Podcasts about disabled people

A Clare disability rights activist had dismissed a new Government strategy for providing better accessibility for disabled people as a "glossy document" and a "distraction". The National Human Rights Strategy for Disabled People, which is a five-year strategy providing a policy framework for the Government's approach to disability issues, has officially been launched. The strategy contains 23 commitments which are under the pillars of learning and education, employment, independent living and active participation in society, wellbeing and health, and transport and mobility. Ennistymon-based disability rights activist Ann Marie Flanagan has been telling Clare FM's Seán Lyons she believes the plan lacks the required legal framework for it to have any impact.

Send us a textThink disabled people don't have sex? Think again.

The Minister of State with Responsibility for Disability outlines the new five-year strategy that aims to provide better accessibility for disabled people.

The Government has announced the publication of the National Human Rights Strategy for Disabled People 2025-2030, but what exactly are the commitments being made?Joining Kieran to discuss is Minister of State at the Department of Children, Equality, Disability, Integration and Youth with responsibility for Disability, Hildegarde Naughton.

A select committee report has recommended going ahead with a referendum on four-year Parliament terms. Māori health providers have brought a case to the High Court asking for a declaration of inconsistency between the Government's disestablishment of Te Aka Whai Ora and Te Tiriti o Waitangi. And the Public Service Commissioner, Sir Brian Roche, is currently considering a “major shakeup” of several ministries, including those for Women, Pacific Peoples, Disabled People, and Māori Development. For our weekly catch-up with the Labour Party, regular Wire Host Caeden spoke to Shanan Halbert about all of these topics.

Jeannette meets Rosaleen Moriarty-Simmonds OBE, a remarkable individual with an inspiring story. Born with phocomelia caused by the drug thalidomide, Rosaleen defied the odds and became a successful businesswoman, equality campaigner, volunteer, author, artist, and inspirational speaker. Rosie joins the show this week to share her journey from overcoming societal barriers and discrimination to finding her passion in disability equality training and becoming a renowned mouth painting artist. KEY TAKEAWAYS Rosie's parents played a crucial role in her upbringing, providing support and encouragement for her to be as independent as possible Rosie faced numerous challenges and rejections in her career, but her determination and drive helped her overcome them and achieve success. Rosie has been actively involved in disability equality training and advocacy, working to raise awareness and improve accessibility for disabled individuals. Rosie's journey as a mother has been a significant part of her life, defying societal expectations and proving that disabled individuals can have fulfilling family lives. BEST MOMENTS "If I can succeed in it, then the doors should be open for other disabled people as well." "I need to do something that I'm passionate about." This is the perfect time to get focused on what YOU want to really achieve in your business, career, and life. It's never too late to be BRAVE and BOLD and unlock your inner BRILLIANCE. If you'd like to jump on a free mentoring session just DM Jeannette at info@jeannettelinfootassociates.com or sign up via Jeannette's linktree https://linktr.ee/JLinfoot VALUABLE RESOURCES Brave, Bold, Brilliant podcast series - https://podcasts.apple.com/gb/podcast/brave-bold-brilliant-podcast/id1524278970      ABOUT THE GUEST Rosaleen (Rosie) Moriarty-Simmonds OBE: A member of many disability and other organisations, Rosie is also a Vice President of the Cardiff Business Club, and protagonist for the Thalidomide Memorial - dedicated in June 2016, which marks the lives and achievements of Thalidomide Impaired people globally.  She is also, Patron of Flamingo Chicks, [national inclusive dance schools where all youngsters can spread their wings.  It gives disabled children the opportunity to explore movement and have fun alongside their non-disabled friends]. Patron of Flat Spaces, [a project providing fully accessible holiday bungalows with state-of-the-art facilities, all around the UK]. and Chairperson of the Equality, Diversity and Inclusion Advisory Board for Cardiff University. Happily married to Stephen with one son [James], Rosie's hobbies are theatre and concert going, and photography. In December 2018, Rosie received an Honorary Doctorate and Honorary Fellowship from Swansea University, again for her equality work. Rosie was the High Sheriff of South Glamorgan from April 2022-2023. ABOUT THE HOST Jeannette Linfoot is a highly regarded senior executive, property investor, board advisor, and business mentor with over 25 years of global professional business experience across the travel, leisure, hospitality, and property sectors. Having bought, ran, and sold businesses all over the world, Jeannette now has a portfolio of her own businesses and also advises and mentors other business leaders to drive forward their strategies as well as their own personal development. Jeannette is a down-to-earth leader, a passionate champion for diversity & inclusion, and a huge advocate of nurturing talent so every person can unleash their full potential and live their dreams. CONTACT THE HOST Jeannette's linktree - https://linktr.ee/JLinfoot https://www.jeannettelinfootassociates.com/ YOUTUBE - https://www.youtube.com/channel/UCtsU57ZGoPhm55_X0qF16_Q LinkedIn - https://uk.linkedin.com/in/jeannettelinfoot Facebook - https://uk.linkedin.com/in/jeannettelinfoot Instagram - https://www.instagram.com/jeannette.linfoot/ Email - info@jeannettelinfootassociates.com

WBBM political editor Geoff Buchholz reports the RTA voted to impose limits on a popular program subsidizing rideshare and cab rides for people with disabilities.

WBBM political editor Geoff Buchholz reports the RTA voted to impose limits on a popular program subsidizing rideshare and cab rides for people with disabilities.

WBBM political editor Geoff Buchholz reports the RTA voted to impose limits on a popular program subsidizing rideshare and cab rides for people with disabilities.

Shabnam is at Wimbledon, talking snooker with fellow reporter Andy Stevenson who was born with no hands, very short arms and only one fully formed leg. Explore the sport of snooker, from its biggest names to sharing stories of the people involved at all levels of the game. With Shabnam Younus-Jewell.

In this episode of "Disabled and Proud," Brooke speaks with Nicole Brennan. Together they explore the complexities of motherhood and disability, exploring the internalised ableism that often accompanies these experiences. The conversation highlights the transformative journey of accepting one's body and identity as a disabled mother, particularly in the face of societal expectations and scrutiny from healthcare professionals. They discuss the creation of the I Am Possible Foundation, aimed at increasing representation and support for individuals with limb differences. KEY TAKEAWAYS Internalised Ableism and Motherhood : The experience of becoming a mother can amplify feelings of inadequacy, especially for those with disabilities. The pressure to conform to societal standards of motherhood can lead to internalised ableism, where individuals question their worth and abilities as parents. Transitioning from Charity to Business : The conversation highlights the shift from viewing disability-focused initiatives as charities to recognising them as legitimate businesses. This change promotes sustainability and autonomy in supporting the disabled community without relying solely on donations. The Importance of Community and Support : Engaging with others who share similar experiences can be empowering. The creation of platforms for sharing stories fosters a sense of community and provides valuable resources for those navigating challenges related to disability and motherhood. BEST MOMENTS "I was just picking on me as a person. It wasn't actually my arm, it felt like it was me as a mum. Like, I'm just not good enough." "I was like, I don't want him to grow up in a world where his mum sees herself the way she does." "It's so fucking lazy to consistently put disabled businesses under the guise of charity." VALUABLE RESOURCES Join the I Am Possible Foundation - https://store.iampossiblefoundation.co.uk/ https://podcasts.apple.com/gb/podcast/disabled-and-proud/id1621152878 HOST BIO Disabled and Proud is the show that brings listeners a different perspective on disability. Each week this podcast highlights an awesome disabled guest speaking about their own disability; why they are proud to be disabled and why they are proud to be themselves. The conversations in this show will look at what challenges these amazing people face socially, mentally, physically and life in general. This show is raw, open, honest, funny, welcoming and educational. Disabled & Proud does exactly what it says on the tin! And whilst we are creating this space for disabled people to be unashamedly themselves, without the need to conform to society, this is also not about toxic positivity. This show will be shining a big, bright light on disability without it being “Paralympic or pity”. As you will hear disability is WHOLE, COMPLETE & PERFECT and whilst the topic of disability can be quite heavy - and we definitely don't shy away from the bad days - this podcast is also about having fun too! Our aim is to play a part in reclaiming the word disability - turning it from inadequacy to perfection! This Podcast has been brought to you by Disruptive Media .https://disruptivemedia.co.uk/

Today we're chatting with Paige Harvey from Special Effect, a charity promoting accessible gaming for players all over the globe. We talk to Paige about the work that Special Effect does with the community, how the charity came to be, and how to go about accessing the services they provide, as well as Paige's love of Retro Gaming and how you can support Special Effect so that they can keep doing the incredible work they're carrying out here in the UK And further afield.

“We are a community affair. We're Autistic, ADHD, OCD, PTSD, Tourettes, schizophrenic, bipolar, apraxic, dyslexic, dyspraxic, dyscalculic, non-speaking, and more. We've collectively experienced rare diseases, organ transplants, various cancers, many surgeries and therapies, and lots of ableism and SpEd. We've experienced #MedicalAbleism, #MedicalMisogyny, #MedicalRacism, #MedicalTrauma, and #MedicalGaslighting. We understand chronic pain, chronic illness, and the #NEISvoid “No End In Sight Void”. We know what it's like to be disabled and different in our systems. We know what it is like to live with barriers and what it means to not fit in and have to forge our own community. Disabled and neurodivergent people are always edge cases, and edge cases are stress cases. We can help you design for the edges, because we live at the edges. We are the canaries. We are “the fish that must fight the current to swim upstream.“And that's just the opening statement on Stimpunks.org.Stimpunks has been among HRP's closest allies over the years, and I am so grateful to be joined by an amazing cross section of Stimpunks today -- Ryan Boren, Chelsea Adams, Norah Hobbs, and Helen Edgar, who also runs Autistic Realms – to speak to their roll your own, DIY, Mutual Aid and Human-Centered Learning for Neurodivergent and Disabled People.Chelsea had to step away during recording so you'll hear her voice just in the first half. This episode was a long time coming, and I hope you enjoy it. You can connect with Stimpunks and find all of the resources mentioned in this episode at Stimpunks.org.Mentioned in this episode:Stimpunks WebsiteCommunity DiscordMutual-AidMap of Monotropic ExperiencesThe Five Neurodivergent Love Languages/Locutions10 Obstacles to Neurodiversity Affirming Practice

Guardian columnist Frances Ryan on the reality of being disabled in the UK and the impact of the government's proposed cuts. Help support our independent journalism at theguardian.com/infocus

From benefits to AI, Emma Tracey looks through the headlines with BBC tech reporter Paul Carter, as well as sharing a few unexpected stories from their personal lives as innocent-looking 'smugglers'.And comedian Rosie Jones with actor and reporter Ruben Reuter join Emma to talk about Pushers - the new Channel 4 sitcom written by Rosie about a disabled woman who becomes a drug pusher through desperation after losing her benefits money. Sound recording and mix: Dave O'Neill Producers: Alex Collins and Emma Tracey Series Producer: Beth Rose Editor: Damon Rose

Barriers to Employment and Progression in Dance for Disabled People short report audio by People Dancing

A 39-year-old woman in Tokyo has been working to help disabled people get jobs in an effort to create a society that recognizes the value of all people.

Today: A new report shows how, throughout its history, Massachusetts failed thousands of disabled residents living in institutions, and then tried to cover their tracks with bureaucratic stonewalling decades later.GBH's Megan Smith joins alongside Alex Green, vice-chair of the commission behind this report. And, naturalist Sy Montgomery is back to talk about axolotls, as researchers at Northeastern look into whether humans could ever tap into their secrets around limb regeneration.

Barriers to Progression & Employment in Dance for Disabled People: Detailed Report Audio by People Dancing

In this episode, I chat with the absolutely incredible Amy Butterworth - or as she's known online, Long COVID Rockstar. Amy lives with long COVID, and what she shares about rest, identity, and the invisible cost of simply existing in a capitalist world? It hit me hard.We talk about what it's like to live in a society that tells you your worth is tied to how much you can produce -  and what happens when your body says no more. Amy gets honest about disability, burnout, ego vs. grace, and the internal work it takes to stop apologising for existing.Together, we explore:

When the cost of survival outweighs the cost of death, something has gone deeply wrong. In this sobering and eye-opening episode, Mitch, living with cerebral palsy and chronic pain, shares his harrowing journey through a Canadian healthcare and social system that he argues is failing its disabled citizens. From the challenges of inadequate education and inaccessible post-secondary programs, to the emotional toll of societal stigma and the bureaucratic obstacles in pursuing intimacy, Mitch exposes the gaps that leave many disabled individuals isolated, under-resourced, and overlooked. He bravely discusses everything from systemic failures and addiction to sex work and survival strategies — reminding us how much dignity and independence are shaped by equity, not charity.You can watch this entire episode over on YouTube.Follow Sickboy on Instagram, TikTok and Discord!

When the cost of survival outweighs the cost of death, something has gone deeply wrong. In this sobering and eye-opening episode, Mitch, living with cerebral palsy and chronic pain, shares his harrowing journey through a Canadian healthcare and social system that he argues is failing its disabled citizens. From the challenges of inadequate education and inaccessible post-secondary programs, to the emotional toll of societal stigma and the bureaucratic obstacles in pursuing intimacy, Mitch exposes the gaps that leave many disabled individuals isolated, under-resourced, and overlooked. He bravely discusses everything from systemic failures and addiction to sex work and survival strategies — reminding us how much dignity and independence are shaped by equity, not charity.You can watch this entire episode over on YouTube.Follow Sickboy on Instagram, TikTok and Discord!

DWI has recently rebranded to help continue its mission to help people with developmental disabilities. Student Reporter Cody Miller talked to Glenn Guzman, sales and marketing director, about the organization.

On both sides of the Atlantic disabled people are protesting, despite the sometimes tricky logistics.In the UK, a mass lobby event was held on 21 May at Westminster to enable disabled people to 'green card' their MP. That means the MP is informed their constituent is waiting for them in Parliament and they should go and meet them. The hot topic for this event was the £5bn welfare cuts announced in the Spring Statement. But how successful was it? Access All's Alex Collins goes to meet those who have travelled from across the country to be there and Emma Tracey chats with Svetlana Kotova from disabled peoples organisation, Inclusion London. Across the Atlantic, American activists have also been out in force. Last week 26 disabled people were arrested in Congress when they disrupted a debate around Medicaid and who gets government-funded health and social care. Domonique Howell, from US disability advocacy organisation Adapt, was one of those to be arrested and talks about her experience, while veteran protester, Julie Farrar, talks about the importance of direct action.Plus Ellie Simmonds: Should I Have Children? That's the thought-provoking title of the Paralympian come TV presenter's new documentary, which explores the decisions parents make when told their unborn child could be disabled. She chats about how it shaped her feelings around having children as a woman with an impairment that could be passed on, and what she learned by spending time with couples at a specialist foetal medicine unit.Presented by Emma Tracey Producer and reporter: Alex Collins Sound by Dave O'Neill Editors: Damon Rose and Beth Rose

Clare has been awarded over €3 million in funding for housing adaptation grants. Just under €2.7 million of this has been provided to this county through exchequer funding while a further 476,000 is estimated to be contributed by the local authority. It forms part of a national total of €117 million, with an increase of €10,000 in the maximum grant available under the Housing Adaption Grant for Disabled People also announced. Ennistymon-based disability rights activist, Ann Marie Flanagan, says the funding is welcome but is hopeful in time the full cost of works will be covered under the grant.

In this episode of "Disabled and Proud," Brooke talks with Scott Whitney in a thought-provoking discussion about the recent reforms to Personal Independence Payment (PIP) and universal credit in the UK. He highlights the misconceptions surrounding disability benefits, particularly the unfounded belief in widespread fraud, and emphasises the importance of PIP as a means to maintain independence rather than merely an out-of-work benefit. The conversation delves into the challenges faced by disabled individuals in navigating the assessment process, the potential dangers of tightening benefit structures, and the urgent need for businesses to adapt their hiring practices to be more inclusive. Scott also shares insights from his own journey as a disabled person and discusses the initiatives of his organisation, All4Inclusion, which aims to reduce loneliness within the disability community by fostering safe spaces for open conversations. The episode concludes with a powerful reminder that being proud of one's disability should translate into action and advocacy for change. KEY TAKEAWAYS PIP Reforms and Misconceptions : The discussion highlights the misconception that Personal Independence Payment (PIP) is often fraudulently claimed. Research indicates that only 0.04% of all benefit fraud is related to disability benefits, suggesting that the focus on tightening PIP is misguided. Importance of Training for Assessors : Many decisions regarding PIP claims are made by individuals without adequate medical training. This can lead to incorrect assessments, as seen in personal experiences where medical evidence was overlooked. PIP as a Means of Independence : PIP is not an out-of-work benefit; rather, it is designed to help individuals maintain their independence, whether they are working or not. The removal of such support could lead to severe consequences for those who rely on it for daily living. Impact of Reforms on Vulnerable Populations : The potential reforms could disproportionately affect individuals with invisible disabilities, such as mental health conditions, who may struggle to prove their need for support. This could lead to increased poverty and destitution among disabled individuals. Community and Activism : There is a call for collective action, emphasizing the need for both disabled and non-disabled allies to advocate for the rights of disabled individuals. Engaging in conversations, writing to MPs, and participating in protests are essential steps to address the challenges faced by the disabled community. BEST MOMENTS "The only way we're going to get disabled people into work is by training, supporting businesses to go, well, actually, this is how we need to interview people." - Scott "PIP isn't an out-of-work benefit; it's something that people use to allow them to go to work." - Scott "The ultimate danger is that people die... it would be because people... wouldn't be able to eat, my diet would be worse." - Scott "Hundreds of thousands more women than men will end up going into poverty and out of the workforce." - Interviewer "If we're proud, what are we doing about it? It's time... to do actions, not words." - Scott VALUABLE RESOURCES https://podcasts.apple.com/gb/podcast/disabled-and-proud/id1621152878 HOST BIO Disabled and Proud is the show that brings listeners a different perspective on disability. Each week this podcast highlights an awesome disabled guest speaking about their own disability; why they are proud to be disabled and why they are proud to be themselves. The conversations in this show will look at what challenges these amazing people face socially, mentally, physically and life in general. This show is raw, open, honest, funny, welcoming and educational. Disabled & Proud does exactly what it says on the tin! And whilst we are creating this space for disabled people to be unashamedly themselves, without the need to conform to society, this is also not about toxic positivity. This show will be shining a big, bright light on disability without it being “Paralympic or pity”. As you will hear disability is WHOLE, COMPLETE & PERFECT and whilst the topic of disability can be quite heavy - and we definitely don't shy away from the bad days - this podcast is also about having fun too! Our aim is to play a part in reclaiming the word disability - turning it from inadequacy to perfection!INSTAGRAM! https://www.instagram.com/disabledandproudpodcast/?hl=en: https://www.instagram.com/disabledandproudpodcast/?hl=en

In this episode of Robot Unicorn, Jess and Scott sit down with their close friend and colleague, Brooklyn Marx, a disabled psychotherapist, to explore how to talk about disability honestly and openly with children. Brooklyn shares her personal journey with Spinal Muscular Atrophy (SMA), the challenges of growing up with a disability, and the evolution of her personal identity.Whether you're a disabled parent, a parent of a disabled child, or simply someone interested in nurturing inclusivity, this episode provides real-world advice and heartfelt insights that encourage us all to view disability as a natural, integral part of human diversity.Get 10% OFF parenting courses and kids' printable activities at Nurtured First using the code ROBOTUNICORN.We'd love to hear from you! Have questions you want us to answer on Robot Unicorn? Send us an email: podcast@robotunicorn.net. Credits:Editing by The Pod Cabin Artwork by Wallflower Studio Production by Nurtured First  Learn more about The Anger Course here!

The UK's chancellor has announced a £5bn cut to benefits, much of which will be borne by those on long-term disability allowance. Gerry McCartney, professor of wellbeing economy at Glasgow University explains about why these cuts will not only hurt the most vulnerable, but will be counterproductive to the government's wish to get people back to work. Also, Suzanne O'Sullivan, consultant neurologist and author, joins us to talk about her new book "Age of Diagnosis". The book used clinical cases to explore the issues of medicalisation, and Suzanne explains why overdiagnosis doesn't mean that care isn't needed.   Reading list; UK welfare reforms threaten health of the most vulnerable Guardian edited extract from "The Age of Diagnosis: Sickness, Health and Why Medicine Has Gone Too Far"  

In this episode, host Samuel Goldsmith is joined by Dr Shani Dhanda, a prominent disability activist and broadcaster. Shani shares her journey, from her roots in a devout Sikh household to her career in events management and her inspiring activism. Additionally, she highlights the significance of the Sikh festival of Vaisakhi, shares delicious cooking tips, and talks about her love for traditional and modern cuisines. Plus, how Nadiya Hussain taught her how to cook. This episode offers a blend of social advocacy, cultural education, and culinary delight. Dr Shani Dhanda is a multi-award-winning disability inclusion specialist, thought leader, and social entrepreneur. She founded Diversability, the Asian Woman Festival, and the Asian Disability Network to combat global social inequality. Over the past year, she has worked with 100+ clients as a keynote speaker and inclusion consultant. Recognized among the most influential women in leadership, she was a BBC 100 Women Laureate and a Changemaker to Watch by CEO Magazine. Shani has featured on LinkedIn's first TV advert, Nadiya Hussain's Time to Eat (BBC) and EastEnders. A prominent broadcaster, she's contributed to Rip Off Britain, This Morning, and major news outlets. She advocates for disability rights, influencing policies and launching an internship program for disabled people. With seven executive roles and five ambassadorships, Shani is a catalyst for change in disability inclusion. Subscribers to the Good Food app via App Store get access to the show ad-free, and with regular bonus content such as interviews recorded at the good food show. To get started, download the Good Food app today. Learn more about your ad choices. Visit podcastchoices.com/adchoices

Send us a textMany young disabled adults are not fulfilling their potential because of a lack of government support. That's according to the founder of a charity that helps those young people achieve their ambitions. Jane Holmes set up Building for the Future because of her own experiences after her daughter, Kitty, was born 24 years ago. Building for the Future supports around 500 families but is running out of space and plans to expand by 2026 to better serve young adults transitioning from education. These young people often face isolation when care packages prove insufficient, leading parents in their 50s to abandon careers to provide necessary support. With the charity receiving no government funding and concerns about proposed cuts to disability benefits, Jane calls for longer-term thinking from policymakers.https://www.bftf.org.uk/Hi listener. I thought you might enjoy Don Anderson's podcast. Missing Pieces - NPE Life is a podcast that curates stories of and about people who find out, usually through a home DNA test, that someone in their family tree isn't who they thought. They also tell stories of adoptees who've found lost family, or are looking. The host, Don Anderson, found out in 2021 that his dad wasn't his dad. It changed his life. NPE stands for Not Parent Expected or Non Paternity Event.Support the showhttps://www.angelawalkerreports.com/

If there's one scapegoat the government loves to roll out when it's doing poorly, it's the benefits thief. This imaginary person uses loopholes and caveats to steal tax money to buy themselves tellies and holidays in Lanzarote. In the UK, the new-ish-ly elected Labour party has announced new budget reforms that plays into this trope with an especially sinister new edge - tightening the pursestrings of the benefit system specifically against disabled people.In this week's episode, hosts Ione and Gina break down what's actually being proposed by our Chancellor, Rachel Reeves, the need to work being framed as life's purpose and the ableism that has always been inherent in capitalist society.Support our work and become a Polyester Podcast member

Alan interviews Garrett Brown. Inspired by his dad's invention - Garrett grew up to be a serial inventor. As a youth, Garrett went from folk singing to film making. He invented the Steadicam that is used globally in film making. Recently he invented the Zeen - a mobility device to enable disabled people to stand and walk. Make sure to subscribe to the podcast at Apple Podcasts, or wherever you get your podcasts, so you won't miss a single episode. Website: www.GoZeen.com    

A Clare disability activist fears it's becoming a widely accepted belief that being disabled and living in poverty go hand in hand. A new report published by the Irish Human Rights and Equality Commissionand the Economic and Social Research Institute has found that households with a disabled member face "significant" financial burdens and have a "very high" risk of poverty rates. It's estimated that households with a disabled member require up to 59% more disposable income to achieve the same standard of living as a similar households with no disabled member. Speaking on Clare FM's Morning Focus, Ennistymon native Ann Marie Flanagan says there's a risk that society could become complacent and refuse to imagine the situation changing.

We're sweating! We're hyperfixating! Because a bunch of conservative attorneys general have filed a lawsuit trying to weaken or eliminate Section 504 of the Rehabilitation Act, which served as a precursor to the Americans with Disabilities Act.This week, Jess and Imani get into the conservative legal movement's attempts to roll back Section 504—and how it could constitute government-sponsored eugenics. And even though conservatives are pretending that they're really just targeting trans folks, why should we believe them?Rewire News Group is a nonprofit media organization, which means that episodes like this one are only made possible with the support of listeners like you! If you can, please join our team by donating here.And sign up for The Fallout, a weekly newsletter written by Jess that's exclusively dedicated to covering every aspect of this unprecedented moment.

We're sweating! We're hyperfixating! Because a bunch of conservative attorneys general have filed a lawsuit trying to weaken or eliminate Section 504 of the Rehabilitation Act, which served as a precursor to the Americans with Disabilities Act.This week, Jess and Imani get into the conservative legal movement's attempts to roll back Section 504—and how it could constitute government-sponsored eugenics. And even though conservatives are pretending that they're really just targeting trans folks, why should we believe them?Rewire News Group is a nonprofit media organization, which means that episodes like this one are only made possible with the support of listeners like you! If you can, please join our team by donating here.And sign up for The Fallout, a weekly newsletter written by Jess that's exclusively dedicated to covering every aspect of this unprecedented moment.

How California can prepare disabled people for the next disaster. Also, CapRadio's new series focusing on Sacramento's diverse environment and wildlife. Finally, a gothic fairytale show “The Lost One.” Helping Disabled People During Disasters

Half a million disabled New Zealanders aren't getting what they need to live a good life. The findings come from the first comprehensive set of disability statistics collected in more than a decade.

Head Over Wheels is a one-year-old company which visited Prague last December for a joint workshop. This British company describes itself as a disabled and non disabled circus company and through its performances or educating art spaces is widening the borders of inclusivity in circus. Listen to the interview with Tilly Lee-Kronick and Johny Leitch hosted by Barbora Schneiderová. Author: Barbora Schneiderová Editor: Veronika Jošková Štefanová

An organization's origin story reveals so much about its founders' principles and vision for generating transformational change. In the case of New Disabled South, co-founders Dom Kelly and Kehsi Iman Wilson knew that they were creating a space that didn't exist, a movement for disability justice in the American South. They focused first on their internal infrastructure, developing human resources and operational policies that support the sustainability of staff, all of whom are disabled, as is the board of directors, as they conduct research, build coalitions and advocate for policy change in city halls and states houses across 14 states. In this episode of Power Station, I am joined by the exceptional movement builder e.k. hoffman who leads New Disabled South Rising, the 501c4 advocacy companion to NDS. E.k shares how punishing asset limits, failure by states to expand Medicaid and government hearings that are inaccessible diminish civil liberties. And as a disabled person who is also trans, e.k. navigates the realities of intersectionality. We talk about the rise of horrible rhetoric coming from the White and the necessity of experiencing disabled joy. New Disabled South is an essential space we should all see, hear and support.

If you are not worried about programs that come from the Federal government, you are not paying attention. Supports for people with disabilities are on the chopping block, everything from Food Stamps to Meals on Wheels to Social Security and Medi-Care. All of it is under threat from the heavy hand of Elon Musk. For our brothers and sisters overseas, these threats became a nightmare in actuality with the Trump Administration's “Stop Work” order for all International Aid on January 28. Disabled children lost the ability to attend school at the same time food supplies were cut. It's been a disaster for disabled refugees, disability organizations, and many others. We talk with Peter Fremlin Torres about what his international contacts told him about the effect of this order. There have been legal challenges and protests in support of the staff at the USAID agency, but in many countries outside the U.S., the damage is real and likely to spread. Join us to learn more about the billionaire's war on disabled people around the world. Peter Torres Fremlin is a disabled man who writes the weekly Disability Debrief newsletter which is archived at disabilitydebrief.org. He's spent 10 years studying, working, and language-learning in Brazil, Bangladesh, Switzerland, and Egypt. He currently resides in Colchester, England, where he grew up. Disability Debrief signup page: https://www.disabilitydebrief.org/signup Link to the article on the Stop Work order: https://www.disabilitydebrief.org/debrief/stop-work/ Inclusive Development Partners: https://www.inclusivedevpartners.com/  Their crowdfunding site: https://www.gofundme.com/f/urgent-support-for-idps-global-mission Peter Torres Fremlin Linkedin: https://www.linkedin.com/in/peter-torres-fremlin/ Note: The artist who painted the picture below was Tan Kuan Aw, who sadly passed away recently. A link to his work on the Debrief is here. Hosted and Produced by Adrienne Lauby. Audio editing by Dominick Trevethan, Denny Daughters, and Jacob Stanton. Peter Torres Fremlin The post The Billionaire's War on Disabled People – Pushing Limits – February 14, 2025 appeared first on KPFA.

Inclusive Rainbow Voices is a community led, intersectional Disabled People's Organisation, by and for LGBTIQA+ people with disability. The organisation works at the forefront of local, national and international movements towards equity and justice for LGBTIQA+ people with disability. Cal Hawk speaks with CEO Katherine Marshall about: How IRV defines disability justice and how this informs the organisation's approach Some of the strong themes to come from community consultation in the past year The barriers to data collection specifically relating to LGBTIQA+ people with disability, and more. Check out our other JOY Podcasts for more on LGBTIQ+ health and wellbeing at joy.org.au/wellwellwell. If there's something you'd like us to explore on the show, send through ideas or questions at wellwellwell@joy.org.au Find out more about LGBTIQ+ services and events in Victoria at thorneharbour.org and in South Australia at samesh.org.au.

A first-of-its-kind study has found disabled people are more likely to be stopped by police, have force used against them, and ultimately end up in the courts.

Our expert panel looks ahead to what 2025 is likely to bring for disabled people and mental health service users. On the panel are: John Pring, founder and editor of Disability News Service; Richard Taylor of the disability equality charity Scope and Lucy Schonehevel of Rethink Mental Illness. They discuss ongoing issues which are likely to carry on making headlines in 2025 – such as the Assisted Dying Bill and changes to disability benefits. We also hear from disabled BBC correspondents in the worlds of sport and entertainment on what's coming up. Presenter: Emma Tracey Producers: Daniel Gordon, Alex Collins Editors: Farhana Haider, Beth Rose Recorded and mixed by Dave O'Neill

Forty years after India's Bhopal disaster, local residents are still suffering from its aftermath. The gas explosion at a chemical plant caused toxic waste to contaminate the water in nearby areas, causing locals to develop numerous health issues. Today, second and third-generation victims of the gas leak are grappling with its effects. Activists are battling to secure justice for the victims. FRANCE 24's Khansa Juned and Martin Bathla report.

In 1970, while a junior in Cornell University's College of Engineering, Ken Kunken broke his neck making a tackle on a kick-off in a lightweight football game against Columbia University. Ken sustained a spinal cord injury at the C 4-5 level, rendering him a quadriplegic, almost totally paralyzed from the shoulders down. Ken spent more than 9 months in various hospitals and rehabilitation facilities. While still a patient, Ken testified before a United States Senate Sub-Committee on Health Care, chaired by Senator Edward Kennedy.  In 1971, almost 20 years before the Americans with Disabilities Act, Ken returned to the Cornell campus, where he completed his undergraduate degree in Industrial Engineering. Ken estimates that he had to be pulled up or bounced down close to 100 steps just to attend his first day of classes.  Ken is the first quadriplegic to graduate from Cornell University.  Upon graduation, Ken decided to change his career goal. He wanted to work with and help people, particularly those with disabilities. Ken went on to earn a Master of Arts degree at Cornell in education and a Master of Education degree at Columbia University in psychology. Ken is the first quadriplegic to earn a graduate degree from Cornell University.  In 1977, Ken was hired by Abilities Inc. in Albertson, NY to be its College Work Orientation Program Coordinator. Ken coordinated a program which provided educationally related work experiences for severely disabled college students. He also maintained a vocational counseling caseload of more than 20 severely disabled individuals.  While working at the Center, Ken became a nationally certified rehabilitation counselor and made numerous public presentations on non-discrimination, affirmative action and employment of the disabled. In 1977, Ken was named the Long Island Rehabilitation Associations “Rehabilitant of the Year” and in 1979 Ken was the subject of one of the Reverend Norman Vincent Peale's nationally syndicated radio broadcasts “The American Character”.  Wanting to accomplish still more, Ken enrolled in Hofstra University's School of Law, where he earned a Juris Doctor degree in 1982. Ken then went to work as an assistant district attorney in Nassau County, Long Island.  Ken was promoted a number of times during his more than 40 years with the District Attorney's Office, eventually becoming one of the Deputy Bureau Chiefs of the County Court Trial Bureau, where he helped supervise more than 20 other assistant district attorneys. In addition, over his years working in the Office, Ken supervised more than 50 student interns.  In 1996 Ken received the Honorable Thomas E. Ryan, Jr. Award presented by the Court Officers Benevolent Association of Nassau County for outstanding and dedicated service as an Assistant District Attorney. In 1999, Ken was awarded the George M. Estabrook Distinguished Service Award presented by the Hofstra Alumni Association, Inc.  Beginning in 2005, for nine consecutive years, “The Ken Kunken Most Valuable Player Award” was presented annually by The Adirondack Trust Allegiance Bowl in Saratoga Springs, NY, in recognition of Ken's personal accomplishments, contributions to society and extraordinary courage.  In 2009, Ken became a member of the Board of Directors of Abilities Inc., and in 2017 he became a member of the Board of Directors for the parent company of Abilities Inc., the Viscardi Center.  In 2020, Ken was inducted into “The Susan M. Daniels Disability Mentoring Hall of Fame,” as a member of the class of 2019.  In March 2024, Ken was named one of the Long Island Business News Influencers in Law.  Ken retired from full-time employment in 2016, but continued to work with the District Attorney's Office for the next eight years in a part time capacity, providing continuing legal education lectures and litigation guidance.  For years, Ken has tried to inspire people to do more with their lives. In October 2023, Ken's memoir “I Dream of Things That Never Were: The Ken Kunken Story” was published.  In 2003 Ken married Anna and in 2005 they became the proud parents of triplet boys: Joey, Jimmy and Timmy. On June 23, 2023 the triplets graduated from Oceanside High School, fifty-five years after Ken had graduated from the same school. 3 Top Tips 1 . Try to improve your knowledge, your skills and your performance. Get the best education possible, and never stop learning. Don't be satisfied with the status quo.  2 . Strive to make the impossible, possible. Just because something has not been done before, does not mean that you cannot do it now.  3 . Find time to help others. Years from now be able to say that you did everything you possibly could to make not only your life, but the lives of those around you better as well. Social Media https://www.facebook.com/ken.kunken  https://www.instagram.com/ken.kunken/  https://www.linkedin.com/feed/

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The Budget is done and dusted and the US elections about to start. How do disabled people fit in to these big political events? Chancellor Rachel Reeves has delivered her budget. Bethany Dawson from Politico and disability charity Scope's head of policy, James Taylor,talk us through the bits disabled people care about. They discuss the increase in the minimum wage and a rise in what carers can earn before their carer's allowance gets stopped. Will any of the chancellor's announcements help disabled people with their household bills? And how significant is the £1 Billion Reeves has promised for special educational needs and disabilities?The experts break it down for us. As Over 40 million disabled Americans head to the polls to vote for their next president, Trump supporter and disability policy expert Melissa Ortiz and disability activist and Harris supporter Mia Ives Rublee predict what their candidate will do for this community if they win. Our guests also give us an insight into how Trump and Harris treat disabled people when the cameras are off.. Presented by Emma Tracey Produced by Alex Collins and Emma Tracey. Edited by Damon Rose and Sara Wadeson.

Transcript: rmad.ac/AIAe064Katherine Beattie is a Los Angeles born television writer/producer and action sports enthusiast. While she has spent most of her professional career writing police procedurals, she considers herself a comedian at heart. But regardless of what she's writing, Katherine is a champion for authentic and nuanced portrayals of Disabled People and other historically excluded communities on screen, and for their inclusion behind the scenes.As one of the pioneers of wheelchair motocross (WCMX), Katherine was the first woman in the world to land a backflip on a wheelchair. She competes on the Adaptive Surfing Professionals World Tour, and is a member of USA Surfing's parasurfing national team. She will represent Team USA at her 4th ISA World Parasurfing Championships this November in Huntington Beach.Connect with Katherine:Katherine Beattie (@ktbeattie) • Instagram photos and videosConnect with the Rocky Mountain ADA Center at RockyMountainADA.org or find us on social media. Don't forget to subscribe, rate and review us on Apple Podcasts, Stitcher, Spotify, or anywhere else you get your podcasts!

Text Us!In this episode we tell parents of typical children:Why they should be having an intentional, continuous conversation with their kids about people with disabilities,What they should teach their children to do and say (and what not to do as well),and we shared opinions from our listeners and fellow caregivers about what they wish you were teaching your kids about their disabled child.Special thanks to the following friends of the show for their comments:lovetoemmaalvesmomkickingcaskemily_mommato4happygolandrysaratothebethAracely GinnspecialneedsparentjourneyHeidi WaltonRuby Moseleyannabusby1daidrahamlintheunboxedfamily disorderrarediseasefilmsunbalancedraremomannabethburnhamvalcirino1 hkwoodleyPlease subscribe, leave a review, and follow us on social media to know about upcoming episodes and to participate in this podcast.Instagram - @raisingdisabledpodcastFacebook - Raising Disabled Podcast