Podcasts about Disability

Share this program with friends by going to www.joniradio.org! --------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.

Learn more on how to serve people living with disabilities at www.joniandfriends.org. -------- 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.

A shorter episode this week. There are only so many ways to say disability ≠ sickness.Support the showWebsite: 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

Six projects will share $200,000 to help disability communities prepare for a changing climate.

It sounds strange but thank your trials for enriching your life with your wealth of knowledge about Christ. -------- 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.

A nurse who worked at a disability support facility in Sakai, Osaka Prefecture, filed a lawsuit claiming it was unlawful for the facility to dismiss them after they made a public-interest whistleblower report about problems at the facility. The Sakai branch of the Osaka District Court ruled that the dismissal was invalid, finding that it was intended to remove the nurse from the workplace, and ordered the facility to pay unpaid wages and damages. The court ordered the facility to pay the three plaintiffs a total of more than ¥20 million in unpaid wages, damages, and other compensation. Episode notes: ‘Sakai District Court Rules Dismissal of Whistleblower Nurse at Disability Facility Invalid': https://barrierfreejapan.com/2026/07/31/sakai-district-court-rules-dismissal-of-whistleblower-nurse-at-disability-facility-invalid/

In This episode Darcy Celebrates the Release of Spider-Man Brand New Day in his own special way. While he, Dritain and Phoebe finally discus their Guilty PleasuresDonate to SYN: http://syn.org.au/donate-to-syn/See omnystudio.com/listener for privacy information.

See why Joni says being as “wise as serpents” is actually the smart thing to do. -------- 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.

A total of 278 disability care facilities in Kumamoto Prefecture have been affected by the powerful earthquake that struck the region earlier this week, Kyodo reported on July 31, citing the Health, Labour and Welfare Ministry. Episode notes: ‘278 disability care facilities affected by Kumamoto earthquake': https://barrierfreejapan.com/2026/08/01/278-disability-care-facilities-affected-by-kumamoto-earthquake/

Fairy tales are as old as time, moralistic stories that have influenced our understanding of the world, and not always for the better. Amanda Leduc's 2020 novel Disfigured: On Fairy Tales, Disability, and Making Space explores the power of fairy tales and their historically problematic depiction of disability.See omnystudio.com/listener for privacy information.

Share this program with a friend or family member at www.joniradio.org!  --------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.

Episode 163ALL ABOUT NONSPEAKERS: REFLECTIONS ON AUTISM SPECTRUM NEWS ISSUE WITH AMY LAURENT AND JEN LEPAPEThe discussion focused on the recent issue of Autism Spectrum News dedicated to non-speaking individuals. Topics in the issue included common misunderstandings about supporting non-speakers, including the concept of presuming competence, the role of neuromotor issues, and concerns about communication authenticity and influence. The discussion highlighted that many non-speaking individuals can learn to communicate effectively through methods like spelling and typing, though it requires time and proper support. The guests emphasized that the issue contains 40 articles, including 17 authored or co-authored by non-speakers, covering topics from mental health to legal issues to practical support strategies, demonstrating the complexity of supporting non-speaking individuals beyond simple debates about authenticity.Find out 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.

Today I had the honor of speaking with Sarah Iengo and Lixon Nelson of ACES. ACES  (www.acesmiami.org) is dedicated to empowering individuals with disabilities, youth, families, and underserved members of the community through education, employment support, mentorship, advocacy, and access to meaningful resources. Our mission is to help individuals build confidence, independence, and pathways toward long-term success. Our vision is to create a more inclusive community where every person has the opportunity to grow, lead, and reach their full potential.

Lachi is a distinguished figure in the music and media industries, known for her work as an award-winning recording artist, producer, and advocate. She has a dynamic career that includes a Grammy-nominated album, hosting the PBS series Renegades, and founding the organization RAMPD (Recording Artists and Music Professionals with Disabilities). Lachi is also a national trustee of the Recording Academy and she identifies as blind and neurodivergent.In this riveting episode of Think Inclusive, host Tim Villegas engages in a profound conversation with the multitalented Lachi, who uses her platform to advocate for disability pride and accessibility in the music industry. The episode dives deep into how language shapes our understanding of disability, and why Lachi chooses to “identify as blind,” a declaration that challenges societal norms and sparks dialogue about the disabled community versus the disabled population.Joining this dialogue, Lachi shares her experiences growing up with blindness and neurodivergence, highlighting how these challenges shaped her career as a musician and advocate. This episode is rich with insight into Lachi's philosophy on inclusion and her journey to remove stigmas attached to disabilities. Her reflections on navigating the industry, establishing RAMPD to support disabled music professionals, and the importance of speaking to individuals with dignity and respect offer a thoughtful critique on how society views and engages with disability.Complete show notes and transcript: https://mcie.org/think-inclusive/i-identify-as-blind-lachi-on-disability-language-identity-and-why-words-matter-in-schools-1340/

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: Brittany Palmer – CoFounder and CEO – Ability Lane And – Managing Partner – Adaptation Ventures Website: https://abilitylane.com Screen Time Story: https://n.pr/4w39rld INDATA Full […]

God's promises are never to be rushed. So, take heart and wait on the Lord. -------- 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.

July is Disability Pride Month, and to mark the occasion we're talking about the state of disability rights and what still needs to be done.

Hear us out: An awkward sex scene can actually be better than a frictionless one. Take the examples Sanj and Tyler cite from Business or Pleasure and Act Your Age, Eve Brown! Then, Riss M. Neilson shares her experiences writing chronic illness and disability and delivering romance to characters who deserve love and steam. Plus, a what-we’ve-consumed-this-month roundup ending with a wildly bad Italian accent courtesy of a rewatch of The Wedding Planner. Most-memorable sex scene mentions: Business or Pleasure by Rachel Lynn Solomon and Act Your Age, Eve Brown by Talia Hibbert. Riss M. Neilson is the author of A Love Like the Sun and The Bridge Back to You. Her rec: Reel by Kennedy Ryan. What we’ve consumed this month: The Invite, Lisa Kleypas’s The Wallflower series, Fossil Feud by Maggie North, Chase Me If You Can by Heather Francis, and The Wedding Planner. See omnystudio.com/listener for privacy information.

Go to https://joniandfriends.org/volunteer/ to see how you can serve today! --------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.

LeDerick Horne is a spoken word poet, advocate, and speaker known for his work in special education and disability advocacy. He serves as the board chair of All In for Inclusive Education and is co-author of “Empowering Students with Hidden Disabilities: A Path to Pride and Success.” LeDerick has performed his poetry at high-profile venues, including the White House, and is the co-host of the “Black and Dyslexic Podcast.” His work primarily revolves around exploring his dual identity as a Black man with a learning disability, utilizing poetry to advocate for inclusive education practices.In this insightful episode of Think Inclusive, Tim Villegas is joined by LeDerick Horne, a distinguished advocate for inclusive education and a spoken word poet. The conversation delves into the implications of labeling in education and the transformative power of truly inclusive environments. As someone who has navigated the challenges of a learning disability, Horne shares his journey and the significance of acknowledging disability as a political identity.The dialogue explores how educators can effectively support students with hidden disabilities such as dyslexia. With an emphasis on collaboration among teachers and acknowledging gaps in knowledge, Horne asserts that integration within classrooms should not merely be about co-location but about genuine collaboration and support. Furthermore, the episode includes a compelling discussion on the intersectionality of race and disability, urging educators to demystify neurodiversity and challenge systemic segregation in schools.Complete show notes and transcript: https://mcie.org/think-inclusive/navigating-identity-poetry-disability-and-inclusion-advocacy-with-lederick-horne-1339/

Nothing is more calming, more quieting, more hopeful to the troubled mind than rehearsing how deep and wide the love of God really is. -------- 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.

Watch the video version on YouTube: https://youtu.be/HHWS6KTKcTU Keith and Jodi interview Meier Galblum Haigh, Executive Director of Disability Culture Lab, about the summer streetwear collection "We're Still Here: Fashion Against Fascism," shaped by conversations with more than 40 disabled people and a North Star visioning process exploring what "winning" and liberation look like. Meier explains Disability Culture Lab's mission to build disabled-led communications infrastructure because "bad stories lead to bad policy," and describes themes behind the collection—interdependence and care, disabled leadership and power, disabled joy, and the harms of oppressive systems—along with tensions around non-disabled parents driving harmful narratives. The Deep Cut segment reviews Netflix's "All the Light We Cannot See" through a disability lens, discussing authentic casting of blind/low-vision actors, shortcomings in character depth and historical context of Nazi violence against disabled people, the value of audio description, and the need for agency, complexity, access, and disabled involvement behind the camera. Disability Culture Lab Website: https://www.disabilityculturelab.org/ Instagram: https://instagram.com/disabilityculturelab BlueSky: https://bsky.app/profile/disabilitylab.bsky.social Store: https://shop.disabilityculturelab.org/

Psychiatrist Dr Tanveer Ahmed joined Tom Elliott to talk about recent data which reported over 1/4 of Australian school students received exemptions due to disability for tests and exams in 2025. See omnystudio.com/listener for privacy information.

Visit www.joniradio.org for more inspiration and encouragement! --------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.

This month on Laura Flanders & Friends we're lifting up the people, the stories, and the ideas driving disability justice forward.  This week we revisit a Peabody Award–winning documentary about a summer camp that helped spark a disability revolution—reminding us that transformation often begins with community. This show is made possible by you! To become a sustaining member go to LauraFlanders.org/donate Description:  Crip Camp is a Peabody Award-winning documentary from Netflix and Higher Ground Productions that tells the story of Camp Jened, a summer camp in the 1960s where disabled youth could be themselves. The film follows several former campers who went on to be leaders of the Disability Rights Movement. Laura speaks with the directors and producers of Crip Camp about how they are using the film to advance the next step in the revolution: Disability Justice, a movement that centers the leadership of disabled queer, trans, Black, Indigenous, and people of color. If the inclusive culture of Camp Jened could help transform American society in the second half of the 20th century, what could a truly intersectional Disability Justice Movement change for us all today? Plus thoughts from Laura on interdependence. Guests: • Jim LeBrecht, Co-Director Crip Camp: A Disability Revolution;  Founder Berkeley Sound Artists • Nicole Newnham, Co-Director Crip Camp: A Disability Revolution;  • Andraéa LaVant, Impact Producer Crip Camp: A Disability Revolution;  And President and Chief Inclusion Officer of LaVant Consulting Inc.   Watch the episode released on YouTube; PBS World Channel 11:30am ET Sundays and on over 300 public stations across the country (check your listings, or search here via zipcode). Listen: Episode airing on community radio (check here to see if your station airs the show) & available as a podcast.   RESOURCES: Related Laura Flanders Show Episodes: • Disability Justice:  Alice Sheppard & Jess Thom • Policy Demands for #DisabilityRights:  An Animated Explainer w/Dara Baldwin • Special Report:  Ableism Out, Independent Living Now! • Ableism Separated Disabled People from Autonomy:  Kelly Buckland and vilissa Thompson • Design For Justice:  Disabled Hackers Are Leading The Way • Tech:  Existential Threat or Life Support?   Related Articles and Resources: • The Crip Camp Educational Curriculum • Crip Camp 2020:  The Virtual Experience • The Defense of Black Lives Must Include Disability Justice by Andraéa LaVant, The Root • 10 Principles of Disability Justice by Sins Invalid • This manager is working toward diversity in Hollywood — and that includes those with disabilities by Anousha Sakoui,   Featured ‘Music in the Middle' of the Podcast: “Badass and Blind” the title track of Raul Midón's album released on Mack Avenue Records. Check out our feature with Raul Midón: “Creative Adaptation and Covid-19”   Listen and Read More   Laura Flanders and Friends Crew: Laura Flanders-Executive Producer, Writer; Sabrina Artel-Supervising Producer; Jeremiah Cothren-Senior Producer; Veronica Delgado-Video Editor, Janet Hernandez-Communications Director; Jeannie Hopper-Audio Director, Podcast & Radio Producer, Audio Editor, Sound Design, Narrator; Sarah Miller-Development Director, Nat Needham-Editor, Graphic Design emeritus; David Neuman-Senior Video Editor, and Rory O'Conner-Senior Consulting Producer. FOLLOW Laura Flanders and FriendsInstagram: https://www.instagram.com/lauraflandersandfriends/Blueky: https://bsky.app/profile/lfandfriends.bsky.socialFacebook: https://www.facebook.com/LauraFlandersAndFriends/Tiktok: https://www.tiktok.com/@lauraflandersandfriendsYouTube: https://www.youtube.com/channel/UCFLRxVeYcB1H7DbuYZQG-lgLinkedin: https://www.linkedin.com/company/lauraflandersandfriendsPatreon: https://www.patreon.com/lauraflandersandfriendsACCESSIBILITY - The broadcast edition of this episode is available with closed captioned by clicking here for our YouTube Channel

Hey comrades! Laura Piper Lee comes on the podcast to talk her latest release, stoner romcom, POT SHOT, her experience with Crohn's and weed, and disability representation in romance. Enjoy the show! Connect with Laura: website; Insta Preorder DOOMSDATE; see Laura on tour   SUPPORT THE PODCAST by visiting my Bookshop.org Storefront to get any book mentioned in the episode. If you use this link or go directly from my store, I earn a small commission. You can also buy me a coffee, shop some WRION merch, or grab something from my sapphic, bookish Etsy shop! FOLLOW THE PODCAST on Instagram/Threads @wereaditonenight or FOLLOW ME on Instagram @thealisonfinch Facebook: We Read It One Night Email: wereaditonenight [at] gmail.com

On the Tip of My Tongue: Jonathan Hirons on Aphasia, Advocacy, and PodcastingThis episode, Marv sits down with Jonathan Hirons, host of the podcast On the Tip of My Tongue, to talk about aphasia — a communication disorder that affects language but not intelligence or memory — and how it shaped his life and work.Jonathan shares the story of the sudden stroke that left him with aphasia, the speech and language therapy that followed, and the vital role his wife played early on using flashcards to help rebuild his vocabulary. He and Marv discuss why aphasia remains so poorly understood despite affecting more people than Parkinson's disease, and why groups and community support make such a difference for people relearning to communicate.The conversation also traces how Jonathan's aphasia documentary evolved into a podcast, why he brought on co-host Rob Edwards to handle scripted segments, and how the show balances lived experience with expert insight. They wrap up comparing notes on production workflows, episode artwork, and the "teaser hook" technique both shows use to draw listeners in.In This Episode● What aphasia is, and why it's known as a "hidden disability"● Jonathan's personal story: sudden onset, hospitalization, and diagnosis● The road through speech therapy and relearning to read, write, and speak● Why community groups are key to rebuilding confidence● How a documentary film became a podcast● Behind-the-scenes: recording with Zoom, editing in Reaper, publishing via Buzzsprout● The importance of podcast artwork and episode "teasers"● Where to find On the Tip of My Tongue and how to support the showLinks & ContactOn the Tip of My Tongue: tipofmytonguefilm.comEmail Jonathan: hello@tipofmytonguefilm.comFind Jonathan on Instagram, Facebook, and LinkedInPods Like UsContact: podslikeus@gmail.comAll links and socials: themarvzone.org

Hear Joni share an amazing story about how a wheelchair was the perfect fit for a man in Kenya. -------- 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.

This summer, we're revisiting some of Hina and Marla's greatest hits from the first 11 seasons of The LowDOWN. On season 8, episode 6 of The LowDOWN: A Down Syndrome Podcast, Rose Reif gives us the lowdown on helping people with Down syndrome process grief.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.

Discover how blind tech enthusiasts navigate listener emails, share hilarious real-life stories, and explore accessibility in healthcare, music, and multi-line braille technology like the Monarch. In this engaging episode of Double Tap, Steven Scott and Shaun Preece dive into their inbox to discuss heartfelt and eclectic listener messages. From Pam's unforgettable prosthetic eye and spaghetti dinner story to Gordon's online shopping frustrations, each email sparks candid conversations about life, blindness, and technology. Listeners share experiences with hospital fall-risk protocols, privacy concerns, and how societal perceptions of disability affect daily life. The hosts also explore multi-line braille reading with the HumanWare Monarch, Orion smart glasses, and the Suno app for AI-generated music. Packed with humour, reflection, and practical advice, this episode highlights the importance of accessibility, self-advocacy, and community in the blind tech world. ----Follow on:YouTube: https://www.doubletaponair.com/youtubeX (formerly Twitter): https://www.doubletaponair.com/xInstagram: https://www.doubletaponair.com/instagramTikTok: https://www.doubletaponair.com/tiktokThreads: https://www.doubletaponair.com/threadsFacebook: https://www.doubletaponair.com/facebookLinkedIn: https://www.doubletaponair.com/linkedinSubscribe to the Podcast:Apple: https://www.doubletaponair.com/appleSpotify: https://www.doubletaponair.com/spotifyRSS: https://www.doubletaponair.com/podcastiHeadRadio: https://www.doubletaponair.com/iheartAbout Double TapHosted by the insightful duo, Steven Scott and Shaun Preece, Double Tap is a treasure trove of information for anyone who's blind or partially sighted and has a passion for tech. Steven and Shaun not only demystify tech, but they also regularly feature interviews and welcome guests from the community, fostering an interactive and engaging environment. Tune in every day of the week, and you'll discover how technology can seamlessly integrate into your life, enhancing daily tasks and experiences, even if your sight is limited."Double Tap" is a registered trademark of Double Tap Productions Inc. Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Black autistic Brazilian activist Luciana Viegas has advocated for the rights and protections of people with disabilities and Black folks in Brazil for many years. We go over some of the milestones.See omnystudio.com/listener for privacy information.

Go to https://joniandfriends.org/volunteer/ to see how you can serve today! --------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.

Rebecca Bloom is a former employee benefits and executive compensation attorney who spent more than 25 years helping women navigate cancer, work, insurance, disability coverage, and financial survival. She is the founder and author of When Women Get Sick, a book built from decades inside the legal, workplace, and patient advocacy systems most people only discover after diagnosis.Bloom started in Big Law at Simpson Thacher handling employee benefits and compensation work she originally chose to pay off student loans. Then her mother was diagnosed with breast cancer. Suddenly the language she used in corporate law offices became the language of survival at home. Explanation of benefits forms. Coverage disputes. Second opinions. Disability protections. Medical leave. Bills no one could explain.That collision changed the direction of her life.In this episode, Bloom explains how serious illness quietly turns patients into unpaid administrators managing paperwork, logistics, financial risk, and emotional labor while trying to survive treatment. She breaks down how employer based health insurance shapes nearly every aspect of cancer care in America and why women often carry the invisible burden of protecting everyone else from discomfort while they themselves fall apart.The conversation digs into workplace power, the illusion of the healthcare “safety net,” caregiver exhaustion, and the class divide hiding underneath patient empowerment culture. Bloom explains why educated, insured women with resources still struggle to navigate healthcare bureaucracy and what happens to patients without those advantages.This episode explores cancer care, health insurance, employee benefits, patient advocacy, workplace protections, caregiving, and the structural incentives that force sick people to become project managers of their own survival.RELATED LINKSRebecca BloomWhen Women Get SickBay Area Cancer ConnectionsSimpson Thacher & BartlettFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

In addition to making media accessible and centering disabled storytelling through podcasting and other creative forms, it is essential that we make visible the views of disabled people on critical issues of the day. In this important conversation with Sara Luterman of the 19th, we discussed Sara's reporting on a first of its kind poll by Data for Progress about disabled people's views on abortion. These views are diverse and complex, rooted in histories of institutionalization, forced sterilization, and the use of abortion to erase disability. This type of polling highlights the critical importance of cross-movement solidarity between the movements for disability justice and reproductive justice, to ensure that the battle for reproductive autonomy is not just about the right to abortion, but also the right to bear children, and to effectively care for ourselves and our families. These issues are more important than ever, in the wake of the Supreme Court's 2022 decision in Dobbs v. Jackson Women's Health, which overturned Roe v. Wade and the Constitutional right to abortion, resulting in a massive erosion in access to reproductive healthcare for birthing people.--Let us know what you think with a comment or review!Visit our website⁠ ⁠for⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ transcripts⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠.⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Subscribe to Qudsiya's Substack, ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Getting Down To It⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Support the team behind the podcast ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠with a donation⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠

Part 3: Creating the Conditions for Disclosure What makes disability disclosure feel safe, supported, and meaningful in healthcare? In the final episode of the Disclosureseries, we move beyond the barriers to examine the conditions that allow disclosure to lead to access, trust, and belonging. Through the perspectives of medical students, physician assistant students, fellows, physicians, and educators, this episode explores how institutional systems, responsive accommodations, inclusive leadership, and everyday acts of advocacy shape disclosure experiences across medical training and practice. Contributors reflect on the importance of flexible accommodation processes, proactive communication, faculty and peer support, and the role of community in fostering psychological safety. Together, these stories demonstrate that while policies create opportunities for access, people create the conditions for trust—and that building environments where disabled learners and clinicians can thrive ultimately strengthens healthcare for everyone. Featured Contributors Anonymous Physician Assistant Student Khaja Siddiqui Anonymous Medical Student Anonymous Fellow Dr. Andrea Lendaris Dr. Karla Castro-Frenzel Transcript https://docs.google.com/document/d/1vgn-NGI52buG-xXUxIOCBMhd3oM6Jyz-9W0KDP-KwG0/edit?usp=sharing Keywords Disability disclosure Disability accommodations Medical education Clinical accommodations Medical students with disabilities Residents with disabilities Healthcare workplace culture Psychological safety Faculty advocacy Inclusive leadership Accessibility in medicine Physicians with disabilities Health professions education Disability inclusion Healthcare culture Community and belonging Identity safety Production Team Developer, Writer, Executive Producer: Sofia Schlozman Co-Producers: Rylee Betchkal and Lisa Meeks Co-Producer, Sound Selection and Editing: Gabe Abrams Sound Production: Next Day Podcast Digital Media: Katie Sullivan

God's Word has the power to change everything – even your depression. -------- 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.

Paid work can be a pathway to independence, purpose, and connection — but Australians with disability are far less likely to be employed than everyone else, especially those with high support needs. Many who do work are paid well below the minimum wage, some as little as $3.31 an hour. How do we build a system for disabled workers that opens up better jobs and fairer wages? In this podcast, Grattan Associate Ben Jefferson talks to Grattan Disability Program Director Sam Bennett and Senior Associate Owain Emslie about our report, Opening doors: Better jobs and fairer wages for disabled workers, which sets out a pragmatic path to better employment outcomes for disabled people with high support needs — while ensuring no one is left behind. Read our report: https://grattan.edu.au/report/opening-doors-better-jobs-and-fairer-wages-for-disabled-workers/ Thanks for listening to the Grattan Podcast. Our research, reports and analysis are freely available thanks to the donations of listeners like you. Please consider making a regular or one-off donation at grattan.edu.au/donate. You can follow us on LinkedIn and Instagram, and sign up to our newsletter on our website to stay up to date with Grattan's news. Thanks again for listening. Instagram: www.instagram.com/grattaninstitute/ LinkedIn: www.linkedin.com/company/grattan-institute/

As part of the 2026 Developmental Disabilities Conference, Corinne Melon, Managing Director, Phamaly Theatre Company, talks about accessible theater for people with disabilities. Series: "Developmental Disabilities Update" [Health and Medicine] [Show ID: 41468]

As part of the 2026 Developmental Disabilities Conference, Corinne Melon, Managing Director, Phamaly Theatre Company, talks about accessible theater for people with disabilities. Series: "Developmental Disabilities Update" [Health and Medicine] [Show ID: 41468]

As part of the 2026 Developmental Disabilities Conference, Corinne Melon, Managing Director, Phamaly Theatre Company, talks about accessible theater for people with disabilities. Series: "Developmental Disabilities Update" [Health and Medicine] [Show ID: 41468]

When you have nowhere to turn, you're not alone because the very presence of God stands with you there and will bring you through it. -------- 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.

Torina Gedler is a musician who is also known as DEĀ EX MACHINĀ, which means "Goddess from the machine" in Latin. With their lush synth-pop sound, DEĀ EX MACHINĀ promotes harmony and inclusion in society through authentic Disability representation in music.  DEĀ EX MACHINĀ advocates for the arts, LGBTQIA+ rights and Environmental and Disability Justice. Their debut EP, APO/THECARY, comes out on July 29, 2026. During this episode, DEĀ EX MACHINĀ discusses: Their work as a musician before and after being disabled by a brain injury Why it's important to have disability representation in music The main themes of their debut EP How joining RAMPD (Recording Artists and Music Professionals with Disabilities) influenced their work as a musician Their EP release party on July 29 in Des Moines, Iowa Learn more about DEĀ EX MACHINĀ at www.DeaExMachina.music and listen to their music on Subvert, Spotify, Apple Music and Bandcamp. Learn more about Recording Artists and Music Professionals with Disabilities (RAMPD) at RAMPD.org. Listen to other Beyond 6 Seconds episodes with neurodivergent musicians: Adin Boyer (episode 227):  https://www.beyond6seconds.net/227  Kaishawna (episode 187):  https://www.beyond6seconds.net/187   Support or sponsor this podcast: BuyMeACoffee.com/Beyond6Seconds Watch the video of this interview on YouTube: youtube.com/watch?v=IldZ1PQYP4E Read the episode transcript: carolynkiel.com/podcast/dea-ex-machina Follow the Beyond 6 Seconds podcast in your favorite podcast player: pod.link/1336740192 Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes: mailchi.mp/f9f6e8356138/insider  *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations. These episodes are for informational purposes only and do not substitute for professional medical advice. Consult a medical professional or healthcare provider if you are seeking medical advice, diagnoses, or treatment.*

Disability and breast cancer intersect in more than one direction. Some people develop long-term effects like lymphedema, neuropathy or cognitive changes because of treatment — effects recognized as disabilities under the Americans with Disabilities Act. Others are already living with a disability, of any kind, when a breast cancer diagnosis enters the picture. This July, in recognition of Disability Pride Month, Krista Park Berry, Director of Susan G. Komen's Breast Care Helpline, returns to Real Pink to talk about how the Helpline supports people through their breast health experience no matter when their disability started, and what that support looks like for women of color in particular. Key takeaways No two disability experiences are the same Disability can exist before or develop after breast cancer treatment The Komen Breast Care Helpline provides personalized support and resources Accessible, whole-person care improves quality of life and health outcomes Chapters 00:00 – Understanding disability and breast cancer 02:08 – Treatment-related disabilities and ADA protections 06:26 – Supporting people living with metastatic breast cancer 08:11 – Navigating breast cancer with a pre-existing disability 12:11 – Health equity, women of color, and closing care gaps 13:36 – Why asking for help can change everything

Meet the team from DARS and Enabled Intelligence and hear the employer's perspective. The post The Employer’s Perspective | 2026 Disability Innovation Fund Project Directors’ Conference | Podcast appeared first on VR Workforce Studio.

One day, Jesus will rid the world of wickedness and bring peace to this troubled planet. What a glorious day that will be! -------- 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.

Are we ready to have a disabled person in a position of power? Trick question! We already have.Support the showWebsite: 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

From disability metaphors to narratives structured around bodies presented as aberrant, early medieval English thoughtworlds conveyed the promise of resurrection and the hope of salvation through crip and disabled bodies. Light of the Everlasting Life: Disability and Crip Eschatology in Old English Literature (U Michigan Press, 2025) argues that early medieval Christian eschatology, as manifested in Old English literary texts, was a crip eschatology: a theology of the afterlife that relied upon disabled bodies and concepts related to disability in order to convey promises of resurrection and salvation. In addition to demonstrating how literature manifested theological approaches to the afterlife, Leah Pope Parker articulates the ways of thinking about bodies and disability that were available to ordinary early medieval people, many of whom experienced their bodies in ways that resonate with what we call disability today, but who rarely appear in the historical record. By analyzing Old English texts, including Alfredian translations, Ælfric's saints' lives, and poetry from the Exeter and Vercelli Books, Parker introduces novel ways of characterizing disability's effects in literature. "Spiritual prosthesis" reveals rhetorical, narrative, and theological reliance upon disability to convey the promise of a Christian afterlife. "Systems of aberrance" emerge as a result, in which bodies marked as deviant--including disabled, monstrous, heroic, saintly, and dead bodies--form a network of embodiments that reinforce the narratives they inhabit and that of Christian salvation history. Locating crip eschatology in early medieval literature, Light of the Everlasting Life rewrites standard histories of disability, of the body, and of medieval Christian eschatology. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/new-books-network

Watch this wonderful video of the amazing Katherine Wolf here. --------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.

At the age of 15, the filmmaker and actor Kyla Harris had an accident that forever changed what her body could do, and what it couldn't. From then on, she needed someone with her 24 hours a day to help her with things like going to the bathroom, cooking and showering.  Family members, friends, romantic partners and personal assistants have all played a role in Kyla's care over the years. She's had to learn to communicate, in exceptionally clear terms, how her body feels and what it needs, at any hour of the day or night.  Kyla is a creator and the star of the BBC TV show “We Might Regret This,” and her character, Freya, has the same disability that Kyla does. While the show depicts a fictional world, its complex web of remarkably close, interdependent relationships is, in part, inspired by Kyla's life. In this episode of “Modern Love,” Kyla tells Anna Martin what it's been like to approach every want and need as a group project. This dynamic becomes especially interesting when it comes to Kyla's thriving sex life, from dance-floor makeouts to long-term partnerships. Kyla discusses getting creative with her body — and the occasional prop —  and takes a deep dive into what intimacy can really mean.   How to submit a Modern Love EssayHow to submit a Tiny Love Story Subscribe today at nytimes.com/podcasts or on Apple Podcasts and Spotify. You can also subscribe via your favorite podcast app here https://www.nytimes.com/activate-access/audio?source=podcatcher. For more podcasts and narrated articles, download The New York Times app at nytimes.com/app. Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.