Podcasts about Disability

S9 E3 — What is the good life? Is it a life marked by money and success and achievement? Or a life marked by love? Author and professor Kelly Kapic joins Amy Julia Becker to rethink our obsession with productivity and self-reliance. They explore:Why “independence” is not the idealHow love—not intelligence or achievement—defines our humanityHow receiving our limits can lead to rest, belonging, and deeper joySubscribe to Amy Julia's Substack newsletter: amyjuliabecker.com/subscribe/00:00 Exploring Humanity's Limits and Gifts 04:30 The Distinction Between Limits and Brokenness 09:35 Redefining Human Value Beyond Achievement 12:16 The Role of Love in Defining Humanity 19:45 The Gift of Humble Dependence in Relationships 26:03 Recognizing and Cultivating Gifts 28:21 The Good Life: Beyond Material Success and Happiness 34:33 Embracing Limits within Work, Rest, and Love 39:16 Practices for Accepting Limits and Cultivating Love__MENTIONED IN THIS EPISODE:Books: You Were Never Meant to Do It All, You're Only Human, and Embodied Hope by Kelly KapicFour Thousand Weeks by Oliver BurkemanWhen Helping Hurts by Steve Corbett and Brian Fikkert Becoming Whole by by Brian Fikkert and Kelly KapicWorld Happiness ReportI Corinthians 13__WATCH this conversation on YouTube: Amy Julia Becker on YouTubeSUBSCRIBE to Amy Julia's Substack: amyjuliabecker.substack.comJOIN the conversation on Instagram: @amyjuliabeckerLISTEN to more episodes: amyjuliabecker.com/shows/_ABOUT OUR GUEST:Kelly M. Kapic (PhD, King's College, University of London) is professor of theological studies at Covenant College in Lookout Mountain, Georgia, where he has taught since 2001. He is a popular speaker and the award-winning author or editor of more than fifteen books, including the devotional You Were Never Meant to Do It All, The God Who Gives, and the Christianity Today Book Award winners You're Only Human and Embodied Hope: A Theological Meditation on Pain and Suffering. Kapic has been featured in Christianity Today and The Gospel Coalition and has worked on research teams funded by the John Templeton Foundation. He also contributes to the Journal of Spiritual Formation and Soul Care and various other journals. kellykapic.com___We want to hear your thoughts. Send us a text!Connect with me: Instagram Facebook YouTube Website Thanks for listening!

If you're neurodivergent and considering starting your own business, boy, have I got the episode for you!Follow my guest, Kaylie Chandler, on social media:Instagram: @kaybowzieThreads: @kaybowzieTikTok: @kaybowzieYouTube: @kaybowzieSupport the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

Send us a textDr Astrid Birgden is a consultant Forensic/Clinical Psychologist and NDIS Behaviour Support Specialist who has years of experience working in corrections and disability settings. Astrid's career is quite extraordinary. She is a trailblazer in behaviour intervention support in Australia and worked overseas on international projects. She has even been an assistant sheriff/warden of a remand centre in New Orleans.We caught up with Astrid at the Complex Needs Conference in March 2025 where she was part of a panel discussion on Integrating mental health, disability, and human rights for comprehensive support.ermha365 provides mental health and disability support for people in Victoria and the Northern Territory. Find out more about our services at our website.Helplines (Australia):Lifeline 13 11 14QLIFE 1800 184 52713 YARN 13 92 76Suicide Callback Service 1300 659 467ermha365 acknowledges that our work in the community takes place on the Traditional Lands of many Aboriginal and Torres Strait Islander Peoples and therefore respectfully recognise their Elders, past and present, and the ongoing Custodianship of the Land and Water by all Members of these Communities.We recognise people with lived experience who contribute to GET REAL podcast, and those who love, support and care for them. We recognise their strength, courage and unique perspective as a vital contribution so that we can learn, grow and achieve better outcomes together.

Send us a textIn a lavish hotel suite where a marble threshold trips the host, a painful fall sparks a million-dollar claim. Can an architect be liable despite code compliance?Learn why safety is more important than style, how well-crafted details can help your defense, and why juries favor sympathy.Connect with Pro-Demnity: Leave a Review Follow us on LinkedIn Access our Risk Education Library Speak with a Risk Services Expert if you're an Ontario architect seeking guidance for a risk management issue. Thank you for listening.

Episode Notes On Episode 401, Andrew sits down with disabled entrepreneur Zoey Schvan as they tell us all about their experiences with Familial Dysautonomia, why they created their business The Spoonie Table and their life as a disabled parent and partner + so much more. Enjoy! Help Disabled Americans w/ Food Insecurity: www.feedingamerica.org Connect with Zoey and Spoonie Table at www.spoonietable.ca Episode Sponsors Do you wanna turn b*tt stuff up a notch. Go to bvibe.com and use code AFTERDARK to receive 20% off orders of $100 (including bundles, discounted items and more). Disability content creation doesn't have to be hard. Follow @seated.perspectives on Instagram to learn how to make content creation a gentle, easy, accessible experience. Are you looking for attendant care when you need it at your convenience? Check out your team, on tap www.whimble.ca Get 15% off your next purchase of sex toys, books and DVDs by using Coupon code AFTERDARK at checkout when you shop at trans owned and operated sex shop Come As You Are www.comeasyouare.com Order Notes From a Queer Cripple and hire him to speak on it by e-mailing andrew@andrewgurza.com US: https://us.jkp.com/products/notes-from-a-queer-cripple Canada: https://www.ubcpress.ca/notes-from-a-queer-cripple Support the show with a donation: https://patreon.com/disabilityafterdark This podcast is powered by Pinecast.

 Disability Employment MonthDante Q. Allen was appointed by Governor Newsom to his new role of Deputy Director of the California Department of Rehabilitation Services on April 18, 2025 and sworn in by Director Kim Rutledge on May 5, 2025 Congratulations Danté!The U.S. Senate approved the nomination of Danté Quintin Allen to lead the U.S. Department of Education's Rehabilitative Services Administration (RSA). Until his confirmation, Allen had been serving as executive director for CalABLE, California's ABLE Act savings and investment program for people with disabilities. Under his five-year leadership, CalABLE was the fastest growing ABLE Act program in the country. Prior to leading CalABLE, Allen was a communications leader for organizations including Kaiser Permanente and the California Department of Public Health's Office of Health Equity. A fulltime wheelchair user, Allen is a well-known advocate for disability rights and equity. Upon his confirmation, Secretary of Education Miguel Cardona remarked, “I look forward to working together with Mr. Allen to provide individuals with disabilities and all students with equitable access to the education and training they need to find good-paying jobs; achieve economic security; and lead healthy, independent lives.”© 2025 Building Abundant Success!!© 2025 All Rights ReservedJoin Me on ~ iHeart Media @ https://tinyurl.com/iHeartBASJoin me on Spotify: https://tinyurl.com/yxuy23baAmazon Music ~ https://tinyurl.com/AmzBASAudacy:  https://tinyurl.com/BASAud

In 2024, a landmark review of the School Education Act 1999 was undertaken in Western Australia. Why? Because our education laws — drafted over 25 years ago — haven't kept pace with modern understandings of disability, inclusion, or the rights of children and families.This review, driven by an expert panel with deep experience in education, disability, and human rights, was driven by one clear question: Does our law support every child to access and thrive in school — or are there too many barriers to access and inclusion for students with disability?What followed was an in-depth consultation with families, clinicians, educators, and young people with lived experience, resulting in 15 recommendations that aim to remove barriers — from enrollment gatekeeping, to inconsistent support, to exclusionary discipline, replacing them with legal obligations for inclusion, voice, and access.For allied health clinicians, this matters. Because so often, we're working with children whose ability to engage in school is shaped by systems, not just skills. Today, we unpack what this report means — and what could change if we get this right.

En este episodio converso con la Dra. Laura Mena García, optometrista e investigadora del Instituto de Oftalmobiología Aplicada (IOBA) de la Universidad de Valladolid. Su trabajo ha contribuido al desarrollo de nuevos programas de neurorrehabilitación visual para pacientes con hemianopsia y otros déficits campimétricos derivados del daño cerebral adquirido. Hablamos sobre cómo el cerebro procesa la información visual más allá del lóbulo occipital, los mecanismos anatómicos y funcionales que explican las hemianopsias, y las diferencias con otros trastornos como la heminegligencia. La Dra. Mena expone con claridad los fundamentos y la evidencia actual de las terapias compensatorias, restitutivas y sustitutivas, y comparte su experiencia clínica en el diseño de programas de rehabilitación visual basados en el reentrenamiento de los movimientos oculares y la atención visual. Una conversación que abre un campo poco explorado en la neurorrehabilitación: la visión desde una perspectiva cerebral. Recomendable ver el episodio en YouTube para ver diapositivas e imágenes que hacen alusión a la entrevista y que aportan mucho. Referencias de interés: 1) Mena-Garcia, L., Pastor-Jimeno, J. C., Maldonado, M. J., Coco-Martin, M. B., Fernandez, I., & Arenillas, J. F. (2021). Multitasking Compensatory Saccadic Training Program for Hemianopia Patients: A New Approach With 3-Dimensional Real-World Objects. Translational vision science & technology, 10(2), 3. https://doi.org/10.1167/tvst.10.2.3 (https://pubmed.ncbi.nlm.nih.gov/34003888/). 2) Mena-Garcia, L., Maldonado-Lopez, M. J., Fernandez, I., Coco-Martin, M. B., Finat-Saez, J., Martinez-Jimenez, J. L., Pastor-Jimeno, J. C., & Arenillas, J. F. (2020). Visual processing speed in hemianopia patients secondary to acquired brain injury: a new assessment methodology. Journal of neuroengineering and rehabilitation, 17(1), 12. https://doi.org/10.1186/s12984-020-0650-5 (https://pubmed.ncbi.nlm.nih.gov/32005265/). 3) Felleman, D. J., & Van Essen, D. C. (1991). Distributed hierarchical processing in the primate cerebral cortex. Cerebral cortex (New York, N.Y. : 1991), 1(1), 1–47. https://doi.org/10.1093/cercor/1.1.1-a (https://pubmed.ncbi.nlm.nih.gov/1822724/). 4) Macaluso, E., Frith, C. D., & Driver, J. (2007). Delay activity and sensory-motor translation during planned eye or hand movements to visual or tactile targets. Journal of neurophysiology, 98(5), 3081–3094. https://doi.org/10.1152/jn.00192.2007 (https://pubmed.ncbi.nlm.nih.gov/17898151/). 5) Pollock, A., Hazelton, C., Rowe, F. J., Jonuscheit, S., Kernohan, A., Angilley, J., Henderson, C. A., Langhorne, P., & Campbell, P. (2019). Interventions for visual field defects in people with stroke. The Cochrane database of systematic reviews, 5(5), CD008388. https://doi.org/10.1002/14651858.CD008388.pub3 (https://pubmed.ncbi.nlm.nih.gov/31120142/). 6) Postuma, E. M. J. L., Heutink, J., Tol, S., Jansen, J. L., Koopman, J., Cornelissen, F. W., & de Haan, G. A. (2024). A systematic review on visual scanning behaviour in hemianopia considering task specificity, performance improvement, spontaneous and training-induced adaptations. Disability and rehabilitation, 46(15), 3221–3242. https://doi.org/10.1080/09638288.2023.2243590 (https://pubmed.ncbi.nlm.nih.gov/37563867/). 7) IOBA: https://www.ioba.es/ LinkedIN: https://www.linkedin.com/company/iobauva/posts/?feedView=all

My guest today is Lux Raven, author of the Siren's duology that starts with Siren's Mark, which came out – together – in early October. Lux wanted to join me on the podcast to talk about disability portrayals in romance, and about her own journey to diagnosis and how it influenced her writing – and vice versa.We talk a lot about the pernicious ableism in the writing of disabled characters, and about writing your catnip when you desperately want to see your experience in a romance.Last week was Invisible Disabilities Week, and we timed this episode on purpose. So if you're dealing with an invisible disability, we see you. You are loved and if no one has told you today, you're fabulous.TW/CW: at 16:50, we discuss antifat bias and misogyny in medical care, and if you'd like to skip over that, it's about 1 minute total.Music:purple-planet.com Hosted on Acast. See acast.com/privacy for more information.

My guest today is Lux Raven, author of the Siren's duology that starts with Siren's Mark, which came out – together – in early October. Lux wanted to join me on the podcast to talk about disability portrayals in romance, and about her own journey to diagnosis and how it influenced her writing – and vice versa.We talk a lot about the pernicious ableism in the writing of disabled characters, and about writing your catnip when you desperately want to see your experience in a romance.Last week was Invisible Disabilities Week, and we timed this episode on purpose. So if you're dealing with an invisible disability, we see you. You are loved and if no one has told you today, you're fabulous.TW/CW: at 16:50, we discuss antifat bias and misogyny in medical care, and if you'd like to skip over that, it's about 1 minute total.Music:purple-planet.com Hosted on Acast. See acast.com/privacy for more information.

Your weekly dose of information that keeps you up to date on the latest developments in the field of technology designed to assist people with disabilities and special needs. Special Guest: Owen McGirr – Founder and Developer – Switchify Find out more: switchifyapp.com Look for Switchify on the Google Play Store Follow Switchify on LinkedIn […]

Some Minnesota disability service providers are concerned about the state's plan to pause payments during an audit of Medicaid program billings.And a closely watched case involving a Minnesota gun law won't get sped up to the state's top court.Those stories and more in today's evening update from MPR News. Hosted by Emily Reese. Music by Gary Meister.

What do we learn about disability and the resurrection body from the works of Flannery O'Connor? The Rev. Dr. Scott Stiegemeyer (Associate Professor of Theology and Bioethics at Concordia University Irvine and author of "Disability and the Resurrection Body in Light of the Works of Flannery O'Connor" in the Concordia Theological Quarterly) joins Andy and Sarah to talk about who Flannery O'Connor was and the Southern Grotesque style she wrote, what value we find in reading things that shock us to reality, how Flannery O'Connor reacts to the Enlightenment personal autonomy mindset through her writing, what we learn from her perspective on disability and suffering, what we learn from Scripture and the Church Fathers on suffering and the resurrection, and where we find our ultimate hope. Download a PDF of Dr. Stiegemeyer's article at ctsfw.net/media/pdfs/StiegemeyerDisabilityAndTheResurrection.pdf or find the landing page for the article at media.ctsfw.edu/Text/ViewDetails/21656. As you grab your morning coffee (and pastry, let's be honest), join hosts Andy Bates and Sarah Gulseth as they bring you stories of the intersection of Lutheran life and a secular world. Catch real-life stories of mercy work of the LCMS and partners, updates from missionaries across the ocean, and practical talk about how to live boldly Lutheran. Have a topic you'd like to hear about on The Coffee Hour? Contact us at: listener@kfuo.org.

Meet Hollis Peirce, a Canadian writer, disability advocate, and the inspiring voice behind the 21st Century Disability podcast. After surviving a life-threatening respiratory crisis in 2021, Hollis now lives in a long-term care hospital—yet continues to create, advocate, and thrive. In this episode, we explore how he finds purpose through writing, why representation matters in disability spaces, and what others often get wrong when talking about accessibility.Hollis is a testament to the power of persistence—not in spite of his circumstances, but within them.Connect with Hollis at:Website: https://www.21stcenturydisability.com/Instagram: https://www.instagram.com/21stcenturydisability/Facebook: https://www.facebook.com/21stcenturydisability/You Will Learn:How one life-altering medical crisis transformed Hollis's understanding of purposeThe surprising challenges (and freedoms) of long-term careWhy universal design isn't just for people with disabilities—it's for everyoneLizbeth's links Want to comment on the show? Connect at Lizbeth's author/podcast Facebook page Wanting great guests for your podcast, or to be a great guest on someone else's show? Join PodMatch here! Unmapped: Solo Women Travelers – Bold Journeys of Healing, Resilience, and Self-Discovery. Half of author royalties support the YWCA's work with survivors of domestic abuse and their families, and to combat racism. https://www.amazon.com/dp/B0FTSNM997 Paperback Amazon https://www.amazon.com/dp/B0FS9DX6HF Draft2Digital ebook https://books2read.com/u/312rlw Lizbeth's memoir Pieces of Me: Rescuing My Kidnapped Daughters can be ordered where books are sold, and is now a TV movie, #Stolen By Their Father on Lifetime.Lizbeth's second book, Grounded in Grit: Turn Your Challenges Into Superpowers is available to order wherever books are sold! Tilka Faces the Odds, One Man at a Time, new release novel https://books2read.com/u/4j760X Sign up to stay in the know on L...

Chapters00:00 Introduction to Romance Writing and Disability05:49 Life Changes During the Pandemic11:53 Writing Romance with Chronic Illness17:55 Representation of Disability in Romance24:35 The Viral Success of a Romance Novel31:07 Writing as a Form of Self-Discovery36:06 Navigating Writing with Disabilities49:59 The Journey of Training a Service DogSummaryIn this conversation, the speakers delve into the intersection of romance writing and disability representation, particularly focusing on the experiences of chronically ill individuals. They discuss the impact of the pandemic on their lives, the process of writing romance novels that feature disabled characters, and the importance of authentic representation in literature. The conversation also touches on the viral success of one speaker's romance novel, the emotional journey of writing, and the practical challenges of writing with disabilities. Additionally, they explore the journey of training a service dog and how it has positively influenced their lives.TakeawaysThe pandemic led to significant life changes and new diagnoses.Writing romance novels became a creative outlet during difficult times.There is a need for authentic representation of disabled characters in romance.Readers appreciate seeing themselves reflected in literature.The success of a romance novel can be validating for writers.Writing can be a form of self-discovery and healing.Navigating the writing process with disabilities requires adaptation and support.Service dogs can provide emotional and physical support for their owners.Community and connection are vital for those with chronic illnesses.The journey of self-publishing can be empowering despite challenges. Hosted on Acast. See acast.com/privacy for more information.

In this episode, Julia speaks with Unnati and Jenny, two women who joined the Women Emerging expedition on leading with a disability or chronic condition, about what it means to lead when your body demands a different pace, and how that changes everything about how you lead yourself and your team. They start by exploring the pressure to push through pain, mask discomfort, and pretend you're fine, especially when you're the one in charge. Both share the emotional cost of ignoring your limits, and what happens when you don't give your team permission to share their pain and limitations. From there, the conversation moves into the nuance of vulnerability. What do you share about your condition? When does it build trust and when does it start to center you too much? Listen to this episode to rethink what strength looks like and to discover how self-awareness, emotional literacy, and forming a relationship with your body might just be the leadership shift we all need. About the Guests: Unnati Joshi is a development professional with over a decade of experience in community outreach, partnerships, and program management. Currently serving as a Senior Program Officer at Mountaintop International, she holds a degree in Psychology, an MBA in Marketing, and certifications in Counseling Psychology, CBT, and Adolescent Guidance. Committed to education and community development, she collaborates with social leaders and engages youth and women through storytelling circles, fostering spaces for connection and growth. An advocate for mental well-being, Unnati focuses on holistic development and community resilience while pursuing personal and professional growth. Jenny is an advocate for ‘Systematic Inclusion', bringing to life the criticality of accessibility if we are to become an equitably safe and sustainable world. Jenny is dyslexic and has ADHD and believes that “the way that my brain is wired differently is an asset”. This led her to leading the Heathrow Inclusive Learners Partnership to ensure equitable pathways for learners to gain experience, internships and work. Jenny advocates that each person should have an equitable seat at the table and creating an environment that is safe for everyone; to challenge and improve the way we interreact and build the world around us.

On Season 11, Episode 9 of The LowDOWN: A Down Syndrome Podcast, Sarah and Carlo Paqueo give us the lowdown on life with their son Ronin.Support the showThe LowDOWN: A Down Syndrome Podcast is produced by the Down Syndrome Resource Foundation. Learn more and support the podcast at DSRF.org.Follow @DSRFCanada on Facebook, Instagram, and Twitter.Leave us a rating and review on Apple Podcasts.

On this Foresight Radio recording of Tech Tuesday, host Steve Moran sits down with Jake Rothstein, founder of Papa and now Upside (formerly UpsideHom), to rethink what "aging in place" really means. Starting from his grandparents' journey, Jake shares how Upside became a "housing easy button" for health plans — matching vulnerable members to safe, affordable apartments and support without laying a single brick. We cover the 5 D's trigger events, why case managers are pivotal, how flex funds unlock moves (deposits, movers, utilities, furniture), and why housing stability delivers a clear ROI for insurers. Jake also gets candid about early failures (hello, Golden Girls co-living) and tells a powerful success story about Joanna, who went from an unsafe unit to long-term stability. If you're a senior living operator, hear how Upside can fill your buildings by transitioning the right residents from SNFs and the community. Plus: Steve teases a big announcement coming later this week… Top Takeaways Aging-in-the-right-place > aging-in-place: Most older adults want to stay home—until a trigger (the 5 D's: Death, Disaster, Divorce, Disability, and Downsizing) makes it unsafe or unsustainable. Housing as healthcare: Upside partners with Medicare Advantage/Medicaid plans; stable housing cuts risk and cost, creating measurable insurer ROI. The "easy button" for case managers: Health plans refer members with housing instability; Upside rapidly matches them via a national network (multifamily, single-family, rooms, Section 8). Resources many seniors miss: Upside helps unlock SNAP, benefits, and plan flex funds (deposits, movers, utilities, furniture) to make moves possible. What didn't work (and why): Early "Golden Girls" co-living in single-family homes didn't scale—apartment partnerships and tech to track real-time inventory did. Operators benefit: Upside transitions qualified members from SNFs to IL/AL/MC, helping communities increase occupancy—including private-pay options from unlocked assets. Advocacy + access wins: Beyond units, families need navigation; the right advocate turns a confusing system into sustainable stability.

Families raising children with disabilities face great challenges, and programs like Family Retreat provide crucial rest, encouragement, and support. -------- Thank you for listening! Your support of Joni and Friends helps make this show possible.     Joni and Friends envisions a world where every person with a disability finds hope, dignity, and their place in the body of Christ. Become part of the global movement today at www.joniandfriends.org   Find more encouragement on Instagram, TikTok, Facebook, and YouTube.

Have a comment or question? Click this sentence to send us a message, and we might answer it in a future episode.Welcome to Season 5, Episode 36 of Winning Isn't Easy. In this episode, we'll dive into the complicated topic of "Frozen, Torn, or Unstable: Proving Shoulder Disability Claims."Most people think that getting disability benefits for shoulder problems is as simple as showing medical proof - MRI results, surgical records, or doctor's notes about your pain and limited motion. But when it comes to Long-Term Disability claims, that's just the beginning. Insurance carriers often twist the facts, using your own records, treatment notes, or even your words against you to argue that you're “better” or “should have recovered by now.” In this episode of Winning Isn't Easy, disability law expert Nancy L. Cavey breaks down what really happens when shoulder disorders collide with the claims process. You'll learn how the shoulder actually works, and why even a “minor” injury can make it impossible to perform the essential duties of your job. Nancy covers the most common conditions that lead to claims, from rotator cuff tears and frozen shoulder to chronic instability and dislocations, and explains how insurers use tactics like “medical improvement” arguments, surveillance, and Activities of Daily Living forms to undermine your case. You'll also hear practical advice on how to document your symptoms, treatment progress, and job limitations so your claim tells the full story - not the version your insurance company wants to tell. If your carrier says you've recovered, or insists you should be able to work through the pain, this episode shows you how to push back with medical evidence, clarity, and confidence. When it comes to shoulder disabilities, understanding your body, and your rights, can make all the difference. Winning Isn't Easy, but with the right strategy, you can keep your claim strong and your benefits protected.In this episode, we'll cover the following topics:One - Understanding Shoulder Disorders, Anatomy, and the Claims ProcessTwo - Rotator Cuff Disorders and Long-Term DisabilityThree - Frozen Shoulder and Long-Term DisabilityFour - Shoulder Instability and Dislocation in Disability ClaimsWhether you're a claimant, or simply seeking valuable insights into the disability claims landscape, this episode provides essential guidance to help you succeed in your journey. Don't miss it.Listen to Our Sister Podcast:We have a sister podcast - Winning Isn't Easy: Navigating Your Social Security Disability Claim. Give it a listen: https://wiessdpodcast.buzzsprout.com/Resources Mentioned in This Episode:LINK TO ROBBED OF YOUR PEACE OF MIND: https://mailchi.mp/caveylaw/ltd-robbed-of-your-piece-of-mindLINK TO THE DISABILITY INSURANCE CLAIM SURVIVAL GUIDE FOR PROFESSIONALS: https://mailchi.mp/caveylaw/professionals-guide-to-ltd-benefitsFREE CONSULT LINK: https://caveylaw.com/contact-us/Need Help Today?:Need help with your Long-Term Disability or ERISA claim? Have questions? Please feel welcome to reach out to use for a FREE consultation. Just mention you listened to our podcast.Review, like, and give us a thumbs up wherever you are listening to Winning Isn't Easy. We love to see your feedback about our podcast, and it helps us grow and improve.Please remember that the content shared is for informational purposes only, and should not replace personalized legal advice or guidance from qua

In this illuminating episode of Walk and Roll Live – Disability Stories, Doug and Addie sit down with leaders from the San Francisco Disability Business Alliance (SFDBA) — the first organization in the Bay Area dedicated entirely to supporting entrepreneurs with disabilities. From helping people with disabilities start and grow their own businesses to breaking down barriers in access to capital and inclusion, SFDBA is proving that disability and entrepreneurship go hand in hand. Discover how they're empowering individuals to build independence, economic freedom, and community impact — one small business at a time. Join us as we explore the programs behind their success, including the Future Entrepreneur Cohort and Boost Awards, and hear real stories of resilience, innovation, and opportunity. Whether you're an aspiring entrepreneur, advocate, or simply someone who believes in equal access to success, this episode is packed with insight, hope, and empowerment. Walk and Roll Live 

The cost of paying out Veterans Administration disability claims is more than the budget of the entire U.S. Army. Craig Whitlock is an investigative reporter who specializes in national security issues for The Washington Post. He joins host Krys Boyd to discuss how the veteran disability claim process works, the wide array of conditions covered and why administrators are reluctant to change how it operates. His article is “How some veterans exploit $193 billion VA program, due to lax controls.” Learn about your ad choices: dovetail.prx.org/ad-choices

Grey's Anatomy isn't a stranger to disability-related storylines. So why was this time different?Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

There is a lot to consider when a child receives a new diagnosis for an intellectual/developmental disability (IDD). For caregivers, families, and even providers, the conversations and planning can be overwhelming!   If you have received a new diagnosis, or maybe you are interested in beginning the process, use this podcast episode featuring Licensed Clinical Social Worker, Lauren Mowrey, to understand the diagnosis process, next steps, and most importantly, take a deep breath!

(00:00:00) Encountering Disability is a series of free events over three days focused on community health and public policy as well as community inclusion and spirituality. Asia speaks with keynote speakers Marisa Brown and Michael Gamel-McCormick, as well as Rev. David Peck who spearheaded the initiative. (00:22:04) Consumer Affairs recently published a report covering the top metros in the U.S. with the worst housing shortages. These areas were found after researchers at the site calculated metrics like the vacancy ratio for the 200 most populous metro areas in the country. Not one, not two, but three spots in the Keystone State were ranked amongst the top 10: York in second; Harrisburg in fifth; and Lancaster in ninth.Support WITF: https://www.witf.org/support/give-now/See omnystudio.com/listener for privacy information.

Disability advocate and self-advocate Cameron Bloomfield shares what it’s like to be a gay man with an intellectual disability. He talks about self-advocacy, pride, and challenging the misconception that people with disability aren’t sexual or part of the LGBTIQ+ community. Connect:Peta HookeInstagram: @petahookeWebsite: www.icantstandpodcast.comEmail: icantstandpodcast@gmail.com Episode Transcript: www.icantstandpodcast.comSee omnystudio.com/listener for privacy information.

In this episode of the ListenABLE with Karni Liddell she opens up about her incredible journey from being diagnosed with a neuromuscular condition at birth to becoming a world class Paralympian, advocate, and mother. Karni reflects on her experiences in elite sport, the evolution of disability representation, and the personal challenges that shaped her strength and perspective. She speaks candidly about the realities of motherhood with a disability, the significance of the Paralympics in shifting public perception, and the ongoing fight to ensure people with disabilities are supported and seen. Follow Karni: https://www.instagram.com/karniliddell/ https://au.linkedin.com/in/karniliddell Key Takeaways• Karni was diagnosed at birth with a neuromuscular wasting disease and was told she wouldn't live a long life.• Sport became a powerful avenue for confidence, independence, and connection.• The Paralympic movement has transformed dramatically over the past 25 years.• Motherhood brought new purpose along with new challenges.• Visibility and media representation play a critical role in changing perceptions. Chapters00:00 Introduction to the Podcast and Guest05:37 Karni Liddell’s Journey with Disability18:38 Motherhood and Disability24:39 Celebrating 25 Years of the Paralympics25:39 Reflections on the 1996 Paralympics28:11 The Impact of Sydney 200030:00 The Evolution of Disability Representation32:54 The Future of Paralympic Sports35:39 Challenges and Triumphs in Swimming37:30 The New Generation of Paralympians40:10 Representation in Media and Personal Identity Karni Liddell, Paralympian, disability advocacy, motherhood, neuromuscular disease, Paralympic movement, representation, inclusion, athlete stories, resilienceSee omnystudio.com/listener for privacy information.

In this episode of Celiac Straight Talk, Beyond Celiac Chief Scientific Officer Dr. Debra Silberg fact-checks celiac disease myths and misconceptions. She answers our questions about who can get celiac disease (answer: just about anyone!), as well as some unique symptoms that present in celiac disease, and whether or not you can grow out of it.    Thank you to Dr. Silberg for taking the time to answer our questions! Thank you so much to Takeda Pharmaceuticals for their continued support of our disease awareness campaign and research towards treatments for celiac disease.    Learn more about Beyond Celiac at beyondceliac.org! Find us on social media at @BeyondCeliac on all platforms. 

Kate Reynolds , also known as the Lavender Librarian, is the founder and director of Storytime Solidarity. Based in Ontario, Canada, Kate has been working in public libraries since 2010. She is also a sought after international keynote speaker, trained opera singer, patient advocate, writer, and content creator with a large social media following. Kate's international advocacy has brought her to high-level events in Sweden, Hungary, Canada, and the United States. Kate holds masters degrees in musicology and library science at Western University as well as a bachelor of music in vocal performance at the University of Windsor. Openly disabled and autistic, Kate is working to make the world a kinder place, one storytime at a time.Learn more on our WebsiteSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Send us a text Get £5 off the Richmond Marathon with the code BADBOY5Love the podcast and these videos? Buy us a beer! https://www.buymeacoffee.com/badboyrunning Join the Bad Boy Running Facebook group: https://www.facebook.com/groups/badboyrunning Visit the Bad Boy Running store for merchandise: https://store.badboyrunning.com Join the Bad Boy Running Club here: https://club.badboyr...

Your weekly dose of information that keeps you up to date on the latest developments in the field of technology designed to assist people with disabilities and special needs. Special Guest: Breanna Emmett – Art Specialist – Adult Day Program – Noble Find out more: Website: www.mynoblelife.org/art Email for more information: r.davis@mynoblelife.org or b.emmett@mynoblelife.org Link […]

When your days revolve around medical routines, sleepless nights, and endless caregiving, marriage can start to feel more like project management than partnership. In this episode, Madeline and Alyssa unpack all the ways that marriage is impacted amidst  medical and disability parenting—the disconnection, resentment, and chronic stress that test relationships, and the deepened understanding, teamwork, and shared strength that can come from walking through it together.Whether you think your marriage has struggled, beenstrengthened, or maybe experienced a little bit of both, this episode has something you can relate to.Links:Listen to Ep156: Should I Get a Divorce?Listento Ep 187: Do you Miss Who You Used to Be?Listento Ep 159: Sharing the Mental Load.Listento Ep 147: Sexual Intimacy.Listento Ep 171: Financial Strain.Listento Ep 99: Family Planning.Listento Ep 146: The Dad Episode.Listento Ep 139: In-Home Nursing.Listento Ep 135: Careers.Join The Rare Life newsletter andnever miss an update!Fill out our contact form to joinupcoming discussion groups!Follow us on Instagram @the_rare_life!Donateto the podcast or Contactme about sponsoring an episode.Follow the Facebook page. Join the Facebook group Parents of Children with Rare Conditions.Access the transcript on the website here. And if you love this podcast, please leave usa rating or review in your favorite podcast app

Madison Tevlin is an actor, advocate, and podcaster known for her breakout role in the film Champions and her viral YouTube performances. Madison's work centers on authentic representation in media, advocating for inclusion that goes beyond disability. She is the host of the upcoming podcast 21 Questions, which celebrates identity, energy, and connection. Madison's advocacy extends to inclusive classrooms and authentic storytelling, and she is passionate about being recognized for her personality and talents rather than her diagnosis.In this episode, host Tim Villegas talks with Madison Tevlin about her journey as a performer and advocate. Madison shares insights from her experiences on inclusive film sets, the importance of being seen for who you are, and her vision for representation in media. The conversation explores Madison's creative process, her new podcast 21 Questions, and her advice for educators on fostering authentic inclusion in schools. Madison's story is a powerful reminder that the least interesting thing about a person is their diagnosis, and that true inclusion means celebrating everyone's unique identity.Complete show notes and transcript: https://mcie.org/think-inclusive/how-madison-tevlin-redefines-disability-in-media-and-hollywood-1308/

Suzy and Diana revisit Pixar's Finding Nemo to talk about how the film hits differently as parents. They unpack Marlin's trauma and anxiety, Dory as a thoughtful nod to neurodiversity, why “family” is bigger than blood, and how to balance protection with independence. They also put Nemo through the Disney Moms Gone Wrong Hall of Fame criteria and land on a verdict.00:00 Welcome, “Hidden Mickey” kid cameos, why Nemo is on repeat at home02:00 2003 shocker, quick plot refresher03:40 Dory's humor and what she represents for neurodivergent listeners10:24 The parenting balance between protection and letting kids grow16:32 Marlin and Nemo's relationship shift from fear to trust21:07 Safe risks, helicopter parenting, and real life boundaries25:04 Family beyond blood: Bruce, Crush, Squirt, and the tank crew as a village31:39 Most emotional moments and why they land as parents38:31 Nemo's fin and talking about disability with care and support43:02 Hall of Fame debate and verdict46:01 Scheduling notes, shoutouts, sign offMarlin's overprotection is rooted in trauma and love, not control. Naming that helps parents reframe their own anxiety.Dory reads as a warm, respectful reflection of neurodiversity, reminding us that different brains belong in the story.Kids need safe space to try, stumble, and grow. Guardrails beat bubble wrap.“Family” is the people who show up. Nemo's helpers along the way model a real village.Disability is part of the world, not an afterthought. Nemo's fin is handled with empathy, not pity.Verdict: Yes to the Disney Moms Gone Wrong Hall of Fame for cultural impact and emotional storytelling, even without iconic songs.“The balance between protecting your kids and letting them grow up is real, and it's hard.”“Family is more of a feeling than DNA.”“Safe risks matter. You can supervise without smothering.”“Dory reminds us that different ways of thinking have a place in the journey.”If this episode resonated with you, please follow, rate, and review the show. Share it with a friend and tag us with #DisneyMomsGoneWrong so we can find your post.GeekFreaksPodcast.com – Our home base and the source of all news discussed on our showsMovie referenced: Finding Nemo (2003), PixarDisney Moms Gone Wrong: IG: @disneymomsgonewrongGeek Freaks: Instagram: @geekfreakspodcast, Threads: @geekfreakspodcast, Twitter: @geekfreakspod, Facebook: Geek Freaks Podcast, Patreon: GeekFreaksPodcastWhat parenting moment in Finding Nemo hit you the hardest, and why? Send your questions or topic ideas for future episodes to our socials or through GeekFreaksPodcast.com. We'll feature a few on the next show.Apple Podcasts Tags: Disney Moms Gone Wrong, Finding Nemo, Pixar, Parenting, Neurodiversity, Disability Representation, Family, Movie Review, Animation, Geek Freaks NetworkTimestamps and TopicsKey TakeawaysQuotesCall to ActionLinks and ResourcesFollow UsListener Questions

October is National Disability Employment Awareness Month! Learn how Goodwill and @TexasWorkforce are helping young adults with disabilities gain independence with local employers in the latest episode of GoodCast!

Episode 123: Evaluating Disability-Inclusive Content on U.S. Medical Schools' Websites—A National Study Interviewees: Ifeoma Ikedionwu, MD — Psychiatry and Internal Medicine Dual Intern, UT Southwestern Dominique Cook — Fourth-Year Medical Student, University of South Florida Interviewer: Lisa Meeks, PhD, MA — Guest Editor, Academic Medicine Supplement on Disability Inclusion in Undergraduate Medical Education Description: In this episode of Stories Behind the Science, Dr. Lisa Meeks sits down with Dr. Ifeoma Ikedionwu and Dominique Cook, co-authors of the first national study examining how medical school websites communicate disability inclusion. Their paper, Evaluating Disability-Inclusive Content on U.S. Medical Schools' Websites: A National Study, is part of the Academic Medicine supplement on Disability Inclusion in Undergraduate Medical Education. What do medical schools' digital front doors say about who belongs? The conversation explores how public-facing messages shape applicants' sense of access, belonging, and possibility—and why visibility is the first step toward equity. Ikedionwu and Cook share how their lived experiences as medical students with and without disabilities inspired a research project that merges advocacy, analysis, and systemic change. Together, they unpack the challenges of quantifying inclusivity, the nuance of intersecting identities, and the powerful role of student-led research in shaping institutional accountability. The episode underscores how every mission statement, technical standard, and accessibility page sends a message—and how aligning those messages with institutional values can create a more inclusive path for future physicians. Listeners will leave with actionable insights: Audit your institution's website for clarity, tone, and accessibility. Engage learners with lived experience in reviewing public materials. Translate inclusion from policy into practice—and from practice into visibility. Because as Ikedionwu reminds us, “It's not enough to do the work—you have to share it, so others can find their way.” Transcript: https://docs.google.com/document/d/1UmiXVs8wESM28eRYAM-d13IuJTV6VzR2khagExHF12A/edit?usp=sharing Resources: Article from Today's Talk: Ikedionwu I, Cook D, Kim N, Cotts J, Case B, Meeks LM. Evaluating Disability-Inclusive Content on U.S. Medical Schools' Websites: A National Study. Academic Medicine. 2025;100(10S):S60–S67. Read the full article here → Related Reading: Equal Access for Students with Disabilities: The Guide for Health Science and Professional Education (2nd Ed). Meeks LM, Jain NR, & Laird EP. Springer Publishing, 2020.

On Season 11, Episode 8 of The LowDOWN: A Down Syndrome Podcast, Eleni Bakolias gives us the lowdown on providing truly inclusive childcare.Support the showThe LowDOWN: A Down Syndrome Podcast is produced by the Down Syndrome Resource Foundation. Learn more and support the podcast at DSRF.org.Follow @DSRFCanada on Facebook, Instagram, and Twitter.Leave us a rating and review on Apple Podcasts.

In Honor Of Disability Month - A story of finding peace, connection, and meaning even in the midst of change.What do you do when life as you knew it suddenly disappears? When the things that once came easy — walking, working, feeling independent — are gone, and you're left wondering what's left of “you”? That's where Rosemarie found herself after a devastating accident left her paralyzed, and yet she somehow turned that loss into a life filled with impact and meaning. In this episode, she shares the mindset shifts and practical lessons that helped her move from frustration to freedom. If you've ever felt stuck between who you were and who you're becoming, her story will remind you that it's possible to create a life that still feels full, no matter what changes come your way. What You'll Learn:The best way to start rebuilding your life.How Rosemarie turned her wheelchair into a classroom for leaders, builders, and designers.The one mindset shift that helped her move from self-pity to possibility.What Christopher Reeve taught her about hope long before she needed it.How to find joy again when your body no longer does what it used to.Why lowering your expectations of others can actually bring more peace and connection.The simple phrase Rosemarie keeps on her desk that changed how she lives every day.

Scott Hamilton is one of the most recognizable and decorated figure skaters in the world — an Olympic Gold Medalist and four-time World Champion who has earned more than 70 titles and honors, including inductions into both the U.S. Olympic and World Figure Skating Hall of Fame.His journey, however, goes far beyond the ice. In 1997, Scott was diagnosed with testicular cancer — just 20 years after losing his mothe to cancer. In the years that followed, he battled three brain tumors with the same courage and resilience that defined his skating career.Today, Scott channels that spirit into his mission off the ice — raising awareness and funding for cancer research and patient support through the Scott Hamilton CARES Foundation.Download my FREE Coaching Beyond the Scoreboard E-book www.djhillier.com/coach Download my FREE 60 minute Mindset Masterclass at www.djhillier.com/masterclassDownload my FREE top 40 book list written by Mindset Advantage guests: www.djhillier.com/40booksSubscribe to our NEW YouTube channel: https://www.youtube.com/@MindsetAdvantagePurchase a copy of my book: https://a.co/d/bGok9UdFollow me on Instagram: @deejayhillierConnect with me on my website: www.djhillier.com

What if disability isn't something to fix, but a way to see God and one another more clearly? Theologian John Swinton joins Amy Julia Becker to explore how our ideas of perfection, healing, and humanity can distort—or deepen—our understanding of the good life. Together, they imagine a church and a world that welcomes every body as good, beloved, and whole. They explore:How culture shapes (and distorts) our perceptions of disability and beautyWhat it means for a world to be both wounded and belovedWhy the difference between goodness and perfection mattersHow interdependence includes both beauty and a cost__TAKE THE NEXT STEP PODCAST: amyjuliabecker.com/step/SUBSCRIBE to Amy Julia's newsletter: amyjuliabecker.com/subscribe/__00:00 Introduction02:54 Significance of Disability in Faith05:50 Cultural Perceptions of Disability08:50 The Image of God and Human Relationships11:45 Understanding Goodness vs. Perfection18:18 Goodness and Suffering23:55 The Power of Naming and Identity27:38 Relationality and the Cost of Interdependence35:38 Resisting Culture's Distortions of the Image of God__MENTIONED IN THIS EPISODE:Christianity Today essay: “It Was Good, Not Perfect.”Genesis 1-3_WATCH this conversation on YouTube: Amy Julia Becker on YouTubeSUBSCRIBE to Amy Julia's Substack: amyjuliabecker.substack.comJOIN the conversation on Instagram: @amyjuliabeckerLISTEN to more episodes: amyjuliabecker.com/shows/_ABOUT OUR GUEST:John Swinton is Professor in Practical Theology and Pastoral Care and Chair in Divinity and Religious Studies at the University of Aberdeen. For more than a decade John worked as a registered mental health nurse. He also worked for a number of years as a hospital and community mental health Chaplain alongside of people with severe mental health challenges who were moving from the hospital into the community. In 2004, he founded the University of Aberdeen's Centre for Spirituality, Health and Disability. He has published widely within the area of mental health, dementia, disability theology, spirituality and healthcare, end of life care, qualitative research and pastoral care. John is the author of a number of monographs including Finding Jesus in the Storm: The spiritual lives of people with mental health challenges. (Eerdmans 2020) which won the Aldersgate prize for outstanding interdisciplinary work within theology. His book Dementia: Living in the memories of God won the Archbishop of Canterbury's Ramsey Prize for excellence in theological writing. We want to hear your thoughts. Send us a text!Connect with me: Instagram Facebook YouTube Website Thanks for listening!

Have a comment or question? Click this sentence to send us a message, and we might answer it in a future episode.Welcome to Season 5, Episode 35 of Winning Isn't Easy. In this episode, we'll dive into the complicated topic of "The Hidden Role of Job Skills in Winning (or Losing) Your ERISA Disability Claim."Most people think that winning a Long-Term Disability claim is all about proving you're sick or injured, with medical records, doctor's notes, or diagnostic tests. But in ERISA claims, that's only half the story. What often makes or breaks your case isn't just your health - it's your job skills. Insurance companies know that every job leaves you with transferable abilities: skills, knowledge, and experience that could, in theory, be used in another line of work. And they use that to their advantage. By arguing that you can apply your past skills to a new occupation, carriers can deny or terminate benefits even when you clearly can't return to your old job. In this episode of Winning Isn't Easy, disability law expert Nancy L. Cavey explains how your work history and skill classification can shape the outcome of your claim. You'll learn what “own occupation” really means, how insurers decide whether your work is skilled, semi-skilled, or unskilled, and how those labels can be twisted to fit their narrative. Nancy also discusses how vocational experts and work history forms are used, and sometimes misused, during the claims process, along with practical strategies to document your true job duties and protect your benefits. If your disability carrier says you can “do other work,” this episode shows you how to fight back with facts, clarity, and confidence. In disability law, understanding your skills isn't just helpful - it's essential. Winning Isn't Easy, but with the right approach, you can make your story and your skills work for you.In this episode, we'll cover the following topics:One - The Own and Any Occupation Stages and Why Skills MatterTwo - How Carriers Classify Job SkillsThree - Work History, Vocational Experts, and Fighting BackWhether you're a claimant, or simply seeking valuable insights into the disability claims landscape, this episode provides essential guidance to help you succeed in your journey. Don't miss it.Listen to Our Sister Podcast:We have a sister podcast - Winning Isn't Easy: Navigating Your Social Security Disability Claim. Give it a listen: https://wiessdpodcast.buzzsprout.com/Resources Mentioned in This Episode:LINK TO ROBBED OF YOUR PEACE OF MIND: https://mailchi.mp/caveylaw/ltd-robbed-of-your-piece-of-mindLINK TO THE DISABILITY INSURANCE CLAIM SURVIVAL GUIDE FOR PROFESSIONALS: https://mailchi.mp/caveylaw/professionals-guide-to-ltd-benefitsFREE CONSULT LINK: https://caveylaw.com/contact-us/Need Help Today?:Need help with your Long-Term Disability or ERISA claim? Have questions? Please feel welcome to reach out to use for a FREE consultation. Just mention you listened to our podcast.Review, like, and give us a thumbs up wherever you are listening to Winning Isn't Easy. We love to see your feedback about our podcast, and it helps us grow and improve.Please remember that the content shared is for informational purposes only, and should not replace personalized legal advice or guidance from qualified professionals. 

Jaz races in the Hanse 303 and RS Venture Connect SCS classes, and sails an Albin Vega 27, in which she recently became the first wheelchair user to sail solo and unassisted around Great Britain and Ireland, and doing so confronted and overcame great difficulties. She lives with Ehlers-Danlos Syndrome,  which means her connective tissue does not function properly, and this also effects her internal organs, and her condition is terminal. Regardless, Jaz is now preparing to compete in the 2026 Worldstar, in which she will attempt to sail solo nonstop unassisted around the world. We talk about her introduction to sailing on a cold wet day in the Cornish Harbor, her obsession with the ocean, growing up with a difficult home situation, being homeless as a child and living on the street, then sleeping in the boats at the sailing club, dealing with fear, living on a shorter time line, finding a new family, comparing the Albin Vega to performance boats, heaving-to, sleeping while solo, hallucinations, breakages, preventers, Project Fear, how the circumnavigation of Britain and Ireland changed her, the extents of her mobility, foul-weather gear, beautiful moments, wildlife, running aground 50 nm from the finish and kedging off, the WorldStar 2026, and more. Photos and links are on the podcast shownotes page Support the show through Patreon

Stories, perspectives, and wisdom from folks in our own community.

Today we have the Sex & Disability Superfile, where we hear from past guests Claire AH, Andrew Gurza, Rachel Rose, Graham Isador, Stella Palikorova, and Daniel James.  Brought to you By: The Sonar Network https://thesonarnetwork.com/

Pastor Nicoletti, in an interlude lesson between series, gives an introduction to disability theology.

Australia has its first new cancer screening programme in 20 years, this time for lung cancer. Today we'll be discussing this new programme in depth as well as the role of primary care and the supports available in delivering the programme.This podcast is Sponsored by the Australian Government National Lung Cancer Screening Program.Professor Vivienne Milch is Medical Director, at Cancer Australia. Professor Milch is also Medical Advisor to the Australian Commonwealth Department of Health, Disability and Ageing on cancer screening policy.Professor Milch holds a Master's degree in Health Policy and is an Adjunct Clinical Associate Professor in the School of Medicine, Sydney Campus at The University of Notre Dame, Australia and Professorial Fellow at the Caring Futures Institute at Flinders University in Adelaide. Prior to joining Cancer Australia, Professor Milch was a General Practitioner and clinical researcher at the Garvan Institute of Medical Research, Sydney. Relevant links: the Investigating Symptoms of Lung Cancer guide Healthcare Provider Toolkit The NLCSP website Program Guidelines GP guide resource Reducing stigma in the program Low-dose CT Scan request form eLearning modules developed by Lung Foundation Australia Actionable additional findings guidelines

Mainstream adaptive fashion lines are relatively new, but creating clothes to fit and flatter a range of bodies has long been part of disability culture. Anita meets three disabled fashionistas who design with disabled bodies as a starting point, not an afterthought.Meet the guests:- Dr. Ben Barry is the Dean of Fashion at Parsons School of Design who's pushing for further inclusion in fashion – particularly when it comes to the ways clothing is designed, marketed and modeled for folks with disabilities-  Sky Cubacub is a Chicago-based fashion designer focused on making size-inclusive garments for queer and trans disabled folks through their company, Rebirth Garments- Samantha Jade Durán is a designer and influencer also known by the handle “A Disabled Icon"Read the transcript | Review the podcast on your preferred platformFollow Embodied on Instagram Leave a message for EmbodiedPlease note: This episode originally published November 7, 2024.Update: Samantha Jade Durán launched a disability and chronic illness awareness merch brand called Thanks Icon. She plans on expanding to adaptive clothing and accessories in the future.

The government shutdown continues apace, Virginia AG candidate Jay Jones fields another scandal, and almost 100k veterans are receiving disability checks for acne. Get the facts first with Evening Wire. - - - Wake up with new Morning Wire merch: https://bit.ly/4lIubt3 Learn more about your ad choices. Visit megaphone.fm/adchoices