Podcasts about disabled people

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

Health and Human Services Secretary Robert F. Kennedy Jr. Wednesday declared that autism is a rapidly growing "epidemic" in the U.S. and vowed to identify the "environmental toxin" he says is to blame.Erica Stanford stands behind Education Review Office research to include compulsory consent education as a part of the high school Sex-ed curriculum.A deep dive from The Conversation by authors Rachelle Martin & Kaaren Mathias looks at research into the exclusion of disabled people in health research.That and more to send you off into this Easter weekend!=================================Come support the work we're doing by becoming a Patron of ⁠⁠#BHN⁠⁠ www.patreon.com/BigHairyNews⁠=================================Merch available at www.BHNShop.nz Like us on Facebookwww.facebook.com/BigHairyNews Follow us on Twitter.@patbrittenden @Chewie_NZFollow us on BlueskyPat @patbrittenden.bsky.socialChewie @chewienz.bsky.socialEmily @iamprettyawesome.bsky.socialMagenta @xkaosmagex.bsky.social

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

The US has imposed an import ban on solar salt products produced by a Korean company, citing “forced labour.” This is the first time that a foreign government has banned the import of a Korean company's products for the reason that they were made using forced labour. Since 2014, suspicions of human trafficking and forced labor of intellectually disabled people have emerged in salt fields in Sinan-gun, including Taipyeong Salt Fields. In 2022, victims of forced labour in salt fields spoke to the media, saying things like "I ran away but was caught" and "I was beaten." The US has imposed an import ban on solar salt products produced by a Korean company, citing "forced labour." This is the first time that a foreign government has banned the import of a Korean company's products for the reason that they were made using forced labour. Episode Notes: ' “Disabled people forced to work at Taepyeong Salt Fields in Korea” – US Imposes Import Ban': https://barrierfreejapan.com/2025/04/08/disabled-people-forced-to-work-at-taipyeong-salt-fields-in-korea-us-imposes-import-ban/

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.

The Japan Branch of the NPO Disabled People' International (DPI), located in Chiyoda-ku, Tokyo, will hold an online rally on the theme of “Prisoners with disabilities and their right to use wheelchairs” on Saturday, April 5, 2025. The rally is being held in response to a ruling handed down in a lawsuit seeking ‘reasonable accommodation' in Gifu, a lawsuit concerning an alleged human rights violation in which an inmate with walking difficulties was denied wheelchair access at Gifu Prison for over 10 years. On October 30, 2024, the Gifu District Court did not recognize the denial of wheelchair access as illegal and ruled against the plaintiff. Episode notes: ‘Disabled People International Japan Branch to Hold ‘Online Rally' on “Prisoners with Disabilities and the Right to Use Wheelchairs” ': https://barrierfreejapan.com/2025/02/26/disabled-people-international-japan-branch-to-hold-online-rally-on-prisoners-with-disabilities-and-the-right-to-use-wheelchairs/ DPI Website: https://www.dpi-japan.org/blog/events/disabled-inmates-and-wheelchair-access-rights-rally/

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/

It's claimed people with disabilities in Clare are unable to enjoy an equal social life due to a lack of accessible facilities. The local authority has called on the outgoing Taoiseach and Minister for Finance to establish a grant scheme to allow for universal toilets to be installed in cafés, bars and restaurants. The issue has been widely highlighted in Kilrush, where 791 people are currently living with some form of disability. Kilrush Independent Councillor Ian Lynch says the lack of suitable infrastructure has led to very demoralising situations for locals.

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Twelve years ago, Mandy McCracken's life changed overnight, leaving her with limited guidance on how to navigate her new reality as a disabled person. Now, through Get Started Disability Support Australia, Mandy is on a mission to help others who have just acquired a disability, providing the practical advice and support she wishes she had.  Connect with Mandy:  Website: https://www.getstarteddisability.org.au Facebook: https://www.facebook.com/GetStartedDisability Instagram: https://www.instagram.com/getstarteddisability/ Connect with Peta: Instagram: @petahooke Website: www.icantstandpodcast.com Email: icantstandpodcast@gmail.com Episode Transcript:https://www.icantstandpodcast.comSee omnystudio.com/listener for privacy information.

The rise of right-wing power in the U.S. is the culmination of a 50 year plan to seize the reins of government power in the U.S. It has succeeded in the Supreme Court and, who knows, could take the Presidency and both House and Senate at Tuesday's election. As the plan becomes actualized, the Heritage Foundation has gifted us with the next step – a plan for a radical restructuring of our legal and regulatory bodies written in a document called Project 2025. Unless you are inclined to policy wonky-ness, it's hard to tell how the Project 2025 changes could affect people with disabilities.  Fortunately for us, our guest for this program has the knowledge and experience to translate these bureaucratic maneuvers into the devilish details that are set to make our lives much more difficult. Claudia Center is the Legal Director of Disability Rights Education and Defense Fund (DREDF). She litigates cases that increase civil rights and civil liberties for persons with disabilities, and represents the disability community in legislative, policy, amicus, and appellate work. Claudia Center Project 2025 lays out drastic cuts to Medi-Caid (MediCal), the end of equity in K-12 schooling for disabled kids, less eligible injuries for Veteran services, and so much more. Halloween will be over by the time this program airs but it's not too late to be very scared. Want to know more?  Our community members are working to make it easy for you: 1. Claudia Center's analysis with page numbers in the Project 2025 document.so you can read what it says yourself. 2. Instragram post by DREDF. 3. Lainey Feingold's great hub with all the Project 2025 content from a disability perspective. Produced and hosted by Adrienne Lauby. Audio Editing by Adrienne Lauby and Denny Daughters. Production assistance by Tina Pinedo. The post Devilish Details for Disabled People: Project 2025 – Pushing Limits – November 1, 2024 appeared first on KPFA.

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!

Anna Smith speaks to Lily Ahree Siegel, director of Equal Play, a new short documentary that discusses the importance of equal access to school sports for disabled children. Anna is also joined by Lindsey Dryden, director, writer, producer, executive producer, as well as co-founder of FWD-DOC, and Clare Baines, the BFI's Inclusion Partner, to talk about equal access within the film industry and the bigger issues touched on in Equal Play. First, Clare discusses her personal connection to the documentary, revealing to Anna how losing her eyesight at 15 affected her ability to participate in school sports. Clare also advocates the importance of educating kids about their bodies. As a disabled woman in the film industry, Lindsey highlights the inaccessibility of disabled people entering the world of entertainment. She questions the disparity between disabled stories in documentaries vs narratives and encourages more joyous cinematic portrayals of the disabled experience. Lindsey and Clare share their favourite film depictions that capture the disabled experience. They also call for a disability revolution including more on-screen celebrations about disabilities. Next up, Lily Ahree Siegel discusses her background within the arts and what inspired her to become a documentary filmmaker. Lily highlights access to PE and sports as an issue affecting kids worldwide, discusses the importance of inclusion passports, and shares her favourite moment on set. Equal Play is available to watch on Channel 4 - https://www.channel4.com/programmes/equal-play A reminder that you can read a transcript of our episodes on Apple Podcasts by clicking the ‘transcript' option in settings in the episode description. This episode is brought to you by Harder Than You Think. Films/TV Shows/Books mentioned: The Gleaners and I (Agnes Varda) We Might Regret This (created by Kyla Harris) - available on BBC The Callers (Lindsey Dryden) Lost In Sound (Lindsey Dryden) Coda (Sian Heder) Trans In America (produced by Lindsey Dryden and Shaleece Haas) Unrest (Jennifer Brea) Patrice: The Movie (Ted Passon) - available on Hulu and showing at LFF 2024 Crip Camp (James Lebrecht and Nicole Newnham) - available on Netflix I Didn't See You There (Reid Davenport) - available to rent on Apple TV, Prime Video, and Google Play Is Anybody Out There (Ella Bee Glendining) - available on ITVX and Netflix The Tube Thieves (Alison O'Daniel) - available on PBS Feminist, Queer, Crip by Alison Kafer Websites mentioned: TV Access - https://www.channel4.com/4producers/creative-equity/tv-access-project Sins Invalid - https://www.sinsinvalid.org/blog/10-principles-of-disability-justice FWD-DOC - https://www.fwd-doc.org/ TripleC - https://triplec.org.uk/ DANC - https://triplec.org.uk/danc/ Deaf and Disabled People in TV - https://www.ddptv.org/ Sign up to the Girls On Film newsletter below: http://eepurl.com/iEKaM-/ or email girlsonfilmsocial@gmail.com to be signed up. Become a patron of Girls On Film on Patreon here: www.patreon.com/girlsonfilmpodcast Follow us on socials: www.instagram.com/girlsonfilm_podcast/ www.facebook.com/girlsonfilmpodcast www.twitter.com/GirlsOnFilm_Pod www.twitter.com/annasmithjourno Watch Girls On Film on the BFI's YouTube channel: www.youtube.com/playlist?list=PLX…L89QKZsN5Tgr3vn7z Girls On Film is an HLA production. Host: Anna Smith Executive Producer: Hedda Lornie Archbold Producer: Charlotte Matheson Assistant Producer: Jade Evans Intern: Anna Swartz Audio editor: Benjamin Cook band: MX Tyrants © HLA Agency

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

Shownotes:Being an advocate for equity and inclusion requires a certain level of self-awareness, humility and an appetite to be a lifelong learner. Especially considering that the vocabulary around DEIB/DEIBA or whatever you choose to call it is constantly evolving, there is more we don't know than we know.My chance encounter with Caroline Collier, CEO Inclusion Barnet happened over a LinkedIn recruitment post and my subsequent message to her regarding the language. She was gracious in her response educating me about why they were using ‘disabled person' (instead of person first language). I was slightly mortified but glad that I had the opportunity to engage with Caroline to better understand why they subscribe to the social model of disability. I am grateful to Caroline for making time for this important conversation (a learning opportunity for me). In the episode we spoke about Inclusion Barnet and why it describes itself as a Deaf and Disabled People's organisation, deaf being separate from disabled in deference to the cultural model of deafness. We also spoke at length about the ‘social model of disability; harnessing lived experiences for social change; acceptable language; role of the private sector in opening up opportunities; what allies can do to support; and the just launched ‘Campaign for Disability Justice' calling for a) Opportunity b) Security c) Respect.Did you know that care in the UK is based on a ‘medical model' that frames the body or mind of disabled person as something that needs to be fixed?“We see disability through the ‘social model', where being Disabled is a political term that describes our experience of marginalisation, not individual impairments. The social model allows us to come together to fight back against a world that we can't navigate safely without care and support. This model helps us understand that a flourishing social care system should give us access to choices and the freedom to live independently.We want a system that enables us to live independently, rather than generating a list of ‘care tasks' our local authority can charge us for. The struggle for a better, more equal system should unify us all to talk about intersectionality and disability justice alongside the crucial demands for fair conditions for both paid and unpaid carers, wholesale changes to the gendered imbalance of care responsibilities, and the need to tackle the looming climate crisis, which will affect our capacity to care for one another.” Caroline Collier, CEO Inclusion Barnet Episode Transcript:Sudha: Good morning, Caroline. It's wonderful to have you today as a guest on the Elephant in the Room podcast. Thank you for being hereCaroline: Thank you. Really pleased to be asked, so thank you so much.Sudha: Let's start with a quick introduction to who you are and what you do.Caroline: I'm Caroline Collier. I'm CEO of a deaf and disabled persons' organization called Inclusion Barnet. My background is varied. I started after college working in libraries. Then I ended up in my thirties writing about the construction industry, unusually enough. That changed in 2009 when I became really ill with what turned out to be bipolar. I had a bit of a rethink just because I wanted to find something with a little bit more purpose, and I was incredibly lucky to end up working in the organization that is now...

About 300 people, chanting "nothing about us, without us", have marched through central New Plymouth protesting changes to disability services.The government is restructuring Whaikaha, the Ministry of Disabled People. It's losing responsibility for delivering support services, which will move to the Ministry of Social Development, Taranaki Whanganui reporter Robin Martin was at the protest.

Today on the show Steven and Shaun dive into the inbox for the first in our weekly series of “App of the Week” featuring your favourite apps and why others might liike them. We also welcome disability and technology advocate Colin Hughes back to discuss the upcoming Apple Event and why he thinks Meta are missing a trick when it comes to their Ray-Ban smart glasses. As always, the show begins with a catchup between Steven and Shaun, with Shaun telling us about his weekend away coming up at a rather fancy hotel. They both share their packing plans when going away, and discuss the best way to assess and use the features of a hotel room. In our new “App of the Week” feature, listeners Gordon and Dennis share their lists of favourite apps including Be My Eyes, Seeing AI, OoTunes and Mona for Mastodon. Get in touch using the details below to share your suggestions. Our special guest today is Colin Hughes, a long time disability and technology advocate, who talks to Steven about his experience of the Apple beta software ahead of its launch over the next month, as well as discussing his annoyance at the Apple Watch as a person who lives with muscular dystrophy, and why he believes Meta need to better understand the value their Ray-Ban smart glasses can have on the disability community. Get in touch with Double Tap by emailing us feedback@doubletaponair.com or by call 1-877-803-4567 and leave us a voicemail. You can also find us across social media. Double Tap is available daily on AMI-audio across Canada, on podcast worldwide and now on YouTube. Chapter Markers: 0:00 - Intro 0:37 - Hotels & Tech 11:50 - App Of The Week 14:06 - E-mail - Gordons Essential App List 18:09 - E-mail - Dennis Essential Apps 25:46 - Contact Us 25:57 - Colin Hughes Interview - Apple Event Preview & Meta Ray Bans YouTube Video Chapter Adjustments. 18:59 - E-mail - Dennis Essential Apps 26:36 - Contact Us 26:47 - Colin Hughes Interview - Apple Event Preview & Meta Ray Bans

The parents of a man with severe disabilities said they've lost the ability to plan for his future thanks to changes in the way his care is funded. Their advocate said the situation is cruel and inhumane, but the Ministry of Disabled People, Whaikaha, says it's just an interim arrangement. Ryan Cook's family have for the past few years received an annual budget for his care. But in June, it wasn't renewed and instead they're now receiving funding for six weeks at a time. The family employ four staff to care for Ryan, so the change means they no longer have any long-term certainty that his care can continue, Jimmy Ellingham reports.

In this episode of the You First Podcast, hosts Maddie and Keith talk with disabled activist and attorney Marissa Ditkowsky about the challenges and inequities faced by disabled women in healthcare, employment, and financial freedom. Marissa discusses her role as Disability Economic Justice Council at the National Partnership for Women and Families and shares insights on systemic oppression, the impact of disability on financial stability, and the importance of intersectional advocacy. The episode also addresses issues like reproductive rights, bodily autonomy, and the overturning of Roe v. Wade. Relevant links:  National Partnership for Women & Families Website: https://nationalpartnership.org/ National Partnership for Women & Families social media: Twitter: https://x.com/npwf, or @npwf Instagram: https://www.instagram.com/npwf/, or @npwf Facebook: https://www.facebook.com/nationalpartnership/ TikTok: https://www.tiktok.com/@npwf?lang=en, or @npwf Marissa's Twitter: @mditkowsky (https://x.com/mditkowsky) Systems Transformation Guides: https://nationalpartnership.org/report/disability-economic-justice-systems-transformation/ The Intersection of Disability and Reproductive Justice - with Morénike Giwa Onaiwu, Rebecca Cokley, Keith Jones, and Heather Watkins: https://disabilityrightsflorida.org/podcast/story/episode_38 Buck v Bell: https://disabilityjustice.org/right-to-self-determination-freedom-from-involuntary-sterilization #FreeBritney and Disability: https://www.hrw.org/news/2021/02/17/freebritney-shines-light-problematic-guardianship-systems How State Abortion Bans Harm Disabled Women: https://nationalpartnership.org/report/state-abortion-bans-harm-disabled-women/ What Disability Reproductive Equity Day Means to Me: https://nationalpartnership.org/what-disability-reproductive-equity-day-means-to-me/ National Women's Law Center's resource about Forced Sterilization of Disabled People in the United States: https://nwlc.org/resource/forced-sterilization-of-disabled-people-in-the-united-states/ American Progress's article ‘Rethinking Guardianship to Protect Disabled People's Reproductive Rights: https://www.americanprogress.org/article/rethinking-guardianship-to-protect-disabled-peoples-reproductive-rights/

For our weekly catch-up with the Labour Party Wire Host Caeden spoke to Carmel Sepuloni about Labour MP Greg Connor's comments on benefit sanctions and the dismantling of parts of the Whaikaha.

Ella Houston's book Advertising Disability (Routledge, 2024) invites Cultural Disability Studies to consider how advertising, as one of the most ubiquitous forms of popular culture, shapes attitudes towards disability. The research presented in the book provides a much-needed examination of the ways in which disability and mental health issues are depicted in different types of advertising, including charity 'sadvertisements', direct-to-consumer pharmaceutical advertisements and 'pro-diversity' brand campaigns. Textual analyses of advertisements from the eighteenth century onwards reveal how advertising reinforces barriers facing disabled people, such as stigmatising attitudes, ableist beauty 'ideals', inclusionism and the unstable crutch of charity. As well as investigating how socio-cultural meanings associated with disability are influenced by multimodal forms of communication in advertising, insights from empirical research conducted with disabled women in the United Kingdom and the United States are provided. Moving beyond traditional textual approaches to analysing cultural representations, the book emphasises how disabled people and activists develop counternarratives informed by their personal experiences of disability, challenging ableist messages promoted by advertisements. From start to finish, activist concepts developed by the Disabled People's Movement and individuals' embodied knowledge surrounding disability, impairments and mental health issues inform critiques of advertisements. Its critically informed approach to analysing portrayals of disability is relevant to advertisers, scholars and students in advertising studies and media studies who are interested in portraying diversity in marketing and promotional materials as well as scholars and students of disability studies and sociology more broadly. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/new-books-network

When Fred Trump III asked his uncle Donald Trump for money to help with his disabled son's medical care, he says the former U.S. president suggested letting the young man die instead. Fred talks to guest host Susan Bonner about the incident and his new book All in the Family: The Trumps and How We Got This Way.

https://linktr.ee/doweknowthem In today's episode, for once we don't have anything too dark, just some TikTok drama. First we discuss Jessi's recent travel fiasco before reacting to a TikTok couple who felt that they missed their flight not due to lack of planning but due to elderly people in wheelchairs that took too long... yeah. Then we move on to more wedding drama but this time regarding an artist who paints live portraits at the reception. Let's just say TikTok ... is not a fan of her work. 00:00 Introduction/Jessi's Travel Fiasco 14:35 Airport Couple Blames Disabled People for Missing Flight 49:56 Wedding Portrait Disaster 1:18:30 We Love the Internet We hope you enjoyed this episode! Please let us know on Twitter or Instagram if you have any topic suggestions for next Sunday! (@lily_marston & @jessismiles__) Business Inquiries: doweknowthempodcast@gmail.com

Emma Tracey interviews representatives from all the major parties to find out what they are pledging when it comes to disability and mental health, ahead of the general election on 4 July.In this edition, we hear from Mims Davies, the Minister for Disabled People, Health and Work for the Conservative Party. Kate Lamble, from More or Less, a Radio 4 programme all about numbers, also offers some analysis on how the plans add up.Production: Daniel Gordon, Alex Collins and Natasha MayoSound recording and editing: Dave O'NeillEditors: Farhana Haider and Beth RoseAt the time of recording, all the statistics provided by the Disability Policy Centre, around the number of disabled candidates were correct. The DPC says it will continue to collate the information and will have a final tally shortly after the election.Get in touch, we really want to hear from you. You can email us at accessall@bbc.co.uk or message @bbcaccessall on X or Instagram. Our WhatsApp number is 0330 123 9480, please begin your message with the word ACCESS.

Episode Notes While I am still on my summer hiatus, today we take a look back at E69 of the show and explore why planning for sex is so much more accessible than spontaneity for disabled folks. Enjoy! Episode Sponsors  Clone-A-Willy or Clone-A-Pussy all your own and get 20% off sitewide by using coupon code ANDREWGURZA at Checkout. www.cloneawillycom.  Get 15% off your next purchase of sex toys, books and DVDs by using Coupon code AFTERDARK at checkout when you shop at trans owned and operated sex shop Come As You Are www.comeasyouare.com  Join the Patreon and get the show days early and ad free at www.Patreon.com/disabilityafterdark  This podcast is powered by Pinecast.

Rachel Stevens was one of the founding members of S Club 7, the pop band that took the world by storm in the early 2000s. She joins Anita to talk about her memoir Finding my Voice: A story of strength, belief and S Club, which covers her time in the hit-making band, her solo career and what it's been like being in the public eye.In a special extended 90 minute programme, Nuala McGovern hosted the Woman's Hour Election Debate. Senior women from the main political parties of Great Britain outlined their priorities for women and answered your questions.Taking part were: Scottish National Party spokesperson for Consular Affairs and International Engagement Hannah Bardell; Reform UK candidate Maria Bowtell; Green Party spokesperson for Housing and Communities Ellie Chowns; Deputy Leader of the Liberal Democrats Daisy Cooper; Conservative Minister of State for Disabled People, Health and Work Mims Davies; Labour's Shadow Minister for Industry and Decarbonisation Sarah Jones and Plaid Cymru's Westminster Leader Liz Saville Roberts.Actor Jill Halfpenny has starred in popular TV series such as Byker Grove, Coronation Street, EastEnders and The Cuckoo. She won an Olivier Award for her role in the musical Legally Blonde and she won the second series of BBC 1's Strictly Come Dancing. But, two tragic events have framed Jill's life story; when she was four years old her dad died suddenly of a heart attack. Then in 2017, in similarly tragic circumstances, her partner Matt died. Jill talks to Clare about confronting her grief head-on, something she examines in her new book, A Life Reimagined.For over a century, many Americans believed that interracial marriage was illegitimate and until the late 1960s, the American legal system supported that belief. Wedding Band: A Love/Hate Story in Black and White is a play written in the 1960s that explores the impact of these laws. Anita is joined by Monique Touko, the director of a new production of the play, and American historian Dr Leni Sorensen who had a black father and white mother in 1940s California.Can you ever really be just best friends with the love of your life? Laura Dockrill talks to Nuala about the thrills and awful heartache of first love, the inspiration for her first adult novel, ‘I love you, I love you, I love you.'Presenter Clare McDonnell Producer: Annette Wells Editor: Louise Corley

In a special extended 90 minute programme, Nuala McGovern hosts the Woman's Hour Election Debate. Senior women from the main political parties of Great Britain outline their priorities for women and answer your questions. Taking part are: Scottish National Party spokesperson for Consular Affairs and International Engagement Hannah Bardell; Reform UK candidate Maria Bowtell; Green Party spokesperson for Housing and Communities Ellie Chowns; Deputy Leader of the Liberal Democrats Daisy Cooper; Conservative Minister of State for Disabled People, Health and Work Mims Davies; Labour's Shadow Minister for Industry and Decarbonisation Sarah Jones and Plaid Cymru's Westminster Leader Liz Saville Roberts.

Rishi Sunak finally ‘got Rwanda done' after a long and dramatic night as his Safety of Rwanda Bill ping-ponged between the Common and the Lords. Our guest, the Green MP Caroline Lucas, tells Coco what it was like to be in Westminster that night and criticises Rishi Sunak for holding a drinks party while the Bill - which she describes as “a piece of performative cruelty” - was still being debated in the Lords. She also discusses her new book about why the left needs to speak up for ‘Englishness', and explains why she's training to become a death doula.Nish and Coco provide an indispensable guide to next week's local elections, talking about why they're important and analysing what they might mean for Tory and Labour prospects at a general election. They also discuss whether the new rules on voter ID are an attempt by the Conservative Party to suppress the vote.For our hero and villain of the week, Nish is appalled by Rishi Sunak's attack on the sick and disabled, while Coco has been enjoying The Menstrual Cramps! Plus what would happen if Nish and Rishi Sunak met at notorious Berlin club Berghain?Pod Save the UK is a Reduced Listening production for Crooked Media. Contact us via email: PSUK@reducedlistening.co.ukWhatsApp: 07494 933 444 (UK) or + 44 7494 933 444 (internationally)Insta: https://instagram.com/podsavetheukTwitter: https://twitter.com/podsavetheukTikTok: https://www.tiktok.com/@podsavetheukFacebook: https://facebook.com/podsavetheukYouTube: https://www.youtube.com/podsavetheworldGuest:Caroline Lucas, Green MP for Brighton PavillionAudio credits:parliamentlive.tvSky News Useful links:https://www.electoralcommission.org.uk/voting-and-elections/voter-idhttps://www.bethknight.com/https://crooked.com/podcast-series/pod-save-america/