Podcasts about Disability

See behind the scenes of Joni's portrait of depression here. --------Thank you for listening! Your support of Joni and Friends helps make this show possible. Joni and Friends envisions a world where every person with a disability finds hope, dignity, and their place in the body of Christ. Become part of the global movement today at www.joniandfriends.org. Find more encouragement on Instagram, TikTok, Facebook, and YouTube.

Send Us Your Prayer Requests --------Thank you for listening! Your support of Joni and Friends helps make this show possible. Joni and Friends envisions a world where every person with a disability finds hope, dignity, and their place in the body of Christ. Become part of the global movement today at www.joniandfriends.org. Find more encouragement on Instagram, TikTok, Facebook, and YouTube.

A Joni and Friends Family Retreat is a little slice of heaven on earth! Learn how you be part of providing a Christ-centered, accessible week of respite for families living with disability here. --------Thank you for listening! Your support of Joni and Friends helps make this show possible. Joni and Friends envisions a world where every person with a disability finds hope, dignity, and their place in the body of Christ. Become part of the global movement today at www.joniandfriends.org. Find more encouragement on Instagram, TikTok, Facebook, and YouTube.

This week, Qudsiya speaks with Professor Jamelia Morgan, an award-winning and acclaimed scholar and teacher at the Northwestern Pritzker School of Law, where she also directs the Center for Racial and Disability Justice. Professor Morgan's work focuses on the intersection of race, gender, disability, and criminal law and punishment. Qudsiya and Jamelia talked about her personal path to studying these issues, the particular harms that people of color with disabilities face when it comes to policing and mass incarceration, and her transformative vision for a world that prioritizes justice and inclusion over violence and punishment.--Let us know what you think with a comment or review!Visit our website⁠ ⁠for⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ transcripts⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠.⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ Subscribe to Qudsiya's Substack, ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Getting Down To It⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ Support the team behind the podcast ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠with a donation⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠

At least 10 percent of parents in the U.S. are disabled, but Andrea can't seem to find parenting advice on disability and accessibility. On this episode of How To!, Carvell Wallace brings on Jessica Slice, author of the new book Unfit Parent: A Disabled Mother Challenges an Inaccessible World, to help Andrea reimagine parenthood.  If you liked this episode check out: How To Date With a Disability and How To Become a Parent Overnight.  Do you have a problem that needs solving? Send us a note at howto@slate.com or leave us a voicemail at 646-495-4001 and we might have you on the show. Subscribe for free on Apple, Spotify, or wherever you listen. How To! is produced by Rosemary Belson, with Kevin Bendis. Our technical director is Merritt Jacob and our supervising producer is Joel Meyer. Learn more about your ad choices. Visit megaphone.fm/adchoices

Guardian journalist Archie Bland describes the day his seven-week-old son stopped breathing, and the life he has led in the two years since. Help support our independent journalism at theguardian.com/infocus

DONATE to the Sam Allen Scholarship: details coming soon--check back later :)APPLY for the Sam Allen Scholarship: https://dbatvirginiabeach.com/index.php/sam-allen-scholarshiphttps://elizabethrivertrail.org/https://www.shoelesspodcast.com/season-three/02

Find out why the weak are indispensable by listening to this radio program. -------- 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.

In this Memorial Day episode of Hope for the Caregiver, I open up about one of the hardest—and most overlooked—struggles caregivers face: resentment. After more than 40 years in this journey, I've learned that it's not just the physical exhaustion that wears us down—it's the internal striving, the bitterness, and the sense of being forgotten. In this episode, I talk about: The difference between sleep and true rest Why striving leaves us drained and bitter A quote from my new book, A Caregiver's Companion, and the hymn that goes with it How gratitude becomes the antidote to resentment And what one surprising verse in Matthew 1:6 reveals about God's justice, memory, and hope for caregivers I also share a story from the hospital room—something small, but sacred—that brought the Gospel into sharp focus for me. If you're weary, grieving, or stuck in resentment, I hope this message will point you toward the rest only Christ can give.

Influencers are using AI filters to appear to have Down Syndrome in order to promote their OnlyFans. If you think that's gross, wait till you hear the Liver King talking about the first time he ejaculated. Plus, JoJo (not that one) wrote a memoir.Video episodes, bonus episodes and our premium series WAWU—we're currently covering The Osbournes—are on Patreon.Pot Psych merch is available at Pipe Dreams.Check out potential drama and our Diamond Girls on our Instagram. ★ Support this podcast on Patreon ★

Visit the Radio Ministry online to find the photos Joni mentioned in today's program. --------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.

As a mental health educational professional advocate, and as a black autistic mother of neurodivergent children, Dr. Destiny Huff brings her extensive knowledge of the law, her in depth, understanding of educational systems, and on the ground experience to her work. Destiny, Barry and Dave discuss the challenges that all parents face, but especially parents of color, in advocating for their child, while navigating the complications caused by various roles that parents may play in the process of interfacing with educational systems.Find out more on our websiteSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

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: Kimberly Cline – Director of Sales USA & Canada – LVI America Inc. Kimberly Email: kimberly.cline@lviamerica.com Kimberly Cell: 702-468-6611 Website: www.lviamerica.com LVI Phone: 888-781-7811 […]

In this episode of the Brain & Life Podcast, co-host Dr. Katy Peters is joined by disability advocate, content creator, and speaker with a focus on accessibility, equity, and innovation in spinal cord injury research Jessie Owen. Jessie is a quadriplegic mother of twins and shares some candid insights on life, parenting, and navigating systemic barriers with humor and authenticity with Dr. Peters. Dr. Peters is then joined by Dr. Shelly Hsieh, attending physician and Assistant Professor, Physical Medicine and Rehabilitation at Montefiore Einstein. Dr. Hsieh's discusses outpatient care for people living with spinal cord injury and related disorders and shares some exciting upcoming treatment options.   Additional Resources Jessie's Story What is Spinal Cord Injury? A Spinal Cord Injury Survivor Opens an Affordable Rehab Center   Other Brain & Life Podcast Episodes on This Topic “Roll with Cole & Charisma" On Building a Life Together as an Interabled Couple How Disability Advocate Wesley Hamilton Became Empowered by Adversity   We want to hear from you! Have a question or want to hear a topic featured on the Brain & Life Podcast? Record a voicemail at 612-928-6206   Social Media: Guests: Jessie Owen @itswheelyjess; Dr. Shelly Hsieh @montefiorehealthsystem Hosts: Dr. Daniel Correa @neurodrcorrea; Dr. Katy Peters @KatyPetersMDPhD

In this episode, Eva and Chloe discuss why and how to set up a disability accommodation policy if your farm employee manual. We get into why and how to use your employee manual to communicate about disability accommodations effectively and equitably with all of your farm employees to promote a healthy workplace while protecting against the risk of a discrimination claim. Recommended Resources:Episode 77: Accommodating Employee Disabilities on the Farm and RanchModel Farm Employee ManualThat's Unreasonable! Making Sense of the ADA on the FarmThis material is based upon work supported by USDA/NIFA under Award Number 2023-70027-40444.

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Police reform advocates in Minneapolis are denouncing the Trump administration's attempt to drop the federal consent decree.And a working group on the human services budget bill at the Minnesota Legislature is meeting privately to iron out differences. As they do, advocates for disabled people in the state held a rally this morning to push against possible cuts for disability waivers.Those stories and more in today's evening news update. Hosted by Emily Reese. Music by Gary Meister.

Guy Harris from AccessiblePRS explains why accessible housing is important, what the key considerations are and how to deliver it well. He also shares his experience of designing his own house as a wheelchair user. Check out the show notes for more information.

The salvation of Christ can reach to the ends of the earth. -------- 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.

Planning a trip to Disney World with a disability? Whether you're traveling with a mobility device, need sensory accommodations, or want to learn more about Disney's Disability Access Service (DAS), we've got you covered.

Figuring out if your multiple sclerosis is changing from the relapsing remitting to the secondary progressive stage can be murky. Signs of progression are discussed like slower walking and worsening memory. The underlying reasons for progression are revealed including nervous system injury, remyelination failure, chronic inflammation and aging. Practical ways to improve progressive symptoms are shared. Successful trials for disease-modifying therapy for secondary progressive multiple sclerosis (SPMS) are highlighted. Tolebrutinib, under expedited review by the FDA, has been shown to slow down progression in SPMS patients by targeting cells in the central nervous system causing chronic inflammation. Introducing our new co-host Jamie Holloman MD from The MS Center for Innovations in Care!  Dr. Holloman completed in neurology residency at Washington University, followed by a 3-year fellowship at the Cleveland Clinic.  He interviews: Christopher Laganke MD, Founder of the Joanne P. LaGanke MS Center, Cullman, Alabama Barry Singer MD, Director of The MS Center for Innovations in Care, Missouri Baptist Medical Center, St. Louis    

What could you achieve if you let go of all excuses and limiting beliefs? In this deeply motivational episode, Nicole Jansen welcomes Lawrence “Stoney” Stone—a remarkable martial arts grandmaster, published author, stunt coordinator, rock band singer, and cancer survivor whose life story is anything but ordinary. Born with congenital hip problem, later with CMT (Charcot-Marie-Tooth Neuropathy) a degenerative nerve disease, Stoney has faced significant physical challenges since birth, yet has refused to let them define or limit him. From building future champions in his dojo to serving as an executive protection consultant, Stoney's impact ripples across countless lives and disciplines. Join us as Stoney opens up about the powerful lessons learned from his “spanking grandma,” and his real-life journey of overcoming adversity with purpose, faith, and fierce love. He shares how mentorship, tough love, a sense of responsibility, and unwavering honesty have fueled his legacy—prompting us all to step up, stop making excuses, and love with conviction. Whether you're searching for inspiration, seeking actionable leadership insights, or grappling with challenges of your own, this conversation will leave you empowered and ready to tackle whatever comes next. What We Discuss in This Episode How did Stoney overcome significant physical limitations to become a martial arts grandmaster and mentor to champions? What role did family and “tough love” play in shaping his unstoppable mindset? How do you guide others—especially young people—out of victimhood and toward responsibility and growth? What does it mean to “not own” your challenges or diagnoses? How can leaders and mentors balance empathy with calling others to greatness? Why is authenticity and emotional expression crucial for true leadership? What does it look like to surrender to purpose and let go of micromanaging your life's plan? How do faith and spirituality underpin resilience and transformation? What lasting advice does Stoney offer for living a meaningful, impactful life? 10 Key Takeaways Lead by Example: Young people and mentees learn most from who you are and what you do—not just what you say or teach. Tough Love Builds Resilience: Support combined with high expectations (“spanking grandma”) pushes us to unprecedented growth. Refuse to “Own” Limitations: Don't take on negative identities around illness or labels—claim victory and move forward. Surround Yourself with Greatness: Your environment and your circle shape your possibilities and determination. Your Challenges Are Your Strength: Facing adversity builds the grit and wisdom necessary to help others. Balance Compassion and Accountability: True mentors love fiercely AND hold people to a higher standard. Embrace Vulnerability: Emotional honesty and caring openly are strengths, not weaknesses, for leaders. Purpose Over Perfection: Focus on finding and fulfilling your unique design rather than achieving flawlessness. Take Responsibility: We must model and teach personal responsibility; excuses perpetuate victimhood and stagnation. Keep Growing and Giving: Growth is a lifelong journey—keep learning, serving, and evolving no matter your stage or circumstances. Favorite Quotes "I've never really relied on or counted on being different. I've never been afraid to stand in front of people and tell them I care. And that makes a difference." — Lawrence Stone "Because I didn't know I was different, because I didn't accept that—I'm just me. I love me. I love what I do. I love who I am, where I am, and why I am." — Lawrence Stone "If I don't believe in me, how can I expect someone else to believe in me? You have to believe in yourself first, no matter what the world says." — Lawrence Stone This episode is a rich tapestry of wisdom, humor, and heart. Tune in—and rediscover what's possible when you stop making excuses and start living your purpose. Episode Show Notes: https://leadersoftransformation.com/podcast/mindset/535-unbreakable-spirit-the-inspiring-journey-of-martial-arts-grandmaster-lawrence-stone/ Check out our complete library of episodes and other leadership resources here: https://leadersoftransformation.com ________

Josh and Amelie discuss various situations where people have limits to savings amounts due to governmental programs such as Medicaid or Disability. Top takeaways: Many of the limits are state-specific. Figure out what someone in this situation would need an emergency fund for–it might be fewer things than you think. Do not think of “savings” as a monolith–each individual problem should be tackled individually. ABLE accounts are similar to retirement accounts except that they're for disabled people and their families to be able to pay for specific expenses. Want help building or growing a successful financial coaching business? Find resources below based on where you're at in your journey: - Deciding whether Financial Coaching is right for you? Join our free Facebook Community with over 5000 current and aspiring financial coaches! https://www.facebook.com/groups/financialcoachescommunity - Already decided you're going to be a Financial Coach and want to learn more? Get 30+ tips and best practices in our free 8-part email series! https://www.financialcoachesnetwork.com/pre-launch-email-series - Ready to Launch your Financial Coaching business? Join FCN Launch, our step-by-step program that will help you successfully launch your business in four months and grow it to a consistent part-time income. https://www.financialcoachesnetwork.com/launch - Are you already coaching clients and want to grow your business to a full-time income? Join FCN Grow, our program that helps you scale your business to a full-time income. https://www.financialcoachesnetwork.com/grow

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 18 of Winning Isn't Easy. In this episode, we'll dive into the complicated topic of "Should Your Workers' Compensation Records Be Part of Your ERISA Disability Carrier's File."What seems like a routine paperwork decision could quietly sabotage your ERISA Long-Term Disability claim. Join attorney Nancy L. Cavey, a nationally recognized expert in disability law, as she explores a critical - but often misunderstood - question: should your workers' compensation records be included in your ERISA disability file? It's not just red tape. When both claims stem from the same injury or illness, what goes into your file - and what stays out - can shape the entire outcome of your case. We'll examine how the two systems interact, why adding workers' compensation records might work for you in some cases but backfire in others, and the troubling reality of selective use: when insurers cherry-pick damaging details from your records but leave out the parts that could actually help you. This is one of those behind-the-scenes moves that can define your financial future - and most claimants never see it coming. Tune in to learn how to navigate this legal gray area, avoid common traps, and make informed decisions about what belongs in your disability file.In this episode, we'll cover the following topics:One - The Relationship Between Workers' Compensation and ERISA Disability ClaimsTwo - When Workers' Compensation Records Help or Hurt Your ERISA ClaimThree - The Problem of Selective Omission by Disability CarriersWhether 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. 

As part of the 2025 Developmental Disabilities Conference, Sneha Dave talks about future healthcare as young adults with chronic and rare medical conditions grow older. Series: "Developmental Disabilities Update" [Health and Medicine] [Show ID: 40606]

As part of the 2025 Developmental Disabilities Conference, Season Goodpasture, Founder and Executive Director, Acorns to Oak Trees, talks about improving access and equity in tribal communities. Series: "Developmental Disabilities Update" [Health and Medicine] [Show ID: 40607]

The waiting list for assessments of need is expected to soar to almost 25 thousand by the end of the year, according to new figures from the HSE. We get rection to this with Alan Kelly Labour TD who obtained the figures.

What beliefs, hopes, worries, and questions would you have if your unborn baby was given a diagnosis of a disability? It's something retired paralympic swimmer Ellie Simmonds has spent a lot of time considering.In this chat with Fearne, Ellie explains what she's learnt from talking to both her parents and her birth mum about their experience of her dwarfism, as well as debating the pros and cons of modern genetic testing.They also chat about Ellie's decision to retire from swimming: how will you know when it's time to call something quits, and how can you then cultivate new passions? Plus, how to untangle self-worth and self-esteem from achievements...Ellie Simmonds: Should I Have Children? will be available to watch on ITV from the 27th of May.CONTENT WARNING: This episode contains frank chat about baby loss and abortion, so do take care while listening.If you liked this episode of Happy Place, you might also like:Liberty MillsSophie MorganSamantha Renke Hosted on Acast. See acast.com/privacy for more information.

Learn why it’s important to be aware of the needs of people with disabilities (and their families) when providing end-of-life and bereavement care. My guest Carrie Batt is an end-of-life doula and the founder of SEOL Care which offers disability-competent end-of-life care, support and planning for people with a disability and their families. She advocates… Continue reading Ep. 501 Disability-Informed End-of-Life Care with Carrie Batt

Dr. Susan Kansagra, ASTHO Chief Medical Officer, provides updates on Measles and the Avian Flu; Dr. Ralph Alvarado, Commissioner of the Tennessee Department of Health and an ASTHO Member, explains how Tennessee is building a better healthcare system for older Americans; on May 22nd, ASTHO's next INSPIRE: Readiness webinar focused on data-ready ecosystems will take place; and Dr. Puthiery Va, ASTHO Member and the Maine CDC Director, recently spoke about youth mental health at an event. Older Americans Month Web Page Tennessee Web Page: Department of Disability and Aging Tennessee Department of Health Web Page: Office of Healthy Aging ASTHO Webinar: INSPIRE – Readiness – Building a Data-Ready Ecosystem for Public Health Response  

Speak wise words of truth to families like Obed's. -------- 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.

EP 179: Coverage for Every Chapter: Life, Disability, and Long-Term Care Insurance”

The entertainment industry needs to stop pretending that there are disabled actors available to fill disabled roles and start admitting that it just doesn't want to put in the effort to find them.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

We would love to hear from you! Please send us your comments here. --------Thank you for listening! Your support of Joni and Friends helps make this show possible. Joni and Friends envisions a world where every person with a disability finds hope, dignity, and their place in the body of Christ. Become part of the global movement today at www.joniandfriends.org. Find more encouragement on Instagram, TikTok, Facebook, and YouTube.

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: Tim Yates – Research and Innovation Executive – Drake Music drakemusic.org Bridging Apps: bridgingapps.org To Register for INDATA Full Day Trainings: https://www.eastersealstech.com/our-services/fulldaytraining/ News Story: Wristband Story: […]

Don't let fear rob you from blessing another with an opportunity to serve. -------- 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.

Send us a textWhat happens when a football tackle changes everything? Ken Kunken's life pivoted dramatically in 1970 when he broke his neck during a Cornell University football game, leaving him almost completely paralyzed from the shoulders down. Doctors delivered a devastating prognosis—they didn't expect him to survive the week. If he did, they predicted a shortened life in a nursing home.Ken refused to accept these limitations. Just eleven days after hospital discharge, he returned to Cornell—navigating a campus with no wheelchair accessibility—and became the first quadriplegic to graduate from the university. This was merely the beginning of his boundary-breaking journey.Through raw, honest conversation, Ken shares how he earned two master's degrees and faced crushing employment discrimination despite his impressive credentials. When over 200 job applications went unanswered, he finally found opportunity at Abilities Inc., counseling others with disabilities. But Ken wasn't finished redefining possibility—he graduated from law school and spent over 40 years as an Assistant District Attorney, even though he couldn't initially fit through the courtroom doors in his wheelchair.Perhaps most powerfully, Ken opens up about finding love later in life and becoming a father to triplet sons through in vitro fertilization. Now in their twenties and attending prestigious universities, his sons represent the life Ken was told would be impossible.Throughout our conversation, Ken's philosophy shines through: "Just because something has not been done before doesn't mean you cannot do it now." His memoir, "I Dream of Things That Never Were," captures this spirit of relentless possibility. Whether you're facing challenges or simply need inspiration, Ken's story proves that with determination and support, extraordinary achievements are possible regardless of physical limitations.Subscribe to Glass Half Full for more conversations that challenge assumptions and celebrate the resilience of the human spirit.Please reach Ken: www.kenkunken.com,  kennethkunken@gmail.com. Also, is via messenger connected to facebook (https://www.facebook.com/ken.kunken/) Support the show

Welcome to Episode 144 of the Think UDL podcast: Accessible Workplaces with Connor Duignan. Connor Duignan is a Technical Software Developer at Innopharma Education. I met Connor at the AHEAD (Association On Higher Education and Disability) conference in Dublin, Ireland. His talk “Tertiary Education as Accessible Workplaces” beautifully summarized what accommodations and structures we have in higher education could also be transferred to the workplace to make a better working environment for all involved. In our conversation, we discuss principles that should be in place to make the workplace more flexible and accessible. This episode hits on the major ideas of Connor's thesis with some excellent talking points for employers and employees to follow. Additionally, we had a wonderful time talking about the Irish language and its renaissance in Ireland, and why language itself is so important to a people and a culture. This is important to identity, culture, and individuality which is also linked to learner variability, and why we need to have places where everyone can bring their best selves in any environment, from higher ed to the workplace and everywhere else.

One in five Americans have a disability. That’s according to the United States Census Bureau. The Trump administration has released statements promising to protect programs like medicaid, medicare and Social security - programs that people with disabilities rely on everyday. But in his recommendation for funding for fiscal year 2026, President Trump proposed cuts to housing for persons with disabilities and cuts to the National Institute of Disability. Today, we hear about the future of disability services from people living with disabilities. GUESTS: Tom Cosker: Disability Advocate at Disability Rights Connecticut Corey Pheez Lee: More Than Walking Peer Mentor Coordinator, Hip-hop artist and host "Super Adaptables" Podcast with More Than Walking Colin Killick: Executive Director of the Autism Self-Advocacy Network Support the show: http://wnpr.org/donateSee omnystudio.com/listener for privacy information.

Dr. Brandon Crawford, a prominent neurologist and researcher, discusses his journey into the field of developmental functional neurology and how through the use of PhotoBioModulation, incorporated with traditional neurological treatments, revolutionizes brain injury recovery.   He is renowned in the field of  photobiomodulation, or laser therapy, and its role in accelerating neuroplasticity and enhancing brain function.  Influenced by personal as well as professional experiences, Dr. Crawford explains the differences between traditional and functional neurology; all the time focusing on brain function, neuroplasticity, energy management,  getting to the root cause of neurological dysfunction, and holistic approaches. Additional topics include brain health, hormonal imbalances that can lead to strokes, inflammatory load, immune components and most importantly post-injury care. Listeners are challenged to investigate new, novel therapies as well as grasp the fact that recovery and brain adaptation are ongoing processes and not time limited.Support the showNew episodes drop every other Thursday everywhere you listen to podcasts.

Leah breaks down the often-overlooked condition of Dry Eye Syndrome (DES) and its significant impact on veterans. She explains the symptoms, causes, and heightened prevalence of DES in the veteran population, especially among those with PTSD, depression, or who underwent refractive surgeries like LASIK or PRK during active duty. Leah supports her insights with peer-reviewed studies and provides practical advice on how veterans can pursue VA disability claims for DES, either as a primary or secondary condition. She emphasizes the importance of getting medical documentation, understanding legal nuances, and seeking support from accredited claims agents. This informative video aims to empower veterans with knowledge that could help them secure benefits they may not realize they're entitled to.

Learn how you can reach families like Alejandro's by visiting www.joniradio.org and planning your next Wheels for the World trip. -------- 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.

In this powerful episode of Wheels of Change, we sit down with author, accessibility advocate, and community leader Jenna Udenberg. A lifelong resident of Minnesota's Northshore, Jenna has used a manual wheelchair since the age of 8 due to Juvenile Idiopathic Arthritis — and has been rolling through life with unstoppable determination ever since. Jenna spent 19 years as a music educator, inspiring students in and out of the classroom. Now, she uses her voice to uplift others through her deeply personal and thought-provoking column Local View from 4 foot 2 in the Lake County Press. Recognized as a 2017 Blandin Foundation Community Leader and a 2020 Bush Fellow, Jenna brings both insight and heart to every space she enters. From the challenges of accessibility to the joy of LEGO robotics, this conversation dives into what it means to live boldly, lead with purpose, and create a life that motivates change — no matter your perspective.Jenna Udenberg is an author, accessibility advocate, and former music educator who calls Minnesota's Northshore home. Diagnosed with Juvenile Idiopathic Arthritis at age 8, she has used a manual wheelchair for most of her life and continues to be a powerful voice for inclusion and representation. Jenna is the author of the Local View from 4 foot 2 column in the Lake County Press, where she shares raw, insightful reflections on life from a seated perspective. She was named a Blandin Foundation Community Leader in 2017 and received a prestigious Bush Fellowship in 2020 for her work in advocacy and community building. When she's not writing or speaking, Jenna enjoys the outdoors, playing games with friends, fishing, and coaching the Robo Dweebs — a LEGO robotics team full of future innovators. Her mission is simple but impactful: to create space for every voice, every perspective, and every story.https://www.aboveandbeyondwithu.org/Become a supporter of this podcast: https://www.spreaker.com/podcast/i-am-refocused-radio--2671113/support.

Qudsiya sits down with Joe Shapiro, investigative correspondent for National Public Radio. Joe was one of the first journalists to cover the disability civil rights movement and the passage of the Americans with Disabilities Act. In this episode, Qudsiya and Joe talk about how Joe came to cover disability issues, his observations about how the movement has evolved over time, and his perspectives on disability coverage today.--Let us know what you think with a comment or review!Visit our website⁠ ⁠for⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ transcripts⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠.⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ Subscribe to Qudsiya's Substack, ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Getting Down To It⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ Support the team behind the podcast ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠with a donation⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠

Dr. Wendy is offering her Wendy wisdom with her drive by makeshift relationship advice. PLUS we are talking about the Bold of Beauty Project at UCLA promoting beauty of people with disabilities with Dr. Eva Ritvo. It's all on KFIAM-640!!!

Episode SummaryIn this episode, actor and voiceover artist Miguel Gabriel shares his journey from struggling with impaired speech to finding his voice, literally and creatively. Thoughtful and grounded beyond his years, Miguel opens up about overcoming bullying, staying true to himself, and how kindness—his self-described superpower—has shaped his path. His reflections on rejection, faith, and friendship offer wisdom that resonates at any age.About MiguelMiguel Gabriel, an American actor of Spanish-Filipino and Hungarian descent, has been captivating audiences since he began his career in theater at the tender age of five. After a series of successful appearances in popular shows like "How to Get Away with Murder" and lending his voice to animated films like "Puss in Boots: The Last Wish," Miguel has made an exciting leap into his first feature film, "Camera." In this pivotal role as Oscar, he stars alongside Hollywood royalty, Beau Bridges, marking a significant milestone in his acting journey.From This EpisodeWatch Camera: https://linktr.ee/camerathemovieRelated episode of Wisdom Shared: Blessed With Support with Miguel's mom, MicheleRelated episode of Wisdom Shared: Finding Voice Through a Camera with filmmaker Jay SilvermanMiguel's Instagram: @officialmiguelgabrielMiguel's IMDB page Find and Follow Carole and Wisdom Shared:https://www.caroleblueweiss.com/Subscribe to YouTube channelFollow and send a message on FacebookFollow and send a message on LinkedInFollow on InstagramFollow on TikTokFollow on ThreadsThe Wisdom Shared TeamAudio Engineering by Steve Heatherington of Good Podcasting WorksCo-Producer and Marketing Coordinator: Kayla NelsonProduction Assistant: Becki Leigh

We would love to hear from you! Please send us your comments here. --------Thank you for listening! Your support of Joni and Friends helps make this show possible. Joni and Friends envisions a world where every person with a disability finds hope, dignity, and their place in the body of Christ. Become part of the global movement today at www.joniandfriends.org. Find more encouragement on Instagram, TikTok, Facebook, and YouTube.

Janeen Herskovitz has worn two hats over two decades, as a mother of an adult son and a daughter who are neurodivergent, and as a therapist and former special educator who supports families, parents and neurodivergent individuals. Initially, she took the path of attempting to cure her son and questioned if vaccinations caused her son's autism, but then evolved into following a different path in understanding of her children's conditions. She now uses her experiences and her training as a therapist to support others. Barry, Dave and Janeen discuss her journey.FIND OUT MORE ON OUR WEBSITESee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.