Podcasts about Ableism

Send us a texthe conversation moves through a fast, chaotic blend of social commentary, sexual humor, political cynicism, and personal reflection. It begins with discussion about the resurgence of collectible items and how AI and capitalism may force people back into simpler, more human activities. That leads into a critique of money, crypto, billionaires, and the concept that nearly everything in modern society is essentially fake. The dialogue expands into global politics—sanctions, coups, oil interests, and the U.S. acting as an unchecked global power.From there, the tone shifts into absurd humor about farming, insemination, and how people who fist cows often hold conservative anti-LGBT views. The conversation spirals into kink culture: leather scenes, pups, masks, fetishes, and why certain communities exist. This includes uncomfortable, explicit questions about fisting, bodily functions, sexual progression, and why some people enjoy extreme acts.The discussion then swerves to everyday life: talking to dogs like children, dogs' pack behavior, the contrast with aloof cats, and the bizarre reality of pets living indoors. Food prices, inflation, and the shrinking size of groceries become a point of frustration. The conversation returns to personal growth, aging, creative phases, past podcast eras, and how both hosts have changed since earlier episodes. Nostalgia for past creative periods emerges, along with recognition of personal evolution.Interwoven is a thread about filmmaking: the beginning of a documentary project, motivations behind solo travel, the meta-process of documenting the making of a documentary, and how it ties to self-reflection. The dialogue continues into aging, nightlife shifting into quiet routines, and the strange dissonance between adult responsibilities and the outrageous conversations they still have.Overall, the transcript jumps from existential dread to explicit gay sexual comedy, from geopolitical collapse to pet parenting, from leather festivals to the price of soup—all narrated with unfiltered honesty, sarcasm, and vulgar humor.Support the showAs always you can write us at nowellpodcast@gmail.com or call us at ‪(614) 721-5336‬ and tell us your Not Wells of the week InstagramTwitterBobby's Only FansHelp us continue to grow and create amazing content, like a live tour or just help fund some new headphones when needed. Any help is appreacited. https://www.buzzsprout.com/510487/subscribe#gaypodcast #podcast #gay #lgbtq #queerpodcast #lgbt #lgbtpodcast #lgbtqpodcast #gaypodcaster #queer#instagay #podcasts #podcasting #gaylife #pride #lesbian #bhfyp #gaycomedy #comedypodcast #comedy #nyc #614 #shesnotdoingsowell #wiltonmanor #notwell

As medical advancements continue to shape the detection, diagnosis, and treatment of disability and illness, technology is often presented as a path to autonomy. Rebecca Monteleone shows how such technologies contribute to a cruel double bind, forcing disabled people to be accountable for adapting to a world built by and for nondisabled people while dismissing their lived experiences in favor of medical expertise. In the new book The Double Bind of Disability, Monteleone explores anecdotes about prenatal genetic screening, deep brain stimulation, and do-it-yourself artificial pancreas systems, exposing new relationships among disability, authority, knowledge, and responsibility. Monteleone is joined here in conversation with Ashley Shew. Rebecca Monteleone is associate professor of disability and technology at the University of Toledo and author of The Double Bind of Disability: How Medical Technology Shapes Bodily Authority.  Ashley Shew is a professor of science, technology, and society at Virginia Tech and author of Against Technoableism: Rethinking Who Needs Improvement.EPISODE REFERENCES:-Ally Day-“Transmobility: Possibilities in Cyborg (Cripborg) Bodies,” Mallory Kay Nelson, Ashley Shew, and Bethany Stevens / Catalyst: Feminism, Theory, Technoscience -Jackie Leach Scully-Dana Lewis-Biomedicalization: Technoscience, Health, and Illness in the U.S. / Adele E. Clarke, Laura Mamo, Jennifer Ruth Fosket, Jennifer R. Fishman, Janet K. Shim, editorsPraise for the book:"A generous, timely, and essential contribution to understanding the current politics that shape medical technology and disability in the context of neoliberal ableism. A book that I will be thinking-making-feeling with for many years to come!"—Laura Forlano, Northeastern University The Double Bind of Disability: How Medical Technology Shapes Bodily Authority by Rebecca Monteleone is available from University of Minnesota Press. Thank you for listening.

In this powerful episode of the BIG Home Ed Conversations Podcast, Kelly and Ashley sit down with author, educator and neurodivergent advocate Helen Daniel to unpack ableism in the education system through the lens of SEND and neurodivergence. Drawing on Helen's experience as a teacher, academic and author of Neurosensory Divergence: Autistic Languages, they explore how a system built on standardisation often fails autistic and otherwise neurodivergent children – and what more equitable, sensory-aware education could look like, both in school and in home ed. Together they dive into: How curriculum changes and raised targets (times tables, Shakespeare, early formal writing) pushed more neurodivergent children “outside the norm.” Why standardisation is the enemy of equity – and why one-size-fits-all schooling doesn't work for diverse brains. EHCPs, SEND provision and why the system feels broken for so many families. Sensory profiles, overload and meltdowns: what's really going on beneath “behaviour.” Practical examples of small, powerful accommodations (movement, video learning, headphones, flexible seating.) How home ed groups can unintentionally replicate ableism – and how to design more inclusive spaces. Teaching all children (ND and NT) compassion, curiosity and respect for different needs. This is a validating, eye-opening listen for: Parents of autistic, ADHD, PDA or otherwise neurodivergent children. Home educating families navigating SEND needs. Teachers who feel the system is wrong but don't know how to change it. Any parent wanting to raise more compassionate, neuro-affirming kids. Guest Spotlight: Find Helen's book Neurosensory Divergence: Autistic Languages in all the usual places for a deeper dive into sensory processing, autistic communication and building truly equitable lives for autistic children. Find Helen at https://outsidetheboxsensory.com/ or on social media @otbsensory. (New website coming soon though!) Join the conversation: Has this episode resonated with your family's experience of SEND or neurodivergence? Share your stories or questions with us on Instagram or TikTok @bighomeedpodcast, or head to the blog www.offroadingmotherhood.co.uk/blog for more resources and episode notes. Keywords: SEND and ableism, neurodivergent children, autism and education, EHCPs UK, sensory needs in school, home education UK, inclusive home ed, trauma-informed education, alternative education, autistic-friendly learning, neurosensory divergence

Send us a textThis Not Well episode is chaotic, funny, and wildly inappropriate in true Bobby-and-Jim fashion. It bounces from self-deprecating body talk and aging jokes to dark humor about ancestry, suicide, and religion—before spiraling into AI obsession, first-class flight hacks, uncut dick curiosity, fungal infections, and political outrage. The second half dives into everything from dementia couples and priest trauma to SNAP benefits, U.S. corruption, and gay community hypocrisy, closing with drunk theater reviews and existential crises. It's part therapy session, part stand-up set, and entirely unfiltered.Support the showAs always you can write us at nowellpodcast@gmail.com or call us at ‪(614) 721-5336‬ and tell us your Not Wells of the week InstagramTwitterBobby's Only FansHelp us continue to grow and create amazing content, like a live tour or just help fund some new headphones when needed. Any help is appreacited. https://www.buzzsprout.com/510487/subscribe#gaypodcast #podcast #gay #lgbtq #queerpodcast #lgbt #lgbtpodcast #lgbtqpodcast #gaypodcaster #queer#instagay #podcasts #podcasting #gaylife #pride #lesbian #bhfyp #gaycomedy #comedypodcast #comedy #nyc #614 #shesnotdoingsowell #wiltonmanor #notwell

It's surprisingly easy for people to think labels don't mean anything, but they can actually be quite powerful.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

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

Da einige in unserem Team aktuell krank sind, gibt es diese Woche leider keine neue Folge. Dafür haben wir in unserem Archiv diese starke Folge aus dem Mai 2022 gefunden, die wir euch sehr ans Herz legen wollen.Luisa L'Audace erlebt aufgrund ihrer Behinderung schon ihr ganzes Leben Diskriminierung – als Frau und noch mal verstärkt als Frau mit Behinderung. Ableismus nennt sich diese Form der strukturellen Diskriminierung. Lena geht mit Luisa der Frage nach, wieso Ableismus in feministischen Diskursen so oft vergessen – oder teilweise sogar reproduziert wird. Dabei geht es nicht nur um barrierearme Zugänge zu feministischen Veranstaltungen oder Demonstrationen, sondern auch um sexuelle Selbstbestimmung, Reproduktionsrechte und Fetischisierung.Danke an alle, die den Lila Podcast unterstützenHelft uns, damit unsere Arbeit fair bezahlt werden kann! Alle Infos darüber, wie ihr den Lila Podcast supporten könnt, haben wir für euch hier gesammelt.Links und HinweiseLuisa L'AudaceAngry CripplesBMFSFJ zur Gewalt an Frauen mit Behinderung:Essay zu Schönheit und Körper mit BehinderungenLuisa L'Audace im Spiegel über Risikogruppen in der Corona-PandemieEingeschränkte Solidarität – Feminismus zwischen Ableism und Intersektionalität von Kirstin AchtelikMord an Menschen mit Behinderung in PotsdamPodcastempfehlung: Die neue NormAktuelle Werbepartner und weitere Infos zum PodcastWeitere tolle Accounts und Bücher über Inklusion und AbleismusKatrin AimeeRaul KrauthausenNatalie Dedreux Jasmin DickersonBuch: „Bist du behindert, oder was?“Wir freuen uns sehr, euch ein Transkript zur Sendung zur Verfügung stellen zu können. Es wurde automatisch erstellt. Ihr findet es auf unserer Website. Hosted on Acast. See acast.com/privacy for more information.

When we talk about equality, we often forget one of its biggest missing pieces: disability. For many, ableism is a word they've never heard, yet it shapes how millions of people live, work, and are treated every single day. Today, I'm sitting down with Celia Chartres-Aris and Jamie Shields, two unapologetic truth-tellers who are breaking the silence and giving us the language—and the courage—to finally unlearn ableism.Featured in 'The Beautiful Edition' of AwareNow Magazine: www.awarenowmagazine.comGuest: Chartres-Aris & Jamie ShieldsHost: Allié McGuireMusic by: Yehezkel RazProduced by: AwareNow Media

Movie reviews #55Eight movies today, can you believe it.1 (Brewster Mcloud 1970) Very early Robert Altman film here where the amazing Margret Hamilton plays a racist jerk. Another early 70's offering that's quite trippy and political 2 (Three sisters 1970) A hard to watch production of an Anton Chekhov novel, I may have slept through this in high school. It is cool to me only because It stars the Grandma mechanic from (I love you to death),3 (Legend of Boggy Creek 1972) Tagline, Rated G Hick, Bigfoot movie, barely.4 (Man who fell to Earth 1976) Rip Torn, Buck Henry, and Candy Clark star in this sci if classic, that we should all see in the theater once. Almost forgot about the guy who wants the baby in Labyrinth, he's here too. JK fam Bowie's cool (rest in space).5 (Sammy 1977) These Jesus films crack me up as a recovering Catholic it always amuses me, among other things. This one got a theatrical release. please listen to hear how much money it made opening weekend, I believe it will put a smile on yer face. 6 (Soldier of Orange 1977) Our first Paul Verhoeven film. I remember this being very good, but not much else. the guy who wants “more life, fucker.” In Blade Runner is young and joins the Dutch resistance.7 (Yesterdays Child 1977) This made for tv movie is deliciously bizarre. Starring the mom of the Partridge family and the General from Planet of the Apes 5.8 (Dummy 1979) Worf's human brother, Geordie La'Forge, and the dip shit cop who goes after John Jay Rambo and doesn't bring a bunch O body bags, star in this rad film about tryin to fight Ableism in the halls of justice. Thanks for listening.

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

RFK Jr.'s autism claims aren't about helping anyone—they're about deciding who gets to exist in America.

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - Neredeyse her beş Avustralyalıdan biri engelli. Ancak bu büyük ve çeşitli grup, orantısız düzeyde ayrımcılık ve ön yargıyla karşı karşıya...

Disagree with me or not, it's a hill I will die on: Pregnancy is not a disability.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

Support the Northwest Regional SCI System by donating at www.acceleratemed.org/SCI. After listening, give us your feedback using this quick survey: redcap.link/sciforumpod Presented at the SCI Forum on March 26, 2025 After a spinal cord injury, people must adapt to changes in their physical abilities while also navigating structural ableism—a system of policies, institutions, and societal norms that disadvantage disabled individuals. How does ableism shape their interactions and self-perception? And how does ableism intersect with sexism? This forum will feature a panel of women sharing their experiences with ableism after acquired disability, discussing its personal and professional effects, and exploring how it appears and is addressed in different settings. Please join us to share your thoughts, perspectives, and questions on navigating ableism after spinal cord injury. The discussion will be moderated by Whitney Morean, PhD, a postdoctoral fellow in rehabilitation psychology at UW.

Matthew Shapiro, founder and CEO of Six Wheels Consulting, joins hosts Lily Newton and Erin Hawley for a candid conversation about language, work culture, and the everyday practice of access. Matthew unpacks how assumptions show up in daily life, why “disabled” is a valuable identifier, and what it means to balance personal energy with public advocacy.The conversation moves from nuance in calling out ableism to concrete advice for workplaces. Matthew shares practical examples that help everyone, like standing desks and curb cuts, and invites leaders to start with simple changes that reduce friction. He challenges listeners to rethink design from the ground up and to see access as standard, not a special add-on.Across the episode, Lily and Erin connect language to outcomes. They underline that asking for what you need benefits teams, and that many improvements cost more thought than money. The result is a grounded roadmap for anyone ready to begin, learn, and keep going.Key Moments03:36 Assumptions and the myth of “needing to be fixed”07:18 The push-pull of advocacy and fatigue13:31 “Own the word”: why Matthew identifies as a disabled person17:08 Ableism on social media and finding useful nuance31:15 Standing desks, curb cuts and designing spaces that work for all41:42 How to begin: start, listen, and make a plan you will actually use45:19 It is not as daunting as people thinkConnect with Matthew ShapiroLinkedIn: https://www.linkedin.com/in/matthew-shapiro-16abb932 Instagram: https://www.instagram.com/6wheelsconsulting/ Six Wheels Consulting website: https://www.6wheelsconsulting.com/ 

I hope my SSA examiner doesn't listen to this episode.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

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - Higit sa isa sa bawat limang Australyano ay may kapansanan. Ngunit sa kabila ng dami nila at pagkakaiba ng grupong ito, madalas pa rin silang makaranas ng diskriminasyon.

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - بیش از یک‌پنجم آسترالیایی‌ها دارای معلولیت هستند، اما این گروه بزرگ و متنوع با میزان بالای تبعیض و نفرت مواجه‌اند.

You might be surprised to learn I'm not automatically on the side of the disabled person in a given situation.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

Send us a textBobby and Jim return after a chaotic few weeks with an unfiltered, hilarious deep dive into the apocalypse, neighborhood drama, and America's collective psychosis. From “RaptureTok” lunatics leaving their clothes out for Jesus to MAGA cults worshiping the golden calf, nothing is off limits. The boys spiral through religion, politics, tailgating chaos, and dog poop wars on their street—all while high, ranting, and trying not to get arrested. It's equal parts stand-up, meltdown, and sermon for the end times.Support the showAs always you can write us at nowellpodcast@gmail.com or call us at ‪(614) 721-5336‬ and tell us your Not Wells of the week InstagramTwitterBobby's Only FansHelp us continue to grow and create amazing content, like a live tour or just help fund some new headphones when needed. Any help is appreacited. https://www.buzzsprout.com/510487/subscribe#gaypodcast #podcast #gay #lgbtq #queerpodcast #lgbt #lgbtpodcast #lgbtqpodcast #gaypodcaster #queer#instagay #podcasts #podcasting #gaylife #pride #lesbian #bhfyp #gaycomedy #comedypodcast #comedy #nyc #614 #shesnotdoingsowell #wiltonmanor #notwell

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - กว่าหนึ่งในห้าของชาวออสเตรเลียมีความพิการ แต่กลุ่มคนที่มีจำนวนมากและหลากหลายนี้กลับเผชิญกับการเลือกปฏิบัติและอคติ

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - 호주인 5명 중 1명 이상이 장애를 가지고 있습니다. 하지만 장애인 집단의 크기와 다양성에도 불구하고 이들 집단은 불균형적인 수준의 차별과 편견에 직면해 있습니다.

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - Hơn một trong năm người Úc sống chung với khuyết tật. Nhưng nhóm người đông đảo và đa dạng này lại phải đối mặt với mức độ phân biệt đối xử và định kiến thường xuyên.

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - प्रत्येक पाँच मध्ये एक भन्दा बढी अस्ट्रेलियन अपाङ्गताका साथ बाँचिरहेका छन्। तर यो ठुलो र विविध समूहले असमान रूपले भेदभाव र पूर्वाग्रह भोगिरहेको बताइन्छ।

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - ஆஸ்திரேலிய மக்கள் தொகையில் கிட்டத்தட்ட 22% பேர் மாற்றுத்திறனாளர்கள். உண்மையில், ஆஸ்திரேலியர்களில் ஐந்தில் ஒருவர் மாற்றுத்திறனுடன் வாழ்கிறார். ஆனால் அவர்களில் பலரின் அனுபவங்கள் — குறிப்பாக அவர்கள் அடிக்கடி சந்திக்கும் துன்புறுத்தல்கள் — எவருக்கும் தெரியாமல், கேட்கப்படாமலேயே உள்ளன.

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - Инвалидность есть у более чем каждого пятого австралийца. Но даже такая большая и разнородная группа сталкивается с непропорционально высоким уровнем дискриминации и предвзятости.

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - Lebih dari satu dari lima warga Australia menyandang disabilitas. Namun, kelompok yang besar dan beragam ini menghadapi tingkat diskriminasi dan prasangka yang tidak proporsional.

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - ਪੰਜ ਵਿੱਚੋਂ ਇੱਕ ਤੋਂ ਵੱਧ ਆਸਟ੍ਰੇਲੀਅਨ ਲੋਕਾਂ ਨੂੰ ਅਪੰਗਤਾ ਹੈ। ਪਰ ਇਸ ਵੱਡੇ, ਵਿਭਿੰਨ ਸਮੂਹ ਨੂੰ ਵਿਤਕਰੇ ਅਤੇ ਪੱਖਪਾਤ ਦੇ ਅਸਾਧਾਰਨ ਪੱਧਰ ਦਾ ਸਾਹਮਣਾ ਕਰਨਾ ਪੈਂਦਾ ਹੈ।

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - ប្រជាជនអូស្ត្រាលីជាងម្ភៃភាគរយមានពិការភាព។ ប៉ុន្តែក្រុមចម្រុះដ៏ធំនេះប្រឈមមុខនឹងកម្រិតនៃការរើសអើង និងការប្រកាន់វិសមាមាត្រគ្នា។

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - オーストラリアでは、5人に1人以上が障害を抱えながら生活しています。そして障害を持つ方々は、日々さまざまな形で差別と偏見に直面しているのです。

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - 超過五分之一的澳洲人有殘疾。但這龐大且多元的群體，卻面臨著不成比例的歧視與偏見。

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - Австралийн таван хүн тутмын нэг нь хөгжлийн бэрхшээлтэй. Гэвч энэ том, олон гарал үүсэлтэй хүмүүс нь харьцангуй өндөр түвшний ялгаварлалтай нүүр тулдаг.

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - প্রতি পাঁচজন অস্ট্রেলিয়ানের মধ্যে একজনেরও বেশি প্রতিবন্ধী। কিন্তু তাদের অনেকের অভিজ্ঞতাই অদৃশ্য আর অশ্রুত থেকে যায়। অক্ষমতার কারণে বৈষম্যের মুখোমুখি প্রতিবন্ধী মানুষেরা যে নিয়মিত নির্যাতন সহ্য করেন সেটাও অজ্ঞাত থেকে যায়।

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - 澳大利亚每五个人中就有一人是残障人士。然而，这个庞大而多样的群体却面临着远高于平均水平的歧视和偏见。 （点击上方收听音频）

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - يعاني أكثر من 20 في المائة من الأستراليين من إعاقة، لكن تجاربهم غالبا تبقى غير مسموعة وغير مرئية. وتقول الرئيسة التنفيذية لمنظمة الأشخاص ذوي الاحتياجات الخاصة في أستراليا ميغان سبيندلر سميث، ، إن هذه الفئة تتعرض لمعدلات عنف وعداء تقارب الضعف مقارنة بغيرها. ويؤكد مهاجرون من ذوي الاحتياجات الخاصة أن معاناتهم تتضاعف مع الوصمة الثقافية والصور النمطية، فيما تدعو أصواتهم إلى مزيد من التضامن لمواجهة التمييز.

More than one in five Australians have a disability. But this large, diverse group faces disproportionate levels of discrimination and prejudice. - پانچ میں سے ایک سے زائد آسٹریلین کسی نہ کسی معذوری کا شکار ہیں۔ لیکن یہ بڑا اور متنوع گروپ عدم مساوات اور تعصب کاغیر متناسب سطح کا سامنا کرتا ہے۔

In another move to demonize the autistic community, the Trump administration has announced that Tylenol is linked to autism, despite very little evidence to suggest it.Sources used in this episode:https://www.cbsnews.com/news/trump-rfk-jr-distort-facts-autism-tylenol-vaccines/https://people.com/what-is-leucovorin-the-supplement-rfk-jr-claims-treats-autism-11814634Support 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

Interviewees: Kirsten Brown, PhD Assistant Professor of Health Professions Education at the Uniformed Services University of the Health Sciences; as a short disclaimer, Kirsten's views do not represent the official policy or position of her employer.  Dionna Bidny, MD, MMUS  a first-year resident in Physical Medicine and Rehabilitation at the University of Pittsburgh Medical Center, currently completing her Transitional Year; and Abby Konoposky, PhD Senior Director of Medical Education Research in the Department of Psychiatry at Northwell Health. Interviewer:  Lisa Meeks, PhD, MA, Guest Editor, Academic Medicine Supplement on Disability Inclusion in UME. Description: This episode of Stories Behind the Science brings you an intimate conversation with Dr. Kirsten Brown (Uniformed Services University of the Health Sciences), Dr. Dionna Bidny (University of Pittsburgh Medical Center), and Dr. Abby Konopasky (Northwell Health), co-authors of Disability in Undergraduate Medical Education in the United States: A Scoping Review, part of the Academic Medicine supplement on Disability Inclusion in Undergraduate Medical Education. Drawing from over 80 publications, their study traces how disability in medical education has too often been framed through deficit and legal models, while leaving intersectionality and the voices of disabled learners largely absent. Together, we explore why this framing matters, what the literature reveals about gaps and progress, and how a critical perspective can re-shape the field. Our guests share the personal and professional motivations behind this ambitious review, the surprises and challenges they encountered, and their hopes for how this work can serve as both roadmap and catalyst. Whether you are a researcher, faculty member, disability resource professional, or student, this episode offers insights into the state of the field and inspiration for charting new directions. Resources and links to the open-access article, Disability Resource Hub, and related tools are in the show notes. Transcript: https://docs.google.com/document/d/1iUYE0Q-2TA1flXiMU6rum1S3dO-obE5DoA9J0mFmHlE/edit?usp=sharing Bios:   Kirsten Brown, PhD Dr. Kirsten Brown's research examines the intersection of disability, power, and social systems. Her work has appeared in the Journal of College Student Development, the Journal of Diversity in Higher Education, and Journal of Higher Education. She co-authored the book Disability in Higher Education: A Social Justice Approach. Dr. Brown prepared this chapter during non-work hours as an independent scholar and this publication did not receive funding from the federal government. The views expressed are solely those of the author and do not represent the official policy or position of the Uniformed Services University of the Health Sciences, the Henry M. Jackson Foundation for the Advancement of Military Medicine, the Department of Defense, or the U.S. Government.  Abigail Konopasky, PhD Abigail Konopasky holds doctorates in educational psychology from George Mason University and in linguistics from Princeton University. She is currently an Associate Professor and Director of Medical Education Research and Scholarship in the Psychiatry Department at Northwell Health. She conducts critical qualitative and mixed methods research in health professions education, with a focus on equity, Black feminism, and critical disability studies using functional linguistic and narrative methods and theories of agency. She serves on the editorial boards of Teaching and Learning in Medicine, Perspectives on Medical Education, and Advances in Health Sciences Education. Dionna Bidny, MD, MMus  Dionna is a first year resident at the University of Pittsburgh Medical Center in Physical Medicine and Rehabilitation (currently  in her  Transitional Year). She has a BS in biomedical engineering and an  MMus in Musicology; she incorporated her interest in accessibility in arts, sports, and healthcare spaces through research during both degrees. In medical school, she continued to study and lecture in the space of disability  justice and its intersections with art, identity,  and healthcare experience, all  while navigating  chronic illness and pursuit of her own  accommodation and access needs. In residency, she aims to continue her work in accessibility within arts and sports through community engagement and engineering innovation. Key Words:   Disability in medical education Undergraduate medical education (UME) Disability inclusion Scoping review Academic Medicine supplement Deficit model vs. asset model Legal framing of disability Intersectionality in medicine Disabled learners' voices Critical perspectives in medical education Equity in medical training Accommodations in medical education Disability justice Ableism in medicine Representation in health professions Research roadmap Diversity and inclusion in medicine Disability studies in medical education Inclusive curriculum Systemic barriers in medical education Resources:  Article from Today's Talk Maggio, Lauren A. PhD; Brown, Kirsten R. PhD; Costello, Joseph A. MSIS; Konopasky, Aaron PhD, JD; Bidny, Dionna MD, MMus; Konopasky, Abigail PhD. Disability in Undergraduate Medical Education in the United States: A Scoping Review. Academic Medicine 100(10S):p S64-S73, October 2025. | DOI: 10.1097/ACM.0000000000006154 https://journals.lww.com/academicmedicine/fulltext/2025/10001/disability_in_undergraduate_medical_education_in.5.aspx   The Docs With Disabilities Podcast https://www.docswithdisabilities.org/docswithpodcast

Medicare is going to introduce a pilot program using AI to determine claims and denials for patients. What could possibly go wrong?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

In which Jess and Ellie discuss the pitfalls of internalized ableism, as well as the concept of 'nothing for us without us.'Schedule coaching and speaking www.CoachJessicaMichaels.comcontact us GiftedKidMessyAdult@gmail.com

Send us a textThis episode of Not Well is chaotic, funny, and raw—Bobby and Jim dive into everything from soccer games and drag shows to conspiracy theories and neighborhood drama. It kicks off with banter about attending a USA vs. Japan match and Bobby's struggle with overstimulation in large crowds. They move into cultural commentary: Japan's heat, high-speed trains vs. America's broken transit, and the hypocrisy of U.S. politics around alcohol, weed, and guns.From there, the conversation spirals through:The Trump/Epstein files controversy and censorship.Weird political alignments (liking Marjorie Taylor Greene tweets “against their will”).The broken state of America and the absurdity of “jobs just to keep jobs.”A disastrous drag show at Kemba, drinking mishaps, and weight-loss meds.Jazz nights at an LGBTQ-friendly church, with a white singer butchering Brazilian lyrics.A breakdown of “stan culture,” Eminem's Stan, and K-pop superfans.The gay undertones of wrestling and male friendships disguised as “bromance.”A neighbor feud escalating into harassment notes and police calls.Random sundries: hating Indian summers, wanting hoodie weather, planning trips, art frustrations, and Bobby admitting Penis Friends might be losing steam.The episode closes with a mix of edible-fueled rambling, travel talk (Mexico, Ireland), crafts, and a GoPro request for scuba diving.Support the showAs always you can write us at nowellpodcast@gmail.com or call us at ‪(614) 721-5336‬ and tell us your Not Wells of the week InstagramTwitterBobby's Only FansHelp us continue to grow and create amazing content, like a live tour or just help fund some new headphones when needed. Any help is appreacited. https://www.buzzsprout.com/510487/subscribe#gaypodcast #podcast #gay #lgbtq #queerpodcast #lgbt #lgbtpodcast #lgbtqpodcast #gaypodcaster #queer#instagay #podcasts #podcasting #gaylife #pride #lesbian #bhfyp #gaycomedy #comedypodcast #comedy #nyc #614 #shesnotdoingsowell #wiltonmanor #notwell

Florida's intention to do away with vaccine mandates has terrible implications for all of us, but especially for vulnerable populations.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

In this episode, we wrestle with the discriminatory notion of Ableism.

In this conversation, disability advocate, artist, and author Jayne Mattingly joins Dr. Marianne to explore body grief: the very real mourning that happens when your body, health, or identity do not match the life you imagined. Jayne traces how she coined the term from years of counseling work in eating disorders and body image, and from her own shift into disability after sudden illness and 19 brain and spine surgeries. Together, we unpack how ableism, intersectionality, and systemic oppression shape what we grieve about our bodies and how we heal. You will hear practical ways to name body grief, honor it, and build community care that creates room for joy, creativity, and resistance. This episode covers body grief, disability advocacy, chronic pain, eating disorders, antifat bias, medical dismissal, grief phases, and neurodivergent-affirming, sensory-attuned care. We discuss how ableism and overlapping identities influence recovery, why harm reduction and community care matter, and practical tools for regulation, access planning, and self-advocacy. CONTENT CAUTION We discuss medical trauma, dismissal in healthcare, chronic pain, disability, diet culture, and systemic oppression. Please listen with care and pause when needed. WHAT WE COVER What “body grief” means and why naming it matters How eating disorders can function as regulation and why recovery can feel like loss Jayne's personal story of sudden illness, surgeries, vision loss, and becoming a wheelchair user Everyday ableism and why language like “non-disabled” helps decenter harmful norms The seven phases Jayne observes in body grief and how people move through them Dismissal in medical settings, internalized dismissal, and how to advocate for yourself Why body grief grows inside systems of racism, antifat bias, sexism, homophobia, and ageism Neurodivergence, disability, and how a more accessible world would change the grief we carry Community care, harm reduction, and finding light without forcing a tidy destination KEY TAKEAWAYS Body grief is universal. We all live in bodies that change. Naming the grief opens space for honesty, compassion, and skills. Oppression intensifies grief. Systems teach us which bodies are “acceptable.” Healing includes unlearning those messages and changing the conditions around us. Hope and grief can coexist. Progress is nonlinear. You can move in and out of phases and still build a meaningful life. Language matters. Shifting to terms like “non-disabled” helps challenge ableist defaults. Community care is protective. Healing grows when we practice access, mutual support, and self-advocacy together. FAVORITE MOMENTS Jayne on seeing ableism inside “love your body for what it can do” messages and why that left disabled people out The dismissal chapter story that shows how easily young people internalize “you're fine” when they are not fine “If you design for disabled people first, everyone benefits.” Body grief as a unifier that crosses political lines through storytelling and clear psychoeducation PRACTICAL TOOLS MENTIONED Name your current phase of body grief and set one tiny supportive action for today Track dismissal patterns you have internalized and write one replacement script for your next appointment Build a personal access plan: sensory needs, mobility needs, communication needs, and who can help Use harm-reduction mindset for recovery work and daily life Create a small “joy and regulation” list that is available on hard days ABOUT JAYNE Jayne Mattingly is a nationally recognized disability advocate, body image speaker, and author of This Is Body Grief. She founded The AND Initiative to shift conversations around accessibility, ableism, and healing. Jayne is also the artist behind Dying for Art, a bold abstract series created in partnership with her changing body and chronic pain. She lives in Charleston, South Carolina with her service dog Wheatie. Find Jayne: Instagram @jaynemattingly, janemattingly.com, and Substack This Is Body Grief. RELATED EPISODES ON BODY GRIEF & ABLEISM Body Grief & Body Peace with Leslie Jordan Garcia @liberatiwellness on Apple & Spotify. Fat Positivity, Accessibility, Body Grief, & Emotions with @bodyimagewithbri Brianna Campos, LPC on Apple & Spotify. Size Inclusivity & Ableism: Why Body Acceptance is More Than Just "Loving Your Curves" on Apple & Spotify. Ableism and Common Myths About Diabetes with Kim Rose, RD @the.bloodsurgar.nutritionist on Apple & Spotify. RESOURCES & LINKS Book: This Is Body Grief by Jayne Mattingly — available wherever books are sold The AND Initiative: education and advocacy on accessibility and ableism Dying for Art: Jayne's abstract painting series CONNECT WITH DR. MARIANNE If you're struggling with restriction, food obsession, or atypical anorexia and are seeking affirming, experienced support, Dr. Marianne offers therapy in California, Texas, and Washington, D.C. Her approach is weight-inclusive, neurodivergent-affirming, sensory-attuned, and trauma-informed. Get started here:

An episode about a deceptively simple topic: restaurant seating.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

 Emmy Award Winner ArtistNetflix's ground-breaking Paralympic documentary ‘Rising Phoenix' won two prestigious Sports Emmy Awards Keith Jones is the President and CEO of SoulTouchin' Experiences LLC,. It is an organization aimed at bringing a perspective to the issues of access inclusion and empowerment, which affect him as well as others who are persons with and without disabilities. To achieve this multicultural, cross-disability education and outreach efforts he collaborates and conducts trainings with the purpose of strengthening efforts to provide services and information for people with disabilities. The issues he tackles are wide ranging from immigration, criminal justice reform, health care and environmental justice just to name a few. Paralleling with his policy and social justice work Mr. Jones is a multitalented artist who along with Leroy Moore and Rob Temple founded Krip Hop Nation which is an international collection of artists with disabilities. Krip Hop Nation is currently celebrating 14 years with the recent Emmy Award winning success of their title song for the Netflix documentary of the Paralympic Games, Rising Phoenix and its critical  acclaimed sound track.  © 2025 Building Abundant Success!! 2025 All Rights Reserved Join Me on ~ iHeart Media @ https://tinyurl.com/iHeartBAS Spot Me on Spotify: https://tinyurl.com/yxuy23ba Amazon Music ~ https://tinyurl.com/AmzBAS Audacy:  https://tinyurl.com/BASAud

In this episode of This Is Getting Old: Moving Toward an Age-Friendly World, I welcome Ashton Applewhite, a leading voice in the global movement against ageism. Ashton challenges the cultural myths that equate aging and disability with decline, showing how these biases harm us all in health care, the workplace, and even in the way we see ourselves. Her talk, Still Kicking: Confronting Ageism and Ableism in the Pandemic's Wake, highlights the importance of intersectionality and reminds us that ageism is not inevitable—it's a social construct we can change. Together, we explore how dismantling ageism and ableism is not just about supporting older adults or people with disabilities—it's about building a world where everyone is valued at every stage of life. This conversation is both empowering and practical, offering a vision of cultural change rooted in equity, inclusion, and age pride.

Oxford Dictionary defines ableism as: “discrimination in favor of able-bodied people.” And on today's episode, we're defining ableism with our own examples:When someone is shocked by our child's capabilitiesWhen someone is suprised by our strong connection to our childrenWhen someone volunteers for a disabilities organization believing they're a heroA lot of ableism is just actions and systems that we may have never questioned.. until being affected by disability. So what do we do when we experience ableism in our communities? Lets unpack it in this week's episode. SHOW NOTESFollow @open_future_learning on Instagram!Follow @ndss on Instagram!Follow @shaneburcaw on Instagram!Disability Euphemisms video from @blairimani Listen to 172. Defining Ableism, Allyship & Advocacy + Redefining "Inclusion" - ft. Dr. Priya LalvaniSPONSORS National Down Syndrome SocietyiCanShine ProgramsDown for GreensRods Heroes

Breaking Down Internalized Ableism  Summary In this conversation, Patricia explores the concept of internalized ableism, particularly among neurodivergent individuals. She discusses how societal stigma and expectations can lead to negative self-perceptions and feelings of inadequacy. Patricia shares personal experiences and insights on how internalized ableism manifests in various aspects of life, including relationships, self-acceptance, and the pressure to conform to neurotypical standards. She emphasizes the importance of unlearning these hurtful beliefs and embracing one's neurodivergent identity with compassion and understanding.   HIGHLIGHTS   ·       Internalized ableism is the unconscious adoption of negative beliefs about oneself due to societal stigma. ·       Neurodivergent individuals often feel pressure to conform to neurotypical standards, which can lead to trauma. ·       Resting is a valid need and should not be seen as a failure. ·       Asking for accommodations is essential for well-being and should not induce guilt. ·       The concept of 'high functioning' can be harmful and does not reflect true capabilities. ·       Time agnosia is a common experience for neurodivergent individuals. ·       Self-compassion is crucial in overcoming internalized ableism. ·       Relationships can be affected by the fear of being a burden. ·       Unlearning internalized ableism involves recognizing and challenging societal expectations. ·       Embracing neurodivergence includes acknowledging strengths and practicing self-acceptance. 115 SPECIFIC POINTS DISCUSSED 1.     How internalized ableism shows up in everyday life o   Masking, pushing through burnout, or feeling "lazy" when you're resting. 2.     Messages we absorbed growing up o   From school, parents, peers, or media about being "too much," "distracted," "weird," or "wrong." 3.     Perfectionism and people-pleasing as survival o   How needing to be “better” or “easy to manage” is often rooted in internalized shame. 4.     The trap of “not disabled enough” or “faking it” o   How we invalidate our own struggles because we don't “look” stereotypically disabled. 5.     ADHD, autism, OCD & “high-functioning” narratives o   The myth of being “high functioning” and how it reinforces ableist expectations. 6.     Feeling guilt for needing accommodations or rest o   That voice that says “you're being difficult” when you ask for what you actually need. 7.     Shame around executive dysfunction o   Struggling to start tasks, follow through, or manage time — and blaming yourself. 8.     Rejecting your own needs to fit in o   Forcing eye contact, avoiding stimming, hiding rituals, not using noise-canceling headphones in public, etc. 9.     The pressure to be “independent” all the time o   How internalized capitalism + ableism equates needing support with being a failure. 10.  Comparing yourself to neurotypical peers ·       Especially in productivity, relationships, or emotional regulation. 11.  “If I can do it sometimes, I should always be able to” myth ·       Inconsistent ability = inconsistent worth? Nope. Talk about spoon theory and fluctuating capacity. 12.  How OCD-specific traits are misunderstood or mocked ·       And how that seeps into how you see yourself (e.g., feeling “crazy,” “irrational,” or “a burden”). 13.  Internalized ableism in dating & relationships ·       Fear of being too much, too emotional, or too rigid — and minimizing yourself as a result. 14.  How healing looks like reclaiming your needs unapologetically ·       Self-accommodation, boundaries, rest, and neurodivergent joy as rebellion. 15.  Relearning self-compassion and identity pride ·       Ending with hope: unmasking, connecting with community, and defining success on your own terms.    SOUND BITES ·       "Rest is resistance." ·       "You are not broken." ·       "You deserve rest, joy, and support."    SENSITIVITY IS NOTHING TO APOLOGIZE FOR; IT'S HOW YOUR BRAIN IS WIRED You are not broken. You were shaped by systems that weren't built for you. You deserve rest, joy, and support exactly as you are.    CHAPTERS (please add time for addition of introduction) 00:00 Understanding Internalized Ableism 02:40 The Impact of Societal Expectations 05:31 Navigating Personal Experiences with Internalized Ableism 08:18 The Struggle for Accommodations 10:55 Executive Dysfunction and Inconsistent Abilities 14:01 The Pressure of Productivity 16:53 Feeling 'Not Enough' in Neurodivergence 19:43 Unlearning Internalized Ableism 22:27 Building Self-Compassion and Acceptance  PODCAST HOST Patricia was a Licensed Clinical Social Worker for over 17 years, but she is now exclusively providing coaching. She knows what it's like to feel like an outcast, misfit, and truthteller.  Learning about the trait of being a Highly Sensitive Person (HSP), then learning she is AuDHD with a PDA profile, OCD and RSD, helped Patricia rewrite her history with a deeper understanding, appreciation, and a sense of self-compassion.  She created the podcast Unapologetically Sensitive to help other neurodivergent folks know that they aren't alone, and that having a brain that is wired differently comes with amazing gifts, and some challenges.  Patricia works online globally working individually with people, and she teaches Online Courses for neurodivergent folks that focus on understanding what it means to be a sensitive neurodivergent. Topics covered include: self-care, self-compassion, boundaries, perfectionism, mindfulness, communication, and creating a lifestyle that honors you LINKS Rest Is Resistance: Free yourself from grind culture and reclaim your life by Tricia Hersey. Neurodivergent Online Course-- https://unapologeticallysensitive.com/neurodivergent-online-courses/ Receive the top 10 most downloaded episodes of the podcast-- https://www.subscribepage.com/e6z6e6  To write a review in itunes: click on this link https://itunes.apple.com/us/podcast/unapologetically-sensitive/id1440433481?mt=2 select “listen on Apple Podcasts” chose “open in itunes” choose “ratings and reviews” click to rate the number of starts click “write a review”   Website--www.unapologeticallysensitive.com Facebook-- https://www.facebook.com/Unapologetically-Sensitive-2296688923985657/ Closed/Private Facebook group Unapologetically Sensitive-- https://www.facebook.com/groups/2099705880047619/ Instagram-- https://www.instagram.com/unapologeticallysensitive/ Youtube-- https://www.youtube.com/channel/UCOE6fodj7RBdO3Iw0NrAllg/videos?view_as=subscriber Tik Tok--https://www.tiktok.com/@unapologeticallysensitiv e-mail-- unapologeticallysensitive@gmail.com Show hashtag--#unapologeticallysensitive Music-- Gravel Dance by Andy Robinson www.andyrobinson.com  

Friend of the show Andrew Gurza, host of the podcast Disability After Dark, joins us to talk about ableism. You can buy Andrew's book, “Notes from a Queer Cripple: How to Cultivate Queer Disabled Joy (and Be Hot While Doing It!),” anywhere books are sold. In this episode: News- 4:05 || Main Topic (Ableism)- 13:10 || Guest (Andrew Gurza)- 19:27 || Gayest & Straightest- 1:05:13 Send your questions for our 450th episode to gayishpodcast+450@gmail.com! Remember, we're having our 450th livestream combined with our quarterly Patreon happy hour on Tuesday, August 5 @ 6pm Pacific / 9pm Eastern. Buy our book, You're Probably Gayish, available right now at www.gayishpodcast.com/book! Each chapter dissects one gay stereotype ranging from drugs to gaydar to iced coffee. It's also available as an audiobook on Audible, Spotify, and more. If you want to join Mike and Kyle on their 2027 Mexican Riviera cruise, visit www.gayishpodcast.com/cruise to sign up. Make sure to check Gayish as the podcast you're attending for. On the Patreon bonus segment, Kyle shares with Mike some stereotypes to avoid in reporting on LGBTQ people with disabilities. If you want to support our show while getting ad-free episodes a day early, go to www.patreon.com/gayishpodcast.