Podcasts about disabilities

Watch Joni's video on faith 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 a textIn this thought-provoking episode, Dr. Paulie sits down with Dr. Keith Storey—Professor Emeritus, BCBA-D, and lifelong educator—to explore how PBIS (Positive Behavioral Interventions and Supports) isn't just for schools. They break down how the same strategies that support students in classrooms can be used to empower people with disabilities as they transition into adult life and the workforce.Too often, students with disabilities age out of school and enter “the real world” with minimal support and little preparation for independence. Dr. Storey shares how PBIS strategies can help bridge that gap—creating environments that reinforce dignity, build skills, and increase the likelihood of success in the workplace and beyond.Topics Covered:How PBIS principles apply beyond K-12 to adult employment settingsUsing behavior analysis to increase independence and reduce barriersThe role of teachers and job coaches in shaping meaningful, dignified employmentChallenges in applying PBIS and ABA ethically in adult servicesReal examples of successful workplace inclusionWhy systems-level change is critical to long-term impactTreating adults with disabilities as capable contributors, not passive recipients of supportCheck out Dr. Storey's most recent book POSITIVE BEHAVIOR SUPPORTS FOR ADULTS WITH DISABILITIES IN EMPLOYMENT, COMMUNITY, AND RESIDENTIAL SETTINGS: Practical Strategies That Work (3rd Ed.)

Check out a Family Retreat near you 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.

You may be weak, but you live by God's power. -------- 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.

Explore the unspoken grief parents of children with disabilities experience over lost dreams. Find comfort, validation, and practical coping strategies for special needs parenting in this heartfelt episode. Download your free mindfulness guide.

Roman Abasy was a national Taekwondo champion and human rights advocate in Afghanistan, until the Taliban made him a target. Forced to flee, he rebuilt his life in Australia, turning exile into purpose. We explore Romans powerful journey from athlete to refugee to community leader, using sport, discipline, mental health and advocacy to uplift others, fight for justice and the right to belong. Timestamps added below if you want to skip to your juice.Want to become a Keep Rolling Patron and help further support the channel, hit the Patreon link below and Roll with the Squad!https://www.patreon.com/street_rolling_cheetahAdd, Follow or Contact Roman:LinkedIn: https://www.linkedin.com/in/roman-abasy-702ab2227/Add, Follow or Contact me: Email: streetrollingcheetah@gmail.com Instagram: https://www.instagram.com/street_rolling_cheetah/?hl=enTwitter: https://twitter.com/st_rollcheetahFace book: https://www.facebook.com/StreetRollingCheetah/LinkedIn: https://www.linkedin.com/in/jake-briggs-77b867100/Timestamps(00:00:00)  Welcome (00:03:23)  Introducing Roman Abasy(00:05:25)  Growing up in Kabul during a civil war(00:07:44)  School under the Taliban regime(00:12:27)  Starting into Taekwondo(00:14:40)  Continuing on education(00:16:20)  Regime change in 2001 - freedom (00:18:35)  Life inside and outside of Kabul (00:23:30)  Living with threats(00:25:10)  The normalisation of war(00:27:00)  Disabilities in a war torn country(00:32:45)  Hope Wheels program(00:34:01)  Access to tech vs values(00:37:45)  Leaving Afghanistan - a chaotic time(00:42:15)  Getting help from the Olympic committee(00:45:00)  Making it to Pakistan(00:46:03)  Australia was not by choice(00:48:16)  Learning languages (00:49:18)  Arriving in Sydney & getting support(00:56:10)  Living under different politics(00:58:05)  First job in Australia as a sports coordinator(01:03:42)  The different communities and integration(01:05:26)  Working in the public service(01:07:30)  Addressing local needs (01:10:35)  Youth settlement worker's role - helping with adaptation(01:16:15)  Housing crisis issues(01:18:40)  Comms with people in Afghanistan is controlled(01:22:15)  You can't forget where you came from(01:24:10)  Hope for change in a war torn country(01:31:02)  Local Islamic community - the difference(01:35:00)  Thoughts on Palestine, Israel and Iran(01:36:55)  Thoughts on local support for refugees(01:38:25)  Little Kabul and food talk

Willie O'Brien is famous for his name on Cranes throughout the city. He's sold up, moved on and now is passionate about other bosses seeing skills not disabilities. See also See My Skills Hosted on Acast. See acast.com/privacy for more information.

At an Omaha, Nebraska, festival this summer, new work explores the intersection of art, disability and technology, asking questions like "who has a voice?" and "who gets to be heard?" Senior arts correspondent Jeffrey Brown reports on this unusual undertaking for our arts and culture series, CANVAS. PBS News is supported by - https://www.pbs.org/newshour/about/funders

At an Omaha, Nebraska, festival this summer, new work explores the intersection of art, disability and technology, asking questions like "who has a voice?" and "who gets to be heard?" Senior arts correspondent Jeffrey Brown reports on this unusual undertaking for our arts and culture series, CANVAS. PBS News is supported by - https://www.pbs.org/newshour/about/funders

In this deeply moving episode, Michael reunites with legendary one-handed MLB pitcher Jim Abbott, whose incredible journey is now the focus of the new ESPN documentary "SOUTHPAW". Abbott shares how he overcame bullying, physical limitations, and public doubt to throw a no-hitter for the New York Yankees—and become an icon of resilience. Hear how he inspired thousands of families, mentored kids with disabilities, and changed the way people think about adversity. Plus, callers share their own remarkable stories of triumph over hardship. A must-listen for anyone in need of some real-life inspiration. Original air date 9 July 2025.

Get 10% OFF at elitefts (CODE: TABLE TALK): https://www.elitefts.com/  Shop Bands: https://www.elitefts.com/shop/bands.html   We welcome Chris Vachio to this episode of Dave Tate's Table Talk Podcast!   Chris Vachio has been training with purpose for over 40 years. A true veteran of the iron game, Chris started lifting in the early ‘80s and hasn't let up since. He first made his mark in the 1990s, dabbling in both bodybuilding and powerlifting, but it was Strongman that ultimately became his long-term passion.   For the past 16 years, Chris has dedicated himself to competing in and promoting Strongman events across the country. As a competitor, he's known for his grit, consistency, and old-school training mindset. As a promoter, Chris has earned widespread respect for running top-tier contests that are both lifter-focused and well-organized—helping grow the sport from the grassroots level up.   Check out his Adaptive Strongman competition this October: America's Strongest Athlete with Disabilities 2025 https://ironpodium.com/browse/event/america-s-strongest-athlete-with-disabi… – celebrating it's 10th anniversary!   Chris' IG: https://www.instagram.com/vachio/   THANK YOU TO OUR SPONSORS  Get 10% OFF Your Next Marek Health Labs (CODE: TABLETALK): https://marekhealth.com/ Get a FREE LMNT Sample Pack: https://partners.drinklmnt.com/free-gift-with-purchase?utm_campaign=agwp&am…   Save Up to 20% at Sleepme (CODE: TABLE TALK): https://sleep.me/tabletalk Get 10% OFF RP Hypertrophy App (CODE: TABLE TALK) :https://go.rpstrength.com/hypertrophy-app/  Get 10% OFF at elitefts (CODE: TABLE TALK): https://www.elitefts.com/  Get 10% OFF at Granite Nutrition (CODE TABLETALK): https://granitenutrition.com/?utm_source=podcast&utm_medium=audio&utm_campaign=Dave_Tate Save $250 at the Business of Strength Retreat 2025 (CODE: Elite250): https://bosretreat.com/     SUPPORT THE SHOW    All profits from elitefts Limited Edition Apparel, Table Talk Coffee, and Team elitefts Workouts, Programs, and Training eBooks support Dave Tate's Table Talk Podcast.    elitefts Shop: https://www.elitefts.com/  elitefts IG: https://www.instagram.com/elitefts/    elitefts  Limited Edition Apparel: https://www.elitefts.com/shop/apparel/limited-edition.html

If your life is in turmoil and everything around you is changing, turn to Malachi 3:6. -------- 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.

If you're a parent, educator, or advocate who's ever struggled to support kids with disabilities in school, this episode is a must-listen for real talk, hard truths, and practical ways to do better.More info, resources & ways to connect - https://www.tacosfallapart.com/podcast-live-show/podcast-guests/shannon-addisonIn this episode of Even Tacos Fall Apart, Shannon Addison joins me to talk about disabilities and youth in schools. Shannon is a mom, writer and creator of My Crummy World, a brand built to help kids (especially girls) navigate emotional health, friendships and confidence through story-driven tools like characters, recipes and problem-solving activities. Her work is rooted in her own journey as someone who's watched bullying and relational aggression happen right under the noses of adults who were supposed to be paying attention.Shannon shares how her daughter's chronic illness became a disability that changed everything - from how she participated in school to how peers treated her. She talks candidly about how cruel kids can be, how isolating school can feel when you're “different” and how parents often get thrown into advocacy without a map. We talk about how invisible disabilities, like dysautonomia or anxiety, get overlooked or misjudged because people can't “see” them, and how damaging that can be to a child's sense of safety and self-worth.We also talk about emotional intelligence, or the lack of it, and how schools are missing the mark by cutting out critical tools like social-emotional learning. Shannon shares examples of how storytelling (especially with her characters “The Breadcrumbs”) opens the door for kids to share what they're feeling in a safe and relatable way. Sometimes, she says, a puppet can get kids to talk in ways that a direct question from an adult just can't.We touched on the differences between IEPs and 504s, and how many parents aren't told what resources they have a right to. Shannon emphasizes that being informed and showing up, even when you're overwhelmed, is key. It's not about being perfect or doing everything. It's about being visible and being willing to fight when your kid needs you to.There's also a lot of love for teachers and school staff in this episode - the ones who go above and beyond, like the principal who told Shannon to bring her daughter in for community connection even when she wasn't able to fully return to school. But we also talk about how educators are underpaid, overstretched and often left without the support they need to help every kid succeed.If you've ever had to ask, “Why isn't this system working for my child?” or felt like you were the only one showing up to fight for your kid, this episode will make you feel seen. Shannon's message is clear: empathy can be taught, kids need community and parents don't have to do it all, but we do have to show up!

This episode is disabled and proud, listener! Tina Friml (Comedy Central, The Tonight Show) is an incredible stand up comedian and writer with cerebral palsy that has been taking the internet by storm, but today she's in the apartment GIVING the internet some TIPS on banging in the world of disabilities! We discuss dating with disabilities and its in's and out's, managing social anxieties around your disability, how male gaze affects even male strip clubs, and embracing disability pride because the gay pride flag sucks. Ashley is letting girls into her apartment. Lizzy is having lesbian sex in a straight relationship. Alex is being pimped out for views. Tina taking a break from touring! See her LIVE while you still can: https://linktr.ee/tinafriml  Follow Tina on IG and TikTok: https://www.instagram.com/tinafriml/  https://www.tiktok.com/@tinafriml  SUPPORT OUR PODCAST: Watch this UNCUT: https://www.patreon.com/WHGS Merch: https://shop.merchcentral.com/collections/ashley-gavin Watch on this YouTube: https://youtu.be/XhvnjwrSuXQ  FOLLOW ASHLEY GAVIN @ashgavs TikTok: https://www.tiktok.com/@ashgavscomedy Instagram: https://www.instagram.com/ashgavs/ YouTube: https://www.youtube.com/@ashgavs Twitter: https://twitter.com/ashgavs FOLLOW LIZZY CASSIDY @lizzycassidy TikTok: https://www.tiktok.com/@lizzycassidycomedy  Instagram: https://www.instagram.com/lizzycassidy/  Twitter: https://x.com/lizzaster  Tour Dates & Podcasts: https://linktr.ee/lizzycassidy  PRODUCED BY SWETSHOP: Instagram: https://www.instagram.com/swetshop.tv/ Learn more about your ad choices. Visit podcastchoices.com/adchoices

Through Joni's House programs, Joni and Friends identifies and meets the needs of people living with disabilities through local, Christ-centered support. At international locations across the globe, Joni's House is raising the standard of care for people with disabilities, offering physical, economic, spiritual, and social support, all in the name of Jesus. Learn more 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.

If you feel like your life is hard, keep trusting in God – there's greater glory on the horizon! -------- 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.

Lords: * Mark * https://wyrmburden.bandcamp.com/album/strange-sorcerous * Shirley * https://shop.naturmacht.com/sorcerot-merch/sorceroet-rotten-magick-vinyl-crowdfunding-lim Topics: * Music League * Shaping the Head Like a Japanese Watermelon * Kugelmugel * https://en.m.wikipedia.org/wiki/Kugelmugel * Welcome to Holland by Emily Perl Kingsley * https://www.emilyperlkingsley.com/welcome-to-holland * Using drugs in 2025 * https://en.m.wikipedia.org/wiki/File:UStimeline.Drugsinvolvedinoverdosedeaths.jpg Microtopics: * Wyrm Burden. * Metal bands running out of cool word combinations. * Checking Metal Archives. * Canadian atmospheric sludge metal. * Sorcerot. * Crowdfunding a vinyl pressing because your label refuses to pay for it. * Music that is not on Spotify. * How many Music Leagues you're part of right now. * A competition to see who has the best taste in music. * A song about a horse. * Adversarial Music League. * Posting on the internet with the goal of getting the same number of upvotes and downvotes. * Benign Hypotonia and the Floppy Baby. * Wearing a helmet 23 hours a day to adjust the shape of your skull. * Heads that smell like feet. * A very head-shaped head. * Babies that look like the Gary Oldman character in The Fifth Element. * A cone-shaped otter. * Zorg and Zord. * What kind of gear is this baby on? * Eat clen, tren hard. * Collecting as many physical therapists as possible. * A sweet little guy who's having a great time. * Putting on your resume your first word and the age you first walked. * Parent influencers with bad takes. * A baby that expands to the size of its container, so they'll stay baby sized forever unless you move into a bigger house. * Listen, have you ever evaluated anything? It's not easy. * Vibes-Based Medicine. * Declaring your metal sphere a micronation. * Closing the borders of your 8 meter micronation during COVID. * Building a house that looks like a ball. * Declaring your new house a micronation after the city refuses to grant you a building permit. * Antifascism Square. * Declaring your baby paddock a micronation. * A very good basically-a-poem. * Disabilities that are worse than going to Holland. * Trying to figure out how to live with the life you have. * Making peace with the fact that you didn't achieve all your dreams. * Divisive takes about sleep training. * Outcomes associated with prolonged cortisol exposure. * Category One Squawking. * Spending six years figuring out how to get your kid to fall asleep. * The term they invented to remind parents that just because things are good now, that doesn't mean they stay good forever, which is true for everything, but for children sleeping they have a specific term for it. * Getting real sad and going home. * Trying to take any drug except for fentanyl. * Fentanyl test strips from reliable suppliers. * If Coolio isn't safe, who is? * Narcan vending machines. * Walking down the street like you have Narcan in your pocket. * The terrifying gray line that dominates the entire graph. * A credible threat to a lot of recreational drug users. * Finally inventing the nightmare drug that DARE wanted you to be terrified of. * Nostalgia for street heroin. * The role that dopamine plays in human behavior. * A dogshit drug even from a drug enjoyer's perspective. * The only internet you even like any more.

If you feel like your life is hard, keep trusting in God – there's greater glory on the horizon! -------- 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.

Spin the Spectrum is an innovative, strength-based program music and DJ program for autistic and neurodivergent individuals. Developed by speech language pathologist Courtney Willis, in collaboration with Jay Clipp, a renowned DJ, and Jah born, a Grammy award-winning producer, opportunities are provided for autistic and neurodivergent individuals to engage in music production and creative self expression. Barry and Dave chat with the Spin the Spectrum team about the development and the impact of this program.Learn more on our websiteSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Our guest this week is Steve Harris of Lanesboro, MN a free-lance writer, widower, author and father of two sons with disabilities.  Part 2. Steve and his wife, Susan, have married for 17 years.  Steve and his first wife, Pam, were together for 30 years, before she passed away in 2012 due to a rare neurological disorder.  Steve and Pam had two boys: Matthew who was born in 1980 with Spina bifida and younger son, Andrew, who is 37 and who has Cerebral Palsy. Both boys would eventually be diagnosed with PMD or Pelizaeus Merzbacher Disease, a rare neurological disease, where there is a lack of myelin covering the nerves.Very sadly, Matthew passed away in October 2020 four days short of his 40th birthday. Steve's career included being a pastor, a middle school teacher and for 20 years, director of communications at Twin Cities YMCA .  All along Steve has been a writer who morer recently has published two books: Dads Like Us: A Survival Guide For Fathers Raising Children With Disabilities (2024)Lanesboro, Minnesota (2018)We also learn about a wide range of supporting organizations the family has benefited from, including: Spina Bifida Association,      Boston Children's Hospital, University of MA Medical Center, Genetic Counseling Gillette Children's Hospital (St. Paul),     Wanna Meonie's School (Palo Alto) inclusive, and   MN Accessible sports.One of Steve's superpowers is his resilience through some of life's greatest challenges. This week's episode of the SFN Dad To Dad Podcast is Part 2.Show Links:Phone – (952) 836-7904Email – sharris1962@msn.comLinkedIn –  https://www.linkedin.com/in/steve-harris-44101315/Website – https://steveharrisauthor.com/Books –Dads Like Us: A Survival Guide For Fathers Raising Children With Disabilities  (2024) https://tinyurl.com/mrxact2yLanesboro, Minnesota (2018) https://tinyurl.com/2zfbv24sSpecial Fathers Network -SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 800+ SFN Mentor Fathers, who are raising kids with special needs, have said: "I wish there was something like this when we first received our child's diagnosis. I felt so isolated.  There was no one within my family, at work, at church or within my friend group who understood or could relate to what I was going through."SFN Mentor Fathers share their experiences with younger dads closer to the beginning of their journey raising a child with the same or similar special needs. The SFN Mentor Fathers do NOT offer legal or medical advice, that is what lawyers and doctors do. They simply share their experiences and how they have made the most of challenging situations.Check out the 21CD YouTube Channel with dozens of videos on topics relevant to dads raising children with special needs - https://www.youtube.com/channel/UCzDFCvQimWNEb158ll6Q4cA/videosPlease support the SFN. Click here to donate: https://21stcenturydads.org/donate/Special Fathers Network: https://21stcenturydads.org/  SFN Mastermind Group - https://21stcenturydads.org/sfn-mastermind-group/

Discover what's possible when A is for action.  What does autism support look like across the globe? In part two of our conversation with Dr. Stephen Shore, he delves into how to move from autism awareness to autism acceptance.  We discuss: Autism awareness around the world Challenges in autism acceptance Practicing cultural humility The need for strength-based approaches and recognizing diverse abilities within the autistic community Meaningful inclusion strategies Disclosure and self-advocacy To learn more about Dr. Stephen Shore, please visit: https://drstephenshore.com/. —--------- This conversation with Dr. Stephen Shore was originally released on August 19, 2021.  Dr. Stephen Shore has written several books, including College for Students with Disabilities, Understanding Autism for Dummies, Ask and Tell, and Beyond the Wall. Currently, Dr. Shore serves on the boards of Autism Speaks, the Asperger Syndrome and High Functioning Autism Association, the US Autism and Asperger Association, the Scientific Council of OAR, and other autism related organizations. He formerly headed the Asperger's Association of New England and was on the board of the Autism Society of America. ----more---- We appreciate your time. If you enjoy this podcast and you'd like to support our mission, please take just a few seconds to share it with one person who you think will find value in it too. Follow us on Instagram: @autismpodcast Join our community on Mighty Networks: Global Autism Community Subscribe to our YouTube channel: Global Autism Project We would love to hear your feedback about the show. Please fill out this short survey to let us know your thoughts: Listener Survey. 

When you listen to Victoria (Vickie) Rock, 73, you would believe her life has never seen a difficult day. Yet, the truth is, at times it has been rocky. Turning lemons into lemonade is the perfect phrase to attribute to Vickie. Always upbeat, charitable, and giving, she works tirelessly to elevate each person, client and company that become part of her network.A career in court reporting led her to create a business of her own. When working until 2 or 3 a.m. in the morning became too much she sold out, along with her 75 member- team of court reporters and again could enjoy the basics of the business - meeting with clients, being in the courtroom and building her vocabulary with new and interesting words. Having been in this world for so many years, Vickie now teaches businesses how to tell their stories and win clients.Vickie is quick to give credit to those organizations along the way who have helped her grow: National Association of Women Business Owners (NAWBO), Women's Business Development Center (WBDC) and Goldman Sachs 10,000 Small Business program. Her church and Center for Disabilities & Elder Law remain important organizations she supports.Enjoy our lives: How many Thanksgivings do we have left? - Victoria RockCONNECT WITH VICTORIA ROCK:Email: victoria@victoriarock.bizWebsite: Victoria Rock

Morton ISD is food trucking across the Panhandle. The SPEDTalk team discusses how they got started, what the students are accomplishing, and where they are going.

Join Stef Blackwell and I again for another conversation about sticky topics we have to uncover with our kids. Today we talk about teaching our kids about disabilities, whether they be obvious, physical disabilities or not-so-obvious mental ones. This can be difficult because kids can often not know how to handle seeing someone with a big disability and be unwittingly unkind. They can also be difficult as we teach our kids about boundaries we (or they) may want to set for our children's protection. We pray this episode does not offend or that we do not share something that leads anyone astray. If you have further insight into this topic, please email me at thebetterpartpod@gmail.com.Some resources mentioned in the episode are:Book: Let's Go Play by Shelby McCarthyExpert in autism: Dr. Amanda BlackwellGame: Concept

No matter how disabled, old, or incapacitated you are, you can still live for God and serve others. That is what gives you a great quality of life! -------- 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's full broadcast of Computer Talk Radio includes - 00:00 - Nerd news for normal people - Etsy, 3D printing, TSA, Infinity Train, Windows 10, SoundBlaster - 11:00 - Upsides and downsides of tech - Benjamin covers both sides of how tech is changing our lives - 22:00 - Smartphone disability features - Keith and Benjamin discuss features for disabled we can all use - 31:00 - Marty Winston's Wisdom - Marty talks of the Plaud Note and the Plaud Notepin AI devices - 39:00 - Scam Series - how to protect - Leo advises his mother almost gave bank info, how to protect - 44:00 - Keske on pulse oximeters - Benjamin and Steve talk about infrared uses in medicine - 56:00 - Listener Q&A - Megan asks why smart home devices need different apps - 1:07:00 - Listener Q&A - Darius wants to know why companies prevent fixing ourselves - 1:16:00 - IT Professional Series - 334 - Benjamin warns of recruitment for jobs going cold due to AI - 1:24:00 - Listener Q&A - Max questions why his gaming console lags in multiplayer

Hear Peter and Christy's account on how their experience was at a Joni and Friends Family Retreat. -------- 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.

Our guest this week is Steve Harris of Lanesboro, MN a free-lance writer, widower, author and father of two sons with disabilities.  Part 1.Steve and his wife, Susan, have married for 17 years.  Steve and his first wife, Pam, were together for 30 years, before she passed away in 2012 due to a rare neurological disorder.  Steve and Pam had two boys: Matthew who was born in 1980 with Spina bifida and younger son, Andrew, who is 37 and who has Cerebral Palsy.  Both boys would eventually be diagnosed with PMD or Pelizaeus Merzbacher Disease, a rare neurological disease, where there is a lack of myelin covering the nerves.Very sadly, Matthew passed away in October 2020 four days short of his 40th birthday. Steve's career included being a pastor, a middle school teacher and for 20 years, director of communications at Twin Cities YMCA .  All along Steve has been a writer who morer recently has published two books: Dads Like Us: A Survival Guide For Fathers Raising Children With Disabilities (2024)Lanesboro, Minnesota (2018)We also learn about a wide range of supporting organizations the family has benefited from, including: Spina Bifida Association,      Boston Children's Hospital, University of MA Medical Center, Genetic Counseling Gillette Children's Hospital (St. Paul),     Wanna Meonie's School (Palo Alto) inclusive, and   MN Accessible sports.One of Steve's superpowers is his resilience through some of life's greatest challenges. This week's episode of the SFN Dad To Dad Podcast is Part 1.Show Links:Phone – (952) 836-7904Email – sharris1962@msn.comLinkedIn –  https://www.linkedin.com/in/steve-harris-44101315/Website – https://steveharrisauthor.com/Books –Dads Like Us: A Survival Guide For Fathers Raising Children With Disabilities  (2024) https://tinyurl.com/mrxact2yLanesboro, Minnesota (2018) https://tinyurl.com/2zfbv24sSpecial Fathers Network -SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 800+ SFN Mentor Fathers, who are raising kids with special needs, have said: "I wish there was something like this when we first received our child's diagnosis. I felt so isolated.  There was no one within my family, at work, at church or within my friend group who understood or could relate to what I was going through."SFN Mentor Fathers share their experiences with younger dads closer to the beginning of their journey raising a child with the same or similar special needs. The SFN Mentor Fathers do NOT offer legal or medical advice, that is what lawyers and doctors do. They simply share their experiences and how they have made the most of challenging situations.Check out the 21CD YouTube Channel with dozens of videos on topics relevant to dads raising children with special needs - https://www.youtube.com/channel/UCzDFCvQimWNEb158ll6Q4cA/videosPlease support the SFN. Click here to donate: https://21stcenturydads.org/donate/Special Fathers Network: https://21stcenturydads.org/  SFN Mastermind Group - https://21stcenturydads.org/sfn-mastermind-group/

In this episode, I welcome Shari Pierce—retired special education teacher, author, and sibling of an adult with developmental disabilities. With over 30 years in the classroom, Shari shares practical life skills for parents and teachers, stories from her career, and powerful advice on how we can better support and include people with intellectual disabilities.We explore:* Why inclusion matters in schools and at home* How to talk to your kids about disabilities* Lessons from teaching hands-on life skills* What Shari learned growing up with a disabled siblingThis conversation is a must-watch for parents, educators, and anyone wanting to raise compassionate kids.

We would love to pray for you! Please send us your request here: https://joniandfriends.org/contact-us/?department=Radio --------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.

There aren't many practitioners writing about today's topic. Unless, that is, you look up the collected works of Dr. Bill Dodson. Dr. Dodson is an award-winning board-certified psychiatrist and specialist in adult ADHD and his contributions to the study of Rejection Sensitive Dysphoria bring him to the show today. According to Dr. Dodson, nearly all those living with ADHD live with some level of rejection sensitivity, and thanks to the poor training on the ADHD connections to the condition, patients are going misdiagnosed and mistreated as a result.Today on the show, Dr. Dodson joins Nikki Kinzer and Pete Wright to discuss Rejection Sensitive Dysphoria and provide new language to frame a state those living with ADHD know all too well.About Dr. William DodsonDr. Bill Dodson is a award-winning board-certified psychiatrist and specialist in adult ADHD. While Dr. Dodson has been on the faculties of Georgetown University and the University of Colorado Health Sciences Center he is primarily a clinical practitioner who tries to combine evidence-based practice techniques with practice-based evidence.  In addition to being named a Life Fellow of the American Psychiatric Association, and recipient of the national Maxwell J. Schleifer Award for Distinguished Service to Persons with Disabilities, Dr. Dodson is one of two experts from the US to the World Anti-Doping program for the development of guidelines for the use of ADHD stimulant medications in the world's athletes.Links & NotesDr. William Dodson at Additudemag.com (00:00) - Welcome to The ADHD Podcast (02:24) - Become a Member of The ADHD Community (04:28) - Introducing Dr. William Dodson (05:53) - What is Rejection Sensitive Dysphoria? (10:59) - Defining Characteristics of RSD? (13:37) - Mental health trends (17:23) - RSD and Imposter Syndrome (20:15) - RSD and Gender (25:45) - Treatment paths for RSD (34:14) - RSD and ADHD Coaching (43:44) - Finding Dr. Dodson ★ Support this podcast on Patreon ★

Grace always, always meets you at your point of pain. -------- 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.

Summer is in full swing and so many are flocking to the tees this time of the year - we talked to Joel Comstock with the Minnesota Golf Association and Organizer for the Minnesota Adaptive Open and how they are providing ways for those who struggle with disabilities to enjoy the great game of golf!

God will use your witness to bring your family to saving faith. -------- 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 episode 17, Jess welcomes Kelleen and Kimmy, who are both older siblings of autistic adults. Kelleen is an SLP, and Kimmy is a BCBA, both at the University of Washington's Autism Center. In today's discussion, they share how their experiences with their autistic siblings shaped them as people, but also as compassionate practitioners and advocates in their fields. We look at the joys and challenges they experienced as older siblings and some of the issues that continue to arise as they navigate the present and future. And last, but not least, they offer parents some helpful advice for helping their neurotypical children understand and embrace autism. We hope you enjoy the episode!     Resources –Websites for Siblings: Sesame Street (young children) – http://autism.sesamestreet.org/ Rocking Mountain Sibs – https://www.rmsibs.com/ A Sibling's Guide to Autism – https://www.autismspeaks.org/sites/default/files/2018-08/Siblings%20Guide%20to%20Autism.pdf Siblings of Autism – https://siblingsofautism.org/ Sibling Leadership Network – https://siblingleadership.org/ Sibling Support Project – https://siblingsupport.org/ The Organization for Autism Research has a number of sibling resources – https://researchautism.org/how-we-help/families/sibling-support/ The Arc of New Jersey has several helpful resources for siblings of all ages –  https://www.thearcfamilyinstitute.org/resources/sibling-resources/young-sibs.html Parent to Parent – https://www.p2pusa.org/ The Sibling Transformation Project – https://www.siblingtransformation.org/ Growing Up Alongside a Sibling with a Disability –https://www.nytimes.com/2020/05/11/parenting/children-sibling-disability.html  Books for Parents about Siblings: Siblings of Children with Autism: A Guide for Families by Sandra Harris PhD & Beth Glasberg PhD Autism Spectrum Disorder Sibling Support: 15 Practical Tips for Parents & Caregivers by Trish Thorpe Here are links to picture book lists featuring Autistic children.  Amazon: https://www.amazon.com/shop/maistorybooklibrary/list/14VLE2C1F0T17 Bookshop: https://bookshop.org/lists/autism-acceptance-picture-book-list   Sibling books: Benji, the Bad Day, and Me by Sally J. Pla My Brother Otto by Meg Raby (preschool to early elementary) My Brother Charlie by Holly Robinson Peete & Ryan Elizabeth Peete (elementary age) Leah's Voice by Lori DeMonia (elementary age) Tacos Anyone? By Marvie Ellis (elementary age) - Bilingual book Brotherly Feelings: Me, My Emotions, and My Brother with Asperger's Syndrome by Sam Frender & Rob Schiffmiller (elementary age) What About Me? A book by and for an Autism Sibling by Brennan & Mandy Farmer (elementary age) Understanding Samantha: A Sibling's Perspective of Autism by Dustin Daniels (elementary age) Everybody is Different by Fiona Bleach (elementary/middle school age) Autism: The Invisible Cord by Barbara Cain (middle school) Rules by Cynthia Lord (middle school) The Reason I Jump by Naoki Higashida (middle school) Same but Different: Teen Life on the Autism Express by Holly Robinson Peete, Ryan Elizabeth Peete, & RJ Peete (middle school/high school) The Sibling Survival Guide: Indispensable Information for Brothers & Sisters of Adults with Disabilities by Don Meyer & Emily Holl (high school/adults)  Memoirs by Siblings: Boy Alone: A Brother's Memoir by Karl Greensfeld How to be a Sister: A love story with a twist of autism by Eileen Garvin The Ride Together: A Brother & Sister's Memoir of Autism in the Family by Paul & Judy Karasik At Home in the Land of Oz: My Sister, Autism, and Me by Anne Barnhill Crystal Puzzle: Growing Up with a Sister with Asperger's by Ashley Nance How autism shapes sibling relationships By Emily Laber-Warren

Welcome to Hot Topics! Join host Gabrielle Crichlow in this empowering episode featuring fellow tutorpreneur Renée Peña Lopez as they discuss the essential role of advocacy in your child's development. Together, they delve into key developmental markers for preschool and elementary-aged children, providing parents with the insights needed to recognize and address their child's unique needs.In this episode, you'll learn effective strategies for advocating for your child's educational and emotional support, and discover how to navigate the systems in place to ensure they receive the help they require. Gabrielle and Renée share practical takeaways for when you feel overwhelmed or stuck, empowering you to advocate confidently and effectively.Renée, an early childhood inclusion specialist and special education teacher, shares her personal journey of advocating for her daughter who faced developmental delays. The conversation highlights the importance of understanding and navigating the special education system, including terms like "CPSC" (Committee of Special Education) and "EI" (Early Intervention). The episode emphasizes the significance of developmental milestones for children aged 3-5 years, advocating early, and the collaborative relationship between parents and educators. Renée also addresses the cultural considerations surrounding advocacy, including the stigma some parents face regarding labels and special education.Whether you're a parent, educator, or caregiver, this episode is filled with expert advice and actionable tips to help you become a mighty advocate for your child. Tune in and take the first steps toward making a meaningful difference in their educational journey! Key Takeaways:- Understanding your child's developmental markers.- Strategies for effective advocacy in educational settings.- Importance of documentation and early intervention.- Navigating cultural considerations and overcoming stigma.- Building collaborative relationships with educators.Don't miss this insightful discussion that empowers you to support your child's needs!,Who is Renée Peña Lopez?Renée Peña Lopez is an Early Childhood Inclusion Specialist, and proud Native New Yorker. She is a licensed special education early childhood teacher who has a passion for quirky learners such as herself. Renée attended Bard College for her B.A. in Dance and Integrated Arts (Video and Arts Education). While on her journey, she fell in love with Early Childhood working at an enrichment school, where the director took a chance on her and suggested she go into the field. She decided to attend Mercy College for (Birth-6th with Student with Disabilities). Now, Renée pulls from her creative background in dance and her vast experience in an array of classrooms from museums to progressive spaces to play-based models. She is also a Mama of a quirky and lovely kiddo who works with Families and Teachers of Littles to help them make sense of their Littles play by finding the magic that makes them shine. Together, we rethink inventions!You can find Renée:On the web: https://www.themagicoflittles.com/On Facebook: https://www.facebook.com/TheMagicOfLittles/On Instagram: https://www.instagram.com/themagicoflittlesOn Threads: https://www.threads.net/@themagicoflittlesOn Pinterest: https://www.pinterest.com/themagicoflittles/On LinkedIn: https://www.linkedin.com/in/renee-pena-lopez-9a93957Download "The Mighty Advocate Guide" for free: https://www.themagicoflittles.com/page/619933Purchase digital "Stay on Top of IEPs" Planner with 50% discount for our audience: https://www.themagicoflittles.com/purchase/212062-Stay-on-Top-of-IEPs-Planner/coupon/ASTEPAHEADWatch this episode on YouTube: https://youtube.com/live/Tjw69vLdAIYRate this episode on IMDB: https://m.imdb.com/title/tt36940673/?ref_=ext_shr_lnk********************************************Follow Gabrielle Crichlow:On Facebook: https://www.facebook.com/gabrielle.crichlow On Instagram: https://www.instagram.com/gabrielle.crichlowOn LinkedIn: https://www.linkedin.com/in/gabrielle-crichlow-92587a360Follow A Step Ahead Tutoring Services:On Facebook: https://www.facebook.com/astepaheadtutoringservicesOn Instagram: https://www.instagram.com/astepaheadtutoringservicesOn X: https://www.x.com/ASATS2013On TikTok: https://www.tiktok.com/@asats2013On LinkedIn: https://www.linkedin.com/company/a-step-ahead-tutoring-services/On YouTube: https://www.youtube.com/@astepaheadtutoringservicesOn Eventbrite: https://astepaheadtutoringservices.eventbrite.comVisit us on the web: https://www.astepaheadtutoringservices.comSign up for our email list: https://squareup.com/outreach/a41DaE/subscribeSign up for our text list: https://eztxt.s3.amazonaws.com/534571/widgets/61fc686d8d6665.90336120.htmlCheck out our entire "Hot Topics!" podcast: https://www.astepaheadtutoringservices.com/hottopicspodcastSupport us:Cash App: https://cash.app/$ASATS2013PayPal: https://paypal.me/ASATS2013Venmo: https://venmo.com/u/ASATS2013Become a supporter of this podcast: https://www.spreaker.com/podcast/hot-topics--5600971/support Original date of episode: March 16, 2025

#95 - Mike Pritchett is the founder of Kids With Disabilities Adventures — a nonprofit dedicated to helping kids with disabilities and their families experience the outdoors through turkey hunting, big game, and fishing trips. In this heartfelt episode, Mike shares how the organization got started, the stories that fuel him, and the incredible impact it's had on children, parents, and volunteers. We also talk about fatherhood, mindset, and how the outdoors can heal and connect. Mike even shares his go-to fish recipe for your next lake trip — and yes, it'll convert even the pickiest eaters. Whether you love hunting, community-driven work, or just a dang good story, this one's for you. BONUS: Want to hear from the teachers, volunteers, and Forest Service staff who've been part of KWD? Watch the Voices from the Field bonus video here →  Get our FAVORITE links, codes & more here! EPISODE MENTIONS:  Kids with Disabilities Adventures website HERE Connect w/ KWD Instagram HERE Watch the show on YouTube HERE Submit your stories at thereckoningpodcast.com/submit SHEEPFEET for custom orthotics, the best hunting shoe and the hideout hoodie use code: RECKONING for 10% OFF SHOP HERE MTN OPS for the best supplements and gear. Use code BRITT for 20% OFF your order! RUGGED ROAD COOLER GET 10% OFF your lightweight and organized cooler here or USE CODE: LONG  Have Reckoning create content for your brand, learn more HERE! Follow Us on Social:  Brittney Long IGReckoning IG Affiliate Disclaimer.  Show Notes may contain affiliate links. If you click through my referral link, at no additional cost to you, I may earn a small commission if you make a purchase.  Thank you for supporting RECKONING LLC.  

From Genesis to Revelation, Scripture has profound things to say about disability, worth, and God's purposes. In this episode, hear a personal and biblical exploration of how God sees every person—including those with disabilities—as fearfully and wonderfully made.Discover how:Every person bears God's image regardless of abilityGod's power is perfected in our weaknessThe Church is called beyond inclusion to true belongingPersonal struggles can become channels for God's gloryThis message includes honest conversations about the daily realities families face and challenges the Church to create spaces of genuine connection and care.Key Scriptures:Genesis 1:27 - "So God created mankind in his own image, in the image of God he created them; male and female he created them."Psalm 139:14 - "I praise you because I am fearfully and wonderfully made; your works are wonderful, I know that full well."John 9:3 - "Neither this man nor his parents sinned," said Jesus, "but this happened so that the works of God might be displayed in him."2 Corinthians 12:9 - "But he said to me, 'My grace is sufficient for you, for my power is made perfect in weakness.'"Exodus 4:11 - "The Lord said to him, 'Who gave human beings their mouths? Who makes them deaf or mute? Who gives them sight or makes them blind? Is it not I, the Lord?'"Revelation 21:4 - "He will wipe every tear from their eyes. There will be no more death, or mourning or crying or pain, for the old order of things has passed away."Connect with us at www.grandpoint.church/nextstepsWatch online on YouTubeFollow us on Facebook and InstagramSign up for our free weekly newsletter

The cross cannot be merely taught or reasoned; it must be experienced. -------- 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 part of the 2025 Developmental Disabilities Conference, Peggy McManus with The National Alliance to Advance Adolescent Health/Got Transition talks about barriers, inequities and policy options for youth aging out of public programs. Series: "Developmental Disabilities Update" [Health and Medicine] [Show ID: 40609]

As part of the 2025 Developmental Disabilities Conference, Peggy McManus with The National Alliance to Advance Adolescent Health/Got Transition talks about barriers, inequities and policy options for youth aging out of public programs. Series: "Developmental Disabilities Update" [Health and Medicine] [Show ID: 40609]

The Hidden Lightness with Jimmy Hinton – At the Prospector Theater in Ridgefield, Connecticut, adults with disabilities find meaningful work, from projectionist to digital marketer. Founder Valerie Jensen focuses on potential over limitations, empowering employees known as “Prospects” to develop skills, confidence, and community. This inclusive cinema experience sparks creativity, transforms lives, and offers a replicable model for...

As a developmental pediatrician, Dr. Wendy Ross serves patients who are autistic and neurodivergent and their families, but her work goes well beyond direct clinical care. She believes in having an impact on community understanding, support and inclusion for all people with neurodevelopmental differences. Barry, Dave and Wendy discuss many of her initiatives in the community and at Jefferson Medical Center in Philadelphia, and the types of supports that truly improve quality of life for neurodivergent and autistic children and adults, and their families.Learn 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.

Episode 94: Parenting a Child with Disabilities with Casey Mouton In this episode, Rachael sits down with therapist and mom Casey Mouton to talk about the emotional and complex journey of parenting a child with disabilities. Casey opens up about her son's diagnosis after a stroke at 10 months old, how it impacted her family, and the ways her personal experience shaped her work in maternal mental health. This conversation is a deeply honest look at what it means to face uncertainty, advocate fiercely, and still find moments of joy along the way. Inside this episode: How Casey's postpartum experience shifted her career to focus on maternal mental health The story of her son's stroke and diagnosis with cerebral palsy What grief looks like when you're parenting through it How parenting a child with disabilities can strain relationships and what helps The healing power of support groups and community Tips for advocating in school settings and building inclusive environments Why finding joy amidst challenges isn't just possible…it's necessary Empowering kids to understand their potential and build confidence The importance of empathy and understanding from the outside world And so much more! Mentioned in this episode: Mavida Health: Collaborative care for maternal mental health Follow Casey on Instagram: https://www.instagram.com/mavidahealth/?hl=en  If you enjoyed this episode, please rate 5⭐️ and write us a review! ⬇️ ✨For sleep support and resources, visit heysleepybaby.com and follow @heysleepybaby on Instagram!

If Tamila's story has touched your heart, you can visit joniradio.org today to bless some boys and girls with disabilities around the world. Children like Tamila need Jesus, a child-sized wheelchair, and their family to hear the Gospel. Donate Today --------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.

Ask Joni a question 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.

Kitrael Chin joins guest host Brooke Taylor sharing the profound impact of performing at the 2025 Jubilee of Persons with Disabilities at the Vatican. Elizabeth Wellendorf is an American nurse dedicating her life to serving disabled children at an orphanage in Bethlehem. Her mother Christina shares about her great work.

Joining us on Well Said is Michael Kalberer, licensed social worker and motivational speaker, Dr. Adam Stein, Chairman and Professor of the Department of Physical Medicine and Rehabilitation at the Zucker School of Medicine and Rebecca Kotun, patient and advocate for people in the disabled community. They will be diving into the unique and diverse […]

Take a look at Steve Bundy's book: “Another Kind of Courage” 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.

TAKE THIS PERSONALLY WITH MORGAN: *Part 1 of the disability series* Madeline Cheney shares her origin story & why she started The Rare Life podcast after she received troubling results at her 20-week ultrasound that pointed to a rare syndrome. She details the emotions she had throughout the entire journey and opened up about the highs and lows of having a child with disabilities and medical complexities. Follow Madeline Cheney: @the_rare_life Follow Morgan: @webgirlmorgan Follow Take This Personally: @takethispersonallySee omnystudio.com/listener for privacy information.