Podcasts about Disability

Can you spot the difference between real advocacy and AI fakery? In this week's NeuroSpicy Hot Topic from The Neurodivergent Experience, hosts Jordan James and Simon Scott dive into the disturbing rise of AI-generated disability accounts — fake profiles posing as disabled people to chase likes, sympathy, and cash.From TikTok to Instagram, and from stolen advocacy posts to AI-created faces, we explore:How AI accounts impersonate disabled people and outpace real advocatesThe ethics of “sympathy as currency” online — when does support turn into exploitation?Jordan's experience with stolen posts, fake profiles, and even AI-like accusations against his photographyThe thin line between AI as accessibility (non-speaking advocates finding a voice) and AI as deceptionWhy fakes fuel distrust of genuine disabled creators and advocacy communitiesThe psychology of comments, trolls, and why negativity drowns out thousands of quiet supportersHow AI deepfakes risk eroding trust in images, podcasts, and even our own wordsWhether you're fascinated, fearful, or just fed up with online scams, this conversation blends advocacy, ethics, and plenty of neurospicy humour to ask: what happens when disability itself becomes content to counterfeit?❤️ Support the ShowIf this episode resonated with you:✅ Follow or Subscribe to The Neurodivergent Experience⭐ Leave a quick review on Apple Podcasts or Spotify

Bishop Andrew Cozzens, chairman of the Committee on Evangelization and Catechesis, shares incredible stories of a pilot pilgrimage for the upcoming Eucharistic Congress. Following the bishops' overwhelming approval of the new national pastoral plan, Bishop Oscar Cantú talks with Catholic Current about strengthening Hispanic/Latino Ministry in parishes and dioceses. The bishops have voted to begin a process of consultation and eventual revision of the Ethical and Religious Directives for Catholic Health Care Ministry. Forty-five years after the landmark pastoral letter on disabilities, the USCCB voted to begin drafting a new statement. Bishop Michael Burbidge, episcopal moderator of the National Catholic Partnership on Disability, shares his enthusiasm for the upcoming document. In his opening address to the bishops, the apostolic nuncio Archbishop Christophe Pierre exhorts the baptized to be “ambassadors for Christ.”

In this latest episode, we're joined by Nic Novicki, founder of the Easterseals Disability Film Challenge (EDFC) - an annual competition that gives disabled creatives the chance to showcase their talent in front of and behind the camera. We discuss: Nic's career and the relationship to EDFC And plenty more... Follow or subscribe wherever you get podcasts. Transcripts available at ReidMyMind.com. FB/IG @ReidMyMindRadio

A Nebraska service provider for adults with developmental disabilities is suing the Nebraska Department of Health and Human Services. Integrated Life Choices is alleging DHHS violated due process and separation of powers and is seeking injunctive relief in Lancaster County District Court.

Niamh Ní Hoireabhaird, Disability activist and freelance journalist, assesses the new strategy on rare diseases, published by the Department of Health.

Released 2025.05.28 Making Catholic education inclusive and accessible for students with special needs is a priority for the Committee on Catholic Education. Guests Mary Pat Donoghue, Executive Director of USCCB's Secretariat for Catholic Education, and Maggie Hubbard, Ed. D, with the National Catholic Partnership on Disability, discuss the importance of serving all students in Catholic schools.

When pain drives you to the floor, take heart—God is already there beside you, rebuilding hope from the ashes. -------- 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.

Africa Melane chats to Acting Treasurer of the Western Cape Disability Network Anthony Ghillino, about the outcome of a meeting they had with the City of Cape Town today, following yesterday’s picket regarding budget cuts to the Dial - A - Ride service. Presenter John Maytham is an actor and author-turned-talk radio veteran and seasoned journalist. His show serves a round-up of local and international news coupled with the latest in business, sport, traffic and weather. The host’s eclectic interests mean the program often surprises the audience with intriguing book reviews and inspiring interviews profiling artists. A daily highlight is Rapid Fire, just after 5:30pm. CapeTalk fans call in, to stump the presenter with their general knowledge questions. Another firm favourite is the humorous Thursday crossing with award-winning journalist Rebecca Davis, called “Plan B”. Thank you for listening to a podcast from Afternoon Drive with John Maytham Listen live on Primedia+ weekdays from 15:00 and 18:00 (SA Time) to Afternoon Drive with John Maytham broadcast on CapeTalk https://buff.ly/NnFM3Nk For more from the show go to https://buff.ly/BSFy4Cn or find all the catch-up podcasts here https://buff.ly/n8nWt4x Subscribe to the CapeTalk Daily and Weekly Newsletters https://buff.ly/sbvVZD5 Follow us on social media: CapeTalk on Facebook: https://www.facebook.com/CapeTalk CapeTalk on TikTok: https://www.tiktok.com/@capetalk CapeTalk on Instagram: https://www.instagram.com/ CapeTalk on X: https://x.com/CapeTalk CapeTalk on YouTube: https://www.youtube.com/@CapeTalk567 See omnystudio.com/listener for privacy information.

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 28 of Winning Isn't Easy. In this episode, we'll dive into the complicated topic of "Disability and Disputed Illnesses: Navigating Claims Without Full Medical Recognition."Some medical conditions cause symptoms so real and severe that they disrupt daily life, yet remain disputed or only partly recognized by mainstream medicine. For patients, it is not just a fight to be believed, it is also a fight to secure the disability benefits they need. With ERISA-governed Long-Term Disability insurance, the challenges are even greater. In this episode of Winning Isn't Easy, disability law expert Nancy L. Cavey examines one of the most difficult areas of disability claims: conditions the medical community has not fully accepted. From chronic Lyme disease, fibromyalgia, and chronic fatigue syndrome to mental health diagnoses such as dissociative identity disorder, adult ADHD, and PTSD outside of combat, Nancy explains why these claims are often denied and what you can do about it. You will learn how insurers view subjective symptoms like pain, fatigue, and cognitive fog, why strong documentation and physician support matter, and the strategies that can help prove the impact of these conditions on your ability to work. Nancy also shares a real case example that shows how persistence and preparation can turn the tide. If you are living with a condition the medical world questions but your symptoms are real, this episode will give you the tools to fight for the benefits you deserve. Winning is not easy, but with the right strategy, it is possible.In this episode, we'll cover the following topics:One - Disputed Physical ConditionsTwo - Disputed Mental ConditionsThree - Multiple Chemical Sensitivity (MCS)Whether 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. 

Looking for a more inclusive, accessible way to date while disabled or chronically ill?

The growth in the cost of the National Disability Insurance Scheme is making it financially unsustainable. But is moving some children with autism off the scheme really a good idea? The government plans to have a new program called Thriving Kids in place by July next year to support children with mild to moderate developmental delays and autism. Today, we speak with Jess Otter, whose son has autism and to the ABC's disability affairs reporter Nas Campanella. Featured: Jess Otter, motherNas Campanella, ABC disability affairs reporter

We all buy into at least one conspiracy theory. This one's mine.Support the showNew Website: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

In today's Five Question Friday (FQF) video, we cover the following questions:1. What are the best finance apps for those with a learning disability?2. Is 3% SWR the new 4%?3. How do you model tax-free income in Boldin?4. In what account type should you hold cash you plan to spend in the first few years of retirement?5. What inflation rate should you assume in retirement?ResourcesMonarch Money: https://go.robberger.com/monarch-yt/y... (Use Promo Code ROB50 for 50% off the first year)Simplifi: https://go.robberger.com/simplifi/yt-fqfBoldin: https://go.robberger.com/boldin/yt-fqfFidelity article: https://www.fidelity.com/learning-cen...Shiller PE: https://www.multpl.com/shiller-peKitces article: https://www.kitces.com/blog/the-ratch...Join the Newsletter. It's Free:https://robberger.com/newsletter/?utm...

In this special episode with Sista Creatives Rising, we sit down with guest Chi (they/them), a talented artist, graphic designer, and mental healthcare worker from New York. Chi shares their journey of creating powerful infographics on the impacts of COVID and climate change, specifically as they relate to Indigenous and Palestinian displacement, illness, and disability.Discover how their art serves as a healing experience for marginalized communities. This interview highlights the mission of Sista Creatives Rising—a virtual project founded by a Black, invisibly disabled mother-daughter duo. We champion homebound disabled, queer, and BIPOC creatives, offering free virtual events like our disability-accessible "Art & Mind" series. Tune in for a powerful discussion on community building and liberation through artChE / ChillusionsRole: Graphics Assistant, Creating Infographics on COVID, Climate Issues and Climate Change in relation to Indigenous & Palestinian displacement, Illness & Disability. COVID-Conscious Chi, who uses they/them pronouns, is a 31 year old artist, graphic designer, and mental healthcare worker based in New York State. They have contributed illustrative works to local organizations, mutual aid projects, and virtual advocacy spaces since 2018. For the past 4 years Chi has lived with chronic illnesses and disabilities that impact their ability to create, so through their work they hope to create a healing experience for all by focusing on projects that deal with disability, community building, liberation, and justice for marginalized groups.Links: Instagramhttps://www.instagram.com/chillusions?igsh=MXM2b3VlZXZ2Y3ljcA==Sista Creatives Rising (SCR) is a 100% virtual project (not a non-profit or LLC!) and concept founded by Black, invisibly disabled mother-daughter duo Claire Jones (age 62) and Amaranthia Sepia (age 25). ​SCR seeks to strengthen our community through virtual engagements, including our disability-accessible event, "Art & Mind." Through documentaries, short films, 3D virtual galleries, speaking engagements, and free resources led by therapists and disability activists, "Art & Mind" highlights these artists while fundraising at each event for our microgrant program, The Sistas Uprising Fund. Our first show occurred in 2021, leading to the creation of SCR in 2023. We pride ourselves on working with primarily homebound, disabled, queer, BIPOC creatives & activists. All our "Art & Mind" events are free to ensure that anyone can watch & participate, and people can donate to The Sistas Uprising Fund if they choose. We offer the perspective that virtual content has value and can provide audiences with innovative solutions for the often-overlooked disabled community.She/HerSista Creatives RisingBridging Gaps From the Past to the Present and to the Future___Our Website: SistaCreativesRising.comFiscal Sponsor Donation Page - Directly Support Our Projects!Wanna Tip us? Paypal Donation Page & Ko-Fi (Store Incoming!)Instagram: @SistaCreativesRisingSubstack: Musings of a Black Disabled ElderLinkedIn: Sista Creatives Rising

Recorded live in-studio (CA and PA), Kyle and Sean welcome viewers and then dive into a vulnerable discussion about the transition from walking to using assistive devices like walkers and wheelchairs. Incorporating comments from the audience, they talk honestly about the embarrassment, shame, and pride tied to showing visible signs of disability, as well as the unexpected freedom and safety these tools can bring. The conversation expands into themes of feeling like a burden, hiding pain, struggling with speech in public or professional settings, and ultimately the power of owning one's reality rather than hiding it.

Interviewees: Emily Green, MD and Kelley Volpe, MD Interviewer: Lisa Meeks, PhD, MA Description: In Episode 113, Dr. Lisa Meeks talks with Dr. Emily Green (child psychiatrist, University of Chicago; recent fellow at UIC) and Dr. Kelley Volpe (training director of the Child and Adolescent Psychiatry Fellowship at UIC) about navigating fellowship with ADHD and a learning disability—and how openness, advocacy, and leadership support shaped a successful training experience. Together, they trace Emily's decision-making during the match, the challenges of transitioning from residency to fellowship (and from student to employee), and the unexpected barriers in GME accommodation processes. They unpack how program leadership stepped in when paperwork stalled, why “temporary vs. chronic” misunderstandings of disability remain a problem, and how centering inclusion ultimately benefited both the trainee and the program. Listeners will hear advice for residents and fellows (be specific in accommodation requests, know when disclosure matters, embrace authenticity with patients) and for program directors (be proactive with GME, advocate beyond bureaucracy, and create space for trainees to bring their whole selves to medicine). This episode accompanies the open-access case study From Policy to Practice: Building the Disability Inclusion Infrastructure in Graduate Medical Education (Green & Volpe, Academic Medicine, 2025). Part of the ACGME/DWDI Disability Resource Hub, supported by the Josiah Macy Jr. Foundation Catalyst Award, it's both a roadmap and a reminder that when programs invest in access, everyone wins. Transcript: https://docs.google.com/document/d/1uhs1zRh2QOWVMgYlEFkxbFY-MJQbiqV_/edit?usp=sharing&ouid=104315301750264632478&rtpof=true&sd=true Bios:  Kelly Volpe, MD Dr. Kelley Volpe is the medical director of the Pediatric Stress & Anxiety Disorders Clinic at UI Health. Dr. Volpe currently provides outpatient services that are specialized in the treatment of anxiety disorders, such as generalized anxiety, social anxiety, obsessive compulsive disorder, and selective mutism, in addition to trauma- and stress-related disorders. She is board certified in both General Psychiatry and Child & Adolescent Psychiatry. Emily Green, MD Emily is an Assistant Professor of Psychiatry and Behavioral Neuroscience at the University of Chicago. She specializes in pediatric psychiatry and helps children and adolescents who are struggling with mental well-being. Key Words:   Disability Inclusion Residency Fellowship ADHD Learning Disability Psychiatry Accommodations Program Directors Graduate Medical Education (GME) Produced by: Lisa Meeks  Resources:  Disability Resource Hub: https://dl.acgme.org/pages/disability-resource-hub Case Studies in Disability Resource Hub: https://dl.acgme.org/pages/disability-resource-hub#case_studies UME to GME Toolkit:  https://dl.acgme.org/pages/disability-resource-hub-transitions-toolkit-introduction Policy Toolkit:  https://dl.acgme.org/pages/disability-resource-hub-policy-toolkit Disability in Graduate Medical Education Program:  https://www.docswithdisabilities.org/digme Illinois Lend: https://www.illinoislend.org Case Study: From Policy to Practice: Building the Disability Inclusion Infrastructure in Graduate Medical Education      

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: Vicki Mayo – Founder and CEO – The Touchpoint Solution Website: ilovetouchpoint.com Discount code – assist For more about Bridging Apps: www.bridgingapps.org —————————— If […]

New Medicaid waiver limits threaten significant service cuts to those with disabilities. Indiana Lawmakers cut public funding from $100 million to just $40 million, leading health care leaders to issue a warning that the loss will impact health care costs and outcomes. Governor Braun has taken 11 helicopter rides home in 8 months, costing taxpayers $24,000. Host Brandon Smith is joined by Democrat Ann DeLaney, Republican Mike O'Brien, Jon Schwantes of Indiana Lawmakers, and Oseye Boyd of Mirror Indy to debate and discuss this week's top stories.

See the quilt 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.

Nick Gojcaj grew up in Queens dreaming of becoming an NYPD cop, but after that didn't work out, he spent 20 years in the corporate world before making a drastic career change in his 40s—joining Rikers Island as a corrections officer. For three years he worked inside one of America's most notorious jails, dealing with chaos, violence, and the daily dangers of being a prison guard, until a confrontation with inmates left him permanently disabled. Instead of protecting him, Rikers illegally terminated his job, sparking a legal battle that he's still fighting today. In this episode, Nick opens up about his journey from the academy to life on the inside, the shocking realities of working at Rikers, and how he's now exposing the system that betrayed him. #RikersIsland #PrisonGuard #CorrectionsOfficer #NYCPrisons #RikersStories #PrisonLife #LawEnforcement #CorruptionExposed Hosted, Executive Produced & Edited By Ian Bick: https://www.instagram.com/ian_bick/?hl=en https://ianbick.com/ Presented by Tyson 2.0 & Wooooo Energy: https://tyson20.com/ https://woooooenergy.com/ Use code LOCKEDIN for 20% OFF Wooooo Energy Buy Merch: http://www.ianbick.com/shop Timestamps: 00:00 Prison Realities and Riker's Introduction 00:19 Nick's Unusual Career Path 01:51 Favorite Episodes and Influential People 03:21 Union Perks, Disability, and Department Politics 04:23 Growing Up: Family and Childhood Influences 05:21 School Trouble and Early Aspirations 06:12 Drinking, Gambling, and Avoiding Trouble 08:09 Crime, Arrests, and a Flawed System 09:49 Stable Home vs. Turbulent Friends 10:57 From College Hopes to Law Enforcement Dreams 13:09 College Life and NYPD Rejection 14:35 Corporate World: Two Decades Lost 16:08 Career Pivot: Joining Corrections at 44 17:43 Correctional Academy: Training Realities 20:08 Academy vs. Real World at Rikers 22:47 Early Days on the Job & Learning from Inmates 26:03 Systemic Issues: Contraband, Corruption, and Challenges 29:39 Schedules, Overtime, and Hidden Job Hazards 33:09 Facing Reality: Dangerous Shifts, Staff Politics 36:14 Respect, Dignity, and Handling Inmates 39:41 Violence, Use of Force, and Officer Dilemmas 43:00 The Incident and Long-Term Injury 47:34 Aftermath: Desk Duty, Recovery, and Abrupt Firing 53:46 Legal Fight and Alleged Retaliation 58:39 Department Corruption and Favoritism 01:02:02 Lawsuit, Motivation, and Moving Forward 01:06:10 Advice, Support, and Closing Thoughts Powered by: Just Media House : https://www.justmediahouse.com/ Creative direction, design, assets, support by FWRD: https://www.fwrd.co Learn more about your ad choices. Visit megaphone.fm/adchoices

In this episode of 'Pushing Forward with Alycia,' host Alycia Anderson interviews Treasa Praino, a legally blind disability advocate, university instructor, and human rights and inclusion specialist. Treasa shares her journey from facing discrimination in her youth to becoming a scholar finishing her PhD at Syracuse University. The discussion covers her experiences working in federal probation, education inequities, and her transformative work in South Africa. Treasa highlights the importance of presuming competence, interdependence over independence, and how different cultural contexts shape the experience of disability. The conversation underscores the value of inclusive education and the need for practical applications of disability research. Your Guide Through the Episode 00:00 Introduction to Pushing Forward with Alycia 00:25 Meet Treasa Praino: Disability Advocate and Scholar 02:18 Treasa's Early Life and Career Journey 05:43 Insights from South Africa and the Path to Academia 10:06 Understanding Disability in Different Contexts 20:09 The Importance of Inclusive Education 35:02 Future Vision and Final Thoughts A Quote from Treasa Praino ” Don't be afraid, be curious. People are okay for you to be curious, as long as you're going in with an open mind and not judgmental and presuming that competence.” ~ Treasa Praino Driving Forces of the Discussion

Interviewees: Josh Schammel, MD; Brian Inouye, MD; and Becky Stetzer, MD Interviewer: Justin Bullock, MD, MPH Description: In this episode, Dr. Justin Bullock talks with Dr. Josh Schammel (chief urology resident at Albany Medical Center), Dr. Brian Inouye (associate program director of urology at Albany Med), and Dr. Becky Stetzer (assistant dean of competency development, Albany Med) about navigating remediation, cognitive disability support, and institutional change in residency training. Together, they trace Josh's experience entering urology residency off-cycle, the social and educational challenges that followed, and the turning point that came with honest conversations about expectations and support. They explore how leadership reframed remediation from punitive to restorative, how program culture embraced accommodations even without a formal diagnosis, and how outside expertise in competency development reshaped both Josh's trajectory and the program's systems. Listeners will hear candid reflections on the fear of dismissal, the relief of being given a “do-over” year, and the powerful role of trust and transparency in rebuilding confidence. The team highlights the importance of creating a culture where struggling is not synonymous with failure, but with an opportunity for growth. This episode accompanies the open-access article A Master Adaptive Learner Approach to Cognitive Disability Support in a U.S. Urology Residency (Stetzer et al., Teaching and Learning in Medicine). Part of the ACGME/DWDI Disability Resource Hub, supported by the Josiah Macy Jr. Foundation Catalyst Award, it's a practical and deeply human guide for residents, faculty, and program leaders working to build equitable clinical learning environments. Transcript: https://docs.google.com/document/d/1u-qRRgjrB-lOJnQytGy7C7ByxYppdfju/edit?usp=sharing&ouid=104315301750264632478&rtpof=true&sd=true Key words: Medical education, cognitive disability, residency, accommodations, program director, GME, GME Policy, Disability, Training, PTSD. Bios:   Resources:  Disability Resource Hub: https://dl.acgme.org/pages/disability-resource-hub Case Studies in Disability Resource Hub: https://dl.acgme.org/pages/disability-resource-hub#case_studies UME to GME Toolkit:  https://dl.acgme.org/pages/disability-resource-hub-transitions-toolkit-introduction Policy Toolkit:  https://dl.acgme.org/pages/disability-resource-hub-policy-toolkit Disability in Graduate Medical Education Program:  https://www.docswithdisabilities.org/digme Link to Case Study: A Master Adaptive Learner Approach to Cognitive Disability Support in a U.S. Urology Residency https://www.tandfonline.com/doi/10.1080/10401334.2025.2502670?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%20%200pubmed  

Fetal Alcohol Spectrum Disorders (FASD) is an often-overlooked diagnosis for many people, but it's important to spread awareness to help those who need it get the correct supports. Hear from Marilyn Fausset, who is the Chair of the FASD Awareness Work Group at Illuminate Colorado, as she discusses her family's journey to the diagnosis and all that she's learned since!

In this informative and candid episode of Engage, hosts Captain Laura Woods and First Officer Ryan Argenta sit down with Retirement and Insurance (R&I) experts Captains Scott Bowles and John Doherty to take a deep dive into the often-misunderstood world of disability for Delta pilots. Whether you're navigating a short-term medical issue, a planned procedure, or facing an unexpected long-term event, this conversation covers everything you need to know - from qualifying for disability, using your sick leave and understanding DPMA, to how your 401(k), healthcare, and income are affected.  You'll also hear practical advice about returning to work, how income offsets work, and the importance of staying off ladders (seriously). With real-life examples and clear guidance, this episode is essential listening for pilots at any seniority level. 

For parents of children with disabilities, back to school time can be a mix of excitement and anxiety. They may be navigating complex education plans, arranging for specialized transportation, or making sure the right support staff are in place. For some families, it's a matter of making sure their child has access to therapies; for others, it's about fighting for accommodations they're legally entitled to but don't always get. And behind those hurdles is concern for whether their child will feel included, safe, and understood in a new school year. Our guests discuss their experiences and what resources are available.Our guests: Shenee Elzey, mother of a child who has Holoprosencephaly Kara Georgi, family education specialist at Starbridge Brentaysia Johnson, parent of a child with disabilities Kristen Lopez, communications manager at Starbridge and parent of a child with disabilities

On this week's episode of The 1 Girl Revolution Podcast, we welcome Collette Divitto — entrepreneur, baker, author, speaker, and founder of Collettey's Cookies and Collettey's Leadership Program. You may know Collette from her inspiring story that went viral in 2016, when she turned rejection into fuel for her mission and built a cookie empire. After facing countless job rejections because she was born with Down Syndrome, Collette decided to create her own path and founded Collettey's Cookies — not only to share her delicious “Amazing Cookies” with the world, but also to create meaningful jobs for people with “different abilities.” Since then, Collette has been featured on CNN, Good Morning America, ABC World News, People Magazine, BBC, and many other media outlets. She's sold over 500,000 cookies, built a thriving company in Boston that now employs 15+ people (several with disabilities), and continues to grow her mission of empowerment and inclusion. But Collette's story doesn't end with cookies. Through her nonprofit, Collettey's Leadership Program, she provides entrepreneurship and leadership training to people with disabilities, helping them discover their abilities, build confidence, and pursue their dreams. She also travels the country as a speaker and advocate, and one of her ultimate goals is to work with lawmakers in Washington, D.C. to create more employment opportunities for people with disabilities. In this episode, you'll hear: ✨ Collette's journey growing up with Down Syndrome and discovering her passion for baking; ✨ The story behind her now-famous Collettey's Cookies; ✨ How she turned rejection in the job market into an opportunity to launch her own business; ✨ The growth of Collettey's Cookies and its mission to employ people with disabilities; ✨ Her advocacy work and her dreams for systemic change in the world; ✨ And so much more!

You make God look good when you trust him fully—especially in hard, uncertain moments. Give him all the glory! -------- 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 disability support service is worried the government could be about to cut a travel subsidy that helps people with disabilities get where the need to be. The Total Mobility Scheme is jointly funded by Waka Kotahi the New Zealand Transport Agency, Councils and the government, while card holders pay 25% of a taxi fare. The service is currently under review and Transport Minister Chris Bishop says future funding of the scheme is yet to be decided. Chief executive of Aspire Canterbury, spoke to Lisa Owen.

Sid Ghosh is 18 (going on 81) years old and he just published his first full length book of poems with a major poetry company. He's been given extraordinary praise from renowned authors, and us too of course! Here's what we're talking about today: Sid's poems about his profound experience the world, as an autistic adult who has Down syndrome and uses a communication board (Spellers style!)Why it's important to challenge our comfort zones to get a glimpse into a more fully profound way to be human. What the publishing process was like + where and when you can BUY this book! There's a lot of talk about energies, frequencies, and connectivity in this one too. We hope you join us for this incredible interview with Sid Ghosh, and his mother, Dr. Vaish Sarathy! --SHOW NOTESPurchase Yellow Flower Gills Me Whole by Sid GhoshFollow @downlikesid on InstagramSubscribe to Sid's stubstack newsletterSPONSORS National Down Syndrome SocietyiCanShine ProgramsDown for GreensRods HeroesJOIN THE LUCKY CREWJoin us in celebrating and supporting The Lucky Few Podcast! For just $4.99 a month, you can help us continue shouting worth and shifting narratives for people with Down syndrome. Enjoy bonus episodes where we dive deeper into the most controversial issues, shop discounts, and more! Become an essential part of The Lucky Few movement today! 

In this eye-opening episode of The Common Sense MD, Dr. Tom Rogers welcomes former Social Security disability judge George Evans for a candid conversation about one of the most misunderstood and complex topics in medicine and law: disability. Drawing from his remarkable 27-year career as a disability judge and his current work helping individuals navigate the daunting application process, George breaks down what it actually means to be “disabled” in the eyes of the law, explains the real differences between SSI and Social Security Disability (Title II), and offers vital tips for anyone considering filing a claim.Discover why the system is so difficult to navigate, how cases are evaluated, and why getting representation early is essential. George shares fascinating inside stories—from why some seemingly healthy people may qualify for benefits while others with obvious impairments are denied, to what judges really look for in hearings, and the myths about “easy” disability approvals. They also discuss how having an advocate not only increases your chances of success but can save you from costly mistakes.If you or someone you know is confused about disability, thinking about applying, or just curious about how these crucial decisions are made, this episode will clear up the confusion and provide tools you can use. Learn from real-life examples, get insider knowledge, and arm yourself with common sense advice from the experts.Tune in for clarity, honesty, and practical guidance on a topic that affects millions—but few truly understand.What did you think of this episode of the podcast? Let us know by leaving a review!Connect with Performance Medicine!Check out our new online vitamin store:⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://performancemedicine.net/shop/⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Sign up for our weekly newsletter: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://performancemedicine.net/doctors-note-sign-up/⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Facebook: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠@PMedicine⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Instagram: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠@PerformancemedicineTN⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠YouTube: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Performance Medicine

Reject the lie that disability devalues life. Instead, uphold God's truth that every life—no matter how broken—is sacred and worthy of protection. -------- 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.

Fears are growing in the disability community that a vital travel subsidy scheme could be capped. The Total Mobility Scheme that is co-funded by the government helps disabled people who cant use buses trains or ferries get where they need to go in subsidised taxis. The scheme has been under review for the past two years, with no official word on any changes. Disability groups fear the subsidy will be cut or overall funding capped, seriously restricting options for people who use the scheme. Auckland academic Dr Sally Britnell spoke to Lisa Owen.

Take a look at this amazing quilt 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.

Learn about traveling the world as a deafblind Latina—salsa dancing, sumo-wrestling and becoming a disability advocate. _____________________________ Subscribe to The Maverick Show's Monday Minute Newsletter where I email you 3 short items of value to start each week that you can consume in 60 seconds (all personal recommendations like the latest travel gear I'm using, my favorite destinations, discounts for special events, etc.). Follow The Maverick Show on Instagram ____________________________________ Catarina joins Matt and talks about growing up in the U.S. in an immigrant home with Puerto Rican and Cuban heritage. She reflects on what those identities mean to her as well as her deafblind disability journey with Usher syndrome.  Catarina debunks common misconceptions people have about deafblind people and offers tips on non-disabled people can be better allies to disabled travelers.  She then reflects on how her interest in world travel developed and tells stories from a family trip to Spain in high school and more immersive trips to rural Kentucky, Argentina and Korea in college.  Next, Catarina talks about her first solo-trip with the white cane to Montreal, her love for Salsa dancing around the world, and her recent trip to Japan where she had epic tea experiences and got to try sumo-wrestling.  She then talks about the trip she led to Portugal for disable travelers and reflects and the power and impact of that experience.  Catarina next takes us on her journey of becoming an intersectional activist and building a fully remote company to smash disability stigmas. She explains how she designs her travel lifestyle and offers trips for disabled travelers as well as those traveling with a relationship partner.  And finally Catarina reflects on how traveling to nearly 40 countries has impacted her as a person.  FULL SHOW NOTES INCLUDING DIRECT LINKS TO EVERYTHING DISCUSSED ARE AVAILABLE HERE. ____________________________________ See my Top 10 Apps For Digital Nomads See my Top 10 Books For Digital Nomads See my 7 Keys For Building A Remote Business (Even in a space that's not traditionally virtual) Watch my Video Training on Stylish Minimalist Packing so you can join #TeamCarryOn  See the Travel Gear I Use and Recommend See HowI Produce The Maverick Show Podcast (The equipment, services & vendors I use) ____________________________________ ENJOYING THE SHOW? Please Leave a Rating and Review. It really helps the show and I read each one personally.  You Can Buy Me a Coffee. Espressos help me produce significantly better podcast episodes! :)

Law Professor Ron McCallum was a premature baby in the 1940s. He completed his studies by recording people reading his textbooks aloud onto cassettes. Then an early version of text to speech opened up new possibilities for him.When Ron was born, prospects for blind people to have careers outside sheltered workshops were few.In the late 1970s enormous change swept into Ron's life. He fell in love with fellow lawyer, Mary Crock, and they began a family. Ron became the first totally blind professor of any discipline in Australia with a role at the University of Sydney Law School.He was also chair of the United Nations Committee on the Rights of Persons with Disabilities, and 2011 Senior Australian of the Year.Further informationFirst broadcast July 2019.You can read all about the Conversations origin story on the ABC News website.The researcher on this episode of Conversations was Michelle Ransom-Hughes. The Executive Producer is Carmel Rooney.This episode touches on disability, a career in law, uni, life story, epic life story, premature babies, history and autobiography.To binge even more great episodes of the Conversations podcast with Richard Fidler and Sarah Kanowski go the ABC listen app (Australia) or wherever you get your podcasts. There you'll find hundreds of the best thought-provoking interviews with authors, writers, artists, politicians, psychologists, musicians, and celebrities.

In this message, we'll look at the first triad of miracles that Matthew records, demonstrating Jesus' divine power as the promised Messianic King, who not only has the power to heal, but the power to save.   Scripture: Matthew 8:1-17

In this episode of Hope for the Caregiver, I sit down with DJ and Jessica Rowland to talk about life with Huntington's disease—and what it really means to keep living when the diagnosis is grim. Jessica was diagnosed in 2018 after a season of clumsiness, psychological symptoms, and career struggles. DJ, her husband and primary caregiver, balances running a mobile truck repair business with caring for her needs, adapting their home for safety, and bringing her along when he can. Their support network of family and friends has learned to adjust plans so Jessica can be part of them. We talk about the “incremental grief” of watching someone you love slowly lose abilities, and how they've chosen to push back against fear with adventure—riding motorcycles, taking a hot-air balloon ride, and embracing experiences Jessica once avoided. Their motto says it all: “Fear does not stop death. It stops life.” DJ shares the adjustments they've made for her mobility, swallowing, and pain, and the way the HD community has become a vital source of encouragement despite the heartache of seeing friends decline. Faith plays a role, too. Past experiences with their autistic son being unwelcome at church have kept them away for a while, but they hope to join a congregation after moving to a warmer climate. DJ finds comfort in the “Footprints” poem, and I encouraged them to explore the story behind It Is Well with My Soul. We closed with my caregiver song, I Can Only Hold You Now, and a reminder that the goal isn't simply to avoid death—it's to live fully with the time we have. “A Caregiver's Companion” Release Date 8/20/2025. Click Cover For More!      

I miss the days when my brain functioned like a well-oiled machine. These days it functions more like someone slipping in oil.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

As part of the 2025 Developmental Disabilities Conference, Dr. Raul Gutierrez, Associate Professor of Pediatrics at San Francisco General Hospital, talks about supporting immigrant children. Series: "Developmental Disabilities Update" [Health and Medicine] [Show ID: 40619]

Kevin Allen is a Pulmonary Hypertension Educator, Disability and Patient Rights Advocate, and Legislative Advocate. He serves as State Board Secretary for the Texas Federation of College Republicans and has advanced federal legislation such as SOARS, Help Copays, and the Safe Step Act. Kevin works with Dr. Victor Test and RN Kara Johnson to expand patient education and access across West Texas and has partnered with pharmaceutical companies to improve opportunities in Lubbock and higher education. He has served as faculty with CHEST, spoken at national events, and been featured in medical education materials. In 2025, Kevin was elected Senator-at-Large at Texas Tech. He founded the nationally recognized support group Lone Star Lungs and was honored by the City of Lubbock as a Civil Rights Activist in 2024.Subscribe to Patreon:https://www.patreon.com/c/snakepitstudiosFollow Breaking Hyman with Morgan and Friends :https://www.instagram.com/breakinghymanpod/Follow The Patriot and The Rattlesnake Podcast : https://www.instagram.com/thepatriotandrattlesnakepod/

Over in Easton, the House of Possibilities provides an array of services, training opportunities, and even a respite space for people with disabilities, all in the hopes of helping them find community and live as independently as possible. Recently, HOPe received a major grant from the Yawkey Foundation which they say will be transformative for their work. President and CEO Katie Terino talks with Nichole about their plans for the grant, their "home away from home", and their efforts to promote inclusivity.

EPISODE 138The Development of the Living and Learning Enrichment Center – An Innovative Neuro-Affirming Community, with Rachelle Vartanian.Rachelle Vartanian is the Founder and President of the Living and Learning Enrichment Center, a community that supports neurodivergent individuals and their families in many ways. She began her journey as a special education teacher, and then as a parent, who now has as an adult son on the autism spectrum. These experiences have allowed her to clearly see the priorities that are needed to support individuals like her son and others, and she, Barry and Dave discuss her journey and her innovative center.FIND OUT MORE ON OUR WEBSITE See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

  Interviewees: Tom Pisano, MD PhD and Laura Ashley Stein, MD, MS, Ed. Interviewer: Lisa Meeks, PhD, MA Description: In Episode 111, Dr. Lisa Meeks talks with Dr. Tom Pisano (former Penn neurology resident; now neuro-hospital medicine and neuro-immunology fellow) and Dr. Laura Stein (Adult Neurology Program Director at Penn) about building an accessible neurology residency for a physician who uses a wheelchair—and how trust, planning, and culture made it work. Together, they trace Tom's match-day disclosure strategy and “find-your-people” approach, an accessibility walk-through with tape measures and ADA checks, and the practical creativity of equivalent rotations when sites differ in accessibility. They also unpack a real barrier—a security policy that blocked ED entry during stroke alerts—and how reframing access as patient safety moved the system. Listeners will hear candid advice for residents (hold onto your “why,” communicate early, invite teaching adaptations) and for program directors (start with goals, not habits; assume success; apply the same creativity you offer patients to your trainees). This episode accompanies a written case study and a Mini Grand Rounds conversation in Learn at ACGME. Part of the ACGME/DWDI Disability Resource Hub, supported by the Josiah Macy Jr. Foundation Catalyst Award, it's a practical guide for PDs, residents, and anyone committed to equitable clinical training.   Transcript: https://docs.google.com/document/d/1xB_Cp8EiekJ9ExUZLP61EvE-0y4HUv22LuRp0D6uNB0/edit?usp=sharing Key words: Medical education, physical disability, disability research, residency, accommodations, wheelchair, SCI, medical technology, residency, neurology, program director, GME, GME Policy Bio: Laura Stein I have been involved in the Neurology Residency Program since 2018, and Director of the program since 2024. I teach residents on multiple inpatient services as well as in outpatient continuity clinic and stroke clinics. I also lead didactic sessions and workshops for resident onboarding and in our resident lecture series. I am particularly interested in expanding resident exposure to structured experiences in medical education and quality improvement and currently mentor multiple residents per year in medical education and quality improvement projects. In 2020, I was honored to receive the University of Pennsylvania Neurology Residents teaching award. I received my masters in medical education from the University of Pennsylvania in 2018. I have been a member of the American Academy of Neurology (AAN) Residency-In-Training Examination Committee since 2019. I have also been a member of the American Heart Association (AHA) Stroke Professional Education Committee since 2016 and currently serve as the Vice Chair of this committee. Clinically, I function predominantly as a neurohospitalist and attend on the stroke inpatient and consult services, the neurology ward service, and the PPMC consult service. I am dedicated to ensuring delivery of high-quality neurologic care across our system and currently am the physician co-lead for our neurovascular disease team, which spans our six-hospital network, as well as our HUP inpatient neurology unit-based quality improvement team. Tom Pisano I enjoy weekend bike rides with my wife, followed by trying out a new restaurant. When traveling, if possible, I always try to get in some monoskiing or scuba diving. I would also consider myself a (very) mildly competitive board gamer. I will be pursuing a combined neurohospitalist/neuroimmunology fellowship to develop expertise in myelopathies. My research includes brain-computer interfaces, especially of the spinal cord. Producer:  Lisa Meeks Follow Us: X: @DocsWith Instagram: @DocsWithDisabilities Linked In: https://www.linkedin.com/company/docs-with-disabilities-initiative Resources:  Disability Resource Hub: https://dl.acgme.org/pages/disability-resource-hub Case Studies in Disability Resource Hub: https://dl.acgme.org/pages/disability-resource-hub#case_studies UME to GME Toolkit:  https://dl.acgme.org/pages/disability-resource-hub-transitions-toolkit-introduction Policy Toolkit: https://dl.acgme.org/pages/disability-resource-hub-policy-toolkit Disability in Graduate Medical Education Program:  https://www.docswithdisabilities.org/digme   Link to Case Study: Coming Soon!              

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: Mike Hazlewood – CEO & Co-Founder – SensePilot For More on SensePilot: Website: https://sensepilot.tech/ Email: info@sensepilot.tech Youtube: https://www.youtube.com/@SensePilotTech IG: @sensepilot https://www.instagram.com/sensepilot?igsh=cmQ4Y21teG14aDR3&utm_source=qr FB: @sensepilot https://www.facebook.com/share/19AYKBW3zV/?mibextid=wwXIfr TikTok: […]

**Contains examples of 'othering', including birth abnormalities, and the terms used to describe them historically**Professor Suzannah Lipscomb is joined by Dr. Surekha Davies to discuss how individuals and groups were often classified in the Early Modern period, and how ideas evolved around normality versus 'otherness' - or even 'monstrosity' - evolved. Suzannah and Surekha consider the influence of the four humors on human classification, the portrayal of different peoples in New World exploration, and the entrenchment of racism and sexism through legal and social frameworks. They also touch upon gender fluidity and intersexuality from various cultural perspectives, culminating in a rich discussion on how humans created its own concepts of 'monsters' amongst men.MORE:Unusual Births and Disability in 17th Century EnglandMaking Babies in the 17th CenturyPresented by Professor Suzannah Lipscomb. The audio editor is Amy Haddow and the producer is Rob Weinberg. The senior producer is Anne-Marie Luff.All music courtesy of Epidemic Sounds.Not Just the Tudors is a History Hit podcast.Sign up to History Hit for hundreds of hours of original documentaries, with a new release every week and ad-free podcasts. Sign up at https://www.historyhit.com/subscribe. You can take part in our listener survey here: https://insights.historyhit.com/history-hit-podcast-always-on

What's stopping you from making a life-changing impact—just like John—by serving people with disabilities right now in your own community? Visit joniradio.org to learn more. -------- 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.

Headlines for August 07, 2025; “War in Perpetuity”: M. Gessen Warns Putin Won’t Make Peace with Ukraine Because It Risks His Own Survival; From India to Brazil, Trump Intensifies Trade War Against BRICS Nations as New Tariffs Take Effect; “Tightening the Chokehold”: Amjad Iraqi on Israel’s Plans to “Empty Out” Gaza and Annex West Bank; The Global Plastic Threat: Research Finds Plastics Can Lead to Disease, Disability & Premature Death

How can we learn to trust God when our prayers for healing go unanswered? What does it truly mean for the Church to become a place of belonging and welcome for individuals with disabilities?Dr. Laurie Thompson has deeply engaged with these questions—both personally and academically. At just 14 years old, a devastating car accident left her permanently disabled, marking the beginning of a lifelong journey of wrestling with faith, suffering, and inclusion. Now, as a college professor and academic advisor, Dr. Thompson empowers the next generation to understand that people with disabilities represent the largest minority in the United States—and that our Churches must become more inclusive, welcoming spaces for those navigating life with disabilities.In her latest book, **Disability-Inclusivity: Creating Awareness to Change the Current Trajectory**, Dr. Thompson explores how the Church can become a transformative community for those with disabilities—simply by making intentional adjustments that foster inclusion, dignity, and belonging.In this conversation, Davey sits down with Dr. Thompson to discuss the need for a robust theology of suffering, how to confront the lies that often accompany seasons of pain, and how the Church can reach and embrace people with disabilities through meaningful shifts in mindset and practice.If you're passionate about creating spaces of true belonging, this episode offers practical insights to help your community become a place of gospel-centered inclusion for those who are often overlooked. Instagram: instagram.com/laurieleet Facebook: https://www.facebook.com/laurie.thompson.98096721 Books: Laurie's Story: Discovering Joy In Adversityhttps://amzn.to/41b6TE4 Disability-Inclusivity: Creating Awareness to Change the Current Trajectoryhttps://amzn.to/4fb62Jk Wondering where to get started on your journey towards healing? Join Davey on our next FREE, live Zoom call and find out how you can begin to take back your story and how Nothing is Wasted can help. Sign up today at: www.nothingiswasted.com/starthere Looking for help in navigating the valley of pain and trauma? Our Nothing is Wasted coaches can help: www.nothingiswasted.com/coaching Want a pathway through your pain? The Pain to Purpose Course can lead you through all you've been through: www.nothingiswasted.com/paintoppurpose Learn more about your ad choices. Visit megaphone.fm/adchoices

Headlines for August 07, 2025; “War in Perpetuity”: M. Gessen Warns Putin Won’t Make Peace with Ukraine Because It Risks His Own Survival; From India to Brazil, Trump Intensifies Trade War Against BRICS Nations as New Tariffs Take Effect; “Tightening the Chokehold”: Amjad Iraqi on Israel’s Plans to “Empty Out” Gaza and Annex West Bank; The Global Plastic Threat: Research Finds Plastics Can Lead to Disease, Disability & Premature Death

Squirmy and Grubs are not your typical YouTube stars. One is them is able-bodied. The other is not. How they navigate the challenges that dichotomy presents is the point. So is how normal their lives as an interabled couple really are. The story of Hannah and Shane Burcaws' relationship and others like it is captured in their new book, "Interabled: True Stories about Love and Disability." They joined The Excerpt to talk about what they hope abled couples understand about interabled love. (This episode originally aired on January 22, 2025.)Please let us know what you think of this episode by sending a note to podcasts@usatoday.com.Episode Transcript available hereSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.