Podcasts about Disability

When life doesn't go as planned, it can be hard to see where God is working. In this powerful conversation, Sandra Peoples, author, special needs mom, and ministry leader,  opens up about her journey from growing up with a sister with Down syndrome to parenting a son with autism. Sandra shares how her family's story revealed a gap in the church for families impacted by disability, and how God called her to help fill it. From starting a special needs ministry to creating sensory rooms and buddy systems, Sandra offers practical and spiritual wisdom for pastors, volunteers, and parents alike. Here is some of what we cover:  Disability families are often unreached — the church has an incredible opportunity to serve and love them. Support for the whole family — offer counseling, respite nights, and peer connection for parents and siblings. The church should be a whole picture of the body of Christ including those with disabilities who often enter into worship in the most beautiful ways.  What questions to ask your friends who are hesitant to come to church with their special needs child.  Hope for the mom that feels unseen or hopeless. Psalm 126:5- Those who sow in tears shall reap with shouts of joy! Connect with Sandra Peoples Website: Sandra Peoples: Equipping Churches and Encouraging Families Instagram: Sandra Peoples (@sandrapeoples) Facebook: Sandra Peoples Links Mentioned:   Accessible Church: By Sandra Peoples Held: Learning to Live in God's Grip: By Sandra Peoples Unexpected Blessings: By Sandra Peoples 99 Balloons Related Episodes: Adopting Special Needs :: Alice and Candace [Ep 213] Mothering Autism: Navigating Grief, Marriage, and Community :: Carrie Cariello, Kate Swenson, and Adrian Wood [Ep 515] Parenting Neurodivergent Children–Summer Edition :: Carrie Cassell [Ep 413] Featured Sponsors:  Thrive Causemetics: Complete your fall look. Go to thrivecausemetics.com/DMA for an exclusive 20% off your first order.  StoryWorth Memoirs: Give your loved ones a unique keepsake you'll all cherish for years–Storyworth Memoirs! Right now, save $10 or more during their Holiday sale when you go to storyworth.com/dma !

Over half the employees at the Substance Abuse and Mental Health Services Administration (SAMHSA) who were there in January are now gone, include 12 of the 17 senior leaders. SAMHSA is in charge of distributing and administering mental health programs around the country and the cuts to both staffing and to the programs the agency serves have meant many programs addressing addiction and suicide prevention being severely hobbled or shutting down altogether. In turn, that means fewer people getting help and more people suffering. O. Rose Broderick, Disability and Healthcare Reporting Fellow at Stat, joins us to explain the cuts, why they may be happening, and the extremely fragile state of these programs in America today. Rose also share her own connection to mental health, the struggles her own family has endured, and why all mental health stories are, at their heart, personal matters.Thank you to all our listeners who support the show as monthly members of Maximum Fun.Check out our I'm Glad You're Here and Depresh Mode merchandise at the brand new merch website MaxFunStore.com!Hey, remember, you're part of Depresh Mode and we want to hear what you want to hear about. What guests and issues would you like to have covered in a future episode? Write us at depreshmode@maximumfun.org.Depresh Mode is on BlueSky, Instagram, Substack, and you can join our Preshies Facebook group. Help is available right away.The National Suicide Prevention Lifeline: 988 or 1-800-273-8255, 1-800-273-TALKCrisis Text Line: Text HOME to 741741.International suicide hotline numbers available here: https://www.opencounseling.com/suicide-hotlines

Let's do a quick review of disability insurance!  In this episode of Financial Clarity for Doctors, hosts Rachelle Vanderzanden and Corey Janoff dive into the details of long-term disability insurance.  This coverage is very important for anyone who is still reliant on their income. Discussion topics include: When and why you need this insurance. Different kinds of disability insurance. Details of long-term disability including a breakdown of many common riders. A comparison of employer/group coverage vs. individual coverage. How to apply for coverage. When you may need to increase your coverage and when it's okay to cancel it. No one likes paying for insurance, but insurance allows you to share some larger financial risks with a third party.  Disability insurance is a great example of that.  Most of us feel invincible until we're not. For more financial planning tips from Corey and Rachelle, you can reach out to them at podcast@thefinitygroup.com. They would love to hear your questions and ideas for upcoming episodes. Discussions in this show should not be construed as specific recommendations or investment advice. Always consult with your investment professional before making important investment decisions. Securities offered through Registered Representatives of Cambridge Investment Research, Inc., a broker-dealer, member FINRA/SIPC. Advisory services offered through Cambridge Investment Research Advisors, Inc., a Registered Investment Adviser. Finity Group, LLC and Cambridge are not affiliated. Cambridge does not offer tax or legal advice.

Chris (founding editor of the ERB) spoke with first-time podcast guest (and one of our most-frequently mentioned writers!) Kathleen Norris and returning guest Amy Julia Becker, regarding some common themes in their published writing. They speak about disability, what it means to be human, and their experiences accompanying family members with disabilities. Their conversation is humble, sincere, vulnerable and light-hearted, and listeners will find their honest reflections encouraging.Books Mentioned in this Episode:If you'd like to order any of the following books, we encourage you to do so from Hearts and Minds Books(An independent bookstore in Dallastown, PA, run by Byron and Beth Borger) The Cloister Walk by Kathleen NorrisAcedia & Me: A Marriage, Monks & a Writer's Life by Kathleen NorrisDakota: A Spiritual Geography by Kathleen NorrisAmazing Grace: A Vocabulary of Faith by Kathleen NorrisA Good and Perfect Gift: Faith, Expectations & a Little Girl Named Penny by Amy Julia BeckerRebecca Sue: A Sister's Reflections on Faith, Disability & Love by Kathleen NorrisWhen Helping Hurts: How to Alleviate Poverty Without Hurting the Poor...And Yourself by Steve Corbett and Brian FikkertTo Be Made Well: An Invitation to Wholeness, Healing & Hope by Amy Julia BeckerThe Hospitality of Need: How Depending on One Another Helps Us Heal & Grow Together by Kevan Chandler & Tommy SheltonThe Dignity of Dependence: A Feminist Manifesto by Leah Libresco SargeantHow to Read a Book: A Novel by Monica WoodDo Not Judge Anyone: Desert Wisdom for a Polarized World by Isaac SlaterSmall Things Like These by Claire KeeganGhost Trail (film)

It's surprisingly easy for people to think labels don't mean anything, but they can actually be quite powerful.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

Going out in public became dreadfully uncomfortable for 75-year-old Dave Richards after an accident with a drunk driver four years ago in Devon, England. His bike got caught under the car, dragging him on the asphalt, tearing away much of his face, nose and neck. Surgeons had to remove his eye and cover the damaged area with a skin graft. The accident that nearly took his life, took his confidence until a team of experts at the Bristol 3D Medical Centre stepped in. Using advanced 3D scanning, design, and printing, they are rebuilding Dave Richards' face. Misha Newnham is one of the reconstructive scientists at the first of its kind centre in the UK. She explains this remarkable new technology and how it's pushing the boundaries of reconstructive medicine.

Episode Notes In E402, Andrew does another in the Popcorn & Power Chair series as they review the Netflix film 37 Seconds. It's about Yuma, a 23 year old manga artist with Cerebral Palsy trying to find herself, her sexuality and her independence. Listen to find out why Andrew liked this film, but how it could have been deeper too. Enjoy! Episode Sponsors Do you wanna turn b*tt stuff up a notch. Go to bvibe.com and use code AFTERDARK to receive 20% off orders of $100 (including bundles, discounted items and more). Disability content creation doesn't have to be hard. Follow @seated.perspectives on Instagram to learn how to make content creation a gentle, easy, accessible experience. Are you looking for attendant care when you need it at your convenience? Check out your team, on tap www.whimble.ca Get 15% off your next purchase of sex toys, books and DVDs by using Coupon code AFTERDARK at checkout when you shop at trans owned and operated sex shop Come As You Are www.comeasyouare.com Order Notes From a Queer Cripple and hire him to speak on it by e-mailing andrew@andrewgurza.com US: https://us.jkp.com/products/notes-from-a-queer-cripple Canada: https://www.ubcpress.ca/notes-from-a-queer-cripple Support the show with a donation: https://patreon.com/disabilityafterdark This podcast is powered by Pinecast. This podcast is powered by Pinecast.

Australian Senator Jordon Steele-John joins Dylan Alcott and Angus O’Loughlin to share what life is really like inside Parliament as a wheelchair user and one of the few disabled politicians in Australia. From rushing to Senate votes without extra time allowances to reshaping accessibility in politics, Jordon gives a candid and inspiring look at how inclusion, policy, and representation intersect in Australia’s most powerful building. The conversation spans his journey from a 23-year-old Greens candidate from WA to a national advocate for accessibility, neurodiversity, and disability rights. Jordon opens up about moments of misunderstanding on the campaign trail, how his ADHD and cerebral palsy shape his leadership, and why true inclusion starts with “getting our own house in order.” This episode is full of insight, humour, and practical advice for anyone—disabled or not—who wants to create change in their community. Connect with Jordon: https://www.instagram.com/jordonsteelejohn/?hl=en https://www.linkedin.com/in/jordon-steele-john-656ba917a/ Key Topics Life as a Senator with disability Accessibility barriers in Parliament House Ableism in political systems How Parliament handles (or doesn’t handle) disability inclusion The power of lived experience in politics Jordon’s journey to the Senate at age 23 Disability pride and representation ADHD, cerebral palsy, and leadership Advice for young people with disability wanting to enter politics Building collective action for change Quotes “If Parliament is going to make laws that fix accessibility in the community, we’ve got to literally get our own house in order first.” – Jordon Steele-John “People thought I was collecting for charity, not running for office. That moment showed how deeply society equates disability with needing help, not giving leadership.” – Jordon Steele-John “Politics should represent every voice—including people with intellectual and cognitive disabilities. The system can and should be rebuilt to meet everyone’s access needs.” – Jordon Steele-John About Jordon Steele-John Jordon Steele-John is an Australian Greens Senator for Western Australia and the youngest person ever elected to the Australian Senate. A proud disabled man with cerebral palsy and ADHD, Jordon has been a leading advocate for disability rights, climate justice, and inclusive reform since 2017. His work includes helping establish the Disability Royal Commission and pushing for systemic accessibility across Australian institutions. Jordon Steele-John, Dylan Alcott, Angus O’Loughlin, ListenABLE podcast, Australian Parliament accessibility, disability politics Australia, cerebral palsy, ADHD, Greens Senator WA, disability representation, ableism in politics, Disability Royal Commission, inclusion, accessibility reform, disabled leaders, advocacy AustraliaSee omnystudio.com/listener for privacy information.

District 15 State Senator Paul Bailey (R) sent out a press release urging Governor Lee to fund SNAP benefits for Tennesseans after the federal government shutdown, which halted payments November 1st, affecting more than 690,000 Tennesseans - including 20,635 constituents in district 15. Bailey's concerns stem from a firsthand look at the crisis during an October visit to a local food bank, where he witnessed empty shelves and overwhelming demand. "Tennessee had reached crisis mode before November 1st." Bailey highlighting how "the elderly and working-class families struggling to make ends meet," and relatives raising children not their own have already exhausted local food pantries. Tuesday, Governor Lee announced he is directing $5 million dollars in state funding to food banks across Tennessee, with funding coming from TennCare. Previously, the federal government covered half of the $128 million in administrative costs and allocated $145 million in monthly cash benefits to the state. Under the Big Beautiful Bill Act, Tennessee will now shoulder half of the administrative costs and a portion of the benefit expenses. Bailey acknowledges the $5 million allocation is a good start, but warns it may take up to 2 weeks to fully restore SNAP benefits once the federal shutdown ends. Tennessee is currently conducting budget hearings to identify spending reductions to comply with the Big Beautiful Bill Act. Beyond TennCare/Medicaid cuts and the elimination of the ACA healthcare premium subsidies, the most significant federal funding cuts will impact the TANF program which helps low-income families meet basic needs and move toward self-sufficiency, also programs in the Department of Aging and Disability. Newschannel 5+ can be seen of Comcast/Xfinity Ch. 250, Spectrum/Charter Ch. 182 and over the air on Ch. 5.2. Inside Politics also streams live Fridays at 7pm and Saturdays at 3pm on our website: https://www.newschannel5.com/live3 as well as the NewsChannel 5 Now app on Connected TVs through Roku, AppleTV, AndroidTV, etc. The episode will air throughout the weekend on Newschannel 5+ Sat. at 5:30am, 3pm, Sun. at 1am, 9am, 7pm, Mon. at 2:30pm and Tues., 3pm unless pre-empted.See omnystudio.com/listener for privacy information.

Hildegarde Naughton, Minister of State for Disability and Fine Gael TD for Galway West, Sorca Clarke, Sinn Féin TD for Longford-Westmeath and Paul Murphy, People Before Profit TD for Dublin South West.

We hear from Tara Shine, CEO at Change by Degrees on what happened this week at COP 30 and our panel of Hildegarde Naughton, Minister of State for Disability and Fine Gael TD for Galway West, Sorca Clarke, Sinn Féin TD for Longford-Westmeath and Paul Murphy, People Before Profit TD for Dublin South West.

Our panel this week are Hildegarde Naughton, Minister of State for Disability and Fine Gael TD for Galway West, Sorca Clarke, Sinn Féin TD for Longford-Westmeath and Paul Murphy, People Before Profit TD for Dublin South West.

 Decades before the headlines about Tylenol, moms have always had to worry if they were to blame for their child's autism. Sara Luterman, Disability and Aging Reporter for The 19th, joins host Krys Boyd to discuss the so-called “refrigerator moms” of the 1950s, and what today's rhetoric from the Health and Human Services Secretary mean for mothers struggling to navigate a difficult diagnosis. Her article “This isn't the first time moms have been blamed for their kids' autism.”  Learn about your ad choices: dovetail.prx.org/ad-choices

David Rivera has experienced the need for, and benefits of mentoring in his own life, and has applied his lived experiences to setting up a non-profit for mentoring others. Barry and Dave discuss the various benefits of mentoring with David, and specifically, “Mentoring Autistic Minds”, the non-profit he has created that welcomes autistic and otherwise neurodivergent individuals to benefit from a community that provides opportunities for mentoring relationships.Learn more on our websiteSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Your weekly dose of information that keeps you up to date on the latest developments in the field of technology designed to assist people with disabilities and special needs. Special Guest: Erik Jakobs – R and D Engineer – Dept of Communications Sciences and Disorders – Penn State University Website Link: www.accessnavigator.org More on Bridging […]

Send us a textWhen you meet Tracee Garner, one thing is clear—she's unstoppable. A best-selling author of twenty books, a powerful speaker, and a fierce disability advocate, Tracee brings wisdom, humor, and a can-do spirit that inspires everyone she meets.On this episode of The Cultural Curriculum Chat, I had the privilege of diving deep into her story and the lessons she's learned along the way.TraceeTracee Garner's Website: https://traceegarner.com/⭐️ Resources I Recommend:Explore my Cultural Competency Courses & Mini Courses: www.jebehedmunds.comGrab Free Lesson Plans to spark inclusive learning in your classroom: Jebeh Cultural ConsultingSubscribe to my weekly newsletter The Inclusive Educator: https://tremendous-motivator-3920.kit.com/a46bfbcba3Listen to the Cultural Curriculum Chat Podcast: https://podcasts.apple.com/us/podcast/cultural-curriculum-chat-with-jebeh-edmunds/id1548161373

I detta avsnitt kommer vi att träffa Magdalena Fresk, allmänläkare och medicine doktor, som arbetar på Socialstyrelsen och som nyligen har disputerat på en avhandling hur ICF (International Classification of Functioning, Disability and Health) kan användas i sjukskrivningsprocessen. Hon har studerat olika ICF Core Sets i sjukintyg för patienter med muskuloskeletal smärta och depression och även ICF-kodad ”TIPPA” som är ett funktions- och aktivitets bedömningsinstrument för patienter med långvarig sjukskrivning.

Learn how to pick dental, vision, life, and disability coverage with confidence, and when refinancing a home can actually save you money. Is now a good time to refinance your mortgage? Which open enrollment benefits are worth it this year? Hosts Sean Pyles and Elizabeth Ayoola talk to an expert about the ins and outs of open enrollment in 2026. But first, news Nerd Anna Helhoski joins them to share her conversation with NerdWallet mortgage writer Holden Lewis about falling mortgage rates and what they mean for buyers, sellers, and homeowners. They begin with a discussion of refinancing and today's housing market, with tips and tricks on using a refinance calculator, how much of a rate cut to target, weighing closing costs and the break-even timeline, and other smart reasons to refi. Then, benefits expert April Brasher, knowledge advisor at the Society for Human Resource Management (SHRM), joins Sean and Elizabeth to discuss open enrollment choices beyond health insurance. They discuss what dental and vision plans usually cover and what they don't, how and when to add to group life insurance provided by some workplaces, and how disability insurance works. They also discuss when accidental death and dismemberment (AD&D), hospital indemnity, and critical illness policies can make sense, how to avoid being over-insured, and why taking a quick personal and financial inventory before enrollment deadlines helps you choose only what you need. Want us to review your budget? Fill out this form — completely anonymously if you want — and we might feature your budget in a future segment! https://docs.google.com/forms/d/e/1FAIpQLScK53yAufsc4v5UpghhVfxtk2MoyooHzlSIRBnRxUPl3hKBig/viewform?usp=header In their conversation, the Nerds discuss: mortgage rates, refinance mortgage, refinance break-even, FHA mortgage insurance, remove FHA MIP, conventional vs FHA loan, housing market outlook, best time to buy a house, home buying season, mortgage closing costs, homeowners insurance shopping, lower mortgage payment, Fed rate cuts, housing inventory, open enrollment, dental insurance, vision insurance, life insurance through employer, supplemental life insurance, beneficiary designation, evidence of insurability, AD&D insurance, disability insurance, short-term disability, long-term disability, own occupation vs any occupation, hospital indemnity insurance, critical illness insurance, high deductible health plan, and limited purpose FSA. To send the Nerds your money questions, call or text the Nerd hotline at 901-730-6373 or email podcast@nerdwallet.com. Like what you hear? Please leave us a review and tell a friend. Learn more about your ad choices. Visit megaphone.fm/adchoices

"Being part of something is an essential human need. When you feel excluded, it becomes a real barrier in life. Don't be too afraid to say the wrong thing. Be more focused on asking the right questions." —Hannah PonsfordWhen you're seen as different, every day can feel like an uphill climb—and those closest to you often hurt quietly alongside, trying to bridge two worlds but unsure how. The longing for real acceptance and togetherness runs deep on both sides, and too often, everyone ends up feeling alone.Hannah Ponsford knows this from both sides, having grown up as the sister of someone with a disability and later becoming an advocate and storyteller. She is passionate about spreading the message that small acts of openness and support can nurture true belonging—for everyone involved. Expect real talk about family ups and downs, navigating awkward moments, tips for more welcoming communities, powerful advocacy, school hurdles, and how small actions ripple outward—listen for stories and insights that prove everyone deserves to belong. Connect with Heather: WebsiteFacebook InstagramLinkedInEpisode Highlights:02:24 Living with a Disability in the Family07:08 Breaking the Ice: Social Awkwardness Around Disabilities13:26 Unmasking “Wholesome”— Misconceptions and Social Labels18:16  The Cost of Exclusion: Why Inclusive Schools Matter22:53 Advice to Siblings: Balancing Care, Guilt, and Personal Dreams24:15 Parent Power: What Moms Need to Hear28:08 Our Kind of Normal Resources:

This is an episode all about the media access awards

In this deep and authentic episode of BUILD, Stephen Scoggins sits down with singer-songwriter and speaker Chris Hendricks for an unforgettable conversation on faith, purpose, vulnerability, and the power of community through music.   Chris opens up about living with cerebral palsy, rediscovering his calling, and building a music movement centered around authenticity and impact — not fame or algorithms. Together, Stephen and Chris explore what it means to turn affliction into artistry and pain into purpose.   From battling cerebral palsy to building Perfectly Afflicted and launching the Be Yourself movement, Chris's story is a powerful reminder that your scars are not signs of weakness — they're the evidence of your strength.   We cover: Music is ministry — art becomes powerful when it serves. Your difference is your advantage. Disability is not limitation — it's adaptation and empathy in motion. The future of music is community-powered and purpose-driven.   Chris also treats us to 2 amazing songs so tune in and get inspired!   Know more about Chris Hendricks: https://www.iamchrishendricks.com/ Connect with Chris and follow: IG iamchrishendricks  

What if our well-intentioned efforts to promote mental health inadvertently perpetuate systems that cause mental unwellness? What if the resilience we encourage only equips individuals to endure rather than challenge structures detrimental to their well-being? Why do mental health experiences vary so drastically across cultures, with Western societies seemingly posing the greatest challenges for certain conditions? Against the backdrop of escalating ecological dramas that devastate our world and its climate, do we ever wonder what ecological suffering might imply for our mental health? With this poignant, impassioned book Seeking Sanctuary, Finding Shalom, John Swinton invites us to begin exploring avenues toward addressing these daunting and interrelated issues. John Swinton is a consulting faculty member at Duke Divinity and professor in practical theology and pastoral care and chair in divinity and religious studies at the University of Aberdeen in Scotland. For more than a decade he worked as a registered mental health nurse. He also worked for a number of years as a hospital and community mental health chaplain alongside of people with severe mental health challenges who were moving from the hospital into the community. In 2004, he founded the University of Aberdeen's Centre for Spirituality, Health, and Disability. He has published widely within the area of mental health, dementia, disability theology, spirituality and healthcare, end-of-life care, qualitative research, and pastoral care. Swinton is the author of a number of monographs including a previous book, Finding Jesus in the Storm: The Spiritual Lives of People With Mental Health Challenges (Eerdmans 2020), which won the Aldersgate book price for interdisciplinary theological research, and his book Dementia: Living in the Memories of God, which won the Archbishop of Canterbury's Ramsey Prize for excellence in theological writing. Swinton is a fellow of the Royal Society of Edinburgh and was recently elected as a fellow of the British Academy.

A Clare teaching representative says online bullying is becoming increasingly difficult for schools to tackle. A new UCD report published by the Department of Children, Disability and Equality has found that bulling and family diversity are "significant risks to a child's emotional development and wellbeing". The findings also state that screen time has "increased markedly" for children between the years of 2008 and 2024, with increased time with technology associated with lower levels of wellbeing and physical activity. INTO Rep for Clare, Principal of Sixmilebridge National School Gareth Heagney, says the prevalence of online incidents is a "huge" societal issue.

A Clare teaching representative says online bullying is becoming increasingly difficult for schools to tackle. A new UCD report published by the Department of Children, Disability and Equality has found that bulling and family diversity are "significant risks to a child's emotional development and wellbeing". The findings also state that screen time has "increased markedly" for children between the years of 2008 and 2024, with increased time with technology associated with lower levels of wellbeing and physical activity. INTO Rep for Clare, Principal of Sixmilebridge National School Gareth Heagney, says the prevalence of online incidents is a "huge" societal issue.

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

Have a comment or question? Click this sentence to send us a message, and we might answer it in a future episode.Welcome to Season 5, Episode 37 of Winning Isn't Easy. In this episode, we'll dive into the complicated topic of "Own Occupation vs Any Occupation: Breaking Down Disability Claim Stages."Most people think that winning an ERISA disability claim comes down to proving you're sick or injured enough to stop working. But that's only half the battle. The real fight often happens on the work side of your claim - where insurance carriers dissect your job duties, analyze your skills, and argue that you can still perform “other work,” even if you can't do your old job. In this episode of Winning Isn't Easy, disability law expert Nancy L. Cavey breaks down how carriers use vocational analysis to deny claims - and what you can do to stay one step ahead. You'll learn how insurers evaluate your own occupation versus any occupation, and why these two stages can dramatically change the outcome of your case. Nancy walks through the eight key questions carriers ask, from assessing your residual functional capacity and physical strength to determining how your skills might “transfer” to other jobs. You'll also discover how labor market surveys, transferable skills assessments, and vague job descriptions can be used to distort your work history - and how to push back with detailed, accurate evidence. By the end, you'll understand why your medical records alone aren't enough, and how clear documentation of your job duties, limitations, and vocational profile can make or break your claim. When it comes to ERISA disability claims, knowing how your work is evaluated is just as important as knowing your diagnosis. Because when carriers twist the definition of “work,” you need to be ready to defend the truth. Winning Isn't Easy, but with insight, preparation, and the right strategy, you can protect your benefits and your future.In this episode, we'll cover the following topics:One - The First Four Questions - Proving Disability at the Own Occupation StageTwo - The Next Four Questions - Skills, Transferability, and the Labor MarketThree - The Any Occupation Stage - A Tougher StandardWhether you're a claimant, or simply seeking valuable insights into the disability claims landscape, this episode provides essential guidance to help you succeed in your journey. Don't miss it.Listen to Our Sister Podcast:We have a sister podcast - Winning Isn't Easy: Navigating Your Social Security Disability Claim. Give it a listen: https://wiessdpodcast.buzzsprout.com/Resources Mentioned in This Episode:LINK TO ROBBED OF YOUR PEACE OF MIND: https://mailchi.mp/caveylaw/ltd-robbed-of-your-piece-of-mindLINK TO THE DISABILITY INSURANCE CLAIM SURVIVAL GUIDE FOR PROFESSIONALS: https://mailchi.mp/caveylaw/professionals-guide-to-ltd-benefitsFREE CONSULT LINK: https://caveylaw.com/contact-us/Need Help Today?:Need help with your Long-Term Disability or ERISA claim? Have questions? Please feel welcome to reach out to use for a FREE consultation. Just mention you listened to our podcast.Review, like, and give us a thumbs up wherever you are listening to Winning Isn't Easy. We love to see your feedback about our podcast, and it helps us grow and improve.Please remember that the content shared is for informational purposes only, and should not replace personalized legal advice or guidance from qualified professionals. 

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

In this episode, Pete Horsley, Founder of Remarkable, the disability-tech accelerator powered by Cerebral Palsy Alliance, joins Peta to explore how technology, innovation, and lived experience are reshaping the future of accessibility. Over the past decade, Pete and his team have supported more than 160 startups developing technologies that change disabled people’s everyday lives. Through Remarkable’s partnership with Toyota Australia, the program now contributes over 2,000 hours of engineering and design expertise each year; proving what’s possible when big business and disability innovation truly collaborate. Pete and Peta discuss how inclusive design benefits everyone, and why disability should never be seen as a niche market. They also unpack how government policy could help stimulate demand for disability-led products and share what to expect from the upcoming Disability Tech Summit 2025. Connect: Remarkable: Disability Tech Summit 2025: https://www.remarkable.org/disability-tech-summit-2025Website: remarkable.orgInstagram: @remarkable_tech https://www.toyota.com.au Peta Hooke:Instagram: @petahookeWebsite: www.icantstandpodcast.comEmail: icantstandpodcast@gmail.com Episode Transcript:www.icantstandpodcast.comSee omnystudio.com/listener for privacy information.

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

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

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

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

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

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

In episode 152 of the Federal Retirement Show, Val is breaking down everything federal employees need to know to retire with confidence and peace of mind. Whether you’re just a few months from your retirement date or planning years ahead, this discussion is packed with expert insights and practical steps to help you prepare. Val covers: Proper advice for retiring federal employees — from understanding your retirement eligibility to maximizing your benefits. Completing retirement paperwork on time — what forms you’ll need, how far in advance to file, and tips to avoid common delays. FEHB and Medicare — how your Federal Employees Health Benefits work with Medicare, and what decisions you’ll need to make before age 65. Setting up your TSP for retirement — managing withdrawals, annuities, and investment strategies to make your savings last. Disability in retirement — understanding options and benefits if disability affects your retirement planning. Have questions about retirement planning or other financial topics? Connect with Val and the topic could be featured in future episodes! Don't forget to leave a review and share this podcast with anyone looking to boost their financial knowledge. --- Listen to Previous Episodes: https://federalretirementshow.com/podcasts/ Subscribe to the show’s YouTube channel: www.youtube.com/@americanbenefitsexchange --- Connect with Val: Phone --- (512) 582-6050 Email --- vmajewski@thinkabx.com American Benefits Exchange --- thinkabx.com Federal Retirement Show --- federalretirementshow.com/podcasts LinkedIn --- https://www.linkedin.com/company/american-benefits-exchange/ --- About American Benefits Exchange: American Benefits Exchange focuses on providing solid financial solutions to Federal, postal, and state employees as well as members of the United States Armed Forces and small businesses. American Benefits Exchange brings years of experience and knowledge to support these niche markets. American Benefits Exchange, along with its provider companies, truly understands the needs of civil service employees. A portfolio of products is available to address important financial issues such as planning for retirement, FEGLI Option B replacement, Thrift Savings Plan Rollovers, and Pension Maximization. See omnystudio.com/listener for privacy information.

Vidya Sundar and Debra Brucker, co-principal investigators of the University of New Hampshire's new Disability and Rehabilitation Research Project (DRRP) on Living and Working with Long COVID and Disabilities, funded by the National Institute on Disability, Independent Living, and Rehabilitation Research (NIDLRR), discuss their proposed research activities to be implemented over the next five years. A critical piece of their research is to build on their prior study on the use and impact of “job crafting,” or how individuals can redesign their jobs to better align with their strengths without having to self-identify with a disability and rely on the formal disability accommodation process. To learn more about job crafting, and the other research projects to be implemented relating to people with pre-existing disabilities who have Long COVID, listen to this podcast.

Mason Ameri, associate professor at the Rutgers University Business School, describes how the pandemic has transformed the outlook of disability employment. Tight labor markets have demonstrated an increased willingness by employers to have remote workers, and people with disabilities are helping meet this demand. However, the growth of telework is more likely in white collar jobs, and workers with disabilities are more concentrated in blue collar jobs and service positions. There is a need for more research to understand how employers can restructure jobs where nonessential tasks are done remotely as well as increased understanding of remote work as a reasonable accommodation under the ADA with other supports that make that possible. There remain unanswered questions as to whether remote workers will be put to a different standard in proving performance necessary for career advancement, challenged by less real time interaction face-to-face with supervisors.

Ari Ne'eman, doctoral candidate in health policy at Harvard University, says that the numbers demonstrate the extraordinary impact the COVID-19-induced shift to expanded telework had on the employment opportunities for people with disabilities, but even those don't tell the complete story regarding what remote work means for disability employment. It is a situation reflective of the gains prospective employees with disabilities experienced because of the pandemic and the parallel economic recession, Ari Ne'eman, doctoral candidate in health policy at Harvard University, says in this episode. The overnight shift to remote work for much of the general workforce because of the pandemic has made it more difficult for employers to argue that physical presence in the workplace is an essential component in job duties, Ne'eman points out, and this is the essence of how disability employment has benefited from remote work. That deconstruction of the perceived importance of physical presence in the workplace needs to be normalized.

Jay Burks, Director of Supplier Diversity at the Comcast Corporation, shares about the importance of ensuring that large companies like Comcast buy goods and services from diverse suppliers, including Disability-owned Business Enterprises (DOBEs).

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

Voice actor Maria Pendolino joins Lily for an episode that challenges the narrow way society views disability. Maria shares her experiences as an ambulatory mobility-aid user, explaining how fluctuating conditions are often misunderstood or erased in media and medicine. With candid honesty, she connects her journey of psoriatic arthritis, knee replacements, and self-advocacy to building a career that truly works for her body, through voiceover and a fully accessible home studio.The conversation also takes on fat bias in healthcare, how outdated tools like BMI continue to be used to deny or delay care, and the scripts Maria uses to set boundaries in appointments. Her message: you deserve to be treated as a whole person, not reduced to a number or assumption.Maria details the creation of the Disabled Voice Actors Directory, now housed under the National Association of Voice Actors, which helps casting directors find authentic talent. It's a resource born out of a belief that disabled people don't just deserve representation on-screen, they should be hired behind the microphone, too.Key Moments02:50 Breaking the myth of disability as “all or nothing”06:02 What fluctuating disability really looks like in practice14:16 Age bias in surgery: when doctors refuse joint replacements under 5021:31 Why BMI is flawed and how it blocks real care29:46 Self-advocacy scripts: “I will not be weighed”42:34 The audition turning point: “Are you limping?”46:54 Building an accessible home studio and thriving as a voice actor54:11 Founding the Disabled Voice Actors Directory1:04:11 Know the Facts: fat phobia and systemic barriersConnect with Maria PendolinoWebsite: https://www.voicebymaria.com/ YouTube: https://www.youtube.com/channel/UCGkmvgiBP89fHUl9-8awQRA/videos Maria Pendolino - London Voice Over: https://www.londonvoiceover.com/artists/maria-pendolino/ Maria Pendolino - London Voice Over: https://voice123.com/voice-actor/voicebymaria 

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

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

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

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

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

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

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

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