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    <title>Connecting Disability</title>
    <description>In Connecting Disability, accessibility reporter Meagan Gillmore and her guests consider how experiences of disability help us connect with others and society.</description>
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    <pubDate>Wed, 16 Aug 2023 15:33:14 +0000</pubDate>
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    <itunes:summary>In Connecting Disability, accessibility reporter Meagan Gillmore and her guests consider how experiences of disability help us connect with others and society.</itunes:summary>
    <itunes:author>Accessible Media Inc, Meagan Gillmore</itunes:author>
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      <title>Connecting Disability to… satire and social commentary with Steven Verdile of The Squeaky Wheel</title>
      <description><![CDATA[We are ending the summer in style as we welcome Steven Verdile onto the show today. Steven is a New York City-based designer and writer, but he’s probably best known as the creator of the disability satire website The Squeaky Wheel. We talk about his approach to disability satire and humour, the funniest disability moments we’ve encountered recently, the Barbie movie and more. 

Here are the links to the Squeaky Wheel articles we discussed: 
Wheelchair Barbie Gets Revolutionary 4 Seconds of Fame: https://thesqueakywheel.org/2023/08/02/wheelchair-barbie-gets-revolutionary-4-seconds-of-fame/
Disability Pride May Have Ended, but 11 Months of Disability Shame Are Just Getting Started: https://thesqueakywheel.org/2023/08/01/disability-pride-month-may-have-ended-but-11-months-of-disability-shame-are-just-getting-started/
U.K.’s Largest Benefit Recipient Awarded with Shiny New Hat: https://thesqueakywheel.org/2023/05/06/uks-largest-benefit-recipient-awarded-with-shiny-new-hat/

Visit The Squeaky Wheel at: www.thesqueakywheel.org or Steven Verdile’s website at: www.stevenverdile.com

On a sadder note, this episode marks the final episode of the Connecting Disability podcast. Recent changes at AMI-audio have meant several shows, like this one, are ending. I want to thank all the guests who joined me during the past two years, the technical producers who worked on this show, and Andy Frank and Ryan Delehanty for guiding the podcasts.  And most importantly, thank you to you, the listeners, for joining me on this journey. I loved every minute we spent together. I’m sad to be leaving this show. 

If you want to contact me, you can go to the site formerly known at Twitter @meagangillmore. My messages are open. Or, send a note to feedback@ami.ca, tell them you’d like to get in touch with me, and they’ll pass your message along. I hope we connect again soon! 
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      <pubDate>Wed, 16 Aug 2023 15:33:14 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-satire-and-social-commentary-with-steven-verdile-of-the-squeaky-wheel-iKm_iiH_</link>
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      <itunes:title>Connecting Disability to… satire and social commentary with Steven Verdile of The Squeaky Wheel</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:43:12</itunes:duration>
      <itunes:summary>We are ending the summer in style as we welcome Steven Verdile onto the show today. Steven is a New York City-based designer and writer, but he’s probably best known as the creator of the disability satire website The Squeaky Wheel. We talk about his approach to disability satire and humour, the funniest disability moments we’ve encountered recently, the Barbie movie and more. 

Here are the links to the Squeaky Wheel articles we discussed: 
Wheelchair Barbie Gets Revolutionary 4 Seconds of Fame: https://thesqueakywheel.org/2023/08/02/wheelchair-barbie-gets-revolutionary-4-seconds-of-fame/
Disability Pride May Have Ended, but 11 Months of Disability Shame Are Just Getting Started: https://thesqueakywheel.org/2023/08/01/disability-pride-month-may-have-ended-but-11-months-of-disability-shame-are-just-getting-started/
U.K.’s Largest Benefit Recipient Awarded with Shiny New Hat: https://thesqueakywheel.org/2023/05/06/uks-largest-benefit-recipient-awarded-with-shiny-new-hat/

Visit The Squeaky Wheel at: www.thesqueakywheel.org or Steven Verdile’s website at: www.stevenverdile.com

On a sadder note, this episode marks the final episode of the Connecting Disability podcast. Recent changes at AMI-audio have meant several shows, like this one, are ending. I want to thank all the guests who joined me during the past two years, the technical producers who worked on this show, and Andy Frank and Ryan Delehanty for guiding the podcasts.  And most importantly, thank you to you, the listeners, for joining me on this journey. I loved every minute we spent together. I’m sad to be leaving this show. 

If you want to contact me, you can go to the site formerly known at Twitter @meagangillmore. My messages are open. Or, send a note to feedback@ami.ca, tell them you’d like to get in touch with me, and they’ll pass your message along. I hope we connect again soon! </itunes:summary>
      <itunes:subtitle>We are ending the summer in style as we welcome Steven Verdile onto the show today. Steven is a New York City-based designer and writer, but he’s probably best known as the creator of the disability satire website The Squeaky Wheel. We talk about his approach to disability satire and humour, the funniest disability moments we’ve encountered recently, the Barbie movie and more. 

Here are the links to the Squeaky Wheel articles we discussed: 
Wheelchair Barbie Gets Revolutionary 4 Seconds of Fame: https://thesqueakywheel.org/2023/08/02/wheelchair-barbie-gets-revolutionary-4-seconds-of-fame/
Disability Pride May Have Ended, but 11 Months of Disability Shame Are Just Getting Started: https://thesqueakywheel.org/2023/08/01/disability-pride-month-may-have-ended-but-11-months-of-disability-shame-are-just-getting-started/
U.K.’s Largest Benefit Recipient Awarded with Shiny New Hat: https://thesqueakywheel.org/2023/05/06/uks-largest-benefit-recipient-awarded-with-shiny-new-hat/

Visit The Squeaky Wheel at: www.thesqueakywheel.org or Steven Verdile’s website at: www.stevenverdile.com

On a sadder note, this episode marks the final episode of the Connecting Disability podcast. Recent changes at AMI-audio have meant several shows, like this one, are ending. I want to thank all the guests who joined me during the past two years, the technical producers who worked on this show, and Andy Frank and Ryan Delehanty for guiding the podcasts.  And most importantly, thank you to you, the listeners, for joining me on this journey. I loved every minute we spent together. I’m sad to be leaving this show. 

If you want to contact me, you can go to the site formerly known at Twitter @meagangillmore. My messages are open. Or, send a note to feedback@ami.ca, tell them you’d like to get in touch with me, and they’ll pass your message along. I hope we connect again soon! </itunes:subtitle>
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      <title>Connecting Disability to… living a full life with hidden disabilities with Laura Brydges</title>
      <description><![CDATA[There’s been a lot more talk lately (in Canada, at least) about the disability community as a political unit. But what happens if your disabilities aren’t considered to be disabilities? Laura Brydges has spent years learning and teaching others about the needs of those with hidden disabilities. She joins us to talk about her journey with hidden disabilities, what politics can and cannot do for people with disabilities, and to share some poetry. Laura has a lot of wisdom to share about choosing happiness and living a full life with limitations. I really hope you enjoy spending time with her as much as I did.

A quick editing note: During this conversation, Laura and I talk about a draft accessibility standard from Accessibility Standards Canada that is open for public consultation. That specific standard is the outdoor spaces standard. You can find more information about that standard here: https://accessible.canada.ca/.  The deadline for public feedback is August 11.

Learn more about Laura’s work and the resources she’s developed here: https://hdscanada.wordpress.com/ 
]]></description>
      <pubDate>Wed, 19 Jul 2023 13:54:26 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-living-a-full-life-with-hidden-disabilities-with-laura-brydges-VCsvqHOc</link>
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      <itunes:title>Connecting Disability to… living a full life with hidden disabilities with Laura Brydges</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:40:07</itunes:duration>
      <itunes:summary>There’s been a lot more talk lately (in Canada, at least) about the disability community as a political unit. But what happens if your disabilities aren’t considered to be disabilities? Laura Brydges has spent years learning and teaching others about the needs of those with hidden disabilities. She joins us to talk about her journey with hidden disabilities, what politics can and cannot do for people with disabilities, and to share some poetry. Laura has a lot of wisdom to share about choosing happiness and living a full life with limitations. I really hope you enjoy spending time with her as much as I did.

A quick editing note: During this conversation, Laura and I talk about a draft accessibility standard from Accessibility Standards Canada that is open for public consultation. That specific standard is the outdoor spaces standard. You can find more information about that standard here: https://accessible.canada.ca/.  The deadline for public feedback is August 11.

Learn more about Laura’s work and the resources she’s developed here: https://hdscanada.wordpress.com/ </itunes:summary>
      <itunes:subtitle>There’s been a lot more talk lately (in Canada, at least) about the disability community as a political unit. But what happens if your disabilities aren’t considered to be disabilities? Laura Brydges has spent years learning and teaching others about the needs of those with hidden disabilities. She joins us to talk about her journey with hidden disabilities, what politics can and cannot do for people with disabilities, and to share some poetry. Laura has a lot of wisdom to share about choosing happiness and living a full life with limitations. I really hope you enjoy spending time with her as much as I did.

A quick editing note: During this conversation, Laura and I talk about a draft accessibility standard from Accessibility Standards Canada that is open for public consultation. That specific standard is the outdoor spaces standard. You can find more information about that standard here: https://accessible.canada.ca/.  The deadline for public feedback is August 11.

Learn more about Laura’s work and the resources she’s developed here: https://hdscanada.wordpress.com/ </itunes:subtitle>
      <itunes:keywords>meagan gillmore, laura brydges, blind, accessibility standards canada, ami, partially sighted, podcast, ami-audio, connecting disability, hidden disabilities</itunes:keywords>
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      <title>Connecting Disability to… Paralympic sports, dog training and reinvention with Jess Tuomela</title>
      <description><![CDATA[There are so many things to say about this month’s guest. Jess Tuomela is a four-time Paralympian who has worked as a massage therapist and now as a dog trainer, training dogs in scent discriminate trailing. But while she’s made headlines for her athletic career and dog training, my favourite thing about Jess is the time I got to spend with her several years ago. There’s a lot of laughter in this episode. We hope you enjoy it as much as we did – and Jess, I really hope we get to meet in-person again soon! 

Learn more about True North Canine, Jess’s dog training company, here: https://truenorthk9dogs.com/

More on Jess and Lucy’s work locating an elderly woman: https://www.vancouverislandfreedaily.com/news/saanich-paralympian-finds-missing-person-with-the-help-of-her-dog/

Jess also works as a mental performance strategist: https://www.jessicatuomela.com/

Jess was featured on an episode of the CBC podcast, Player’s Own Voice. Catch that here: https://www.cbc.ca/listen/cbc-podcasts/202-players-own-voice/episode/15796615-jessica-tuomela-paratriathlete-trains-through-the-trials

We talk about the CNIB Lake Joseph Centre a lot on this podcast. You can learn more about the camp here: https://www.cnib.ca/en/programs-and-services/play/cnib-lake-joe?region=on 

]]></description>
      <pubDate>Thu, 22 Jun 2023 15:54:38 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-paralympic-sports-dog-training-and-reinvention-with-jess-tuomela-2ChlZDVS</link>
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      <itunes:title>Connecting Disability to… Paralympic sports, dog training and reinvention with Jess Tuomela</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:32:54</itunes:duration>
      <itunes:summary>There are so many things to say about this month’s guest. Jess Tuomela is a four-time Paralympian who has worked as a massage therapist and now as a dog trainer, training dogs in scent discriminate trailing. But while she’s made headlines for her athletic career and dog training, my favourite thing about Jess is the time I got to spend with her several years ago. There’s a lot of laughter in this episode. We hope you enjoy it as much as we did – and Jess, I really hope we get to meet in-person again soon! 

Learn more about True North Canine, Jess’s dog training company, here: https://truenorthk9dogs.com/

More on Jess and Lucy’s work locating an elderly woman: https://www.vancouverislandfreedaily.com/news/saanich-paralympian-finds-missing-person-with-the-help-of-her-dog/

Jess also works as a mental performance strategist: https://www.jessicatuomela.com/

Jess was featured on an episode of the CBC podcast, Player’s Own Voice. Catch that here: https://www.cbc.ca/listen/cbc-podcasts/202-players-own-voice/episode/15796615-jessica-tuomela-paratriathlete-trains-through-the-trials

We talk about the CNIB Lake Joseph Centre a lot on this podcast. You can learn more about the camp here: https://www.cnib.ca/en/programs-and-services/play/cnib-lake-joe?region=on 
</itunes:summary>
      <itunes:subtitle>There are so many things to say about this month’s guest. Jess Tuomela is a four-time Paralympian who has worked as a massage therapist and now as a dog trainer, training dogs in scent discriminate trailing. But while she’s made headlines for her athletic career and dog training, my favourite thing about Jess is the time I got to spend with her several years ago. There’s a lot of laughter in this episode. We hope you enjoy it as much as we did – and Jess, I really hope we get to meet in-person again soon! 

Learn more about True North Canine, Jess’s dog training company, here: https://truenorthk9dogs.com/

More on Jess and Lucy’s work locating an elderly woman: https://www.vancouverislandfreedaily.com/news/saanich-paralympian-finds-missing-person-with-the-help-of-her-dog/

Jess also works as a mental performance strategist: https://www.jessicatuomela.com/

Jess was featured on an episode of the CBC podcast, Player’s Own Voice. Catch that here: https://www.cbc.ca/listen/cbc-podcasts/202-players-own-voice/episode/15796615-jessica-tuomela-paratriathlete-trains-through-the-trials

We talk about the CNIB Lake Joseph Centre a lot on this podcast. You can learn more about the camp here: https://www.cnib.ca/en/programs-and-services/play/cnib-lake-joe?region=on 
</itunes:subtitle>
      <itunes:keywords>meagan gillmore, blind, jessica tuomela, ami, search and rescue, partially sighted, lucy, podcast, ami-audio, dog training, connecting disability, true north canine</itunes:keywords>
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      <title>Connecting Disability to… What you learn when you Look Both Ways with Brooke</title>
      <description><![CDATA[What do New York Senator campaigns, sociology and the late Christopher Reeve (a.k.a. Superman) all have in common? Our guest: Brooke Ellison. Brooke is an associate professor at Stony Brook University in Stony Brook, New York. She’s also the author of two books: Miracles Happen and her most recent, Look Both Ways. She joined the show to talk about the process of writing this book, the biggest thing she would change about how she’s lived with a disability, and her thoughts about disability’s place in politics. 

You can learn more about Brooke and her work at her website: www.brookeellison.com

Follow her on Twitter: @brookemellison
]]></description>
      <pubDate>Wed, 17 May 2023 15:14:42 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-what-you-lean-when-you-look-both-ways-with-brooke-G0B_Kftz</link>
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      <itunes:title>Connecting Disability to… What you learn when you Look Both Ways with Brooke</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:37:03</itunes:duration>
      <itunes:summary>What do New York Senator campaigns, sociology and the late Christopher Reeve (a.k.a. Superman) all have in common? Our guest: Brooke Ellison. Brooke is an associate professor at Stony Brook University in Stony Brook, New York. She’s also the author of two books: Miracles Happen and her most recent, Look Both Ways. She joined the show to talk about the process of writing this book, the biggest thing she would change about how she’s lived with a disability, and her thoughts about disability’s place in politics. 

You can learn more about Brooke and her work at her website: www.brookeellison.com

Follow her on Twitter: @brookemellison</itunes:summary>
      <itunes:subtitle>What do New York Senator campaigns, sociology and the late Christopher Reeve (a.k.a. Superman) all have in common? Our guest: Brooke Ellison. Brooke is an associate professor at Stony Brook University in Stony Brook, New York. She’s also the author of two books: Miracles Happen and her most recent, Look Both Ways. She joined the show to talk about the process of writing this book, the biggest thing she would change about how she’s lived with a disability, and her thoughts about disability’s place in politics. 

You can learn more about Brooke and her work at her website: www.brookeellison.com

Follow her on Twitter: @brookemellison</itunes:subtitle>
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      <title>Connecting Disability to… Disability Pride with Ben Mattlin</title>
      <description><![CDATA[Ben Mattlin is one of my favourite writers to read about disability, disability policy and life with disability. His latest book, Disability Pride, describes how the Americans with Disabilities Act (ADA) has changed disability advocacy in the United States and provides snapshots of what disability advocacy and culture looks like today. I was so humbled and grateful when he agreed to be on our show and I hope you enjoy this conversation. 
 
Learn more about Ben at www.benmattlin.com   
 
Ben references some different pieces of American legislation. You can read more about the history of the Individuals with Disabilities Education Act here: https://sites.ed.gov/idea/IDEA-History.  
 
The lawsuit Ben refers to where a Florida woman is suing a Maine resort over its lack of ADA compliance is called the Acheson Hotels, LLC, v. Deborah Laufer.  
Read the New York Times reporting on it here: https://www.nytimes.com/2023/03/27/us/supreme-court-maine-disability.html.   
]]></description>
      <pubDate>Wed, 19 Apr 2023 15:52:57 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-disability-pride-with-ben-mattlin-t2D8yFLD</link>
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      <itunes:title>Connecting Disability to… Disability Pride with Ben Mattlin</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:37:51</itunes:duration>
      <itunes:summary>Ben Mattlin is one of my favourite writers to read about disability, disability policy and life with disability. His latest book, Disability Pride, describes how the Americans with Disabilities Act (ADA) has changed disability advocacy in the United States and provides snapshots of what disability advocacy and culture looks like today. I was so humbled and grateful when he agreed to be on our show and I hope you enjoy this conversation. 
 
Learn more about Ben at www.benmattlin.com   
 
Ben references some different pieces of American legislation. You can read more about the history of the Individuals with Disabilities Education Act here: https://sites.ed.gov/idea/IDEA-History.  
 
The lawsuit Ben refers to where a Florida woman is suing a Maine resort over its lack of ADA compliance is called the Acheson Hotels, LLC, v. Deborah Laufer.  
Read the New York Times reporting on it here: https://www.nytimes.com/2023/03/27/us/supreme-court-maine-disability.html.   </itunes:summary>
      <itunes:subtitle>Ben Mattlin is one of my favourite writers to read about disability, disability policy and life with disability. His latest book, Disability Pride, describes how the Americans with Disabilities Act (ADA) has changed disability advocacy in the United States and provides snapshots of what disability advocacy and culture looks like today. I was so humbled and grateful when he agreed to be on our show and I hope you enjoy this conversation. 
 
Learn more about Ben at www.benmattlin.com   
 
Ben references some different pieces of American legislation. You can read more about the history of the Individuals with Disabilities Education Act here: https://sites.ed.gov/idea/IDEA-History.  
 
The lawsuit Ben refers to where a Florida woman is suing a Maine resort over its lack of ADA compliance is called the Acheson Hotels, LLC, v. Deborah Laufer.  
Read the New York Times reporting on it here: https://www.nytimes.com/2023/03/27/us/supreme-court-maine-disability.html.   </itunes:subtitle>
      <itunes:keywords>meagan gillmore, ben mattlin, disability, blind, ami, partially sighted, podcast, legislation, author, ami-audio, connecting disability, disability policy</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>20</itunes:episode>
    </item>
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      <title>Connecting disability to... being a sibling</title>
      <description><![CDATA[Friends, we have a treat of an episode for you this month! The sibling relationship can be the longest and most complicated relationship in someone’s life. Today, we’re chatting about how disability and chronic illness influence siblings. Our guests are sisters Holly and Amy Mathers. Holly is a registered psychotherapist and Amy is a passionate advocate of Canadian teen fiction. They joined me to talk about how Amy’s disability has impacted them throughout their lives and what it took to go from being siblings to friends. (And, yes, since Holly is a psychotherapist, this did feel like therapy sometimes! All the feelings!)  

You can listen to Amy’s podcast about Canadian teen authors, YA Write, on major podcast platforms. Find more info here: https://bookcentre.ca/publications/ya-write  

Learn more about Holly’s work here: https://www.hopeforfamilies.net/ 

Siblings Canada provided crucial support for this episode. Learn more about them here: https://canadiancaregiving.org/siblingscanadea/ 

]]></description>
      <pubDate>Wed, 15 Mar 2023 11:00:00 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-being-a-sibling-INSM1LKX</link>
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      <itunes:title>Connecting disability to... being a sibling</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:38:56</itunes:duration>
      <itunes:summary>Friends, we have a treat of an episode for you this month! The sibling relationship can be the longest and most complicated relationship in someone’s life. Today, we’re chatting about how disability and chronic illness influence siblings. Our guests are sisters Holly and Amy Mathers. Holly is a registered psychotherapist and Amy is a passionate advocate of Canadian teen fiction. They joined me to talk about how Amy’s disability has impacted them throughout their lives and what it took to go from being siblings to friends. (And, yes, since Holly is a psychotherapist, this did feel like therapy sometimes! All the feelings!)  

You can listen to Amy’s podcast about Canadian teen authors, YA Write, on major podcast platforms. Find more info here: https://bookcentre.ca/publications/ya-write  

Learn more about Holly’s work here: https://www.hopeforfamilies.net/ 

Siblings Canada provided crucial support for this episode. Learn more about them here: https://canadiancaregiving.org/siblingscanadea/ 
</itunes:summary>
      <itunes:subtitle>Friends, we have a treat of an episode for you this month! The sibling relationship can be the longest and most complicated relationship in someone’s life. Today, we’re chatting about how disability and chronic illness influence siblings. Our guests are sisters Holly and Amy Mathers. Holly is a registered psychotherapist and Amy is a passionate advocate of Canadian teen fiction. They joined me to talk about how Amy’s disability has impacted them throughout their lives and what it took to go from being siblings to friends. (And, yes, since Holly is a psychotherapist, this did feel like therapy sometimes! All the feelings!)  

You can listen to Amy’s podcast about Canadian teen authors, YA Write, on major podcast platforms. Find more info here: https://bookcentre.ca/publications/ya-write  

Learn more about Holly’s work here: https://www.hopeforfamilies.net/ 

Siblings Canada provided crucial support for this episode. Learn more about them here: https://canadiancaregiving.org/siblingscanadea/ 
</itunes:subtitle>
      <itunes:keywords>meagan gillmore, holly mathers, authors, siblings, ya write, blind, relationship, ami, teen fiction, amy mathers, young adult, partially sighted, podcast, podcast, ami-audio, connecting disability</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>19</itunes:episode>
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      <title>Connecting disability to … life as a Black family</title>
      <description><![CDATA["This month, we are celebrating love and remembering Black History Month with Clovis and Sherron Grant. Clovis and Sherron are the co-founders of Sawubona Africentric Circle of Support, an organization dedicated to helping Black families get the resources they need to support loved ones who live with a disability. Clovis and Sherron have a lot of insight about family life and responding to difficult social expectations. I really hope you learn as much from them as I did.  

You can find their work here: https://www.sawubonaacs.org/
Follow them on Twitter: @sawubonaacs
Read more about how this work started here: https://www.thestar.com/life/parent/2020/12/06/sherron-grant-got-used-to-being-the-only-black-mother-in-support-groups-for-parents-of-autistic-kids-shes-making-sure-other-black-parents-dont-feel-as-lonely-as-she-did.html 
Read more of Clovis’sreflections on fatherhood in the Spring 2022 issue of Autism Matters: https://files.elfsightcdn.com/43cd4e5b-d7d4-4fe6-8e3c-9968aa47e130/db9bbc51-a266-4cff-9ab7-8448da7ac0ae/AM---Spring-2022---FINAL.pdf   "
]]></description>
      <pubDate>Wed, 15 Feb 2023 12:00:00 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-life-as-a-black-family-cKTjuqO8</link>
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      <itunes:title>Connecting disability to … life as a Black family</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:40:02</itunes:duration>
      <itunes:summary>&quot;This month, we are celebrating love and remembering Black History Month with Clovis and Sherron Grant. Clovis and Sherron are the co-founders of Sawubona Africentric Circle of Support, an organization dedicated to helping Black families get the resources they need to support loved ones who live with a disability. Clovis and Sherron have a lot of insight about family life and responding to difficult social expectations. I really hope you learn as much from them as I did.  

You can find their work here: https://www.sawubonaacs.org/
Follow them on Twitter: @sawubonaacs
Read more about how this work started here: https://www.thestar.com/life/parent/2020/12/06/sherron-grant-got-used-to-being-the-only-black-mother-in-support-groups-for-parents-of-autistic-kids-shes-making-sure-other-black-parents-dont-feel-as-lonely-as-she-did.html 
Read more of Clovis’sreflections on fatherhood in the Spring 2022 issue of Autism Matters: https://files.elfsightcdn.com/43cd4e5b-d7d4-4fe6-8e3c-9968aa47e130/db9bbc51-a266-4cff-9ab7-8448da7ac0ae/AM---Spring-2022---FINAL.pdf   &quot;</itunes:summary>
      <itunes:subtitle>&quot;This month, we are celebrating love and remembering Black History Month with Clovis and Sherron Grant. Clovis and Sherron are the co-founders of Sawubona Africentric Circle of Support, an organization dedicated to helping Black families get the resources they need to support loved ones who live with a disability. Clovis and Sherron have a lot of insight about family life and responding to difficult social expectations. I really hope you learn as much from them as I did.  

You can find their work here: https://www.sawubonaacs.org/
Follow them on Twitter: @sawubonaacs
Read more about how this work started here: https://www.thestar.com/life/parent/2020/12/06/sherron-grant-got-used-to-being-the-only-black-mother-in-support-groups-for-parents-of-autistic-kids-shes-making-sure-other-black-parents-dont-feel-as-lonely-as-she-did.html 
Read more of Clovis’sreflections on fatherhood in the Spring 2022 issue of Autism Matters: https://files.elfsightcdn.com/43cd4e5b-d7d4-4fe6-8e3c-9968aa47e130/db9bbc51-a266-4cff-9ab7-8448da7ac0ae/AM---Spring-2022---FINAL.pdf   &quot;</itunes:subtitle>
      <itunes:keywords>meagan gillmore, black history month, blind, ami, partially sighted, resources, podcast, ami-audio, connecting disability, clovis and sherron grant, sawubona africentric circle of support</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>18</itunes:episode>
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      <title>Connecting Disability to… space travel</title>
      <description><![CDATA[Welcome to 2023! We often start a new year with lofty clichés about reaching for the moon or shooting for the stars. But what if that became a reality? Today, we are talking to Denna Lambert. 

Denna is the Space Technology Mission Directorate’s Early Stage Innovations & Partnerships Diversity, Equity, Inclusion and Accessibility lead at NASA. She works with space technology and in December, she got to experience zero-gravity herself when she participated in a flight with AstroAccess. She joins us to talk about how she got to NASA, her hopes for disability inclusion in space travel and what it’s like being a blind Black woman working in STEM. I loved meeting Denna, and I hope you do too! 

Learn more about AstroAccess here: https://astroaccess.org/ 
]]></description>
      <pubDate>Wed, 18 Jan 2023 15:08:40 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-space-travel-PS0UssFz</link>
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      <itunes:title>Connecting Disability to… space travel</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:34:00</itunes:duration>
      <itunes:summary>Welcome to 2023! We often start a new year with lofty clichés about reaching for the moon or shooting for the stars. But what if that became a reality? Today, we are talking to Denna Lambert. 

Denna is the Space Technology Mission Directorate’s Early Stage Innovations &amp; Partnerships Diversity, Equity, Inclusion and Accessibility lead at NASA. She works with space technology and in December, she got to experience zero-gravity herself when she participated in a flight with AstroAccess. She joins us to talk about how she got to NASA, her hopes for disability inclusion in space travel and what it’s like being a blind Black woman working in STEM. I loved meeting Denna, and I hope you do too! 

Learn more about AstroAccess here: https://astroaccess.org/ </itunes:summary>
      <itunes:subtitle>Welcome to 2023! We often start a new year with lofty clichés about reaching for the moon or shooting for the stars. But what if that became a reality? Today, we are talking to Denna Lambert. 

Denna is the Space Technology Mission Directorate’s Early Stage Innovations &amp; Partnerships Diversity, Equity, Inclusion and Accessibility lead at NASA. She works with space technology and in December, she got to experience zero-gravity herself when she participated in a flight with AstroAccess. She joins us to talk about how she got to NASA, her hopes for disability inclusion in space travel and what it’s like being a blind Black woman working in STEM. I loved meeting Denna, and I hope you do too! 

Learn more about AstroAccess here: https://astroaccess.org/ </itunes:subtitle>
      <itunes:keywords>denna lambert, meagan gillmore, space technology mission directorate’s early stage innovations &amp; partnerships diversity, equity, nasa, blind, ami, partially sighted, podcast, inclusion and accessibility, ami-audio, stem, connecting disability, new year</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>17</itunes:episode>
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      <title>Connecting Disability to… finding home after institutionalization</title>
      <description><![CDATA[In time for the holidays, we’re discussing what it means to find a home. This November, Vicky Levack of Halifax finally left the long-term care facility where she had lived since she was 21. She joined Meagan to talk about what it’s like adjusting to life in the community after being institutionalized, why her advocacy isn’t finished, and her pet peeve with princess movies. 

Thank you so much to everyone who joined us and listened in 2022! We will be back in 2023! 

Follow Vicky on Twitter @VickyLevack

Learn more about the Disability Rights Coalition of Nova Scotia at: https://www.disabilityrightscoalitionns.ca/

Read some reporting Meagan did last year about Vicky’s situation here: https://broadview.org/young-people-with-disabilities-long-term-care/ 
]]></description>
      <pubDate>Wed, 21 Dec 2022 15:11:19 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-finding-home-after-institutionalization-0aIvqUUJ</link>
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      <itunes:title>Connecting Disability to… finding home after institutionalization</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:30:07</itunes:duration>
      <itunes:summary>In time for the holidays, we’re discussing what it means to find a home. This November, Vicky Levack of Halifax finally left the long-term care facility where she had lived since she was 21. She joined Meagan to talk about what it’s like adjusting to life in the community after being institutionalized, why her advocacy isn’t finished, and her pet peeve with princess movies. 

Thank you so much to everyone who joined us and listened in 2022! We will be back in 2023! 

Follow Vicky on Twitter @VickyLevack

Learn more about the Disability Rights Coalition of Nova Scotia at: https://www.disabilityrightscoalitionns.ca/

Read some reporting Meagan did last year about Vicky’s situation here: https://broadview.org/young-people-with-disabilities-long-term-care/ </itunes:summary>
      <itunes:subtitle>In time for the holidays, we’re discussing what it means to find a home. This November, Vicky Levack of Halifax finally left the long-term care facility where she had lived since she was 21. She joined Meagan to talk about what it’s like adjusting to life in the community after being institutionalized, why her advocacy isn’t finished, and her pet peeve with princess movies. 

Thank you so much to everyone who joined us and listened in 2022! We will be back in 2023! 

Follow Vicky on Twitter @VickyLevack

Learn more about the Disability Rights Coalition of Nova Scotia at: https://www.disabilityrightscoalitionns.ca/

Read some reporting Meagan did last year about Vicky’s situation here: https://broadview.org/young-people-with-disabilities-long-term-care/ </itunes:subtitle>
      <itunes:keywords>meagan gillmore, disability rights coalition of nova scotia, advocacy, vicky levack, blind, institutionalized, ami, halifax, partially sighted, podcast, long-term care facility, ami-audio, connecting disability</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>16</itunes:episode>
    </item>
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      <title>Connecting Disability to… inclusive advocacy (and peanut butter cups?!?)</title>
      <description><![CDATA[This month, we’re talking about the news; particularly what stories about disability make the news and what it can be like to report on them. We’re joined by Spencer van Vloten, from BCDisability.com, to talk about how he got involved in covering disability policy, the impact of the COVID-19 pandemic on awareness of disability issues and why the disability movement needs to involve people without disabilities. Stick around to the end – we try to make the case that Reese’s Peanut Butter Cups can teach us about advocacy. 

Also, we do talk about medical assistance in dying (MAID) briefly. If you or someone you know is experiencing thoughts of suicide, call Talk Suicide Canada at 1.833.456.4566.  

You can learn more about Spencer’s work at: www.bcdisability.com 

Follow Spencer on Twitter @BcDisability
]]></description>
      <pubDate>Wed, 16 Nov 2022 16:03:43 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-inclusive-advocacy-and-peanut-butter-cups-bGvjp445</link>
      <enclosure length="29458575" type="audio/mpeg" url="https://op3.dev/e/injector.simplecastaudio.com/78be6ee8-1936-48c9-9672-6eb681edd3a6/episodes/bf4eaf39-3b0f-4389-a755-71ee9f9b4220/audio/128/default.mp3?aid=rss_feed&amp;awCollectionId=78be6ee8-1936-48c9-9672-6eb681edd3a6&amp;awEpisodeId=bf4eaf39-3b0f-4389-a755-71ee9f9b4220&amp;feed=KLnjl5ZJ"/>
      <itunes:title>Connecting Disability to… inclusive advocacy (and peanut butter cups?!?)</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:30:41</itunes:duration>
      <itunes:summary>This month, we’re talking about the news; particularly what stories about disability make the news and what it can be like to report on them. We’re joined by Spencer van Vloten, from BCDisability.com, to talk about how he got involved in covering disability policy, the impact of the COVID-19 pandemic on awareness of disability issues and why the disability movement needs to involve people without disabilities. Stick around to the end – we try to make the case that Reese’s Peanut Butter Cups can teach us about advocacy. 

Also, we do talk about medical assistance in dying (MAID) briefly. If you or someone you know is experiencing thoughts of suicide, call Talk Suicide Canada at 1.833.456.4566.  

You can learn more about Spencer’s work at: www.bcdisability.com 

Follow Spencer on Twitter @BcDisability</itunes:summary>
      <itunes:subtitle>This month, we’re talking about the news; particularly what stories about disability make the news and what it can be like to report on them. We’re joined by Spencer van Vloten, from BCDisability.com, to talk about how he got involved in covering disability policy, the impact of the COVID-19 pandemic on awareness of disability issues and why the disability movement needs to involve people without disabilities. Stick around to the end – we try to make the case that Reese’s Peanut Butter Cups can teach us about advocacy. 

Also, we do talk about medical assistance in dying (MAID) briefly. If you or someone you know is experiencing thoughts of suicide, call Talk Suicide Canada at 1.833.456.4566.  

You can learn more about Spencer’s work at: www.bcdisability.com 

Follow Spencer on Twitter @BcDisability</itunes:subtitle>
      <itunes:keywords>meagan gillmore, maid, covid-19, medical assistance in dying, blind, spencer van vloten, ami, reporting, partially sighted, podcast, peanut butter, ami-audio, talk suicide canada, bcdisability.com, connecting disability, disability policy, reese&apos;s peanut butter cups</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>15</itunes:episode>
    </item>
    <item>
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      <title>Connecting Disability to… crossing the Great Lakes</title>
      <description><![CDATA[Water scares many people. Our guest, Mike Shoreman, has conquered this fear. 

Many people know him as the Unbalanced Paddleboarder. In August, Mike became the first person with disabilities to paddle board across all of the Great Lakes. In this conversation, he talks about why he decided to do this, how crossing the Great Lakes resembles a mental health journey and the pros and cons of being called “inspirational.” He also tries to counsel Meagan through aquatic anxiety.  

Follow Mike on Twitter @MikeShoreman 
Follow Mike on Instagram @mike_shoreman

Learn about his book here: https://www.goodreads.com/en/book/show/55240816-diaries-of-the-unbalanced-paddleboarder
Read the CBC article Meagan mentioned: https://www.cbc.ca/2017/what-moving-to-whitehorse-and-back-taught-me-about-my-disability-and-canada-1.4149676
]]></description>
      <pubDate>Wed, 19 Oct 2022 11:00:00 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-parenting-and-compassion-hs-qigaj-fGaPj29m</link>
      <enclosure length="29363300" type="audio/mpeg" url="https://op3.dev/e/injector.simplecastaudio.com/78be6ee8-1936-48c9-9672-6eb681edd3a6/episodes/bce2fb88-2513-4b82-89a0-0a4bf0d5563b/audio/128/default.mp3?aid=rss_feed&amp;awCollectionId=78be6ee8-1936-48c9-9672-6eb681edd3a6&amp;awEpisodeId=bce2fb88-2513-4b82-89a0-0a4bf0d5563b&amp;feed=KLnjl5ZJ"/>
      <itunes:title>Connecting Disability to… crossing the Great Lakes</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:30:34</itunes:duration>
      <itunes:summary>Water scares many people. Our guest, Mike Shoreman, has conquered this fear. 

Many people know him as the Unbalanced Paddleboarder. In August, Mike became the first person with disabilities to paddle board across all of the Great Lakes. In this conversation, he talks about why he decided to do this, how crossing the Great Lakes resembles a mental health journey and the pros and cons of being called “inspirational.” He also tries to counsel Meagan through aquatic anxiety.  

Follow Mike on Twitter @MikeShoreman 
Follow Mike on Instagram @mike_shoreman

Learn about his book here: https://www.goodreads.com/en/book/show/55240816-diaries-of-the-unbalanced-paddleboarder
Read the CBC article Meagan mentioned: https://www.cbc.ca/2017/what-moving-to-whitehorse-and-back-taught-me-about-my-disability-and-canada-1.4149676</itunes:summary>
      <itunes:subtitle>Water scares many people. Our guest, Mike Shoreman, has conquered this fear. 

Many people know him as the Unbalanced Paddleboarder. In August, Mike became the first person with disabilities to paddle board across all of the Great Lakes. In this conversation, he talks about why he decided to do this, how crossing the Great Lakes resembles a mental health journey and the pros and cons of being called “inspirational.” He also tries to counsel Meagan through aquatic anxiety.  

Follow Mike on Twitter @MikeShoreman 
Follow Mike on Instagram @mike_shoreman

Learn about his book here: https://www.goodreads.com/en/book/show/55240816-diaries-of-the-unbalanced-paddleboarder
Read the CBC article Meagan mentioned: https://www.cbc.ca/2017/what-moving-to-whitehorse-and-back-taught-me-about-my-disability-and-canada-1.4149676</itunes:subtitle>
      <itunes:keywords>meagan gillmore, lake ontario, paddle board, great lakes, lake michigan, lake erie, mental health, inspiration, lake superior, blind, ami, lake huron, anxiety, partially sighted, mike shoreman, podcast, ami-audio, connecting disability</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>14</itunes:episode>
    </item>
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      <title>Connecting disability to… trying new things after a loss</title>
      <description><![CDATA[On this first episode of Season 2, I am thrilled to introduce you to Heather Graham. After Heather was diagnosed with multiple sclerosis at age 46, she lost much of her mobility and active lifestyle. A few years ago, she decided to gain it back. Heather joins me from her residence in Calgary to talk about her journey with MS, what living in long-term care looks like before and during a pandemic, and what it means to control your disability. 

Some resources Heather mentioned in this episode: 

Direct MS: www.direct-ms.org
Wahls Diet: https://terrywahls.com/
Overcoming MS: https://overcomingms.org 

These links are provided for your personal research. They do not constitute endorsements or medical advice. 

Meagan’s previous reporting on younger adults living in long-term care: https://broadview.org/young-people-with-disabilities-long-term-care/ 
]]></description>
      <pubDate>Wed, 21 Sep 2022 11:00:00 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-trying-new-things-after-a-loss-wHCLKKr7</link>
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      <itunes:title>Connecting disability to… trying new things after a loss</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:30:40</itunes:duration>
      <itunes:summary>On this first episode of Season 2, I am thrilled to introduce you to Heather Graham. After Heather was diagnosed with multiple sclerosis at age 46, she lost much of her mobility and active lifestyle. A few years ago, she decided to gain it back. Heather joins me from her residence in Calgary to talk about her journey with MS, what living in long-term care looks like before and during a pandemic, and what it means to control your disability. 

Some resources Heather mentioned in this episode: 

Direct MS: www.direct-ms.org
Wahls Diet: https://terrywahls.com/
Overcoming MS: https://overcomingms.org 

These links are provided for your personal research. They do not constitute endorsements or medical advice. 

Meagan’s previous reporting on younger adults living in long-term care: https://broadview.org/young-people-with-disabilities-long-term-care/ </itunes:summary>
      <itunes:subtitle>On this first episode of Season 2, I am thrilled to introduce you to Heather Graham. After Heather was diagnosed with multiple sclerosis at age 46, she lost much of her mobility and active lifestyle. A few years ago, she decided to gain it back. Heather joins me from her residence in Calgary to talk about her journey with MS, what living in long-term care looks like before and during a pandemic, and what it means to control your disability. 

Some resources Heather mentioned in this episode: 

Direct MS: www.direct-ms.org
Wahls Diet: https://terrywahls.com/
Overcoming MS: https://overcomingms.org 

These links are provided for your personal research. They do not constitute endorsements or medical advice. 

Meagan’s previous reporting on younger adults living in long-term care: https://broadview.org/young-people-with-disabilities-long-term-care/ </itunes:subtitle>
      <itunes:keywords>meagan gillmore, ltc, ms, covid-19, pandemic, blind, ami, partially sighted, multiple sclerosis, podcast, heather graham, ami-audio, calgary, connecting disability, long-term care</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>13</itunes:episode>
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      <title>Connecting disability to… music and mentorship</title>
      <description><![CDATA[We’re ending our FIRST YEAR of podcasting on a musical note!

W. Ian Walker has spent his life in music, whether by singing with various musical groups, working in arts administration, or now as a playwright. Ian joins Meagan to talk about turning his memoir, Stirring My Soul to Sing, into a play, how music has influenced his journey with ADHD, his experiences in the church, and the value of mentorship. Meagan reveals her answers to the questions, “Where is it hard for you to connect with your disability?” and, “What has good connection looked like for you?” We also hear about what happens when boy band fans enter middle age.  

Learn more about Ian’s book Stirring My Soul to Sing: https://www.amazon.ca/Stirring-My-Soul-Sing-Overcoming-ebook/dp/B07H4WYH4X

Attention Deficit Disorder Association – http://add.org

Thank you to everyone who has listened and given feedback. You are very appreciated.
]]></description>
      <pubDate>Wed, 17 Aug 2022 11:00:00 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-music-and-mentorship-T7A_z_Wq</link>
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      <itunes:title>Connecting disability to… music and mentorship</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:30:17</itunes:duration>
      <itunes:summary>We’re ending our FIRST YEAR of podcasting on a musical note!

W. Ian Walker has spent his life in music, whether by singing with various musical groups, working in arts administration, or now as a playwright. Ian joins Meagan to talk about turning his memoir, Stirring My Soul to Sing, into a play, how music has influenced his journey with ADHD, his experiences in the church, and the value of mentorship. Meagan reveals her answers to the questions, “Where is it hard for you to connect with your disability?” and, “What has good connection looked like for you?” We also hear about what happens when boy band fans enter middle age.  

Learn more about Ian’s book Stirring My Soul to Sing: https://www.amazon.ca/Stirring-My-Soul-Sing-Overcoming-ebook/dp/B07H4WYH4X

Attention Deficit Disorder Association – http://add.org

Thank you to everyone who has listened and given feedback. You are very appreciated.</itunes:summary>
      <itunes:subtitle>We’re ending our FIRST YEAR of podcasting on a musical note!

W. Ian Walker has spent his life in music, whether by singing with various musical groups, working in arts administration, or now as a playwright. Ian joins Meagan to talk about turning his memoir, Stirring My Soul to Sing, into a play, how music has influenced his journey with ADHD, his experiences in the church, and the value of mentorship. Meagan reveals her answers to the questions, “Where is it hard for you to connect with your disability?” and, “What has good connection looked like for you?” We also hear about what happens when boy band fans enter middle age.  

Learn more about Ian’s book Stirring My Soul to Sing: https://www.amazon.ca/Stirring-My-Soul-Sing-Overcoming-ebook/dp/B07H4WYH4X

Attention Deficit Disorder Association – http://add.org

Thank you to everyone who has listened and given feedback. You are very appreciated.</itunes:subtitle>
      <itunes:keywords>meagan gillmore, mentorship, sing, ian walker, playright, music, attention deficit disorder, blind, ami, partially sighted, podcast, church, ami-audio, stirring my soul to sing, singer, connecting disability, adhd</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
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      <itunes:episode>12</itunes:episode>
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      <title>Connecting disability to… the outdoors</title>
      <description><![CDATA[It’s hard to believe, but summer vacation is nearly half over. So, today we’re talking about the importance of getting outside.

Leona Mattice is an avid birder from Elliot Lake, Ont., who has spent years encouraging those with disabilities to explore the natural world around them. She joins us today to talk about how birding helped her through grief, brought her love and what birds can teach us about life with a disability. We also test her knowledge of bird calls. 
]]></description>
      <pubDate>Wed, 20 Jul 2022 15:54:51 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-the-outdoors-_ZVA0SSm</link>
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      <itunes:title>Connecting disability to… the outdoors</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:28:02</itunes:duration>
      <itunes:summary>It’s hard to believe, but summer vacation is nearly half over. So, today we’re talking about the importance of getting outside.

Leona Mattice is an avid birder from Elliot Lake, Ont., who has spent years encouraging those with disabilities to explore the natural world around them. She joins us today to talk about how birding helped her through grief, brought her love and what birds can teach us about life with a disability. We also test her knowledge of bird calls. </itunes:summary>
      <itunes:subtitle>It’s hard to believe, but summer vacation is nearly half over. So, today we’re talking about the importance of getting outside.

Leona Mattice is an avid birder from Elliot Lake, Ont., who has spent years encouraging those with disabilities to explore the natural world around them. She joins us today to talk about how birding helped her through grief, brought her love and what birds can teach us about life with a disability. We also test her knowledge of bird calls. </itunes:subtitle>
      <itunes:keywords>birder, disabilities, meagan gilmore, outdoors, leona mattice, connecting disability</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>11</itunes:episode>
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      <title>Connecting Disability… to careers and that often-elusive first job</title>
      <description><![CDATA[It’s graduation season, so we turn our focus to employment and job searching. Our guest is Jack McCormick, human resources manager at Microsoft. Jack chats about how his partial sight has impacted his job search and career, and why volunteering is so important. 

And – congrats to the Class of 2022! 

]]></description>
      <pubDate>Wed, 15 Jun 2022 11:55:08 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-careers-and-that-often-elusive-first-job-35D_IqBS</link>
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      <itunes:title>Connecting Disability… to careers and that often-elusive first job</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:31:07</itunes:duration>
      <itunes:summary>It’s graduation season, so we turn our focus to employment and job searching. Our guest is Jack McCormick, human resources manager at Microsoft. Jack chats about how his partial sight has impacted his job search and career, and why volunteering is so important. 

And – congrats to the Class of 2022! 
</itunes:summary>
      <itunes:subtitle>It’s graduation season, so we turn our focus to employment and job searching. Our guest is Jack McCormick, human resources manager at Microsoft. Jack chats about how his partial sight has impacted his job search and career, and why volunteering is so important. 

And – congrats to the Class of 2022! 
</itunes:subtitle>
      <itunes:keywords>meagan gillmore, jack mccormick, microsoft, blind, manager, graduation, ami, partially sighted, podcast, ami-audio, connecting disability, human resources</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>10</itunes:episode>
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      <title>Connecting Disability to… the medical system</title>
      <description><![CDATA[<p>People with disabilities often use the medical system, but what happens when they want to become doctors? On this episode, Quinten Clarke gives us some insight into what the medical profession looks like as a medical resident who has a disability. Quinten is the vice-president and Trainee Group Lead for the Canadian Association of Physicians with Disabilities. Through this work, he advocates for medical learners with disabilities. He’s currently a resident physician at the University of British Columbia. He talked about how he thinks the medical system views disability, and how this can be changed.  </p><p> </p><p>You can learn more about the Canadian Association of Physicians with Disabilities <a href=" capd.ca" target="_blank">here</a></p><p>Check out the Ostomy Canada Society<a href="ostomycanada.ca" target="_blank"> here</a></p><p>Quinten mentions a February 2021 article by Dr. Lisa I. Iezzoni. <a href="https://news.harvard.edu/gazette/story/2021/02/survey-finds-doctors-have-negative-perception-of-patients-with-disability/" target="_blank">Read more about that article here:</a> </p><p><a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722582/" target="_blank">The full article can be accessed here:</a> </p>
]]></description>
      <pubDate>Wed, 25 May 2022 11:00:00 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-the-medical-system-354EKSop</link>
      <content:encoded><![CDATA[<p>People with disabilities often use the medical system, but what happens when they want to become doctors? On this episode, Quinten Clarke gives us some insight into what the medical profession looks like as a medical resident who has a disability. Quinten is the vice-president and Trainee Group Lead for the Canadian Association of Physicians with Disabilities. Through this work, he advocates for medical learners with disabilities. He’s currently a resident physician at the University of British Columbia. He talked about how he thinks the medical system views disability, and how this can be changed.  </p><p> </p><p>You can learn more about the Canadian Association of Physicians with Disabilities <a href=" capd.ca" target="_blank">here</a></p><p>Check out the Ostomy Canada Society<a href="ostomycanada.ca" target="_blank"> here</a></p><p>Quinten mentions a February 2021 article by Dr. Lisa I. Iezzoni. <a href="https://news.harvard.edu/gazette/story/2021/02/survey-finds-doctors-have-negative-perception-of-patients-with-disability/" target="_blank">Read more about that article here:</a> </p><p><a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722582/" target="_blank">The full article can be accessed here:</a> </p>
]]></content:encoded>
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      <itunes:title>Connecting Disability to… the medical system</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:30:53</itunes:duration>
      <itunes:summary>People with disabilities often use the medical system, but what happens when they want to become doctors? On this episode, Quinten Clarke gives us some insight into what the medical profession looks like as a medical resident who has a disability. Quinten is the vice-president and Trainee Group Lead for the Canadian Association of Physicians with Disabilities. Through this work, he advocates for medical learners with disabilities. He’s currently a resident physician at the University of British Columbia. He talked about how he thinks the medical system views disability, and how this can be changed. 

You can learn more about the Canadian Association of Physicians with Disabilities here: capd.ca

Check out the Ostomy Canada Society here: ostomycanada.ca

Quinten mentions a February 2021 article by Dr. Lisa I. Iezzoni. Read more about that article here: https://news.harvard.edu/gazette/story/2021/02/survey-finds-doctors-have-negative-perception-of-patients-with-disability/. The full article can be accessed here: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722582/</itunes:summary>
      <itunes:subtitle>People with disabilities often use the medical system, but what happens when they want to become doctors? On this episode, Quinten Clarke gives us some insight into what the medical profession looks like as a medical resident who has a disability. Quinten is the vice-president and Trainee Group Lead for the Canadian Association of Physicians with Disabilities. Through this work, he advocates for medical learners with disabilities. He’s currently a resident physician at the University of British Columbia. He talked about how he thinks the medical system views disability, and how this can be changed. 

You can learn more about the Canadian Association of Physicians with Disabilities here: capd.ca

Check out the Ostomy Canada Society here: ostomycanada.ca

Quinten mentions a February 2021 article by Dr. Lisa I. Iezzoni. Read more about that article here: https://news.harvard.edu/gazette/story/2021/02/survey-finds-doctors-have-negative-perception-of-patients-with-disability/. The full article can be accessed here: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722582/</itunes:subtitle>
      <itunes:keywords>meagan gillmore, quinten clarke, dr. lisa iezzoni, ostomy canada society, canadian association of physicians with disabilities, university of british columbia, trainee group lead, blind, ami, vice-president, partially sighted, podcast, ami-audio, connecting disability</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>9</itunes:episode>
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      <title>Connecting Disability… to life as a refugee</title>
      <description><![CDATA[It’s been nearly two months since Russia invaded Ukraine. The ongoing war has had devastating impacts on the approximately 2.7 million Ukrainians who have disabilities. Tanya Herasymova knows this well. She’s the project manager of Fight for Right, an organization that advocates for human rights for Ukrainians with disabilities. Tanya joins us to talk about how the war has impacted her life, what it’s like being a refugee with a disability and what her biggest hopes are. 

This is a very raw and honest conversation, and I’m so grateful that Tanya took the time to join us.

You can learn more about Fight for Right’s work here: https://ffr.org.ua/
]]></description>
      <pubDate>Wed, 20 Apr 2022 11:00:00 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-life-as-a-refugee-3hfc6el_</link>
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      <itunes:title>Connecting Disability… to life as a refugee</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:32:23</itunes:duration>
      <itunes:summary>It’s been nearly two months since Russia invaded Ukraine. The ongoing war has had devastating impacts on the approximately 2.7 million Ukrainians who have disabilities. Tanya Herasymova knows this well. She’s the project manager of Fight for Right, an organization that advocates for human rights for Ukrainians with disabilities. Tanya joins us to talk about how the war has impacted her life, what it’s like being a refugee with a disability and what her biggest hopes are. 

This is a very raw and honest conversation, and I’m so grateful that Tanya took the time to join us.

You can learn more about Fight for Right’s work here: https://ffr.org.ua/</itunes:summary>
      <itunes:subtitle>It’s been nearly two months since Russia invaded Ukraine. The ongoing war has had devastating impacts on the approximately 2.7 million Ukrainians who have disabilities. Tanya Herasymova knows this well. She’s the project manager of Fight for Right, an organization that advocates for human rights for Ukrainians with disabilities. Tanya joins us to talk about how the war has impacted her life, what it’s like being a refugee with a disability and what her biggest hopes are. 

This is a very raw and honest conversation, and I’m so grateful that Tanya took the time to join us.

You can learn more about Fight for Right’s work here: https://ffr.org.ua/</itunes:subtitle>
      <itunes:keywords>meagan gillmore, war, advocate, russia, project manager, tanya herasymova, fight for right, blind, ami, ukrainians with disabilities, partially sighted, podcast, ami-audio, ukraine, connecting disability, human rights</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>8</itunes:episode>
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      <title>Connecting Disability to … professional sports and being a fan</title>
      <description><![CDATA[The Beijing Paralympics and Olympics have just wrapped up, and we’re taking this opportunity to reflect on disability and sport. 

In this case, though, we’re looking at how disability connects with professional, able-bodied sports. Chanel Keenan is the intersectionality consultant for the NHL’s Seattle Kraken, which means she’s responsible for making sure the NHL’s newest team considers the needs of fans who are disabled. 

Chanel and Meagan talk about how Chanel got her start in hockey, why professional sports organizations need to consider disability, and why Chanel thinks her disability would make her a good TV detective. This is a really fun conversation, and we hope it gives you the opportunity to think, laugh and enjoy being a fan. 

You can find all the ways to connect with Chanel here: https://linktr.ee/CMoreThanSports

Learn more about one of Chanel’s hockey heroes, the late Joey Moss, here: https://www.joeymossmemorialfund.ca/
]]></description>
      <pubDate>Wed, 16 Mar 2022 11:33:10 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-professional-sports-and-being-a-fan-XuTkAwn4</link>
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      <itunes:title>Connecting Disability to … professional sports and being a fan</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:31:52</itunes:duration>
      <itunes:summary>The Beijing Paralympics and Olympics have just wrapped up, and we’re taking this opportunity to reflect on disability and sport. 

In this case, though, we’re looking at how disability connects with professional, able-bodied sports. Chanel Keenan is the intersectionality consultant for the NHL’s Seattle Kraken, which means she’s responsible for making sure the NHL’s newest team considers the needs of fans who are disabled. 

Chanel and Meagan talk about how Chanel got her start in hockey, why professional sports organizations need to consider disability, and why Chanel thinks her disability would make her a good TV detective. This is a really fun conversation, and we hope it gives you the opportunity to think, laugh and enjoy being a fan. 

You can find all the ways to connect with Chanel here: https://linktr.ee/CMoreThanSports

Learn more about one of Chanel’s hockey heroes, the late Joey Moss, here: https://www.joeymossmemorialfund.ca/</itunes:summary>
      <itunes:subtitle>The Beijing Paralympics and Olympics have just wrapped up, and we’re taking this opportunity to reflect on disability and sport. 

In this case, though, we’re looking at how disability connects with professional, able-bodied sports. Chanel Keenan is the intersectionality consultant for the NHL’s Seattle Kraken, which means she’s responsible for making sure the NHL’s newest team considers the needs of fans who are disabled. 

Chanel and Meagan talk about how Chanel got her start in hockey, why professional sports organizations need to consider disability, and why Chanel thinks her disability would make her a good TV detective. This is a really fun conversation, and we hope it gives you the opportunity to think, laugh and enjoy being a fan. 

You can find all the ways to connect with Chanel here: https://linktr.ee/CMoreThanSports

Learn more about one of Chanel’s hockey heroes, the late Joey Moss, here: https://www.joeymossmemorialfund.ca/</itunes:subtitle>
      <itunes:keywords>meagan gillmore, ice hockey, olympics, paralympics, fans, intersectionality consultant, seattle kraken, blind, ami, partially sighted, podcast, sports fans, nhl, ami-audio, joey moss, hockey, chanel keenan, connecting disability</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>7</itunes:episode>
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      <title>Connecting Disability to… cultural curiosity (and hygiene!)</title>
      <description><![CDATA[This conversation is a vivid example of all the ways disability can bring unexpected opportunities and experiences to our lives. David Achuroa, who is from northern Ghana, contracted polio when he was two. That eventually led him to a rehabilitation centre, which then led to him beginning school. David earned a science degree in community nutrition before moving to Canada to study anthropology at the University of Calgary. He currently lives in Edmonton. 

In this conversation, we talk about different cultural understandings of disability, and how being asked, “What happened to you?” can be a good thing. And, as we approach two years of the COVID-19 pandemic, we reflect on disability accessibility and handwashing. David really challenged the way I think about interactions with strangers, and I hope you learn something form this conversation, too.  

David Akanpentiba Achuroa, a  disability advocate, nutritionist, social anthropologist, and policy analyst, undertakes research that increases our knowledge in social and cultural issues that impact the lives and well-being of people with disabilities. Projects he currently works on empowers people with disabilities in Africa, the UK and Canada. He sits on the management committee of Disability in Wales and Africa in the UK and volunteers with Alberta Disability Pride Foundation and Edmonton Region Immigrant Employment Council. His graduate thesis explored the web of cultural practices and systems that influence parental understanding and caring of children with disabilities among the Bulsa in Northern Ghana.
]]></description>
      <pubDate>Wed, 16 Feb 2022 12:00:00 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-cultural-curiosity-and-hygiene-I2xu_Rku</link>
      <enclosure length="30304566" type="audio/mpeg" url="https://op3.dev/e/injector.simplecastaudio.com/78be6ee8-1936-48c9-9672-6eb681edd3a6/episodes/7cd84a51-2e41-4a1b-a951-cee9a1723085/audio/128/default.mp3?aid=rss_feed&amp;awCollectionId=78be6ee8-1936-48c9-9672-6eb681edd3a6&amp;awEpisodeId=7cd84a51-2e41-4a1b-a951-cee9a1723085&amp;feed=KLnjl5ZJ"/>
      <itunes:title>Connecting Disability to… cultural curiosity (and hygiene!)</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:31:33</itunes:duration>
      <itunes:summary>This conversation is a vivid example of all the ways disability can bring unexpected opportunities and experiences to our lives. David Achuroa, who is from northern Ghana, contracted polio when he was two. That eventually led him to a rehabilitation centre, which then led to him beginning school. David earned a science degree in community nutrition before moving to Canada to study anthropology at the University of Calgary. He currently lives in Edmonton. 

In this conversation, we talk about different cultural understandings of disability, and how being asked, “What happened to you?” can be a good thing. And, as we approach two years of the COVID-19 pandemic, we reflect on disability accessibility and handwashing. David really challenged the way I think about interactions with strangers, and I hope you learn something form this conversation, too.  

David Akanpentiba Achuroa, a  disability advocate, nutritionist, social anthropologist, and policy analyst, undertakes research that increases our knowledge in social and cultural issues that impact the lives and well-being of people with disabilities. Projects he currently works on empowers people with disabilities in Africa, the UK and Canada. He sits on the management committee of Disability in Wales and Africa in the UK and volunteers with Alberta Disability Pride Foundation and Edmonton Region Immigrant Employment Council. His graduate thesis explored the web of cultural practices and systems that influence parental understanding and caring of children with disabilities among the Bulsa in Northern Ghana.</itunes:summary>
      <itunes:subtitle>This conversation is a vivid example of all the ways disability can bring unexpected opportunities and experiences to our lives. David Achuroa, who is from northern Ghana, contracted polio when he was two. That eventually led him to a rehabilitation centre, which then led to him beginning school. David earned a science degree in community nutrition before moving to Canada to study anthropology at the University of Calgary. He currently lives in Edmonton. 

In this conversation, we talk about different cultural understandings of disability, and how being asked, “What happened to you?” can be a good thing. And, as we approach two years of the COVID-19 pandemic, we reflect on disability accessibility and handwashing. David really challenged the way I think about interactions with strangers, and I hope you learn something form this conversation, too.  

David Akanpentiba Achuroa, a  disability advocate, nutritionist, social anthropologist, and policy analyst, undertakes research that increases our knowledge in social and cultural issues that impact the lives and well-being of people with disabilities. Projects he currently works on empowers people with disabilities in Africa, the UK and Canada. He sits on the management committee of Disability in Wales and Africa in the UK and volunteers with Alberta Disability Pride Foundation and Edmonton Region Immigrant Employment Council. His graduate thesis explored the web of cultural practices and systems that influence parental understanding and caring of children with disabilities among the Bulsa in Northern Ghana.</itunes:subtitle>
      <itunes:keywords>meagan gillmore, david achuroa, blind, ami, partially sighted, podcast, ami-audio, connecting disability</itunes:keywords>
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      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>6</itunes:episode>
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      <title>Connecting Disability to … Living with cancer in community</title>
      <description><![CDATA[Welcome to 2022! We’re starting this year with a story of living with hope and resilience in the face of ongoing health challenges.

Clare Li has lived with various autoimmune diseases for most of her life. But it wasn’t until the Vancouver native moved to Montreal that she intently started studying her disabilities – and shortly after she made some hard decisions to increase her independence, she was diagnosed with breast cancer.  

In this conversation, Clare talks about her journey of accepting what happens when an invisible disability becomes visible, and what her cancer diagnosis hasn’t changed. I hope this episode encourages you, whether you’re living with a long-term illness, or know someone who is. 

Resources Clare finds helpful: 

Wildfire Breast Cancer Magazine – for women “too young” for breast cancer: www.wildfirecommunity.org

Rethink Breast Cancer: https://rethinkbreastcancer.com

Personalink – helping connect breast cancer survivors who’ve had mastectomies with tattoo artists: 
https://www.instagram.com/personal.ink/?utm_medium=copy_link

Clare would like to thank UNI Training Montreal for their help and support: 
https://unitraining.ca/

For various reasons, Meagan often looks for good writing about living with cancer. She is especially grateful for Kate Bowler's work on this topic. You can check out Kate's work at: https://katebowler.com
]]></description>
      <pubDate>Wed, 19 Jan 2022 12:00:00 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-living-with-cancer-in-community-7tTuUs7E</link>
      <enclosure length="28851064" type="audio/mpeg" url="https://op3.dev/e/injector.simplecastaudio.com/78be6ee8-1936-48c9-9672-6eb681edd3a6/episodes/d6b8cf0d-f0bd-4772-a779-9049463a2b89/audio/128/default.mp3?aid=rss_feed&amp;awCollectionId=78be6ee8-1936-48c9-9672-6eb681edd3a6&amp;awEpisodeId=d6b8cf0d-f0bd-4772-a779-9049463a2b89&amp;feed=KLnjl5ZJ"/>
      <itunes:title>Connecting Disability to … Living with cancer in community</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:30:02</itunes:duration>
      <itunes:summary>Welcome to 2022! We’re starting this year with a story of living with hope and resilience in the face of ongoing health challenges.

Clare Li has lived with various autoimmune diseases for most of her life. But it wasn’t until the Vancouver native moved to Montreal that she intently started studying her disabilities – and shortly after she made some hard decisions to increase her independence, she was diagnosed with breast cancer.  

In this conversation, Clare talks about her journey of accepting what happens when an invisible disability becomes visible, and what her cancer diagnosis hasn’t changed. I hope this episode encourages you, whether you’re living with a long-term illness, or know someone who is. 

Resources Clare finds helpful: 

Wildfire Breast Cancer Magazine – for women “too young” for breast cancer: www.wildfirecommunity.org

Rethink Breast Cancer: https://rethinkbreastcancer.com

Personalink – helping connect breast cancer survivors who’ve had mastectomies with tattoo artists: 
https://www.instagram.com/personal.ink/?utm_medium=copy_link

Clare would like to thank UNI Training Montreal for their help and support: 
https://unitraining.ca/

For various reasons, Meagan often looks for good writing about living with cancer. She is especially grateful for Kate Bowler&apos;s work on this topic. You can check out Kate&apos;s work at: https://katebowler.com</itunes:summary>
      <itunes:subtitle>Welcome to 2022! We’re starting this year with a story of living with hope and resilience in the face of ongoing health challenges.

Clare Li has lived with various autoimmune diseases for most of her life. But it wasn’t until the Vancouver native moved to Montreal that she intently started studying her disabilities – and shortly after she made some hard decisions to increase her independence, she was diagnosed with breast cancer.  

In this conversation, Clare talks about her journey of accepting what happens when an invisible disability becomes visible, and what her cancer diagnosis hasn’t changed. I hope this episode encourages you, whether you’re living with a long-term illness, or know someone who is. 

Resources Clare finds helpful: 

Wildfire Breast Cancer Magazine – for women “too young” for breast cancer: www.wildfirecommunity.org

Rethink Breast Cancer: https://rethinkbreastcancer.com

Personalink – helping connect breast cancer survivors who’ve had mastectomies with tattoo artists: 
https://www.instagram.com/personal.ink/?utm_medium=copy_link

Clare would like to thank UNI Training Montreal for their help and support: 
https://unitraining.ca/

For various reasons, Meagan often looks for good writing about living with cancer. She is especially grateful for Kate Bowler&apos;s work on this topic. You can check out Kate&apos;s work at: https://katebowler.com</itunes:subtitle>
      <itunes:keywords>meagan gillmore, cancer, clare li, blind, ami, disability advocate, partially sighted, podcast, ami-audio, autoimmune diseases, connecting disability</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>5</itunes:episode>
    </item>
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      <title>Connecting Disability to … Good conversations and Marriage</title>
      <description><![CDATA[To bring some warmth to this winter season, we’re learning about how disability played a role in one couple’s romance. Michelle Hewitt is a disability advocate in British Columbia, and the national co-chair of Disability Without Poverty, an organization dedicated to lifting Canadians with disabilities out of financial poverty. Victor Enns is a poet and author, who spent most of his life living in Manitoba – until this past spring. In this conversation, they tell us about how they met and how disability has impacted their relationship. 

You can read Victor’s work here: victorenns9.com
Follow Victor on Twitter: @enns_victor
Follow Michelle on Twitter: @missingabout 
Learn about Disability Without Poverty here: www.disabilitywithoutpoverty.ca and take a look at this recent petition:  
https://petitions.ourcommons.ca/en/Petition/Details?Petition=e-3656

If you want to read more on this topic, Meagan highly recommends Ben Mattlin’s book In Sickness and in Health. Check him out at www.benmattlin.com or @benmattlin. 
]]></description>
      <pubDate>Wed, 15 Dec 2021 12:00:00 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-good-conversations-and-marriage-qZ_wz8wO</link>
      <enclosure length="27834715" type="audio/mpeg" url="https://op3.dev/e/injector.simplecastaudio.com/78be6ee8-1936-48c9-9672-6eb681edd3a6/episodes/0b80d018-d200-44fa-9969-e2d55c7e4666/audio/128/default.mp3?aid=rss_feed&amp;awCollectionId=78be6ee8-1936-48c9-9672-6eb681edd3a6&amp;awEpisodeId=0b80d018-d200-44fa-9969-e2d55c7e4666&amp;feed=KLnjl5ZJ"/>
      <itunes:title>Connecting Disability to … Good conversations and Marriage</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:28:59</itunes:duration>
      <itunes:summary>To bring some warmth to this winter season, we’re learning about how disability played a role in one couple’s romance. Michelle Hewitt is a disability advocate in British Columbia, and the national co-chair of Disability Without Poverty, an organization dedicated to lifting Canadians with disabilities out of financial poverty. Victor Enns is a poet and author, who spent most of his life living in Manitoba – until this past spring. In this conversation, they tell us about how they met and how disability has impacted their relationship. 

You can read Victor’s work here: victorenns9.com
Follow Victor on Twitter: @enns_victor
Follow Michelle on Twitter: @missingabout 
Learn about Disability Without Poverty here: www.disabilitywithoutpoverty.ca and take a look at this recent petition:  
https://petitions.ourcommons.ca/en/Petition/Details?Petition=e-3656

If you want to read more on this topic, Meagan highly recommends Ben Mattlin’s book In Sickness and in Health. Check him out at www.benmattlin.com or @benmattlin. </itunes:summary>
      <itunes:subtitle>To bring some warmth to this winter season, we’re learning about how disability played a role in one couple’s romance. Michelle Hewitt is a disability advocate in British Columbia, and the national co-chair of Disability Without Poverty, an organization dedicated to lifting Canadians with disabilities out of financial poverty. Victor Enns is a poet and author, who spent most of his life living in Manitoba – until this past spring. In this conversation, they tell us about how they met and how disability has impacted their relationship. 

You can read Victor’s work here: victorenns9.com
Follow Victor on Twitter: @enns_victor
Follow Michelle on Twitter: @missingabout 
Learn about Disability Without Poverty here: www.disabilitywithoutpoverty.ca and take a look at this recent petition:  
https://petitions.ourcommons.ca/en/Petition/Details?Petition=e-3656

If you want to read more on this topic, Meagan highly recommends Ben Mattlin’s book In Sickness and in Health. Check him out at www.benmattlin.com or @benmattlin. </itunes:subtitle>
      <itunes:keywords>meagan gillmore, poet, romance, disability without poverty, blind, british columbia, ami, disability advocate, partially sighted, podcast, author, ami-audio, michelle hewitt, victor enns, connecting disability, manitoba</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>4</itunes:episode>
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      <title>Connecting Disability to … International Adoption</title>
      <description><![CDATA[Disabilities impact families in various ways. It literally expanded Katrina Gossett Kelly’s family. Four years ago, she adopted her son from Bulgaria. 

In this conversation, Katrina talks about how having a disability is both a benefit and a challenge when pursuing adoption, and what her journey is teaching her about what it means to build a community. 

Katrina Gossett Kelly is a lawyer practising in trade secret litigation. She’s also an advocate for people with disabilities in Indiana. 

You can read some of her writing about parenting here: 
https://cdrnys.org/blog/advocacy/navigating-the-wheelchair-accessible-path-to-adoption/?fbclid=IwAR3ybilcY26_A1uRI845OV82xlFYjft1J3WNHMLOnL1MQ9Lsxkqo5-cCaQw 
https://www.cdrnys.org/blog/advocacy/why-are-they-looking-at-me/
]]></description>
      <pubDate>Wed, 17 Nov 2021 19:44:41 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/episode-38-connecting-disability-to-international-adoption-fd53c_ux</link>
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      <itunes:title>Connecting Disability to … International Adoption</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:29:53</itunes:duration>
      <itunes:summary>Disabilities impact families in various ways. It literally expanded Katrina Gossett Kelly’s family. Four years ago, she adopted her son from Bulgaria. 

In this conversation, Katrina talks about how having a disability is both a benefit and a challenge when pursuing adoption, and what her journey is teaching her about what it means to build a community. 

Katrina Gossett Kelly is a lawyer practising in trade secret litigation. She’s also an advocate for people with disabilities in Indiana. 

You can read some of her writing about parenting here: 
https://cdrnys.org/blog/advocacy/navigating-the-wheelchair-accessible-path-to-adoption/?fbclid=IwAR3ybilcY26_A1uRI845OV82xlFYjft1J3WNHMLOnL1MQ9Lsxkqo5-cCaQw 
https://www.cdrnys.org/blog/advocacy/why-are-they-looking-at-me/</itunes:summary>
      <itunes:subtitle>Disabilities impact families in various ways. It literally expanded Katrina Gossett Kelly’s family. Four years ago, she adopted her son from Bulgaria. 

In this conversation, Katrina talks about how having a disability is both a benefit and a challenge when pursuing adoption, and what her journey is teaching her about what it means to build a community. 

Katrina Gossett Kelly is a lawyer practising in trade secret litigation. She’s also an advocate for people with disabilities in Indiana. 

You can read some of her writing about parenting here: 
https://cdrnys.org/blog/advocacy/navigating-the-wheelchair-accessible-path-to-adoption/?fbclid=IwAR3ybilcY26_A1uRI845OV82xlFYjft1J3WNHMLOnL1MQ9Lsxkqo5-cCaQw 
https://www.cdrnys.org/blog/advocacy/why-are-they-looking-at-me/</itunes:subtitle>
      <itunes:keywords>meagan gillmore, adoption, blind, katrina gossett kelly, family, ami, partially sighted, podcast, ami-audio, lawyer, trade secret litigation, bulgaria, connecting disability, indiana</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>3</itunes:episode>
    </item>
    <item>
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      <title>Connecting Disability to … Parenting and compassion</title>
      <description><![CDATA[For many parents, their first significant experience with disability comes when they find out their child has one. Shannon Reaume’s story is different: both she and her son have the same medical condition, central congenital hypoventilation syndrome (CCHS). 

In this conversation, Shannon and Meagan talk about how Shannon’s disability impacted her journey to motherhood, what it’s like to share a diagnosis with your child and what the experience is teaching her about having compassion for her own parents. If you’re considering how to be a disabled parent, wondering what your life will look like with your child’s disability, or reflecting on what your parents taught you about living with a disability–there’s something for you in this conversation. 

Shannon Reaume is a registered social worker and a family advisor on multiple committees and working groups for McMaster Children's Hospital in Hamilton, Ontario, Critical Care Services Ontario, and the Provincial Council of Maternal and Child Health. She’s also a Ph.D candidate at the School of Public Health Sciences in the University of Waterloo where she is a researcher at the ARCH Lab, which stands for Advancing Research in Children’s Health. She was a recipient of the 2021 Holly Bartlett Memorial Award from the National Educational Association of Students with Disabilities. Shannon is passionate about helping children and families live healthy lives with disabilities. She lives with her husband and two children in Elora, Ontario. 

If you want to learn more about CCHS or donate to CCHS research, go to www.cchsnetwork.org. International CCHS Day is November 13. 

If you want to hear how Meagan first met Shannon, you can check out this article from July 2020 about homecare for medically fragile children in Ontario during the first few months of COVID-19 lockdowns: https://www.tvo.org/article/were-forgotten-families-call-on-the-government-to-enforce-home-care-rules.  

And if you feel the urge to look at cute teddy bears–and lots of accessories!–this is the company that Shannon’s son got his teddy bear through: www.buildabear.com. 
]]></description>
      <pubDate>Wed, 20 Oct 2021 13:55:06 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-to-parenting-and-compassion-PMciXn0I</link>
      <enclosure length="29016031" type="audio/mpeg" url="https://op3.dev/e/injector.simplecastaudio.com/78be6ee8-1936-48c9-9672-6eb681edd3a6/episodes/6d335236-cacb-4408-b455-0a2173850b1d/audio/128/default.mp3?aid=rss_feed&amp;awCollectionId=78be6ee8-1936-48c9-9672-6eb681edd3a6&amp;awEpisodeId=6d335236-cacb-4408-b455-0a2173850b1d&amp;feed=KLnjl5ZJ"/>
      <itunes:title>Connecting Disability to … Parenting and compassion</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:30:12</itunes:duration>
      <itunes:summary>For many parents, their first significant experience with disability comes when they find out their child has one. Shannon Reaume’s story is different: both she and her son have the same medical condition, central congenital hypoventilation syndrome (CCHS). 

In this conversation, Shannon and Meagan talk about how Shannon’s disability impacted her journey to motherhood, what it’s like to share a diagnosis with your child and what the experience is teaching her about having compassion for her own parents. If you’re considering how to be a disabled parent, wondering what your life will look like with your child’s disability, or reflecting on what your parents taught you about living with a disability–there’s something for you in this conversation. 

Shannon Reaume is a registered social worker and a family advisor on multiple committees and working groups for McMaster Children&apos;s Hospital in Hamilton, Ontario, Critical Care Services Ontario, and the Provincial Council of Maternal and Child Health. She’s also a Ph.D candidate at the School of Public Health Sciences in the University of Waterloo where she is a researcher at the ARCH Lab, which stands for Advancing Research in Children’s Health. She was a recipient of the 2021 Holly Bartlett Memorial Award from the National Educational Association of Students with Disabilities. Shannon is passionate about helping children and families live healthy lives with disabilities. She lives with her husband and two children in Elora, Ontario. 

If you want to learn more about CCHS or donate to CCHS research, go to www.cchsnetwork.org. International CCHS Day is November 13. 

If you want to hear how Meagan first met Shannon, you can check out this article from July 2020 about homecare for medically fragile children in Ontario during the first few months of COVID-19 lockdowns: https://www.tvo.org/article/were-forgotten-families-call-on-the-government-to-enforce-home-care-rules.  

And if you feel the urge to look at cute teddy bears–and lots of accessories!–this is the company that Shannon’s son got his teddy bear through: www.buildabear.com. </itunes:summary>
      <itunes:subtitle>For many parents, their first significant experience with disability comes when they find out their child has one. Shannon Reaume’s story is different: both she and her son have the same medical condition, central congenital hypoventilation syndrome (CCHS). 

In this conversation, Shannon and Meagan talk about how Shannon’s disability impacted her journey to motherhood, what it’s like to share a diagnosis with your child and what the experience is teaching her about having compassion for her own parents. If you’re considering how to be a disabled parent, wondering what your life will look like with your child’s disability, or reflecting on what your parents taught you about living with a disability–there’s something for you in this conversation. 

Shannon Reaume is a registered social worker and a family advisor on multiple committees and working groups for McMaster Children&apos;s Hospital in Hamilton, Ontario, Critical Care Services Ontario, and the Provincial Council of Maternal and Child Health. She’s also a Ph.D candidate at the School of Public Health Sciences in the University of Waterloo where she is a researcher at the ARCH Lab, which stands for Advancing Research in Children’s Health. She was a recipient of the 2021 Holly Bartlett Memorial Award from the National Educational Association of Students with Disabilities. Shannon is passionate about helping children and families live healthy lives with disabilities. She lives with her husband and two children in Elora, Ontario. 

If you want to learn more about CCHS or donate to CCHS research, go to www.cchsnetwork.org. International CCHS Day is November 13. 

If you want to hear how Meagan first met Shannon, you can check out this article from July 2020 about homecare for medically fragile children in Ontario during the first few months of COVID-19 lockdowns: https://www.tvo.org/article/were-forgotten-families-call-on-the-government-to-enforce-home-care-rules.  

And if you feel the urge to look at cute teddy bears–and lots of accessories!–this is the company that Shannon’s son got his teddy bear through: www.buildabear.com. </itunes:subtitle>
      <itunes:keywords>meagan gillmore, arch lab, shannon reaume, blind, advancing research in children&apos;s health, ami, critical care services ontario, central congenital hypoventilation syndrome, partially sighted, podcast, ami-audio, mcmaster children&apos;s hospital, connecting disability, provincial council of maternal and child health</itunes:keywords>
      <itunes:explicit>false</itunes:explicit>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:episode>2</itunes:episode>
    </item>
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      <title>Connecting Disability to...Storytelling and community</title>
      <description><![CDATA[On the first episode of “Connecting Disability,” Meagan sat down with the journalist who first showed her how experiences with disability can lead to in-depth, thoughtful journalism – and help us consider how one person’s disability can impact several people in related, different ways. 
 
In 2009, Globe and Mail feature writer Ian Brown published The Boy in the Moon, a memoir about his experiences with his son, Walker, who was born with a rare genetic disorder called cardiofaciocutaneous syndrome. The book vividly describes the physical routines of Walker’s life - baths, diaper changes, therapies – and his father’s reactions to them. It also made Meagan realize there can be good journalism about disability that is inspired by personal experiences, but goes beyond them. 
 
In this conversation, Ian and Meagan discuss the power of writing about disability, the difficulty of doing that well, and why vulnerability helps us connect. 
 
Meagan and Ian were both nominated for Digital Publishing Awards in 2021 for writing about disability. 
You can read Ian’s piece, published in the Globe and Mail here: https://www.theglobeandmail.com/canada/article-two-metres-and-a-world-apart-life-in-lockdown-for-me-and-my-disabled/. (It got a silver award in the feature article category.) You can read Meagan’s personal essay about the late author Jean Little, published in the Walrus and featured on AMI-audio’s “Voices of the Walrus” here: https://thewalrus.ca/the-author-who-shaped-the-way-we-represent-disability/. (It didn’t place, but gave Meagan an excuse to get dressed up in the middle of the day to attend a virtual award show.) That link will also take you to the recording. 
 
You can check out Ian Brown’s author page at the Globe and Mail here: https://www.theglobeandmail.com/authors/ian-brown/ and follow him on Twitter @BrownoftheGlobe.  
]]></description>
      <pubDate>Fri, 24 Sep 2021 17:47:35 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-tostorytelling-and-community-2OCJVcx_</link>
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      <itunes:title>Connecting Disability to...Storytelling and community</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:31:41</itunes:duration>
      <itunes:summary>On the first episode of “Connecting Disability,” Meagan sat down with the journalist who first showed her how experiences with disability can lead to in-depth, thoughtful journalism – and help us consider how one person’s disability can impact several people in related, different ways. 
 
In 2009, Globe and Mail feature writer Ian Brown published The Boy in the Moon, a memoir about his experiences with his son, Walker, who was born with a rare genetic disorder called cardiofaciocutaneous syndrome. The book vividly describes the physical routines of Walker’s life - baths, diaper changes, therapies – and his father’s reactions to them. It also made Meagan realize there can be good journalism about disability that is inspired by personal experiences, but goes beyond them. 
 
In this conversation, Ian and Meagan discuss the power of writing about disability, the difficulty of doing that well, and why vulnerability helps us connect. 
 
Meagan and Ian were both nominated for Digital Publishing Awards in 2021 for writing about disability. 
You can read Ian’s piece, published in the Globe and Mail here: https://www.theglobeandmail.com/canada/article-two-metres-and-a-world-apart-life-in-lockdown-for-me-and-my-disabled/. (It got a silver award in the feature article category.) You can read Meagan’s personal essay about the late author Jean Little, published in the Walrus and featured on AMI-audio’s “Voices of the Walrus” here: https://thewalrus.ca/the-author-who-shaped-the-way-we-represent-disability/. (It didn’t place, but gave Meagan an excuse to get dressed up in the middle of the day to attend a virtual award show.) That link will also take you to the recording. 
 
You can check out Ian Brown’s author page at the Globe and Mail here: https://www.theglobeandmail.com/authors/ian-brown/ and follow him on Twitter @BrownoftheGlobe.  </itunes:summary>
      <itunes:subtitle>On the first episode of “Connecting Disability,” Meagan sat down with the journalist who first showed her how experiences with disability can lead to in-depth, thoughtful journalism – and help us consider how one person’s disability can impact several people in related, different ways. 
 
In 2009, Globe and Mail feature writer Ian Brown published The Boy in the Moon, a memoir about his experiences with his son, Walker, who was born with a rare genetic disorder called cardiofaciocutaneous syndrome. The book vividly describes the physical routines of Walker’s life - baths, diaper changes, therapies – and his father’s reactions to them. It also made Meagan realize there can be good journalism about disability that is inspired by personal experiences, but goes beyond them. 
 
In this conversation, Ian and Meagan discuss the power of writing about disability, the difficulty of doing that well, and why vulnerability helps us connect. 
 
Meagan and Ian were both nominated for Digital Publishing Awards in 2021 for writing about disability. 
You can read Ian’s piece, published in the Globe and Mail here: https://www.theglobeandmail.com/canada/article-two-metres-and-a-world-apart-life-in-lockdown-for-me-and-my-disabled/. (It got a silver award in the feature article category.) You can read Meagan’s personal essay about the late author Jean Little, published in the Walrus and featured on AMI-audio’s “Voices of the Walrus” here: https://thewalrus.ca/the-author-who-shaped-the-way-we-represent-disability/. (It didn’t place, but gave Meagan an excuse to get dressed up in the middle of the day to attend a virtual award show.) That link will also take you to the recording. 
 
You can check out Ian Brown’s author page at the Globe and Mail here: https://www.theglobeandmail.com/authors/ian-brown/ and follow him on Twitter @BrownoftheGlobe.  </itunes:subtitle>
      <itunes:keywords>meagan gillmore, writing, journalism, ian brown, disability, the boy in the moon, author, connecting disability, accessible</itunes:keywords>
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      <title>Connecting Disability Premieres on September 22nd!</title>
      <description><![CDATA[ In Connecting Disability, accessibility reporter Meagan Gillmore and her guests consider how experiences of disability help us connect with others and society.
]]></description>
      <pubDate>Mon, 20 Sep 2021 14:52:00 +0000</pubDate>
      <author>podcasts@ami.ca (Accessible Media Inc.)</author>
      <link>https://connecting-disability.simplecast.com/episodes/connecting-disability-premieres-on-september-22nd-su1zQ2Db</link>
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      <itunes:title>Connecting Disability Premieres on September 22nd!</itunes:title>
      <itunes:author>Accessible Media Inc.</itunes:author>
      <itunes:duration>00:00:31</itunes:duration>
      <itunes:summary> In Connecting Disability, accessibility reporter Meagan Gillmore and her guests consider how experiences of disability help us connect with others and society.</itunes:summary>
      <itunes:subtitle> In Connecting Disability, accessibility reporter Meagan Gillmore and her guests consider how experiences of disability help us connect with others and society.</itunes:subtitle>
      <itunes:keywords>meagan gillmore, disability, accessibility, connecting disability</itunes:keywords>
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