your own story, and addressing misconceptions about disability.</p><p><br>Jennifer also highlights her personal growth in accepting help and fostering inclusivity. Her story is a powerful testament to self-acceptance, resilience, and the push for a more inclusive world, providing guidance for anyone navigating their own journey.</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>0:00 Jennifer Gasner’s Story </p><p>10:45 Finding Balance</p><p>20:30 Embracing Change</p><p>30:00 Breaking Barriers</p><p>45:15 Everyday Triumphs</p><p>55:00 Redefining Strength</p><p>1:05:00 Looking Forward</p><p><br></p><p><strong>Connect with Jennifer Gasner</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/jennifer-gasner-4b1aaa50/">https://www.linkedin.com/in/jennifer-gasner-4b1aaa50/</a> </p><p>Website:<a href="https://jennifergasner.com/">https://jennifergasner.com/</a> </p><p>My Unexpected Life by Jennifer Gasner: <a href="https://www.amazon.com/My-Unexpected-Life-Finding-Diagnosis/dp/B0CCCPG1ZJ">https://www.amazon.com/My-Unexpected-Life-Finding-Diagnosis/dp/B0CCCPG1ZJ</a> </p>]]>
      </content:encoded>
      <pubDate>Tue, 08 Oct 2024 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/0ae78269/0798d7b1.mp3" length="96375854" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/1DFMUvYzkYIZGJOjIcz8ccsEKoWoE0ZyfHPBhMnVIJM/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS8zMWUw/M2JmOGNhN2ZmMWY5/Y2IyYjhhZmMxNWY0/OTc1Yy5wbmc.jpg"/>
      <itunes:duration>4005</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>"The journey of self-acceptance is ongoing and deeply personal."</p><p><br></p><p>Jennifer Gasner, author of *My Unexpected Life: Finding Balance Beyond My Diagnosis*,</p><p>shares her journey of self-acceptance and understanding of her own identity. She explores the importance of supportive workplaces, the power of tell your own story, and addressing misconceptions about disability.</p><p><br>Jennifer also highlights her personal growth in accepting help and fostering inclusivity. Her story is a powerful testament to self-acceptance, resilience, and the push for a more inclusive world, providing guidance for anyone navigating their own journey.</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>0:00 Jennifer Gasner’s Story </p><p>10:45 Finding Balance</p><p>20:30 Embracing Change</p><p>30:00 Breaking Barriers</p><p>45:15 Everyday Triumphs</p><p>55:00 Redefining Strength</p><p>1:05:00 Looking Forward</p><p><br></p><p><strong>Connect with Jennifer Gasner</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/jennifer-gasner-4b1aaa50/">https://www.linkedin.com/in/jennifer-gasner-4b1aaa50/</a> </p><p>Website:<a href="https://jennifergasner.com/">https://jennifergasner.com/</a> </p><p>My Unexpected Life by Jennifer Gasner: <a href="https://www.amazon.com/My-Unexpected-Life-Finding-Diagnosis/dp/B0CCCPG1ZJ">https://www.amazon.com/My-Unexpected-Life-Finding-Diagnosis/dp/B0CCCPG1ZJ</a> </p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Amplifying Autistic Voices: Lauren Melissa Ellzey on writing, Autistic representation, and self-advocacy | Episode 12</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>14</itunes:episode>
      <podcast:episode>14</podcast:episode>
      <itunes:title>Amplifying Autistic Voices: Lauren Melissa Ellzey on writing, Autistic representation, and self-advocacy | Episode 12</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">44d4ff58-a56d-41c4-a42d-62b27b0d964e</guid>
      <link>https://share.transistor.fm/s/eb40052e</link>
      <description>
        <![CDATA[<p>Author and Activist, Lauren Melissa, shares a powerful story of resilience and creativity. Diagnosed with autism in her twenties, Lauren Melissa turned the challenges of the COVID-19 pandemic into an opportunity, hand-writing a novel that was later accepted by Bold Strokes Books. </p><p><br></p><p>Based in New York City, she passionately advocates for the representation of queer, BIPOC, and disabled individuals in fiction, bringing to life diverse, multiracial, neurodivergent, and queer characters. Her journey is a powerful testament to the strength found at the intersections of identity and creativity.</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>08:27 Getting Into Writing</p><p>16:03 Having Relatable Characters in Fiction</p><p>21:16 Portraying Neurodiversity in Fiction </p><p>25:09 Getting Published As An Independent Publisher</p><p>33:34 Advocacy on Autism, Race, and Queerness</p><p>44:12 Social Expectations, Codependence, and Autistic Identity</p><p><strong>Connect with Lauren Melissa Ellzey</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/laurenmellzey">https://www.linkedin.com/in/laurenmellzey</a> </p><p>Website: <a href="https://laurenmelissaellzey.com/">https://laurenmelissaellzey.com/</a> </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Author and Activist, Lauren Melissa, shares a powerful story of resilience and creativity. Diagnosed with autism in her twenties, Lauren Melissa turned the challenges of the COVID-19 pandemic into an opportunity, hand-writing a novel that was later accepted by Bold Strokes Books. </p><p><br></p><p>Based in New York City, she passionately advocates for the representation of queer, BIPOC, and disabled individuals in fiction, bringing to life diverse, multiracial, neurodivergent, and queer characters. Her journey is a powerful testament to the strength found at the intersections of identity and creativity.</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>08:27 Getting Into Writing</p><p>16:03 Having Relatable Characters in Fiction</p><p>21:16 Portraying Neurodiversity in Fiction </p><p>25:09 Getting Published As An Independent Publisher</p><p>33:34 Advocacy on Autism, Race, and Queerness</p><p>44:12 Social Expectations, Codependence, and Autistic Identity</p><p><strong>Connect with Lauren Melissa Ellzey</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/laurenmellzey">https://www.linkedin.com/in/laurenmellzey</a> </p><p>Website: <a href="https://laurenmelissaellzey.com/">https://laurenmelissaellzey.com/</a> </p>]]>
      </content:encoded>
      <pubDate>Tue, 17 Sep 2024 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/eb40052e/88cc70a0.mp3" length="89850786" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/lDj-6Leo9yxv_4Hy2K6RmM954-02v_fCEWBC3NNsR-o/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS8wYzFj/N2M5NmIwYjQ0NzJi/MzFkMDdkODI1Yjkx/MmE0Mi5wbmc.jpg"/>
      <itunes:duration>3736</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Author and Activist, Lauren Melissa, shares a powerful story of resilience and creativity. Diagnosed with autism in her twenties, Lauren Melissa turned the challenges of the COVID-19 pandemic into an opportunity, hand-writing a novel that was later accepted by Bold Strokes Books. </p><p><br></p><p>Based in New York City, she passionately advocates for the representation of queer, BIPOC, and disabled individuals in fiction, bringing to life diverse, multiracial, neurodivergent, and queer characters. Her journey is a powerful testament to the strength found at the intersections of identity and creativity.</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>08:27 Getting Into Writing</p><p>16:03 Having Relatable Characters in Fiction</p><p>21:16 Portraying Neurodiversity in Fiction </p><p>25:09 Getting Published As An Independent Publisher</p><p>33:34 Advocacy on Autism, Race, and Queerness</p><p>44:12 Social Expectations, Codependence, and Autistic Identity</p><p><strong>Connect with Lauren Melissa Ellzey</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/laurenmellzey">https://www.linkedin.com/in/laurenmellzey</a> </p><p>Website: <a href="https://laurenmelissaellzey.com/">https://laurenmelissaellzey.com/</a> </p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Oliver Scheier: 19-Year-Old Filmmaker, Artist, and College Sophomore | Episode 11</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>13</itunes:episode>
      <podcast:episode>13</podcast:episode>
      <itunes:title>Oliver Scheier: 19-Year-Old Filmmaker, Artist, and College Sophomore | Episode 11</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">e67792f0-b001-4fb8-bad8-5e3d2b7fdec6</guid>
      <link>https://share.transistor.fm/s/828b488f</link>
      <description>
        <![CDATA[<p>"I don't concern myself with what they get wrong. I like to just show up as myself and then let any preconceived notion, if there is any, flow like, float away”</p><p><br></p><p>Oliver Scheier, is a 19-year-old filmmaker, artist, and sophomore in college. Oliver discusses his approach to authenticity in both his work and personal life. He shares insights on his short film "Read a Page," his journey as a young artist, and how he navigates the perceptions of others.</p><p><br></p><p><strong>Key Moments</strong></p><p>00:00 Embracing individuality</p><p>13:01 Life-changing question</p><p>15:12 Gaelynn Lea's inspiring violin journey</p><p>23:54 Grateful for diverse talent support</p><p>26:59 Joy in directing, beyond acting</p><p>37:43 University program: ADHD, autism support</p><p>49:50 Educators' role in accessibility</p><p><br></p><p><strong>Connect with  Oliver Scheier</strong></p><p>Website: <a href="https://news.tulane.edu/news/tulane-freshman-muscular-dystrophy-finds-joy-and-fulfillment-campus">https://news.tulane.edu/news/tulane-freshman-muscular-dystrophy-finds-joy-and-fulfillment-campus</a> </p><p>Read a Page: <a href="https://www.youtube.com/watch?v=h9SfkFG3lL4">https://www.youtube.com/watch?v=h9SfkFG3lL4</a> </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>"I don't concern myself with what they get wrong. I like to just show up as myself and then let any preconceived notion, if there is any, flow like, float away”</p><p><br></p><p>Oliver Scheier, is a 19-year-old filmmaker, artist, and sophomore in college. Oliver discusses his approach to authenticity in both his work and personal life. He shares insights on his short film "Read a Page," his journey as a young artist, and how he navigates the perceptions of others.</p><p><br></p><p><strong>Key Moments</strong></p><p>00:00 Embracing individuality</p><p>13:01 Life-changing question</p><p>15:12 Gaelynn Lea's inspiring violin journey</p><p>23:54 Grateful for diverse talent support</p><p>26:59 Joy in directing, beyond acting</p><p>37:43 University program: ADHD, autism support</p><p>49:50 Educators' role in accessibility</p><p><br></p><p><strong>Connect with  Oliver Scheier</strong></p><p>Website: <a href="https://news.tulane.edu/news/tulane-freshman-muscular-dystrophy-finds-joy-and-fulfillment-campus">https://news.tulane.edu/news/tulane-freshman-muscular-dystrophy-finds-joy-and-fulfillment-campus</a> </p><p>Read a Page: <a href="https://www.youtube.com/watch?v=h9SfkFG3lL4">https://www.youtube.com/watch?v=h9SfkFG3lL4</a> </p>]]>
      </content:encoded>
      <pubDate>Tue, 27 Aug 2024 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/828b488f/7dc2cedb.mp3" length="79777316" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/6ABMjkbhgQT_szfORi3qzHv0v3Ab2Vd21BoVBH-ulQg/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS8zYzQ0/YjQxMjg0NzA2ZDVi/MmJmODI3MjY5Mzg5/ZDU4Yi5wbmc.jpg"/>
      <itunes:duration>3316</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>"I don't concern myself with what they get wrong. I like to just show up as myself and then let any preconceived notion, if there is any, flow like, float away”</p><p><br></p><p>Oliver Scheier, is a 19-year-old filmmaker, artist, and sophomore in college. Oliver discusses his approach to authenticity in both his work and personal life. He shares insights on his short film "Read a Page," his journey as a young artist, and how he navigates the perceptions of others.</p><p><br></p><p><strong>Key Moments</strong></p><p>00:00 Embracing individuality</p><p>13:01 Life-changing question</p><p>15:12 Gaelynn Lea's inspiring violin journey</p><p>23:54 Grateful for diverse talent support</p><p>26:59 Joy in directing, beyond acting</p><p>37:43 University program: ADHD, autism support</p><p>49:50 Educators' role in accessibility</p><p><br></p><p><strong>Connect with  Oliver Scheier</strong></p><p>Website: <a href="https://news.tulane.edu/news/tulane-freshman-muscular-dystrophy-finds-joy-and-fulfillment-campus">https://news.tulane.edu/news/tulane-freshman-muscular-dystrophy-finds-joy-and-fulfillment-campus</a> </p><p>Read a Page: <a href="https://www.youtube.com/watch?v=h9SfkFG3lL4">https://www.youtube.com/watch?v=h9SfkFG3lL4</a> </p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Understanding Disability Through Community, Books, and Shared Experiences</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>12</itunes:episode>
      <podcast:episode>12</podcast:episode>
      <itunes:title>Understanding Disability Through Community, Books, and Shared Experiences</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">b3c3befc-2101-4c46-ad04-b3c475362fdd</guid>
      <link>https://share.transistor.fm/s/48657755</link>
      <description>
        <![CDATA[<p>Your co-hosts Erin &amp; Lily have a special in-person segment for the first time ever on the podcast. They Kick things off by discussing the significance of Disability Pride Month and the joys of creating content together as friends who are both disabled.</p><p><br>They also discuss some light-hearted topics like newfound interests—Erin’s evolving relationship with pizza and Lily’s dive into the world of fantasy books, including some great disability representation in certain titles. They get real about the power of virtual friendships, especially within the disability community, and how these connections help navigate their experiences authentically.</p><p><br></p><p><strong>Timestamps</strong></p><p><br>09:19 Embracing wheelchair for comfort</p><p><br>21:02 Public perception and aging with disability</p><p><br>26:21 Masculinity, ableism, and disability</p><p><br>31:51 Susan B. Anthony's advocacy</p><p><br>35:09 Government, ableism, and organizing change</p><p><br>48:18 Theater accessibility solutions</p><p><br>52:19 Budget pushback on accessibility</p><p><br>59:55 Theater, friendships, and community<br></p><p><strong>Connect with Lily Newton</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/lily-newton-3b0b5b229">https://www.linkedin.com/in/lily-newton-3b0b5b229</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p><p><strong>Connect with Erin Hawley</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/erinhawley2">https://www.linkedin.com/in/erinhawley2</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com</a></p><p><br></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Your co-hosts Erin &amp; Lily have a special in-person segment for the first time ever on the podcast. They Kick things off by discussing the significance of Disability Pride Month and the joys of creating content together as friends who are both disabled.</p><p><br>They also discuss some light-hearted topics like newfound interests—Erin’s evolving relationship with pizza and Lily’s dive into the world of fantasy books, including some great disability representation in certain titles. They get real about the power of virtual friendships, especially within the disability community, and how these connections help navigate their experiences authentically.</p><p><br></p><p><strong>Timestamps</strong></p><p><br>09:19 Embracing wheelchair for comfort</p><p><br>21:02 Public perception and aging with disability</p><p><br>26:21 Masculinity, ableism, and disability</p><p><br>31:51 Susan B. Anthony's advocacy</p><p><br>35:09 Government, ableism, and organizing change</p><p><br>48:18 Theater accessibility solutions</p><p><br>52:19 Budget pushback on accessibility</p><p><br>59:55 Theater, friendships, and community<br></p><p><strong>Connect with Lily Newton</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/lily-newton-3b0b5b229">https://www.linkedin.com/in/lily-newton-3b0b5b229</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p><p><strong>Connect with Erin Hawley</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/erinhawley2">https://www.linkedin.com/in/erinhawley2</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com</a></p><p><br></p>]]>
      </content:encoded>
      <pubDate>Tue, 20 Aug 2024 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/48657755/dbf8506e.mp3" length="36214798" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/aviTGtYa5NsU1icfewvhkOuYSnfOKXv6f6mJKKuSRO8/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS80Njkz/ZTYyYTgyZGY2YTll/N2ViMTgxZTBlYTM4/MGY5Ni5wbmc.jpg"/>
      <itunes:duration>1504</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Your co-hosts Erin &amp; Lily have a special in-person segment for the first time ever on the podcast. They Kick things off by discussing the significance of Disability Pride Month and the joys of creating content together as friends who are both disabled.</p><p><br>They also discuss some light-hearted topics like newfound interests—Erin’s evolving relationship with pizza and Lily’s dive into the world of fantasy books, including some great disability representation in certain titles. They get real about the power of virtual friendships, especially within the disability community, and how these connections help navigate their experiences authentically.</p><p><br></p><p><strong>Timestamps</strong></p><p><br>09:19 Embracing wheelchair for comfort</p><p><br>21:02 Public perception and aging with disability</p><p><br>26:21 Masculinity, ableism, and disability</p><p><br>31:51 Susan B. Anthony's advocacy</p><p><br>35:09 Government, ableism, and organizing change</p><p><br>48:18 Theater accessibility solutions</p><p><br>52:19 Budget pushback on accessibility</p><p><br>59:55 Theater, friendships, and community<br></p><p><strong>Connect with Lily Newton</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/lily-newton-3b0b5b229">https://www.linkedin.com/in/lily-newton-3b0b5b229</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p><p><strong>Connect with Erin Hawley</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/erinhawley2">https://www.linkedin.com/in/erinhawley2</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com</a></p><p><br></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Redefining Accessibility: Jenna Bainbridge’s Impact on Theater and Disability Representation | Episode 10</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>11</itunes:episode>
      <podcast:episode>11</podcast:episode>
      <itunes:title>Redefining Accessibility: Jenna Bainbridge’s Impact on Theater and Disability Representation | Episode 10</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1499a1f8-0df2-4d27-b0f3-f3b4d74456a5</guid>
      <link>https://share.transistor.fm/s/efcae4e6</link>
      <description>
        <![CDATA[<p>In this episode, hosts Erin and Lily interview Jenna Bainbridge, an actress, singer, and accessibility advocate. Jenna shares her journey as the first wheelchair user to perform in a new musical on Broadway, debuting in the award-winning "Suffs." She discusses her career and daily life as an ambulatory wheelchair user, challenging misconceptions and emphasizing the importance of accessibility and personal freedom.</p><p><br></p><p>Jenna explains how her wheelchair enhances her ability to navigate New York City, offering independence in an often inaccessible environment. She highlights the spectrum of capabilities and needs, breaking down binary views of disability. Her role in "Suffs" underscores the power of collective activism and the importance of every action in contributing to a larger movement.</p><p><br></p><p>The episode also touches on Jenna's work with Consultability, a consulting company she co-founded to make theater spaces more accessible. Her experiences offer a rich discussion on the intersections of art, disability, and advocacy, providing listeners with a deeper understanding of inclusivity's importance in all areas of life.</p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Wheelchair allows freedom and less exhaustion.</p><p><br></p><p>09:19 Embracing wheelchair use for everyday comfort.</p><p><br></p><p>12:06 Navigating public perception of disability is exhausting.</p><p><br></p><p>21:02 Disability euphemisms conceal the reality of aging.</p><p><br></p><p>26:21 Masculinity and ableism </p><p><br></p><p>31:51 Susan B. Anthony's advocacy, protests, and power.</p><p><br></p><p>35:09 Messy government, ableist viewpoints, organizing for change.</p><p><br></p><p>43:06 Inclusion in SUFFs provides representation for disabilities.</p><p><br></p><p>48:18 Theater accessibility efforts focus on practical solutions.</p><p><br></p><p>52:19 Budget pushback about accessibility improvements. </p><p><br></p><p>59:55 Theater creates close friendships and community quickly.</p><p><br></p><p>01:01:42 Interview wrap-up </p><p><strong>Connect with Jenna Bainbridge</strong></p><p>Instagram: <a href="https://www.instagram.com/bainbridgejenna/?hl=en">https://www.instagram.com/bainbridgejenna/?hl=en</a></p><p>Website: <a href="https://www.jennabainbridge.com/">https://www.jennabainbridge.com/</a></p><p>Suff the Musical: <a href="https://suffsmusical.com/">https://suffsmusical.com/</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this episode, hosts Erin and Lily interview Jenna Bainbridge, an actress, singer, and accessibility advocate. Jenna shares her journey as the first wheelchair user to perform in a new musical on Broadway, debuting in the award-winning "Suffs." She discusses her career and daily life as an ambulatory wheelchair user, challenging misconceptions and emphasizing the importance of accessibility and personal freedom.</p><p><br></p><p>Jenna explains how her wheelchair enhances her ability to navigate New York City, offering independence in an often inaccessible environment. She highlights the spectrum of capabilities and needs, breaking down binary views of disability. Her role in "Suffs" underscores the power of collective activism and the importance of every action in contributing to a larger movement.</p><p><br></p><p>The episode also touches on Jenna's work with Consultability, a consulting company she co-founded to make theater spaces more accessible. Her experiences offer a rich discussion on the intersections of art, disability, and advocacy, providing listeners with a deeper understanding of inclusivity's importance in all areas of life.</p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Wheelchair allows freedom and less exhaustion.</p><p><br></p><p>09:19 Embracing wheelchair use for everyday comfort.</p><p><br></p><p>12:06 Navigating public perception of disability is exhausting.</p><p><br></p><p>21:02 Disability euphemisms conceal the reality of aging.</p><p><br></p><p>26:21 Masculinity and ableism </p><p><br></p><p>31:51 Susan B. Anthony's advocacy, protests, and power.</p><p><br></p><p>35:09 Messy government, ableist viewpoints, organizing for change.</p><p><br></p><p>43:06 Inclusion in SUFFs provides representation for disabilities.</p><p><br></p><p>48:18 Theater accessibility efforts focus on practical solutions.</p><p><br></p><p>52:19 Budget pushback about accessibility improvements. </p><p><br></p><p>59:55 Theater creates close friendships and community quickly.</p><p><br></p><p>01:01:42 Interview wrap-up </p><p><strong>Connect with Jenna Bainbridge</strong></p><p>Instagram: <a href="https://www.instagram.com/bainbridgejenna/?hl=en">https://www.instagram.com/bainbridgejenna/?hl=en</a></p><p>Website: <a href="https://www.jennabainbridge.com/">https://www.jennabainbridge.com/</a></p><p>Suff the Musical: <a href="https://suffsmusical.com/">https://suffsmusical.com/</a></p>]]>
      </content:encoded>
      <pubDate>Tue, 06 Aug 2024 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/efcae4e6/28dbdf62.mp3" length="93849035" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/bNdoWqU2rbLCFXvAloBxo6n5vqZPc06kUIffLwcelvM/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS81MmRk/NWU3ZDlhYWIxMTE3/NTk1ZWYyNmI3OTEx/ZjlhOC5wbmc.jpg"/>
      <itunes:duration>3901</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this episode, hosts Erin and Lily interview Jenna Bainbridge, an actress, singer, and accessibility advocate. Jenna shares her journey as the first wheelchair user to perform in a new musical on Broadway, debuting in the award-winning "Suffs." She discusses her career and daily life as an ambulatory wheelchair user, challenging misconceptions and emphasizing the importance of accessibility and personal freedom.</p><p><br></p><p>Jenna explains how her wheelchair enhances her ability to navigate New York City, offering independence in an often inaccessible environment. She highlights the spectrum of capabilities and needs, breaking down binary views of disability. Her role in "Suffs" underscores the power of collective activism and the importance of every action in contributing to a larger movement.</p><p><br></p><p>The episode also touches on Jenna's work with Consultability, a consulting company she co-founded to make theater spaces more accessible. Her experiences offer a rich discussion on the intersections of art, disability, and advocacy, providing listeners with a deeper understanding of inclusivity's importance in all areas of life.</p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Wheelchair allows freedom and less exhaustion.</p><p><br></p><p>09:19 Embracing wheelchair use for everyday comfort.</p><p><br></p><p>12:06 Navigating public perception of disability is exhausting.</p><p><br></p><p>21:02 Disability euphemisms conceal the reality of aging.</p><p><br></p><p>26:21 Masculinity and ableism </p><p><br></p><p>31:51 Susan B. Anthony's advocacy, protests, and power.</p><p><br></p><p>35:09 Messy government, ableist viewpoints, organizing for change.</p><p><br></p><p>43:06 Inclusion in SUFFs provides representation for disabilities.</p><p><br></p><p>48:18 Theater accessibility efforts focus on practical solutions.</p><p><br></p><p>52:19 Budget pushback about accessibility improvements. </p><p><br></p><p>59:55 Theater creates close friendships and community quickly.</p><p><br></p><p>01:01:42 Interview wrap-up </p><p><strong>Connect with Jenna Bainbridge</strong></p><p>Instagram: <a href="https://www.instagram.com/bainbridgejenna/?hl=en">https://www.instagram.com/bainbridgejenna/?hl=en</a></p><p>Website: <a href="https://www.jennabainbridge.com/">https://www.jennabainbridge.com/</a></p><p>Suff the Musical: <a href="https://suffsmusical.com/">https://suffsmusical.com/</a></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Just Between Us: Disability Pride Month</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>10</itunes:episode>
      <podcast:episode>10</podcast:episode>
      <itunes:title>Just Between Us: Disability Pride Month</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1e2f21d3-65c1-47ad-b696-c729d00b5f8f</guid>
      <link>https://share.transistor.fm/s/4c82b05d</link>
      <description>
        <![CDATA[<p>Your co-hosts Erin &amp; Lily have a special segment today called “Just Between Us!” Today’s episode is all about the importance of Disability Pride Month. They share their thoughts on why it's crucial to celebrate being disabled and not just focus on ableism. Erin &amp; Lily also discuss how pride in their identities as disabled people and as friends empowers them. </p><p><br></p><p>We hope you enjoy today’s real (and unfiltered) episode. Happy Disability Pride Month!</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>04:06 Claiming pride in queer and disabled identity.</p><p>06:46 I understand the need to educate, but...</p><p>13:14 Navigating disability pride in online content.</p><p>14:12 Discussion on sharing disabled experiences and challenges.</p><p>18:06 Experience of cultural recognition.</p><p>21:38 Embracing disability pride, simplifying routines for ease.</p><p>28:25 Being proud of oneself fights ableism.</p><p><br></p><p><strong>Connect with Lily Newton</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/lily-newton-3b0b5b229">https://www.linkedin.com/in/lily-newton-3b0b5b229</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p><p><strong>Connect with Erin Hawley</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/erinhawley2">https://www.linkedin.com/in/erinhawley2</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Your co-hosts Erin &amp; Lily have a special segment today called “Just Between Us!” Today’s episode is all about the importance of Disability Pride Month. They share their thoughts on why it's crucial to celebrate being disabled and not just focus on ableism. Erin &amp; Lily also discuss how pride in their identities as disabled people and as friends empowers them. </p><p><br></p><p>We hope you enjoy today’s real (and unfiltered) episode. Happy Disability Pride Month!</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>04:06 Claiming pride in queer and disabled identity.</p><p>06:46 I understand the need to educate, but...</p><p>13:14 Navigating disability pride in online content.</p><p>14:12 Discussion on sharing disabled experiences and challenges.</p><p>18:06 Experience of cultural recognition.</p><p>21:38 Embracing disability pride, simplifying routines for ease.</p><p>28:25 Being proud of oneself fights ableism.</p><p><br></p><p><strong>Connect with Lily Newton</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/lily-newton-3b0b5b229">https://www.linkedin.com/in/lily-newton-3b0b5b229</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p><p><strong>Connect with Erin Hawley</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/erinhawley2">https://www.linkedin.com/in/erinhawley2</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p>]]>
      </content:encoded>
      <pubDate>Wed, 31 Jul 2024 11:05:42 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/4c82b05d/f33221db.mp3" length="48122190" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/l5NDGcz4lKhFnsmD-l6G26jMuSDL8SmPsElezp7eh7U/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS82YTJj/Zjg3YWFhNDhkZWU4/NWQxODk4YjNjM2Jl/OWY5OS5wbmc.jpg"/>
      <itunes:duration>2002</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Your co-hosts Erin &amp; Lily have a special segment today called “Just Between Us!” Today’s episode is all about the importance of Disability Pride Month. They share their thoughts on why it's crucial to celebrate being disabled and not just focus on ableism. Erin &amp; Lily also discuss how pride in their identities as disabled people and as friends empowers them. </p><p><br></p><p>We hope you enjoy today’s real (and unfiltered) episode. Happy Disability Pride Month!</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>04:06 Claiming pride in queer and disabled identity.</p><p>06:46 I understand the need to educate, but...</p><p>13:14 Navigating disability pride in online content.</p><p>14:12 Discussion on sharing disabled experiences and challenges.</p><p>18:06 Experience of cultural recognition.</p><p>21:38 Embracing disability pride, simplifying routines for ease.</p><p>28:25 Being proud of oneself fights ableism.</p><p><br></p><p><strong>Connect with Lily Newton</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/lily-newton-3b0b5b229">https://www.linkedin.com/in/lily-newton-3b0b5b229</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p><p><strong>Connect with Erin Hawley</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/erinhawley2">https://www.linkedin.com/in/erinhawley2</a></p><p>Website: <a href="https://www.easterseals.com/">https://www.easterseals.com/</a></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Amanda McGrory’s Insights on Adaptive Sports and Community on EYK | Episode 9</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>9</itunes:episode>
      <podcast:episode>9</podcast:episode>
      <itunes:title>Amanda McGrory’s Insights on Adaptive Sports and Community on EYK | Episode 9</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">c3d38e48-5d5a-4792-a7a6-5928a9d15963</guid>
      <link>https://share.transistor.fm/s/2477205c</link>
      <description>
        <![CDATA[<p>Amanda McGrory, a four-time Paralympian and seven-time Paralympic medalist shares her journey as an elite athlete. She addresses the pervasive stereotypes and misconceptions surrounding disabled athletes and how they are often misrepresented in the media.</p><p><br></p><p>Throughout the conversation, the importance of authentic representation in media and sports is highlighted, focusing on the significance of community support. She discusses her struggles with eating disorders and finding community through adaptive sports.</p><p><br></p><p>Amanda discusses the critical need for authentic representation in sports and media, highlighting how real portrayals can create a more inclusive society. Her insights reveal that being a disabled athlete is just one facet of her multifaceted identity. Amanda advocates for a broader recognition of the everyday achievements of people with disabilities without sensationalism.</p><p><br></p><p>Erin, Lily, and Amanda discuss disability pride and the power of community. Amanda shares about the lack of control she felt as a child and how that led to her struggles with eating. They talk about the power of finding community with other disabled people and how finding adaptive sports brought Amanda the community that led her to her own healing and sense of pride in her identity. </p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>08:53 Amanda’s athletic career trajectory.</p><p><br></p><p>12:19 Athletes and inspiration are both complex issues.</p><p><br></p><p>19:21 Realizing potential through disability and the inspiration narrative.</p><p><br></p><p>24:55 The harm of overcoming narratives, Disability Pride Month.</p><p><br></p><p>31:14 Amanda’s unexpected career in broadcasting.</p><p><br></p><p>34:12 Lived experience is crucial for understanding disability.</p><p><br></p><p>39:15 Amanda’s experience struggling with eating, finding support, and control.</p><p><br></p><p>48:57 Airline staff often disregard the needs of disabled passengers.</p><p><br></p><p>54:37 The importance of disability history.</p><p><br></p><p>57:16 University of Illinois Galesburg campus program summary.</p><p><br></p><p>01:02:18 Emphasizing the importance of accessibility, University of Illinois Accessibility</p><p><strong>Connect with Amanda McGrory</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/amanda-mcgrory">https://www.linkedin.com/in/amanda-mcgrory</a></p><p>Instagram: <a href="http://www.instagram.com/alittlechipped/?hl=en">https://www.instagram.com/alittlechipped/?hl=en</a></p><p>Website: <a href="http://www.amandamcgrory.com/">http://www.amandamcgrory.com/</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Amanda McGrory, a four-time Paralympian and seven-time Paralympic medalist shares her journey as an elite athlete. She addresses the pervasive stereotypes and misconceptions surrounding disabled athletes and how they are often misrepresented in the media.</p><p><br></p><p>Throughout the conversation, the importance of authentic representation in media and sports is highlighted, focusing on the significance of community support. She discusses her struggles with eating disorders and finding community through adaptive sports.</p><p><br></p><p>Amanda discusses the critical need for authentic representation in sports and media, highlighting how real portrayals can create a more inclusive society. Her insights reveal that being a disabled athlete is just one facet of her multifaceted identity. Amanda advocates for a broader recognition of the everyday achievements of people with disabilities without sensationalism.</p><p><br></p><p>Erin, Lily, and Amanda discuss disability pride and the power of community. Amanda shares about the lack of control she felt as a child and how that led to her struggles with eating. They talk about the power of finding community with other disabled people and how finding adaptive sports brought Amanda the community that led her to her own healing and sense of pride in her identity. </p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>08:53 Amanda’s athletic career trajectory.</p><p><br></p><p>12:19 Athletes and inspiration are both complex issues.</p><p><br></p><p>19:21 Realizing potential through disability and the inspiration narrative.</p><p><br></p><p>24:55 The harm of overcoming narratives, Disability Pride Month.</p><p><br></p><p>31:14 Amanda’s unexpected career in broadcasting.</p><p><br></p><p>34:12 Lived experience is crucial for understanding disability.</p><p><br></p><p>39:15 Amanda’s experience struggling with eating, finding support, and control.</p><p><br></p><p>48:57 Airline staff often disregard the needs of disabled passengers.</p><p><br></p><p>54:37 The importance of disability history.</p><p><br></p><p>57:16 University of Illinois Galesburg campus program summary.</p><p><br></p><p>01:02:18 Emphasizing the importance of accessibility, University of Illinois Accessibility</p><p><strong>Connect with Amanda McGrory</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/amanda-mcgrory">https://www.linkedin.com/in/amanda-mcgrory</a></p><p>Instagram: <a href="http://www.instagram.com/alittlechipped/?hl=en">https://www.instagram.com/alittlechipped/?hl=en</a></p><p>Website: <a href="http://www.amandamcgrory.com/">http://www.amandamcgrory.com/</a></p>]]>
      </content:encoded>
      <pubDate>Tue, 23 Jul 2024 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/2477205c/c32581fd.mp3" length="91593443" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/iBeFPg2x-oRpewiEmTv-p_vQx50E4FlRL7A2i9MeoYo/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9mY2Jh/MzM1YWQxNWNkNGI3/NTFmNzc5Zjk1ZmMy/YWRhOS5wbmc.jpg"/>
      <itunes:duration>3807</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Amanda McGrory, a four-time Paralympian and seven-time Paralympic medalist shares her journey as an elite athlete. She addresses the pervasive stereotypes and misconceptions surrounding disabled athletes and how they are often misrepresented in the media.</p><p><br></p><p>Throughout the conversation, the importance of authentic representation in media and sports is highlighted, focusing on the significance of community support. She discusses her struggles with eating disorders and finding community through adaptive sports.</p><p><br></p><p>Amanda discusses the critical need for authentic representation in sports and media, highlighting how real portrayals can create a more inclusive society. Her insights reveal that being a disabled athlete is just one facet of her multifaceted identity. Amanda advocates for a broader recognition of the everyday achievements of people with disabilities without sensationalism.</p><p><br></p><p>Erin, Lily, and Amanda discuss disability pride and the power of community. Amanda shares about the lack of control she felt as a child and how that led to her struggles with eating. They talk about the power of finding community with other disabled people and how finding adaptive sports brought Amanda the community that led her to her own healing and sense of pride in her identity. </p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>08:53 Amanda’s athletic career trajectory.</p><p><br></p><p>12:19 Athletes and inspiration are both complex issues.</p><p><br></p><p>19:21 Realizing potential through disability and the inspiration narrative.</p><p><br></p><p>24:55 The harm of overcoming narratives, Disability Pride Month.</p><p><br></p><p>31:14 Amanda’s unexpected career in broadcasting.</p><p><br></p><p>34:12 Lived experience is crucial for understanding disability.</p><p><br></p><p>39:15 Amanda’s experience struggling with eating, finding support, and control.</p><p><br></p><p>48:57 Airline staff often disregard the needs of disabled passengers.</p><p><br></p><p>54:37 The importance of disability history.</p><p><br></p><p>57:16 University of Illinois Galesburg campus program summary.</p><p><br></p><p>01:02:18 Emphasizing the importance of accessibility, University of Illinois Accessibility</p><p><strong>Connect with Amanda McGrory</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/amanda-mcgrory">https://www.linkedin.com/in/amanda-mcgrory</a></p><p>Instagram: <a href="http://www.instagram.com/alittlechipped/?hl=en">https://www.instagram.com/alittlechipped/?hl=en</a></p><p>Website: <a href="http://www.amandamcgrory.com/">http://www.amandamcgrory.com/</a></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Learning Self-Love: Chelsea Bear Discusses Disability Pride Month on EYK | Episode 8</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>8</itunes:episode>
      <podcast:episode>8</podcast:episode>
      <itunes:title>Learning Self-Love: Chelsea Bear Discusses Disability Pride Month on EYK | Episode 8</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">3f7a5ea3-44ea-4b04-aaed-5c17a2c38065</guid>
      <link>https://share.transistor.fm/s/c80562ce</link>
      <description>
        <![CDATA[<p>In this episode, Chelsea Bear, a content creator and disability advocate, shares her experiences and challenges as a lifestyle influencer. Chelsea highlights the importance of embracing her disability wholeheartedly and the sense of community and validation it brings. She discusses how Disability Pride Month encourages individuals to own their disabilities proudly, even on tough days.</p><p><br></p><p>The co-hosts Erin and Lily resonate with Chelsea's experiences, sharing their struggles and triumphs in accepting their disabilities, while emphasizing the transformative power of community and shared experiences.</p><p><br></p><p>The episode showcases Chelsea's impactful transition from a public relations professional to a dynamic social media advocate. Her authentic and organic approach to content creation, driven by personal stories and unfiltered passion, sets her apart. Chelsea candidly discusses the pressures of being a disability advocate and the balance between addressing systemic issues and sharing her narrative.</p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Intros and Audio Descriptions</p><p>03:39 Addressing assumptions about living with physical disability.</p><p>08:24 PR career taught communication and brand values.</p><p>11:45 Creating social content to connect and share.</p><p>15:41 Pressure to advocate for disabilities in lifestyle.</p><p>17:29 Learning journey, advocacy, spread awareness, disability, daily impact.</p><p>20:34 Discussion on disability experience and authenticity concern.</p><p>24:25 Welcoming community addressing accessibility and disabilities.</p><p>29:20 Accepting disability empowers connection and self-worth.</p><p>30:50 Taking ownership of identity leads to pride.</p><p>36:38 Social media expanded my disability community connections.</p><p>38:29 Social media can connect and empower people.</p><p>42:37 Learning to navigate health challenges with openness.</p><p>45:53 Medical schools need to be more inclusive.</p><p>49:56 Embracing disability transformed my life positively.</p><p><br></p><p><strong>Connect with Chelsea Bear</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/chelseabear/">https://www.linkedin.com/in/chelseabear/</a> </p><p>Instagram: <a href="https://www.instagram.com/realchelseabear/?hl=en">https://www.instagram.com/realchelseabear/?hl=en</a> </p><p>Website: <a href="https://chelseabear.com/">https://chelseabear.com/</a> </p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this episode, Chelsea Bear, a content creator and disability advocate, shares her experiences and challenges as a lifestyle influencer. Chelsea highlights the importance of embracing her disability wholeheartedly and the sense of community and validation it brings. She discusses how Disability Pride Month encourages individuals to own their disabilities proudly, even on tough days.</p><p><br></p><p>The co-hosts Erin and Lily resonate with Chelsea's experiences, sharing their struggles and triumphs in accepting their disabilities, while emphasizing the transformative power of community and shared experiences.</p><p><br></p><p>The episode showcases Chelsea's impactful transition from a public relations professional to a dynamic social media advocate. Her authentic and organic approach to content creation, driven by personal stories and unfiltered passion, sets her apart. Chelsea candidly discusses the pressures of being a disability advocate and the balance between addressing systemic issues and sharing her narrative.</p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Intros and Audio Descriptions</p><p>03:39 Addressing assumptions about living with physical disability.</p><p>08:24 PR career taught communication and brand values.</p><p>11:45 Creating social content to connect and share.</p><p>15:41 Pressure to advocate for disabilities in lifestyle.</p><p>17:29 Learning journey, advocacy, spread awareness, disability, daily impact.</p><p>20:34 Discussion on disability experience and authenticity concern.</p><p>24:25 Welcoming community addressing accessibility and disabilities.</p><p>29:20 Accepting disability empowers connection and self-worth.</p><p>30:50 Taking ownership of identity leads to pride.</p><p>36:38 Social media expanded my disability community connections.</p><p>38:29 Social media can connect and empower people.</p><p>42:37 Learning to navigate health challenges with openness.</p><p>45:53 Medical schools need to be more inclusive.</p><p>49:56 Embracing disability transformed my life positively.</p><p><br></p><p><strong>Connect with Chelsea Bear</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/chelseabear/">https://www.linkedin.com/in/chelseabear/</a> </p><p>Instagram: <a href="https://www.instagram.com/realchelseabear/?hl=en">https://www.instagram.com/realchelseabear/?hl=en</a> </p><p>Website: <a href="https://chelseabear.com/">https://chelseabear.com/</a> </p>]]>
      </content:encoded>
      <pubDate>Tue, 09 Jul 2024 09:36:18 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/c80562ce/0919e8ce.mp3" length="63861234" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/d1s_Lvbe5X_3ZhAghTER6cBylwPni3EVmAlAjdMBpGI/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9mNGQ3/YzUzNmU4YjdiZmRm/ZWEzNTY0ZjYwYjlj/MjM3Ni5wbmc.jpg"/>
      <itunes:duration>3207</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this episode, Chelsea Bear, a content creator and disability advocate, shares her experiences and challenges as a lifestyle influencer. Chelsea highlights the importance of embracing her disability wholeheartedly and the sense of community and validation it brings. She discusses how Disability Pride Month encourages individuals to own their disabilities proudly, even on tough days.</p><p><br></p><p>The co-hosts Erin and Lily resonate with Chelsea's experiences, sharing their struggles and triumphs in accepting their disabilities, while emphasizing the transformative power of community and shared experiences.</p><p><br></p><p>The episode showcases Chelsea's impactful transition from a public relations professional to a dynamic social media advocate. Her authentic and organic approach to content creation, driven by personal stories and unfiltered passion, sets her apart. Chelsea candidly discusses the pressures of being a disability advocate and the balance between addressing systemic issues and sharing her narrative.</p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Intros and Audio Descriptions</p><p>03:39 Addressing assumptions about living with physical disability.</p><p>08:24 PR career taught communication and brand values.</p><p>11:45 Creating social content to connect and share.</p><p>15:41 Pressure to advocate for disabilities in lifestyle.</p><p>17:29 Learning journey, advocacy, spread awareness, disability, daily impact.</p><p>20:34 Discussion on disability experience and authenticity concern.</p><p>24:25 Welcoming community addressing accessibility and disabilities.</p><p>29:20 Accepting disability empowers connection and self-worth.</p><p>30:50 Taking ownership of identity leads to pride.</p><p>36:38 Social media expanded my disability community connections.</p><p>38:29 Social media can connect and empower people.</p><p>42:37 Learning to navigate health challenges with openness.</p><p>45:53 Medical schools need to be more inclusive.</p><p>49:56 Embracing disability transformed my life positively.</p><p><br></p><p><strong>Connect with Chelsea Bear</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/chelseabear/">https://www.linkedin.com/in/chelseabear/</a> </p><p>Instagram: <a href="https://www.instagram.com/realchelseabear/?hl=en">https://www.instagram.com/realchelseabear/?hl=en</a> </p><p>Website: <a href="https://chelseabear.com/">https://chelseabear.com/</a> </p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Adventures Around the World: Cory Lee on Accessible Travel and Advocacy on EYK | Episode 7</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>7</itunes:episode>
      <podcast:episode>7</podcast:episode>
      <itunes:title>Adventures Around the World: Cory Lee on Accessible Travel and Advocacy on EYK | Episode 7</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">764a21dc-fbad-4590-b201-781c32ed6e77</guid>
      <link>https://share.transistor.fm/s/0a673a3e</link>
      <description>
        <![CDATA[<p>In this episode, Cory shares his experiences exploring the world as a wheelchair user, from group trips to international destinations to navigating the challenges of air travel accessibility. Learn about Cory’s blog, Curb Free with Cory Lee, and its company non-profit, The Curb Free Foundation, which funds dream trips for wheelchair users. Discover practical tips on accessible travel planning, insights on preparing for travel obstacles, and the importance of building a strong community for people with disabilities. </p><p><br></p><p>Cory also talks about his children's books that feature characters with disabilities, aiming to educate and promote inclusivity among young readers. </p><p><br></p><p>Don't miss hearing Cory's positive travel experiences and the joy of accessible tourism. </p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Cory’s work includes a children's book and foundation.</p><p><br></p><p>03:34 Public disregard for me becomes increasingly unsettling.</p><p><br></p><p>09:24 Excited traveler faces job rejection, plans trip.</p><p><br></p><p>10:41 Lack of travel info inspired Curb Free with Cory Lee blog</p><p><br></p><p>14:34 Launched the Curb Free Foundation in 2022.</p><p><br></p><p>17:41 Promote travel to more accessible destinations.</p><p><br></p><p>23:04 Book promotes wheelchair travel and representation for children.</p><p><br></p><p>24:24 Children's books shape perception and combat ableist stereotypes.</p><p><br></p><p>29:40 Wheelchair broke, duct taped, urged DOT report.</p><p><br></p><p>32:24 Air travel for wheelchair users is improving.</p><p><br></p><p>34:17 Switzerland trip with incredible accessibility experiences.</p><p><br></p><p>38:15 Wheelchair user plans trips 6-12 months ahead.</p><p><br></p><p>40:14 Double-sided Velcro and Able Sling improve transfers.</p><p><br></p><p>45:12 Community brings joy and understanding to members.</p><p><br></p><p>47:18 Advocate for visibility and living full lives.</p><p><br></p><p>51:30 Travel insurance with preexisting conditions saves money.</p><p><br></p><p><strong>Connect with Cory Lee</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/cory-lee/">https://www.linkedin.com/in/cory-lee/</a></p><p>Instagram: <a href="https://www.instagram.com/curbfreecorylee/?hl=en">https://www.instagram.com/curbfreecorylee/?hl=en</a></p><p>Website: <a href="https://curbfreewithcorylee.com/">https://curbfreewithcorylee.com/</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this episode, Cory shares his experiences exploring the world as a wheelchair user, from group trips to international destinations to navigating the challenges of air travel accessibility. Learn about Cory’s blog, Curb Free with Cory Lee, and its company non-profit, The Curb Free Foundation, which funds dream trips for wheelchair users. Discover practical tips on accessible travel planning, insights on preparing for travel obstacles, and the importance of building a strong community for people with disabilities. </p><p><br></p><p>Cory also talks about his children's books that feature characters with disabilities, aiming to educate and promote inclusivity among young readers. </p><p><br></p><p>Don't miss hearing Cory's positive travel experiences and the joy of accessible tourism. </p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Cory’s work includes a children's book and foundation.</p><p><br></p><p>03:34 Public disregard for me becomes increasingly unsettling.</p><p><br></p><p>09:24 Excited traveler faces job rejection, plans trip.</p><p><br></p><p>10:41 Lack of travel info inspired Curb Free with Cory Lee blog</p><p><br></p><p>14:34 Launched the Curb Free Foundation in 2022.</p><p><br></p><p>17:41 Promote travel to more accessible destinations.</p><p><br></p><p>23:04 Book promotes wheelchair travel and representation for children.</p><p><br></p><p>24:24 Children's books shape perception and combat ableist stereotypes.</p><p><br></p><p>29:40 Wheelchair broke, duct taped, urged DOT report.</p><p><br></p><p>32:24 Air travel for wheelchair users is improving.</p><p><br></p><p>34:17 Switzerland trip with incredible accessibility experiences.</p><p><br></p><p>38:15 Wheelchair user plans trips 6-12 months ahead.</p><p><br></p><p>40:14 Double-sided Velcro and Able Sling improve transfers.</p><p><br></p><p>45:12 Community brings joy and understanding to members.</p><p><br></p><p>47:18 Advocate for visibility and living full lives.</p><p><br></p><p>51:30 Travel insurance with preexisting conditions saves money.</p><p><br></p><p><strong>Connect with Cory Lee</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/cory-lee/">https://www.linkedin.com/in/cory-lee/</a></p><p>Instagram: <a href="https://www.instagram.com/curbfreecorylee/?hl=en">https://www.instagram.com/curbfreecorylee/?hl=en</a></p><p>Website: <a href="https://curbfreewithcorylee.com/">https://curbfreewithcorylee.com/</a></p>]]>
      </content:encoded>
      <pubDate>Tue, 25 Jun 2024 09:53:05 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/0a673a3e/709083e9.mp3" length="55331836" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/jeF3JFytGyCyYSrzqC1ma1iFmVJ9dtZ6tEE1iresYpw/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS8wMzUy/ODNiZjg4ODllNDRj/MjM3NjVlZGNlM2I0/MmIyZS5wbmc.jpg"/>
      <itunes:duration>3454</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this episode, Cory shares his experiences exploring the world as a wheelchair user, from group trips to international destinations to navigating the challenges of air travel accessibility. Learn about Cory’s blog, Curb Free with Cory Lee, and its company non-profit, The Curb Free Foundation, which funds dream trips for wheelchair users. Discover practical tips on accessible travel planning, insights on preparing for travel obstacles, and the importance of building a strong community for people with disabilities. </p><p><br></p><p>Cory also talks about his children's books that feature characters with disabilities, aiming to educate and promote inclusivity among young readers. </p><p><br></p><p>Don't miss hearing Cory's positive travel experiences and the joy of accessible tourism. </p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Cory’s work includes a children's book and foundation.</p><p><br></p><p>03:34 Public disregard for me becomes increasingly unsettling.</p><p><br></p><p>09:24 Excited traveler faces job rejection, plans trip.</p><p><br></p><p>10:41 Lack of travel info inspired Curb Free with Cory Lee blog</p><p><br></p><p>14:34 Launched the Curb Free Foundation in 2022.</p><p><br></p><p>17:41 Promote travel to more accessible destinations.</p><p><br></p><p>23:04 Book promotes wheelchair travel and representation for children.</p><p><br></p><p>24:24 Children's books shape perception and combat ableist stereotypes.</p><p><br></p><p>29:40 Wheelchair broke, duct taped, urged DOT report.</p><p><br></p><p>32:24 Air travel for wheelchair users is improving.</p><p><br></p><p>34:17 Switzerland trip with incredible accessibility experiences.</p><p><br></p><p>38:15 Wheelchair user plans trips 6-12 months ahead.</p><p><br></p><p>40:14 Double-sided Velcro and Able Sling improve transfers.</p><p><br></p><p>45:12 Community brings joy and understanding to members.</p><p><br></p><p>47:18 Advocate for visibility and living full lives.</p><p><br></p><p>51:30 Travel insurance with preexisting conditions saves money.</p><p><br></p><p><strong>Connect with Cory Lee</strong></p><p>LinkedIn: <a href="https://www.linkedin.com/in/cory-lee/">https://www.linkedin.com/in/cory-lee/</a></p><p>Instagram: <a href="https://www.instagram.com/curbfreecorylee/?hl=en">https://www.instagram.com/curbfreecorylee/?hl=en</a></p><p>Website: <a href="https://curbfreewithcorylee.com/">https://curbfreewithcorylee.com/</a></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Redefining Queer Spaces: Spencer West | Episode 6</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>6</itunes:episode>
      <podcast:episode>6</podcast:episode>
      <itunes:title>Redefining Queer Spaces: Spencer West | Episode 6</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d02baa85-58c1-445c-b741-e9637b5c5293</guid>
      <link>https://share.transistor.fm/s/9cf7cfb1</link>
      <description>
        <![CDATA[<p>In today’s episode, we have Spencer West! From discussing the challenges of accessing queer spaces and nightlife to setting boundaries as a disabled content creator, this conversation sheds light on pivotal issues affecting the LGBTQ+ and disabled communities. </p><p><br></p><p>Spencer shares his personal experiences, advocacy work, and the role of social media in promoting awareness.</p><p><br></p><p>Don't miss this engaging episode with Spencer West!</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Spencer West: Keynote speaker, activist, trailblazer, author.</p><p><br></p><p>06:00 Navigating intersectional identities and privacy boundaries on TikTok.</p><p><br></p><p>12:47 The importance of sharing disabled experiences in media.</p><p><br></p><p>16:24 Relate stories to others, especially healthcare workers.</p><p><br></p><p>17:17 Sharing personal stories, lessons, and avoiding inspiration porn.</p><p><br></p><p>20:41 Learning boundaries from an older mentor, embracing self.</p><p><br></p><p>26:46 Struggles with queer identity in nightlife venues.</p><p><br></p><p>28:16 Toronto has organizations creating accessible spaces.</p><p><br></p><p>36:03 Creating regular content as a revenue stream.</p><p><br></p><p>38:04 Grateful for age and experience in authenticity.</p><p><br></p><p>43:23 Learning about disability justice, confronting internalized ableism.</p><p><br></p><p>46:02 RuPaul's reminder: love yourself, love others.</p><p><br></p><p>48:56 Recognition of mutual support in personal relationships.</p><p><br></p><p>51:34 Privilege of walking, trouble with wheelchair damage.</p><p><br></p><p>54:49 Agreement on disability visibility through social media.</p><p><br></p><p>57:35 Celebrate LGBTQ+ and disability pride this month.</p><p><br></p><p><strong>Connect with Spencer West </strong></p><p>Instagram: <a href="https://www.instagram.com/spencer2thewest/?hl=en">https://www.instagram.com/spencer2thewest/?hl=en</a></p><p>TikTok: <a href="https://www.tiktok.com/@spencer2thewest?lang=en">https://www.tiktok.com/@spencer2thewest?lang=en</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In today’s episode, we have Spencer West! From discussing the challenges of accessing queer spaces and nightlife to setting boundaries as a disabled content creator, this conversation sheds light on pivotal issues affecting the LGBTQ+ and disabled communities. </p><p><br></p><p>Spencer shares his personal experiences, advocacy work, and the role of social media in promoting awareness.</p><p><br></p><p>Don't miss this engaging episode with Spencer West!</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Spencer West: Keynote speaker, activist, trailblazer, author.</p><p><br></p><p>06:00 Navigating intersectional identities and privacy boundaries on TikTok.</p><p><br></p><p>12:47 The importance of sharing disabled experiences in media.</p><p><br></p><p>16:24 Relate stories to others, especially healthcare workers.</p><p><br></p><p>17:17 Sharing personal stories, lessons, and avoiding inspiration porn.</p><p><br></p><p>20:41 Learning boundaries from an older mentor, embracing self.</p><p><br></p><p>26:46 Struggles with queer identity in nightlife venues.</p><p><br></p><p>28:16 Toronto has organizations creating accessible spaces.</p><p><br></p><p>36:03 Creating regular content as a revenue stream.</p><p><br></p><p>38:04 Grateful for age and experience in authenticity.</p><p><br></p><p>43:23 Learning about disability justice, confronting internalized ableism.</p><p><br></p><p>46:02 RuPaul's reminder: love yourself, love others.</p><p><br></p><p>48:56 Recognition of mutual support in personal relationships.</p><p><br></p><p>51:34 Privilege of walking, trouble with wheelchair damage.</p><p><br></p><p>54:49 Agreement on disability visibility through social media.</p><p><br></p><p>57:35 Celebrate LGBTQ+ and disability pride this month.</p><p><br></p><p><strong>Connect with Spencer West </strong></p><p>Instagram: <a href="https://www.instagram.com/spencer2thewest/?hl=en">https://www.instagram.com/spencer2thewest/?hl=en</a></p><p>TikTok: <a href="https://www.tiktok.com/@spencer2thewest?lang=en">https://www.tiktok.com/@spencer2thewest?lang=en</a></p>]]>
      </content:encoded>
      <pubDate>Tue, 18 Jun 2024 11:57:39 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/9cf7cfb1/35e093f5.mp3" length="56917444" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/ZgSSaHjcptDZhGN891Ci3g4So4LcGPFxxzpiffRWw_A/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS84ZTQ0/MDQxNmY4ZWYxN2Nj/M2ViY2M0ZWM1OTBm/YWIxYi5qcGc.jpg"/>
      <itunes:duration>3556</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In today’s episode, we have Spencer West! From discussing the challenges of accessing queer spaces and nightlife to setting boundaries as a disabled content creator, this conversation sheds light on pivotal issues affecting the LGBTQ+ and disabled communities. </p><p><br></p><p>Spencer shares his personal experiences, advocacy work, and the role of social media in promoting awareness.</p><p><br></p><p>Don't miss this engaging episode with Spencer West!</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Spencer West: Keynote speaker, activist, trailblazer, author.</p><p><br></p><p>06:00 Navigating intersectional identities and privacy boundaries on TikTok.</p><p><br></p><p>12:47 The importance of sharing disabled experiences in media.</p><p><br></p><p>16:24 Relate stories to others, especially healthcare workers.</p><p><br></p><p>17:17 Sharing personal stories, lessons, and avoiding inspiration porn.</p><p><br></p><p>20:41 Learning boundaries from an older mentor, embracing self.</p><p><br></p><p>26:46 Struggles with queer identity in nightlife venues.</p><p><br></p><p>28:16 Toronto has organizations creating accessible spaces.</p><p><br></p><p>36:03 Creating regular content as a revenue stream.</p><p><br></p><p>38:04 Grateful for age and experience in authenticity.</p><p><br></p><p>43:23 Learning about disability justice, confronting internalized ableism.</p><p><br></p><p>46:02 RuPaul's reminder: love yourself, love others.</p><p><br></p><p>48:56 Recognition of mutual support in personal relationships.</p><p><br></p><p>51:34 Privilege of walking, trouble with wheelchair damage.</p><p><br></p><p>54:49 Agreement on disability visibility through social media.</p><p><br></p><p>57:35 Celebrate LGBTQ+ and disability pride this month.</p><p><br></p><p><strong>Connect with Spencer West </strong></p><p>Instagram: <a href="https://www.instagram.com/spencer2thewest/?hl=en">https://www.instagram.com/spencer2thewest/?hl=en</a></p><p>TikTok: <a href="https://www.tiktok.com/@spencer2thewest?lang=en">https://www.tiktok.com/@spencer2thewest?lang=en</a></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Model, Actor, and CEO: A Conversation with Lolo Spencer | Episode 5</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>5</itunes:episode>
      <podcast:episode>5</podcast:episode>
      <itunes:title>Model, Actor, and CEO: A Conversation with Lolo Spencer | Episode 5</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">5d93d676-afa1-49e0-a269-8a686171249f</guid>
      <link>https://share.transistor.fm/s/0b5adbfd</link>
      <description>
        <![CDATA[<p>In this episode, hosts Lily Newton and Erin Hawley sit down with actor, model, content creator, and CEO of the lifestyle brand Live Solo,  Lolo Spencer. Known for her advocacy work and trailblazing efforts in changing the narrative around disability, Lolo shares her incredible journey and vision for a more inclusive world.</p><p><br></p><p>We also explore the broader implications of representation in Hollywood and the importance of community building, with Lolo emphasizing the need for disabled actors to be cast in diverse roles. </p><p><br></p><p>Tune in and be part of the movement towards a more inclusive society!</p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Lolo Spencer, actor and disability advocate, succeeds.</p><p><br></p><p>03:26 Misconceptions about ambulatory wheelchair users' disabilities.</p><p><br></p><p>07:51 Difficulty accessing doctor's office due to age.</p><p><br></p><p>10:48 Feeling judged for being young and able.</p><p><br></p><p>14:03 Friends collaborate, enjoy and resonate with humor.</p><p><br></p><p>18:28 Importance of clear communication for disability accommodations.</p><p><br></p><p>19:38 Production must fully support disabled talent's needs.</p><p><br></p><p>25:47 Enhancing audience experience through laughter and enjoyment.</p><p><br></p><p>26:34 Season's exciting trailer, surprisingly, accessible to all.</p><p><br></p><p>30:46 Creating community through inclusive lifestyle brand blog.</p><p><br></p><p>34:34 Bringing community together through events and activities.</p><p><br></p><p>38:19 US healthcare detrimental; bias against black women.</p><p><br></p><p>40:51 Questioning the healthcare system's dismissiveness towards accessibility.</p><p><br></p><p>45:15 Lily searching for EDS diagnosis and medical diversity.</p><p><br></p><p>47:18 Collaboration of traditional and alternative medicine beneficial.</p><p><br></p><p>50:55 Community ties into information sharing and health.</p><p><br></p><p>55:08 Attitude towards disability needs to change.</p><p><br></p><p>57:25 Lolo praised for support and collaboration efforts.</p><p><strong>Connect with Lolo Spencer</strong></p><p>Instagram: <a href="https://www.instagram.com/itslololove/">https://www.instagram.com/itslololove/</a></p><p>Visit Live Solo: <a href="https://www.livesolo.co/">https://www.livesolo.</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In this episode, hosts Lily Newton and Erin Hawley sit down with actor, model, content creator, and CEO of the lifestyle brand Live Solo,  Lolo Spencer. Known for her advocacy work and trailblazing efforts in changing the narrative around disability, Lolo shares her incredible journey and vision for a more inclusive world.</p><p><br></p><p>We also explore the broader implications of representation in Hollywood and the importance of community building, with Lolo emphasizing the need for disabled actors to be cast in diverse roles. </p><p><br></p><p>Tune in and be part of the movement towards a more inclusive society!</p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Lolo Spencer, actor and disability advocate, succeeds.</p><p><br></p><p>03:26 Misconceptions about ambulatory wheelchair users' disabilities.</p><p><br></p><p>07:51 Difficulty accessing doctor's office due to age.</p><p><br></p><p>10:48 Feeling judged for being young and able.</p><p><br></p><p>14:03 Friends collaborate, enjoy and resonate with humor.</p><p><br></p><p>18:28 Importance of clear communication for disability accommodations.</p><p><br></p><p>19:38 Production must fully support disabled talent's needs.</p><p><br></p><p>25:47 Enhancing audience experience through laughter and enjoyment.</p><p><br></p><p>26:34 Season's exciting trailer, surprisingly, accessible to all.</p><p><br></p><p>30:46 Creating community through inclusive lifestyle brand blog.</p><p><br></p><p>34:34 Bringing community together through events and activities.</p><p><br></p><p>38:19 US healthcare detrimental; bias against black women.</p><p><br></p><p>40:51 Questioning the healthcare system's dismissiveness towards accessibility.</p><p><br></p><p>45:15 Lily searching for EDS diagnosis and medical diversity.</p><p><br></p><p>47:18 Collaboration of traditional and alternative medicine beneficial.</p><p><br></p><p>50:55 Community ties into information sharing and health.</p><p><br></p><p>55:08 Attitude towards disability needs to change.</p><p><br></p><p>57:25 Lolo praised for support and collaboration efforts.</p><p><strong>Connect with Lolo Spencer</strong></p><p>Instagram: <a href="https://www.instagram.com/itslololove/">https://www.instagram.com/itslololove/</a></p><p>Visit Live Solo: <a href="https://www.livesolo.co/">https://www.livesolo.</a></p>]]>
      </content:encoded>
      <pubDate>Tue, 11 Jun 2024 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/0b5adbfd/eca81bec.mp3" length="57198099" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/IRw_7t0Sxo0G9g8eNer4yaIA3SJz-WkXbFV3zdyqS8I/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS81Y2Zi/YzUyNjUzMWEyMmQ5/YWUwNWU4ZDg2YzM0/YjJjMC5wbmc.jpg"/>
      <itunes:duration>3571</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In this episode, hosts Lily Newton and Erin Hawley sit down with actor, model, content creator, and CEO of the lifestyle brand Live Solo,  Lolo Spencer. Known for her advocacy work and trailblazing efforts in changing the narrative around disability, Lolo shares her incredible journey and vision for a more inclusive world.</p><p><br></p><p>We also explore the broader implications of representation in Hollywood and the importance of community building, with Lolo emphasizing the need for disabled actors to be cast in diverse roles. </p><p><br></p><p>Tune in and be part of the movement towards a more inclusive society!</p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Lolo Spencer, actor and disability advocate, succeeds.</p><p><br></p><p>03:26 Misconceptions about ambulatory wheelchair users' disabilities.</p><p><br></p><p>07:51 Difficulty accessing doctor's office due to age.</p><p><br></p><p>10:48 Feeling judged for being young and able.</p><p><br></p><p>14:03 Friends collaborate, enjoy and resonate with humor.</p><p><br></p><p>18:28 Importance of clear communication for disability accommodations.</p><p><br></p><p>19:38 Production must fully support disabled talent's needs.</p><p><br></p><p>25:47 Enhancing audience experience through laughter and enjoyment.</p><p><br></p><p>26:34 Season's exciting trailer, surprisingly, accessible to all.</p><p><br></p><p>30:46 Creating community through inclusive lifestyle brand blog.</p><p><br></p><p>34:34 Bringing community together through events and activities.</p><p><br></p><p>38:19 US healthcare detrimental; bias against black women.</p><p><br></p><p>40:51 Questioning the healthcare system's dismissiveness towards accessibility.</p><p><br></p><p>45:15 Lily searching for EDS diagnosis and medical diversity.</p><p><br></p><p>47:18 Collaboration of traditional and alternative medicine beneficial.</p><p><br></p><p>50:55 Community ties into information sharing and health.</p><p><br></p><p>55:08 Attitude towards disability needs to change.</p><p><br></p><p>57:25 Lolo praised for support and collaboration efforts.</p><p><strong>Connect with Lolo Spencer</strong></p><p>Instagram: <a href="https://www.instagram.com/itslololove/">https://www.instagram.com/itslololove/</a></p><p>Visit Live Solo: <a href="https://www.livesolo.co/">https://www.livesolo.</a></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>The Laughing Edge: Changing expectations through comedy with Tina Friml on EYK | Episode 4</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>4</itunes:episode>
      <podcast:episode>4</podcast:episode>
      <itunes:title>The Laughing Edge: Changing expectations through comedy with Tina Friml on EYK | Episode 4</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">02b58b7b-4f96-40bc-8177-651acb770f2c</guid>
      <link>https://share.transistor.fm/s/842381a2</link>
      <description>
        <![CDATA[<p>In today's episode, Erin and Lily are joined by Tina Friml, a New York-based comedian who shares her unique experiences navigating the comedy scene. We'll explore the misconceptions about disabilities, the role of humor and radical self-acceptance, and turning casual ableism into comedy gold.</p><p><br></p><p>From the sometimes illogical things Tina can and cannot do, to her decision to only perform in ADA accessible venues, this episode is packed with insights.</p><p><br></p><p>Get ready to tune in, laugh, and learn as we welcome you to another episode of Everything You Know About Disability is Wrong. Let's get started!</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Disabled with mild cerebral palsy needing accommodations.</p><p><br></p><p>09:39 Challenges of being labeled and misunderstood.</p><p><br></p><p>10:56 Navigating disability and others' perceptions and actions.</p><p><br></p><p>19:37 Comedy often exploits societal expectations for jokes.</p><p><br></p><p>25:25 Some struggle to understand disabilities, affecting interactions.</p><p><br></p><p>29:18 Prioritizing ADA accessibility at event venues promoted.</p><p><br></p><p>34:04 Struggling to find accessible venues in various cities.</p><p><br></p><p>43:59 Unexpectedly positive experience appearing on Jimmy Fallon.</p><p><br></p><p>50:27 Easterseals podcast highlights equity, access, and accommodation.</p><p><br></p><p>51:41 Traveling alone, finding increasing airport accommodations.</p><p><br></p><p>01:00:45 Comedy community support, challenges of being underestimated.</p><p><br></p><p>01:02:22 Disability can be both a benefit and drawback.</p><p><br></p><p><strong>Connect with Tina Friml:</strong></p><p>Instagram: <a href="https://www.instagram.com/tinafriml/?hl=en">https://www.instagram.com/tinafriml/?hl=en</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In today's episode, Erin and Lily are joined by Tina Friml, a New York-based comedian who shares her unique experiences navigating the comedy scene. We'll explore the misconceptions about disabilities, the role of humor and radical self-acceptance, and turning casual ableism into comedy gold.</p><p><br></p><p>From the sometimes illogical things Tina can and cannot do, to her decision to only perform in ADA accessible venues, this episode is packed with insights.</p><p><br></p><p>Get ready to tune in, laugh, and learn as we welcome you to another episode of Everything You Know About Disability is Wrong. Let's get started!</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Disabled with mild cerebral palsy needing accommodations.</p><p><br></p><p>09:39 Challenges of being labeled and misunderstood.</p><p><br></p><p>10:56 Navigating disability and others' perceptions and actions.</p><p><br></p><p>19:37 Comedy often exploits societal expectations for jokes.</p><p><br></p><p>25:25 Some struggle to understand disabilities, affecting interactions.</p><p><br></p><p>29:18 Prioritizing ADA accessibility at event venues promoted.</p><p><br></p><p>34:04 Struggling to find accessible venues in various cities.</p><p><br></p><p>43:59 Unexpectedly positive experience appearing on Jimmy Fallon.</p><p><br></p><p>50:27 Easterseals podcast highlights equity, access, and accommodation.</p><p><br></p><p>51:41 Traveling alone, finding increasing airport accommodations.</p><p><br></p><p>01:00:45 Comedy community support, challenges of being underestimated.</p><p><br></p><p>01:02:22 Disability can be both a benefit and drawback.</p><p><br></p><p><strong>Connect with Tina Friml:</strong></p><p>Instagram: <a href="https://www.instagram.com/tinafriml/?hl=en">https://www.instagram.com/tinafriml/?hl=en</a></p>]]>
      </content:encoded>
      <pubDate>Wed, 29 May 2024 11:39:16 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/842381a2/00d313aa.mp3" length="67038590" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/48MQYsxAgmqScZiwBmXDBO4wrFJ36L7yBZ1f870_0-8/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9iMGMx/YzNhOWYwY2YxOTA3/YzcyZTY4YThjMWEy/YjM1MS5wbmc.jpg"/>
      <itunes:duration>4186</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In today's episode, Erin and Lily are joined by Tina Friml, a New York-based comedian who shares her unique experiences navigating the comedy scene. We'll explore the misconceptions about disabilities, the role of humor and radical self-acceptance, and turning casual ableism into comedy gold.</p><p><br></p><p>From the sometimes illogical things Tina can and cannot do, to her decision to only perform in ADA accessible venues, this episode is packed with insights.</p><p><br></p><p>Get ready to tune in, laugh, and learn as we welcome you to another episode of Everything You Know About Disability is Wrong. Let's get started!</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Disabled with mild cerebral palsy needing accommodations.</p><p><br></p><p>09:39 Challenges of being labeled and misunderstood.</p><p><br></p><p>10:56 Navigating disability and others' perceptions and actions.</p><p><br></p><p>19:37 Comedy often exploits societal expectations for jokes.</p><p><br></p><p>25:25 Some struggle to understand disabilities, affecting interactions.</p><p><br></p><p>29:18 Prioritizing ADA accessibility at event venues promoted.</p><p><br></p><p>34:04 Struggling to find accessible venues in various cities.</p><p><br></p><p>43:59 Unexpectedly positive experience appearing on Jimmy Fallon.</p><p><br></p><p>50:27 Easterseals podcast highlights equity, access, and accommodation.</p><p><br></p><p>51:41 Traveling alone, finding increasing airport accommodations.</p><p><br></p><p>01:00:45 Comedy community support, challenges of being underestimated.</p><p><br></p><p>01:02:22 Disability can be both a benefit and drawback.</p><p><br></p><p><strong>Connect with Tina Friml:</strong></p><p>Instagram: <a href="https://www.instagram.com/tinafriml/?hl=en">https://www.instagram.com/tinafriml/?hl=en</a></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Rawan Tuffaha Unveils the Artistic Journey of ASD Band on Everything You Know | Episode 3</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>3</itunes:episode>
      <podcast:episode>3</podcast:episode>
      <itunes:title>Rawan Tuffaha Unveils the Artistic Journey of ASD Band on Everything You Know | Episode 3</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">4b42f782-e7f8-4fcc-90ca-002669999a6c</guid>
      <link>https://share.transistor.fm/s/945c1a06</link>
      <description>
        <![CDATA[<p>In today's episode, your hosts Lily Newton and Erin Hawley have a heartfelt conversation with our guest, Rawan Tuffaha. Rawan is the lead singer of the ASD Band, a group composed entirely of autistic musicians, which shines a light on talent within the autistic community. Besides her music career, Rawan is an advocate for autism acceptance and disability employment, challenging misconceptions and pushing for more inclusive practices.</p><p><br></p><p>Join us as we delve into Rawan's journey, from forming the ASD Band to her academic pursuits at Metal Works Institute, her experiences with the documentary about her band, and her thoughts on the misconceptions people often have about individuals on the autism spectrum. We'll also hear about her challenging yet rewarding experiences managing school, autism, and her music career, including her exciting upcoming album, "Almost Flawless."</p><p><br></p><p>This episode is not only an exploration of Rawan's personal and professional life but also a broader discussion of the challenges faced by individuals with disabilities as they transition into adulthood, particularly in accessing employment and continuing to receive support.</p><p><br></p><p>Stay tuned as we celebrate the exceptional contributions of individuals like Rawan and discuss how organizations like Easterseals are paving the way for full access, equity, and inclusion for people with disabilities and their families.</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Podcast featuring Rawan Tuffaha, lead of ASD Band.</p><p><br></p><p>04:10 Documentary creation, album release amidst COVID-19 impact.</p><p><br></p><p>08:18 Performed with Roger Hodgson, formed a band and overcame setbacks.</p><p><br></p><p>11:23 Started playing the toy piano and learned by ear.</p><p><br></p><p>14:41 Honest, raw music conveying autistic experience powerfully.</p><p><br></p><p>19:44 Gratitude for positive influences and values learned.</p><p><br></p><p>22:28 Struggle with identity and trust in popularity.</p><p><br></p><p>25:32 Teenagers realize the importance of loyal, caring friends.</p><p><br></p><p>29:47 Passion for the Jonas Brothers, autism acceptance.</p><p><br></p><p>31:58 Struggling with travel plans, rehearsals, and charity.</p><p><br></p><p>35:04 Understanding the travel process with help from family.</p><p><br></p><p>38:26 Autism diagnosis at 1, received varied support.</p><p><br></p><p>40:57 Seeking support in university, aiming for success.</p><p><br></p><p>46:00 Struggles finding a job as an autistic person. Need for inclusion and understanding.</p><p><br></p><p>49:51 Multitasking autism advocate defies stereotypes with grace.</p><p><strong>Connect with Rawan Tuffaha</strong></p><p>Instagram: <a href="https://www.instagram.com/rawansinger/?ref=tablehopper.com">https://www.instagram.com/rawansinger/?ref=tablehopper.com</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>In today's episode, your hosts Lily Newton and Erin Hawley have a heartfelt conversation with our guest, Rawan Tuffaha. Rawan is the lead singer of the ASD Band, a group composed entirely of autistic musicians, which shines a light on talent within the autistic community. Besides her music career, Rawan is an advocate for autism acceptance and disability employment, challenging misconceptions and pushing for more inclusive practices.</p><p><br></p><p>Join us as we delve into Rawan's journey, from forming the ASD Band to her academic pursuits at Metal Works Institute, her experiences with the documentary about her band, and her thoughts on the misconceptions people often have about individuals on the autism spectrum. We'll also hear about her challenging yet rewarding experiences managing school, autism, and her music career, including her exciting upcoming album, "Almost Flawless."</p><p><br></p><p>This episode is not only an exploration of Rawan's personal and professional life but also a broader discussion of the challenges faced by individuals with disabilities as they transition into adulthood, particularly in accessing employment and continuing to receive support.</p><p><br></p><p>Stay tuned as we celebrate the exceptional contributions of individuals like Rawan and discuss how organizations like Easterseals are paving the way for full access, equity, and inclusion for people with disabilities and their families.</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Podcast featuring Rawan Tuffaha, lead of ASD Band.</p><p><br></p><p>04:10 Documentary creation, album release amidst COVID-19 impact.</p><p><br></p><p>08:18 Performed with Roger Hodgson, formed a band and overcame setbacks.</p><p><br></p><p>11:23 Started playing the toy piano and learned by ear.</p><p><br></p><p>14:41 Honest, raw music conveying autistic experience powerfully.</p><p><br></p><p>19:44 Gratitude for positive influences and values learned.</p><p><br></p><p>22:28 Struggle with identity and trust in popularity.</p><p><br></p><p>25:32 Teenagers realize the importance of loyal, caring friends.</p><p><br></p><p>29:47 Passion for the Jonas Brothers, autism acceptance.</p><p><br></p><p>31:58 Struggling with travel plans, rehearsals, and charity.</p><p><br></p><p>35:04 Understanding the travel process with help from family.</p><p><br></p><p>38:26 Autism diagnosis at 1, received varied support.</p><p><br></p><p>40:57 Seeking support in university, aiming for success.</p><p><br></p><p>46:00 Struggles finding a job as an autistic person. Need for inclusion and understanding.</p><p><br></p><p>49:51 Multitasking autism advocate defies stereotypes with grace.</p><p><strong>Connect with Rawan Tuffaha</strong></p><p>Instagram: <a href="https://www.instagram.com/rawansinger/?ref=tablehopper.com">https://www.instagram.com/rawansinger/?ref=tablehopper.com</a></p>]]>
      </content:encoded>
      <pubDate>Tue, 14 May 2024 09:01:14 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/945c1a06/2fef4d8b.mp3" length="52141915" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/snaF0tMhMQZ0N95a2AeFBLuJ2MfHUAq0YxeH1jgQlSs/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS8zMzli/NDZlN2ZhYzI1NTZl/ODJhYWQ4MmI2NDU4/ZTk4My5wbmc.jpg"/>
      <itunes:duration>3259</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>In today's episode, your hosts Lily Newton and Erin Hawley have a heartfelt conversation with our guest, Rawan Tuffaha. Rawan is the lead singer of the ASD Band, a group composed entirely of autistic musicians, which shines a light on talent within the autistic community. Besides her music career, Rawan is an advocate for autism acceptance and disability employment, challenging misconceptions and pushing for more inclusive practices.</p><p><br></p><p>Join us as we delve into Rawan's journey, from forming the ASD Band to her academic pursuits at Metal Works Institute, her experiences with the documentary about her band, and her thoughts on the misconceptions people often have about individuals on the autism spectrum. We'll also hear about her challenging yet rewarding experiences managing school, autism, and her music career, including her exciting upcoming album, "Almost Flawless."</p><p><br></p><p>This episode is not only an exploration of Rawan's personal and professional life but also a broader discussion of the challenges faced by individuals with disabilities as they transition into adulthood, particularly in accessing employment and continuing to receive support.</p><p><br></p><p>Stay tuned as we celebrate the exceptional contributions of individuals like Rawan and discuss how organizations like Easterseals are paving the way for full access, equity, and inclusion for people with disabilities and their families.</p><p><br></p><p><strong>Timestamps</strong></p><p><br></p><p>00:00 Podcast featuring Rawan Tuffaha, lead of ASD Band.</p><p><br></p><p>04:10 Documentary creation, album release amidst COVID-19 impact.</p><p><br></p><p>08:18 Performed with Roger Hodgson, formed a band and overcame setbacks.</p><p><br></p><p>11:23 Started playing the toy piano and learned by ear.</p><p><br></p><p>14:41 Honest, raw music conveying autistic experience powerfully.</p><p><br></p><p>19:44 Gratitude for positive influences and values learned.</p><p><br></p><p>22:28 Struggle with identity and trust in popularity.</p><p><br></p><p>25:32 Teenagers realize the importance of loyal, caring friends.</p><p><br></p><p>29:47 Passion for the Jonas Brothers, autism acceptance.</p><p><br></p><p>31:58 Struggling with travel plans, rehearsals, and charity.</p><p><br></p><p>35:04 Understanding the travel process with help from family.</p><p><br></p><p>38:26 Autism diagnosis at 1, received varied support.</p><p><br></p><p>40:57 Seeking support in university, aiming for success.</p><p><br></p><p>46:00 Struggles finding a job as an autistic person. Need for inclusion and understanding.</p><p><br></p><p>49:51 Multitasking autism advocate defies stereotypes with grace.</p><p><strong>Connect with Rawan Tuffaha</strong></p><p>Instagram: <a href="https://www.instagram.com/rawansinger/?ref=tablehopper.com">https://www.instagram.com/rawansinger/?ref=tablehopper.com</a></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Navigating Independence and Relationships: Subodh and Aarti's Journey on EYK</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>2</itunes:episode>
      <podcast:episode>2</podcast:episode>
      <itunes:title>Navigating Independence and Relationships: Subodh and Aarti's Journey on EYK</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">1654be4b-272d-4710-9b4f-827be6cbb168</guid>
      <link>https://share.transistor.fm/s/2c4cc3d4</link>
      <description>
        <![CDATA[<p><strong>Navigating Independence and Relationships: Subodh and Aarti's Journey on EYK | Season 3, Episode 2</strong></p><p><br></p><p>Welcome to a special episode of Everything You Know, presented by Easterseals. Today, we've got a truly enlightening conversation lined up with our guests, Subodh Garg and his sister, Aarti Garg. Subodh, a charismatic individual diagnosed with autism at the age of 3, shares his journey towards independence, his exceptional memory, and his experiences with dating and social interactions. Aarti, who plays a crucial role in managing Subodh’s social engagements and safety online, provides insight into their sibling dynamics and the support systems that help Subodh navigate his challenges and aspirations.</p><p><br></p><p>In this episode, we delve into the importance of the diverse representation of autism in media, the critical role of technology in improving communication skills, and the universal struggles with dating and social skills. Subodh also discusses his participation in the show Love on the Spectrum, his employment goals in accounting, and his passion for travel. Join hosts Erin Hawley and Lily Newton as they explore these topics and more, offering a broader perspective on neurodiversity and the common human desires for love and connection. </p><p><br></p><p>Stay tuned as we challenge the misconceptions about autism and celebrate the diverse capabilities and aspirations of individuals on the spectrum.</p><p><strong>Timestamps</strong></p><p><br></p><p>0:00 - Introduction to today's episode with hosts Erin Hawley and Lily Newton, featuring guests Subodh and Aarti Garg.</p><p><br></p><p>2:45 - Subodh Garg discusses his journey towards independence and his aspirations in accounting.</p><p><br></p><p>5:20 - Exploring the sibling dynamics between Subodh and Aarti Garg, including the misconceptions about their relationship.</p><p><br></p><p>7:40 - Aarti Garg talks about her role as a manager rather than a caretaker in Subodh's life.</p><p><br></p><p>10:15 - Challenges of making and maintaining friendships as adults, emphasized by Subodh's experiences.</p><p><br></p><p>13:30 - Subodh's take on his participation in Love on the Spectrum and developing his dating skills.</p><p><br></p><p>18:29 - The impact of "Love on the Spectrum" on Subodh’s life, as discussed by Aarti.</p><p><br></p><p>21:10 - Conversation about the universal struggle with dating and social skills.</p><p><br></p><p>24:05 - Subodh and community building: From online dating to maintaining connections with the show's cast.</p><p><br></p><p>27:50 - The transportation hurdles and Subodh's use of Access, a paratransit service.</p><p><br></p><p>30:16 - Subodh’s employment ventures at Teledelis and Insight, and his educational goals.</p><p><br></p><p>33:45 - Lily Newton and Aarti Garg critique the representation of disability in mainstream media and specific TV shows.</p><p><br></p><p>37:12 - The role of digital content in Subodh’s life, including his Instagram engagement and travel posts.</p><p><br></p><p>40:40 - Detailing the disability readathon initiative and its significance, shared by Erin Hawley.</p><p><br></p><p>43:28 - Reflections on maintaining friendships amidst life changes and busy schedules.</p><p><br></p><p>45:35 - Subodh’s exceptional memory skills and affinity for recalling specific dates and personal milestones.</p><p><br></p><p>49:20 - Deep dive into Subodh's past therapies, ongoing supportive services, and aspirations for travel.</p><p><br></p><p>52:15 - Discussion on the broader spectrum of autism and the personal ambitions of individuals with autism.</p><p><br></p><p>55:00 - Closing thoughts, upcoming initiatives, and a thank you to Subodh and Aarti Garg for their participation.</p><p><br></p><p>57:10 - Call to action for disability advocacy and an invitation to listen in to future episodes presented by Easterseals.</p><p><br></p><p><strong>Connect with Subodh Garg</strong></p><p>Instagram: <a href="https://www.instagram.com/traveling_subodh/?hl=en">https://www.instagram.com/traveling_subodh/?hl=en</a></p><p><br></p><p><strong>Connect with Aarti Garg</strong></p><p>Instagram: <a href="https://www.instagram.com/aartipaarty/?hl=en">https://www.instagram.com/aartipaarty/?hl=en</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p><strong>Navigating Independence and Relationships: Subodh and Aarti's Journey on EYK | Season 3, Episode 2</strong></p><p><br></p><p>Welcome to a special episode of Everything You Know, presented by Easterseals. Today, we've got a truly enlightening conversation lined up with our guests, Subodh Garg and his sister, Aarti Garg. Subodh, a charismatic individual diagnosed with autism at the age of 3, shares his journey towards independence, his exceptional memory, and his experiences with dating and social interactions. Aarti, who plays a crucial role in managing Subodh’s social engagements and safety online, provides insight into their sibling dynamics and the support systems that help Subodh navigate his challenges and aspirations.</p><p><br></p><p>In this episode, we delve into the importance of the diverse representation of autism in media, the critical role of technology in improving communication skills, and the universal struggles with dating and social skills. Subodh also discusses his participation in the show Love on the Spectrum, his employment goals in accounting, and his passion for travel. Join hosts Erin Hawley and Lily Newton as they explore these topics and more, offering a broader perspective on neurodiversity and the common human desires for love and connection. </p><p><br></p><p>Stay tuned as we challenge the misconceptions about autism and celebrate the diverse capabilities and aspirations of individuals on the spectrum.</p><p><strong>Timestamps</strong></p><p><br></p><p>0:00 - Introduction to today's episode with hosts Erin Hawley and Lily Newton, featuring guests Subodh and Aarti Garg.</p><p><br></p><p>2:45 - Subodh Garg discusses his journey towards independence and his aspirations in accounting.</p><p><br></p><p>5:20 - Exploring the sibling dynamics between Subodh and Aarti Garg, including the misconceptions about their relationship.</p><p><br></p><p>7:40 - Aarti Garg talks about her role as a manager rather than a caretaker in Subodh's life.</p><p><br></p><p>10:15 - Challenges of making and maintaining friendships as adults, emphasized by Subodh's experiences.</p><p><br></p><p>13:30 - Subodh's take on his participation in Love on the Spectrum and developing his dating skills.</p><p><br></p><p>18:29 - The impact of "Love on the Spectrum" on Subodh’s life, as discussed by Aarti.</p><p><br></p><p>21:10 - Conversation about the universal struggle with dating and social skills.</p><p><br></p><p>24:05 - Subodh and community building: From online dating to maintaining connections with the show's cast.</p><p><br></p><p>27:50 - The transportation hurdles and Subodh's use of Access, a paratransit service.</p><p><br></p><p>30:16 - Subodh’s employment ventures at Teledelis and Insight, and his educational goals.</p><p><br></p><p>33:45 - Lily Newton and Aarti Garg critique the representation of disability in mainstream media and specific TV shows.</p><p><br></p><p>37:12 - The role of digital content in Subodh’s life, including his Instagram engagement and travel posts.</p><p><br></p><p>40:40 - Detailing the disability readathon initiative and its significance, shared by Erin Hawley.</p><p><br></p><p>43:28 - Reflections on maintaining friendships amidst life changes and busy schedules.</p><p><br></p><p>45:35 - Subodh’s exceptional memory skills and affinity for recalling specific dates and personal milestones.</p><p><br></p><p>49:20 - Deep dive into Subodh's past therapies, ongoing supportive services, and aspirations for travel.</p><p><br></p><p>52:15 - Discussion on the broader spectrum of autism and the personal ambitions of individuals with autism.</p><p><br></p><p>55:00 - Closing thoughts, upcoming initiatives, and a thank you to Subodh and Aarti Garg for their participation.</p><p><br></p><p>57:10 - Call to action for disability advocacy and an invitation to listen in to future episodes presented by Easterseals.</p><p><br></p><p><strong>Connect with Subodh Garg</strong></p><p>Instagram: <a href="https://www.instagram.com/traveling_subodh/?hl=en">https://www.instagram.com/traveling_subodh/?hl=en</a></p><p><br></p><p><strong>Connect with Aarti Garg</strong></p><p>Instagram: <a href="https://www.instagram.com/aartipaarty/?hl=en">https://www.instagram.com/aartipaarty/?hl=en</a></p>]]>
      </content:encoded>
      <pubDate>Tue, 30 Apr 2024 09:00:00 -0400</pubDate>
      <author>Easterseals</author>
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      <itunes:author>Easterseals</itunes:author>
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      <itunes:duration>4259</itunes:duration>
      <itunes:summary>
        <![CDATA[<p><strong>Navigating Independence and Relationships: Subodh and Aarti's Journey on EYK | Season 3, Episode 2</strong></p><p><br></p><p>Welcome to a special episode of Everything You Know, presented by Easterseals. Today, we've got a truly enlightening conversation lined up with our guests, Subodh Garg and his sister, Aarti Garg. Subodh, a charismatic individual diagnosed with autism at the age of 3, shares his journey towards independence, his exceptional memory, and his experiences with dating and social interactions. Aarti, who plays a crucial role in managing Subodh’s social engagements and safety online, provides insight into their sibling dynamics and the support systems that help Subodh navigate his challenges and aspirations.</p><p><br></p><p>In this episode, we delve into the importance of the diverse representation of autism in media, the critical role of technology in improving communication skills, and the universal struggles with dating and social skills. Subodh also discusses his participation in the show Love on the Spectrum, his employment goals in accounting, and his passion for travel. Join hosts Erin Hawley and Lily Newton as they explore these topics and more, offering a broader perspective on neurodiversity and the common human desires for love and connection. </p><p><br></p><p>Stay tuned as we challenge the misconceptions about autism and celebrate the diverse capabilities and aspirations of individuals on the spectrum.</p><p><strong>Timestamps</strong></p><p><br></p><p>0:00 - Introduction to today's episode with hosts Erin Hawley and Lily Newton, featuring guests Subodh and Aarti Garg.</p><p><br></p><p>2:45 - Subodh Garg discusses his journey towards independence and his aspirations in accounting.</p><p><br></p><p>5:20 - Exploring the sibling dynamics between Subodh and Aarti Garg, including the misconceptions about their relationship.</p><p><br></p><p>7:40 - Aarti Garg talks about her role as a manager rather than a caretaker in Subodh's life.</p><p><br></p><p>10:15 - Challenges of making and maintaining friendships as adults, emphasized by Subodh's experiences.</p><p><br></p><p>13:30 - Subodh's take on his participation in Love on the Spectrum and developing his dating skills.</p><p><br></p><p>18:29 - The impact of "Love on the Spectrum" on Subodh’s life, as discussed by Aarti.</p><p><br></p><p>21:10 - Conversation about the universal struggle with dating and social skills.</p><p><br></p><p>24:05 - Subodh and community building: From online dating to maintaining connections with the show's cast.</p><p><br></p><p>27:50 - The transportation hurdles and Subodh's use of Access, a paratransit service.</p><p><br></p><p>30:16 - Subodh’s employment ventures at Teledelis and Insight, and his educational goals.</p><p><br></p><p>33:45 - Lily Newton and Aarti Garg critique the representation of disability in mainstream media and specific TV shows.</p><p><br></p><p>37:12 - The role of digital content in Subodh’s life, including his Instagram engagement and travel posts.</p><p><br></p><p>40:40 - Detailing the disability readathon initiative and its significance, shared by Erin Hawley.</p><p><br></p><p>43:28 - Reflections on maintaining friendships amidst life changes and busy schedules.</p><p><br></p><p>45:35 - Subodh’s exceptional memory skills and affinity for recalling specific dates and personal milestones.</p><p><br></p><p>49:20 - Deep dive into Subodh's past therapies, ongoing supportive services, and aspirations for travel.</p><p><br></p><p>52:15 - Discussion on the broader spectrum of autism and the personal ambitions of individuals with autism.</p><p><br></p><p>55:00 - Closing thoughts, upcoming initiatives, and a thank you to Subodh and Aarti Garg for their participation.</p><p><br></p><p>57:10 - Call to action for disability advocacy and an invitation to listen in to future episodes presented by Easterseals.</p><p><br></p><p><strong>Connect with Subodh Garg</strong></p><p>Instagram: <a href="https://www.instagram.com/traveling_subodh/?hl=en">https://www.instagram.com/traveling_subodh/?hl=en</a></p><p><br></p><p><strong>Connect with Aarti Garg</strong></p><p>Instagram: <a href="https://www.instagram.com/aartipaarty/?hl=en">https://www.instagram.com/aartipaarty/?hl=en</a></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Gaelynn Lea - Everything You Know About Disability is Wrong Podcast | Season 3, Episode 1</title>
      <itunes:season>3</itunes:season>
      <podcast:season>3</podcast:season>
      <itunes:episode>1</itunes:episode>
      <podcast:episode>1</podcast:episode>
      <itunes:title>Gaelynn Lea - Everything You Know About Disability is Wrong Podcast | Season 3, Episode 1</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/ef8093a0</link>
      <description>
        <![CDATA[<p>Join our hosts, Lily Newton and Erin Hawley, as they sit down with the riveting Gaelynn Lea, whose voice and violin strings resonate with the force of change, challenging our perceptions of ability and accessibility.</p><p><br></p><p>Imagine being told that your dream career is not designed for someone like you. Now picture breaking that mold and redefining what is possible. Gaelynn Lea did just that. Born with a physical disability, Gaelynn transformed the way the violin is played, gripping it like a cello. With this twist, she orchestrated her way to stardom after winning NPR's Tiny Desk concert. But her journey is more than a story of musical success it's a powerful narrative of breaking barriers and rewriting the stanzas of inclusivity.</p><p><br></p><p>Tune in, and you may just find that the key to unlocking true inclusivity and happiness lies within the stories that defy silence and demand to be heard.</p><p><br></p><p><strong>Key Moments</strong></p><p>10:39 Disability is more than just assumptions.</p><p><br></p><p>12:18 Name experiences, avoid overgeneralizing, and amplify underrepresented voices.</p><p><br></p><p>27:01 Rant on marriage inequality and divorce advice.</p><p><br></p><p>30:49 Advocating for disabled rights and innovation.</p><p><br></p><p>35:18 Teachers adapt instruments without needing deep disability knowledge.</p><p><br></p><p>43:41 Importance of owning your work and feelings.</p><p><br></p><p>46:09 Discovering hidden desires through writing memoirs.</p><p><br></p><p>54:48 Recognize the knowledge gap, educate, and make events accessible.</p><p><br></p><p>56:47 Advocate for accessibility and supporting accessible businesses.</p><p><br></p><p>01:01:52 Inappropriate discussion led to realization and job.</p><p><br></p><p>01:09:53 Disabled community excels; companies should embrace inclusion.</p><p><strong>Connect with Gaelynn Lea</strong></p><p><strong>Instagram:</strong> <a href="https://www.instagram.com/gaelynnlea/">https://www.instagram.com/gaelynnlea/</a></p><p><strong>Website:</strong> <a href="https://violinscratches.com/">https://violinscratches.com/</a></p>]]>
      </description>
      <content:encoded>
        <![CDATA[<p>Join our hosts, Lily Newton and Erin Hawley, as they sit down with the riveting Gaelynn Lea, whose voice and violin strings resonate with the force of change, challenging our perceptions of ability and accessibility.</p><p><br></p><p>Imagine being told that your dream career is not designed for someone like you. Now picture breaking that mold and redefining what is possible. Gaelynn Lea did just that. Born with a physical disability, Gaelynn transformed the way the violin is played, gripping it like a cello. With this twist, she orchestrated her way to stardom after winning NPR's Tiny Desk concert. But her journey is more than a story of musical success it's a powerful narrative of breaking barriers and rewriting the stanzas of inclusivity.</p><p><br></p><p>Tune in, and you may just find that the key to unlocking true inclusivity and happiness lies within the stories that defy silence and demand to be heard.</p><p><br></p><p><strong>Key Moments</strong></p><p>10:39 Disability is more than just assumptions.</p><p><br></p><p>12:18 Name experiences, avoid overgeneralizing, and amplify underrepresented voices.</p><p><br></p><p>27:01 Rant on marriage inequality and divorce advice.</p><p><br></p><p>30:49 Advocating for disabled rights and innovation.</p><p><br></p><p>35:18 Teachers adapt instruments without needing deep disability knowledge.</p><p><br></p><p>43:41 Importance of owning your work and feelings.</p><p><br></p><p>46:09 Discovering hidden desires through writing memoirs.</p><p><br></p><p>54:48 Recognize the knowledge gap, educate, and make events accessible.</p><p><br></p><p>56:47 Advocate for accessibility and supporting accessible businesses.</p><p><br></p><p>01:01:52 Inappropriate discussion led to realization and job.</p><p><br></p><p>01:09:53 Disabled community excels; companies should embrace inclusion.</p><p><strong>Connect with Gaelynn Lea</strong></p><p><strong>Instagram:</strong> <a href="https://www.instagram.com/gaelynnlea/">https://www.instagram.com/gaelynnlea/</a></p><p><strong>Website:</strong> <a href="https://violinscratches.com/">https://violinscratches.com/</a></p>]]>
      </content:encoded>
      <pubDate>Tue, 16 Apr 2024 11:04:53 -0400</pubDate>
      <author>Easterseals</author>
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      <itunes:author>Easterseals</itunes:author>
      <itunes:image href="https://img.transistorcdn.com/D0dCWgqswDAXzMFF3-5Ve7I76ZocfARrXVOGWyKLJc4/rs:fill:0:0:1/w:1400/h:1400/q:60/mb:500000/aHR0cHM6Ly9pbWct/dXBsb2FkLXByb2R1/Y3Rpb24udHJhbnNp/c3Rvci5mbS9mMDcw/NjBhNjkzM2U3MjM2/MmU2N2EyZTMxMTgy/Mzg3ZS5wbmc.jpg"/>
      <itunes:duration>4463</itunes:duration>
      <itunes:summary>
        <![CDATA[<p>Join our hosts, Lily Newton and Erin Hawley, as they sit down with the riveting Gaelynn Lea, whose voice and violin strings resonate with the force of change, challenging our perceptions of ability and accessibility.</p><p><br></p><p>Imagine being told that your dream career is not designed for someone like you. Now picture breaking that mold and redefining what is possible. Gaelynn Lea did just that. Born with a physical disability, Gaelynn transformed the way the violin is played, gripping it like a cello. With this twist, she orchestrated her way to stardom after winning NPR's Tiny Desk concert. But her journey is more than a story of musical success it's a powerful narrative of breaking barriers and rewriting the stanzas of inclusivity.</p><p><br></p><p>Tune in, and you may just find that the key to unlocking true inclusivity and happiness lies within the stories that defy silence and demand to be heard.</p><p><br></p><p><strong>Key Moments</strong></p><p>10:39 Disability is more than just assumptions.</p><p><br></p><p>12:18 Name experiences, avoid overgeneralizing, and amplify underrepresented voices.</p><p><br></p><p>27:01 Rant on marriage inequality and divorce advice.</p><p><br></p><p>30:49 Advocating for disabled rights and innovation.</p><p><br></p><p>35:18 Teachers adapt instruments without needing deep disability knowledge.</p><p><br></p><p>43:41 Importance of owning your work and feelings.</p><p><br></p><p>46:09 Discovering hidden desires through writing memoirs.</p><p><br></p><p>54:48 Recognize the knowledge gap, educate, and make events accessible.</p><p><br></p><p>56:47 Advocate for accessibility and supporting accessible businesses.</p><p><br></p><p>01:01:52 Inappropriate discussion led to realization and job.</p><p><br></p><p>01:09:53 Disabled community excels; companies should embrace inclusion.</p><p><strong>Connect with Gaelynn Lea</strong></p><p><strong>Instagram:</strong> <a href="https://www.instagram.com/gaelynnlea/">https://www.instagram.com/gaelynnlea/</a></p><p><strong>Website:</strong> <a href="https://violinscratches.com/">https://violinscratches.com/</a></p>]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Jameela Jamil</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:episode>6</itunes:episode>
      <podcast:episode>6</podcast:episode>
      <itunes:title>Jameela Jamil</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">642efe97-146b-440d-9338-a708a2e4d44a</guid>
      <link>https://share.transistor.fm/s/192e19a0</link>
      <description>
        <![CDATA[In this exciting episode, Jameela Jamil, actress, activist, and television host, shares how she began to understand her own disability while navigating the entertainment industry. We're working through shame, making our own rules, and creating inclusive spaces together to break barriers. Are you in?]]>
      </description>
      <content:encoded>
        <![CDATA[In this exciting episode, Jameela Jamil, actress, activist, and television host, shares how she began to understand her own disability while navigating the entertainment industry. We're working through shame, making our own rules, and creating inclusive spaces together to break barriers. Are you in?]]>
      </content:encoded>
      <pubDate>Wed, 10 Jan 2024 05:00:00 -0500</pubDate>
      <author>Easterseals</author>
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      <itunes:author>Easterseals</itunes:author>
      <itunes:duration>3422</itunes:duration>
      <itunes:summary>In this exciting episode, Jameela Jamil, actress, activist, and television host, shares how she began to understand her own disability while navigating the entertainment industry. We're working through shame, making our own rules, and creating inclusive spaces together to break barriers. Are you in?</itunes:summary>
      <itunes:subtitle>In this exciting episode, Jameela Jamil, actress, activist, and television host, shares how she began to understand her own disability while navigating the entertainment industry. We're working through shame, making our own rules, and creating inclusive s</itunes:subtitle>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Lachi</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:episode>5</itunes:episode>
      <podcast:episode>5</podcast:episode>
      <itunes:title>Lachi</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
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      <link>https://share.transistor.fm/s/3ccd3947</link>
      <description>
        <![CDATA[Erin and Lily are joined by award-winning recording artist, Youtuber and disability advocate Lachi. Lachi talks about her DEI work in the music industry and the nuances of ableism as it relates to trauma, class, race, and gender.]]>
      </description>
      <content:encoded>
        <![CDATA[Erin and Lily are joined by award-winning recording artist, Youtuber and disability advocate Lachi. Lachi talks about her DEI work in the music industry and the nuances of ableism as it relates to trauma, class, race, and gender.]]>
      </content:encoded>
      <pubDate>Wed, 03 Jan 2024 15:17:00 -0500</pubDate>
      <author>Easterseals</author>
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      <itunes:author>Easterseals</itunes:author>
      <itunes:duration>3385</itunes:duration>
      <itunes:summary>Erin and Lily are joined by award-winning recording artist, Youtuber and disability advocate Lachi. Lachi talks about her DEI work in the music industry and the nuances of ableism as it relates to trauma, class, race, and gender.</itunes:summary>
      <itunes:subtitle>Erin and Lily are joined by award-winning recording artist, Youtuber and disability advocate Lachi. Lachi talks about her DEI work in the music industry and the nuances of ableism as it relates to trauma, class, race, and gender.</itunes:subtitle>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Collette Divitto</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:episode>4</itunes:episode>
      <podcast:episode>4</podcast:episode>
      <itunes:title>Collette Divitto</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">a687ad57-405d-43b1-a693-3f7504eb3d89</guid>
      <link>https://share.transistor.fm/s/8a19940d</link>
      <description>
        <![CDATA[Collette Divitto, founder and CEO of Collettey’s Cookies, turned her love for baking into a successful business where half of the staff has a disability. She joins hosts Erin and Lily to chat about her successes, life as an entrepreneur, and the stigma many disabled people face while building their careers.]]>
      </description>
      <content:encoded>
        <![CDATA[Collette Divitto, founder and CEO of Collettey’s Cookies, turned her love for baking into a successful business where half of the staff has a disability. She joins hosts Erin and Lily to chat about her successes, life as an entrepreneur, and the stigma many disabled people face while building their careers.]]>
      </content:encoded>
      <pubDate>Wed, 03 Jan 2024 15:10:00 -0500</pubDate>
      <author>Easterseals</author>
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      <itunes:author>Easterseals</itunes:author>
      <itunes:duration>3340</itunes:duration>
      <itunes:summary>Collette Divitto, founder and CEO of Collettey’s Cookies, turned her love for baking into a successful business where half of the staff has a disability. She joins hosts Erin and Lily to chat about her successes, life as an entrepreneur, and the stigma many disabled people face while building their careers.</itunes:summary>
      <itunes:subtitle>Collette Divitto, founder and CEO of Collettey’s Cookies, turned her love for baking into a successful business where half of the staff has a disability. She joins hosts Erin and Lily to chat about her successes, life as an entrepreneur, and the stigma ma</itunes:subtitle>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Jillian Mercado</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:episode>3</itunes:episode>
      <podcast:episode>3</podcast:episode>
      <itunes:title>Jillian Mercado</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">4dcf8691-edeb-405b-8be3-6492964aa824</guid>
      <link>https://share.transistor.fm/s/673cc138</link>
      <description>
        <![CDATA[As a fashion model, actress, and disability rights advocate, Jillian has a lot going on! Throughout her career, she has encountered comments from strangers about her disability. Learn about how she became inspired by those experiences to create safe, inclusive spaces on social media.]]>
      </description>
      <content:encoded>
        <![CDATA[As a fashion model, actress, and disability rights advocate, Jillian has a lot going on! Throughout her career, she has encountered comments from strangers about her disability. Learn about how she became inspired by those experiences to create safe, inclusive spaces on social media.]]>
      </content:encoded>
      <pubDate>Thu, 21 Dec 2023 11:43:00 -0500</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/673cc138/ee4859d2.mp3" length="157649575" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:duration>3942</itunes:duration>
      <itunes:summary>As a fashion model, actress, and disability rights advocate, Jillian has a lot going on! Throughout her career, she has encountered comments from strangers about her disability. Learn about how she became inspired by those experiences to create safe, inclusive spaces on social media.</itunes:summary>
      <itunes:subtitle>As a fashion model, actress, and disability rights advocate, Jillian has a lot going on! Throughout her career, she has encountered comments from strangers about her disability. Learn about how she became inspired by those experiences to create safe, incl</itunes:subtitle>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Lindsey Rowe Parker</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:episode>2</itunes:episode>
      <podcast:episode>2</podcast:episode>
      <itunes:title>Lindsey Rowe Parker</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">0ec80d02-756a-42e0-9405-78e82055da56</guid>
      <link>https://share.transistor.fm/s/907a51ee</link>
      <description>
        <![CDATA[Lindsey Rowe Parker, author of the children’s book, “Wiggles, Stomps, and Squeezes Calm My Jitters Down,” joins the podcast to discuss why disability representation is important in children's literature. This episode also explores the often challenging road toward self-acceptance.]]>
      </description>
      <content:encoded>
        <![CDATA[Lindsey Rowe Parker, author of the children’s book, “Wiggles, Stomps, and Squeezes Calm My Jitters Down,” joins the podcast to discuss why disability representation is important in children's literature. This episode also explores the often challenging road toward self-acceptance.]]>
      </content:encoded>
      <pubDate>Wed, 08 Nov 2023 05:00:00 -0500</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/907a51ee/018a8b1c.mp3" length="121315121" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:duration>3033</itunes:duration>
      <itunes:summary>Lindsey Rowe Parker, author of the children’s book, “Wiggles, Stomps, and Squeezes Calm My Jitters Down,” joins the podcast to discuss why disability representation is important in children's literature. This episode also explores the often challenging road toward self-acceptance.</itunes:summary>
      <itunes:subtitle>Lindsey Rowe Parker, author of the children’s book, “Wiggles, Stomps, and Squeezes Calm My Jitters Down,” joins the podcast to discuss why disability representation is important in children's literature. This episode also explores the often challenging ro</itunes:subtitle>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Kaelynn Partlow</title>
      <itunes:season>2</itunes:season>
      <podcast:season>2</podcast:season>
      <itunes:episode>1</itunes:episode>
      <podcast:episode>1</podcast:episode>
      <itunes:title>Kaelynn Partlow</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">d17898f8-579d-4794-8d52-26f044ea0838</guid>
      <link>https://share.transistor.fm/s/d2456890</link>
      <description>
        <![CDATA[Kaelynn Partlow, autistic advocate and Senior Therapist at Project Hope Foundation, Inc., was featured on the Netflix series called, “Love on the Spectrum.” She joins hosts Erin and Lily to chat about neurodiversity, social media advocacy, and more!]]>
      </description>
      <content:encoded>
        <![CDATA[Kaelynn Partlow, autistic advocate and Senior Therapist at Project Hope Foundation, Inc., was featured on the Netflix series called, “Love on the Spectrum.” She joins hosts Erin and Lily to chat about neurodiversity, social media advocacy, and more!]]>
      </content:encoded>
      <pubDate>Wed, 01 Nov 2023 10:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/d2456890/a3f7f275.mp3" length="36101505" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:duration>2257</itunes:duration>
      <itunes:summary>Kaelynn Partlow, autistic advocate and Senior Therapist at Project Hope Foundation, Inc., was featured on the Netflix series called, “Love on the Spectrum.” She joins hosts Erin and Lily to chat about neurodiversity, social media advocacy, and more!</itunes:summary>
      <itunes:subtitle>Kaelynn Partlow, autistic advocate and Senior Therapist at Project Hope Foundation, Inc., was featured on the Netflix series called, “Love on the Spectrum.” She joins hosts Erin and Lily to chat about neurodiversity, social media advocacy, and more!</itunes:subtitle>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Vilissa Thompson</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:episode>6</itunes:episode>
      <podcast:episode>6</podcast:episode>
      <itunes:title>Vilissa Thompson</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">4e68a643-08bc-4218-a4b2-08a57cad5fbd</guid>
      <link>https://share.transistor.fm/s/477084fc</link>
      <description>
        <![CDATA[In this episode, we talk about disability pride with Vilissa Thompson, who is celebrating the 10 year anniversary of her work!]]>
      </description>
      <content:encoded>
        <![CDATA[In this episode, we talk about disability pride with Vilissa Thompson, who is celebrating the 10 year anniversary of her work!]]>
      </content:encoded>
      <pubDate>Tue, 18 Jul 2023 16:10:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/477084fc/4cadfd84.mp3" length="43390666" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:duration>2712</itunes:duration>
      <itunes:summary>In this episode, we talk about disability pride with Vilissa Thompson, who is celebrating the 10 year anniversary of her work!</itunes:summary>
      <itunes:subtitle>In this episode, we talk about disability pride with Vilissa Thompson, who is celebrating the 10 year anniversary of her work!</itunes:subtitle>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Erin &amp; Lily</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:episode>5</itunes:episode>
      <podcast:episode>5</podcast:episode>
      <itunes:title>Erin &amp; Lily</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">e2a2d77c-8cb1-412c-adec-647dcbbb2206</guid>
      <link>https://share.transistor.fm/s/2285c8de</link>
      <description>
        <![CDATA[In this special episode, hosts Erin and Lily bring on their romantic partners to chat about their love origin stories, dealing with conflict as multiply-disabled couples, and the importance of strong communication in a relationship.]]>
      </description>
      <content:encoded>
        <![CDATA[In this special episode, hosts Erin and Lily bring on their romantic partners to chat about their love origin stories, dealing with conflict as multiply-disabled couples, and the importance of strong communication in a relationship.]]>
      </content:encoded>
      <pubDate>Thu, 15 Jun 2023 13:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/2285c8de/3b7d0473.mp3" length="42050840" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:duration>2629</itunes:duration>
      <itunes:summary>In this special episode, hosts Erin and Lily bring on their romantic partners to chat about their love origin stories, dealing with conflict as multiply-disabled couples, and the importance of strong communication in a relationship.</itunes:summary>
      <itunes:subtitle>In this special episode, hosts Erin and Lily bring on their romantic partners to chat about their love origin stories, dealing with conflict as multiply-disabled couples, and the importance of strong communication in a relationship.</itunes:subtitle>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Dom Evans</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:episode>4</itunes:episode>
      <podcast:episode>4</podcast:episode>
      <itunes:title>Dom Evans</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">50c7cae7-a0fb-4367-b943-b2e9eb103de3</guid>
      <link>https://share.transistor.fm/s/36b8b271</link>
      <description>
        <![CDATA[Dom Evans (they/he) is a filmmaker, activist, public speaker, and writer. They dig deep into discussions with Erin and Lily about health care and mental health. Plus, a live declaration of love!]]>
      </description>
      <content:encoded>
        <![CDATA[Dom Evans (they/he) is a filmmaker, activist, public speaker, and writer. They dig deep into discussions with Erin and Lily about health care and mental health. Plus, a live declaration of love!]]>
      </content:encoded>
      <pubDate>Thu, 18 May 2023 13:30:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/36b8b271/8fb6a794.mp3" length="109677768" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:duration>2742</itunes:duration>
      <itunes:summary>Dom Evans (they/he) is a filmmaker, activist, public speaker, and writer. They dig deep into discussions with Erin and Lily about health care and mental health. Plus, a live declaration of love!</itunes:summary>
      <itunes:subtitle>Dom Evans (they/he) is a filmmaker, activist, public speaker, and writer. They dig deep into discussions with Erin and Lily about health care and mental health. Plus, a live declaration of love!</itunes:subtitle>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Emily Ladau</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:episode>3</itunes:episode>
      <podcast:episode>3</podcast:episode>
      <itunes:title>Emily Ladau</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">c6c898cb-d4ed-4b8a-a023-d38f8b99cf9a</guid>
      <link>https://share.transistor.fm/s/b5e3eb31</link>
      <description>
        <![CDATA[Author of Demystifying Disability, Emily Ladau, discusses her experiences with ableism and invasive questions on dating apps, and dealing with breakups. Erin and Lily join Emily in sharing their cringiest first dates and how to know when love is real.]]>
      </description>
      <content:encoded>
        <![CDATA[Author of Demystifying Disability, Emily Ladau, discusses her experiences with ableism and invasive questions on dating apps, and dealing with breakups. Erin and Lily join Emily in sharing their cringiest first dates and how to know when love is real.]]>
      </content:encoded>
      <pubDate>Fri, 14 Apr 2023 06:45:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/b5e3eb31/1088cbed.mp3" length="101273570" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:duration>2532</itunes:duration>
      <itunes:summary>Author of Demystifying Disability, Emily Ladau, discusses her experiences with ableism and invasive questions on dating apps, and dealing with breakups. Erin and Lily join Emily in sharing their cringiest first dates and how to know when love is real.</itunes:summary>
      <itunes:subtitle>Author of Demystifying Disability, Emily Ladau, discusses her experiences with ableism and invasive questions on dating apps, and dealing with breakups. Erin and Lily join Emily in sharing their cringiest first dates and how to know when love is real.</itunes:subtitle>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Nic Novicki</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:episode>2</itunes:episode>
      <podcast:episode>2</podcast:episode>
      <itunes:title>Nic Novicki</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">80c7379a-e565-4823-8497-16e3a898a5f9</guid>
      <link>https://share.transistor.fm/s/182a7a46</link>
      <description>
        <![CDATA[Erin and Lily are in conversation with comedian, actor, and founder of the Easterseals Disability Film Challenge, Nic Novicki. Nic talks about being a father and husband while working in Hollywood, and how your priorities shift when becoming a parent. The group discusses authentic disability representation in movies, popcorn betrayal, and a love story so sweet that it ended up on the big screen!]]>
      </description>
      <content:encoded>
        <![CDATA[Erin and Lily are in conversation with comedian, actor, and founder of the Easterseals Disability Film Challenge, Nic Novicki. Nic talks about being a father and husband while working in Hollywood, and how your priorities shift when becoming a parent. The group discusses authentic disability representation in movies, popcorn betrayal, and a love story so sweet that it ended up on the big screen!]]>
      </content:encoded>
      <pubDate>Fri, 14 Apr 2023 06:30:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/182a7a46/99aac479.mp3" length="33888482" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:duration>2118</itunes:duration>
      <itunes:summary>Erin and Lily are in conversation with comedian, actor, and founder of the Easterseals Disability Film Challenge, Nic Novicki. Nic talks about being a father and husband while working in Hollywood, and how your priorities shift when becoming a parent. The group discusses authentic disability representation in movies, popcorn betrayal, and a love story so sweet that it ended up on the big screen!</itunes:summary>
      <itunes:subtitle>Erin and Lily are in conversation with comedian, actor, and founder of the Easterseals Disability Film Challenge, Nic Novicki. Nic talks about being a father and husband while working in Hollywood, and how your priorities shift when becoming a parent. The</itunes:subtitle>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Jennifer Msumba</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:episode>1</itunes:episode>
      <podcast:episode>1</podcast:episode>
      <itunes:title>Jennifer Msumba</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">5aab46d3-1b9e-4c64-a001-142f213642c0</guid>
      <link>https://share.transistor.fm/s/bfcb23c7</link>
      <description>
        <![CDATA[Erin and Lily speak with award-winning filmmaker, musician, and creator of the Everything You Know About Disability is Wrong theme song, Jennifer Msumba. Jennifer shares her experiences in unrequited love as an autistic woman. The three women chat openly about the awkwardness of dating, being true to yourself, and farts!]]>
      </description>
      <content:encoded>
        <![CDATA[Erin and Lily speak with award-winning filmmaker, musician, and creator of the Everything You Know About Disability is Wrong theme song, Jennifer Msumba. Jennifer shares her experiences in unrequited love as an autistic woman. The three women chat openly about the awkwardness of dating, being true to yourself, and farts!]]>
      </content:encoded>
      <pubDate>Fri, 14 Apr 2023 06:15:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/bfcb23c7/88323e3e.mp3" length="33845118" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:duration>2116</itunes:duration>
      <itunes:summary>Erin and Lily speak with award-winning filmmaker, musician, and creator of the Everything You Know About Disability is Wrong theme song, Jennifer Msumba. Jennifer shares her experiences in unrequited love as an autistic woman. The three women chat openly about the awkwardness of dating, being true to yourself, and farts!</itunes:summary>
      <itunes:subtitle>Erin and Lily speak with award-winning filmmaker, musician, and creator of the Everything You Know About Disability is Wrong theme song, Jennifer Msumba. Jennifer shares her experiences in unrequited love as an autistic woman. The three women chat openly </itunes:subtitle>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
    <item>
      <title>Audio Trailer Episode</title>
      <itunes:season>1</itunes:season>
      <podcast:season>1</podcast:season>
      <itunes:episode>1</itunes:episode>
      <podcast:episode>1</podcast:episode>
      <itunes:title>Audio Trailer Episode</itunes:title>
      <itunes:episodeType>full</itunes:episodeType>
      <guid isPermaLink="false">2850537c-d80c-4f6d-be3a-fd6aca9a768d</guid>
      <link>https://share.transistor.fm/s/880a3af4</link>
      <description>
        <![CDATA[]]>
      </description>
      <content:encoded>
        <![CDATA[]]>
      </content:encoded>
      <pubDate>Fri, 14 Apr 2023 06:00:00 -0400</pubDate>
      <author>Easterseals</author>
      <enclosure url="https://dts.podtrac.com/redirect.mp3/media.transistor.fm/880a3af4/8f03f313.mp3" length="992196" type="audio/mpeg"/>
      <itunes:author>Easterseals</itunes:author>
      <itunes:duration>62</itunes:duration>
      <itunes:summary>
        <![CDATA[]]>
      </itunes:summary>
      <itunes:keywords></itunes:keywords>
      <itunes:explicit>No</itunes:explicit>
    </item>
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