Podcasts about Cerebral palsy

Dr. Patricia Tan serves as Medical Director for Rusk Pediatrics Rehabilitation. Her Certification is from the American Board of Physical Medicine & Rehabilitation. She has been selected as a Fellow by the following organizations: American Academy of Physical Medicine and Rehabilitation; American Academy of Pediatrics; American Academy of Cerebral Palsy and Developmental Medicine; and the Association of Academic Physiatrists. Her medical degree is from the University of Santo Tomas in Manila, Philippines. Dr. Megan Conklin is Associate Director of Rusk Pediatric Therapy Services at NYU Langone. She works collaboratively with an interdisciplinary team across the spectrum of pediatric diagnoses from birth through the transition into adulthood. She has a Doctor of Physical Therapy degree, 20 years of clinical experience at NYU; and is certified as a clinical specialist in pediatric physical therapy by the American Board of Physical Therapy Specialties of the American Physical Therapy Association. Part 2 The discussion included the following topics: quality measures used to determine if desired outcomes are being achieved; challenges or potential downsides associated with a transition from pediatric to adult care; integration of artificial intelligence into pediatric rehabilitation; and current pediatric research conducted at NYU.

All Home Care Matters and our host, Lance A. Slatton were honored to welcome Anne S. Royer & Robert W. Royer as guests to the show.   About Anne S. Royer: Anne's background and interests have included family, volunteering, and her love of art, painting and photography that began while living in Santa Fe and continues today.   About Robert W. Royer: Robert is a semi-retired real estate developer specializing in residential, mixed-use, and resort properties.   About Meal Lifter®: The Meal Lifter® eating aid was created to assist individuals suffering from Parkinson's, Alzheimer's, dementia, Cerebral Palsy, Essential Tremors, autism, strokes, injuries, learning disabilities, and age-related conditions that make it difficult to eat independently.    

Beyond Coping: Radical Healing in a World Not Built for Us – An Interview with José Rosario Curt and Katie chat with José Rosario about radical healing, disability, cultural trauma, and intersectionality. José shares his story as a scholar, practitioner, and activist, and how his lived experience as a disabled person of color who is also queer informs both his clinical work and research. He discusses how healing must move beyond coping, the importance of community engagement, and how therapists can better support clients with marginalized identities. About Our Guest: José Rosario Born to young Puerto Rican parents, José Rosario developed Cerebral Palsy as a premature baby. His family's journey towards equity deeply impacted his mental health. Currently nearing his PhD in Clinical Psychology, his research focuses on cultural trauma in intersectional communities. He is an Interdisciplinary Minority Fellow for the American Psychological Association, member of the Congressional Diversity and Equality Advisory Board for Congressman James Langevin, and member of the Rhode Island Attorney General Community Advisory Board. He has been honored with the Chris Martin Humanitarian Award and the Victoria Lederberg Award for Excellence in Psychology. Key Takeaways for Therapists Radical healing means moving beyond coping to systemic change and community-based healing. Disability, race, and queerness intersect in ways that compound stigma and systemic barriers. Community is both a source of hope and a vital element of healing. Therapists must step outside the therapy room and engage genuinely with the communities they serve. For full show notes and transcripts, visit: mtsgpodcast.com Join the Modern Therapist Community Linktree: https://linktr.ee/therapyreimagined Modern Therapist's Survival Guide Creative Credits Voice Over by DW McCann Music by Crystal Grooms Mangano

You might be surprised to learn I'm not automatically on the side of the disabled person in a given situation.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

How do you build a thriving life while navigating profound personal challenges? This week, we welcome a truly inspiring guest who embodies resilience, Dr. Michelle Taveras, founder of M Taveras, PsyD & Company Psychological Services.Dr. Taveras shares her powerful, intimate journey of earning her doctorate and establishing a respected practice while living with cerebral palsy. It's a candid look at what it truly takes to push past limitations and find your deepest sense of purpose.In this essential mental health break, Dr. Taveras draws on her decades of clinical experience to give you actionable clarity:Stress vs. Anxiety: She breaks down the critical differences between these two common emotional states—and why misdiagnosing yourself is holding you back.The Power of Letting Go: Learn the mental practice required to release what you can't control and redirect your energy toward constructive change.When to Get Help: Dr. Taveras offers clear guidance on recognizing the signs that you've moved past self-help and need to seek professional support.The Root Cause: Discover her belief that comprehending the origin of your emotional experiences is the most effective path to lasting empowerment.This is an episode about achieving your fullest potential, regardless of the challenges you face. Tune in for expert psychological insight and a dose of real-world inspiration.Support the showHave a question for the host or guest? Want their freebee? Are you looking to become a guest or show partner? Email Danica at PodcastsByLanci@gmail.com.This show is brought to you by Coming Alive Podcast Production.CRISIS LINE: DIAL 988

Stepping away from our studio setting, we're bringing you a special "speedcast" from the bustling Abilities Expo in Chicago where we met Mikaylah, a remarkable young woman navigating life with dystonic cerebral palsy while pursuing her dreams.Mikaylah, a creative writing major at the University of Illinois Urbana-Champaign, offers a candid glimpse into her world. She manages her condition with a deep brain stimulator (a device similar to a pacemaker but connected to her brain) and medication regimens. What stands out immediately is her matter-of-fact approach to these medical realities – they're simply part of her daily experience, not limitations that define her potential.When our conversation turns to literature, Mikaylah's passion ignites. She recommends "Unmasked" by Kendra Merritt, praising how the author authentically incorporates disability into fantasy fiction. This representation matters deeply to Mikaylah's, who notes the scarcity of disabled characters in the books she encountered growing up. Now, she's crafting her own stories, adding her voice to this essential narrative space. The most revealing moment comes when she shares a troubling high school incident – administrators placed her service dog's photo on her student ID instead of her own picture, a dehumanizing error that speaks volumes about how society often fails to see disabled individuals as complete persons.Michaela's parting wisdom resonates deeply: "Just keep living. Life goes on. Life is precious. You only get one." Connect with us on social media, share your thoughts, and subscribe to hear more stories that challenge perspectives and celebrate the full spectrum of human experience.

In this episode of ListenABLE, hosts Dylan Alcott and Angus O’Loughlin sit down with Carly Salmon – athlete, teacher, and captain of the Para Matildas. Carly opens up about her journey with cerebral palsy, how sport shaped her identity, and why representation in disability sport matters now more than ever. From her early years in athletics to leading Australia’s Para Matildas, Carly shares the highs and lows of competing, teaching, and empowering others. She reflects on the impact of women’s football, the importance of mental health in sport, and her mission to inspire young people to see their disabilities as strengths. Follow their journey: Carly's Instagram: https://www.instagram.com/carlysalmon ParaMatildas: https://www.instagram.com/paramatildas/ Para Volley: https://www.instagram.com/ausparavolley/ Key Takeaways Diagnosed with cerebral palsy at 18 months, Carly has grown into a leader in sport and education. Represented Australia in athletics before transitioning into football. Captain of the Para Matildas, leading by example on and off the field. Teaching is central to her advocacy – showing kids that disability doesn’t limit potential. Women’s football’s rise has created more visibility and momentum for para athletes. Advocates strongly for funding and support to grow para sports in Australia. Believes sport is a powerful way to build identity, community, and empowerment. Chapters 00:00 – Introduction to the Podcast and Guests03:09 – Carly Salmon's Journey with Cerebral Palsy05:55 – Teaching and Impact on Students08:59 – Realizations of Disability in School11:43 – Finding Strength in Disability14:46 – Transitioning from Athletics to Football17:49 – Leadership in Team Sports20:44 – The Rise of Women's Football and Its Impact23:49 – Pride in Disability Beyond Sports26:37 – Future Goals for the Para Matildas29:56 – Addressing Funding and Support for Para SportsSee omnystudio.com/listener for privacy information.

Trajectories of Fidgety Movements in Infants with and without medical complexity.This paper is a finalist for AACPDM's highest honour - the Gayle G Arnold award, chosen and highlighted by the scientific review committee for it's high quality.We look ahead at The American Academy for Cerebral Palsy and Developmental Medicine (AACPDM) Conference - the 79th Annual Meeting!“Celebrating Resilience” October 15-18, 2025, to be held in New Orleans, LA. 

The Tim Conway Jr. Show is No. 43 on the list of top podcasts at iHeartMedia! There's an Apple iPhone update, iOS26 is here! Let's check out all the bells and whistles on this latest iPhone release. Apparently, the folks are nice as Hemet. And it's Fat Bear Week in Alaska! California's High-Speed Rail continues to travel in the wrong direction. Twenty-four percent of the nation's homeless population – that's 187,000 people – live in California – it's an outrage! A food delivery bot went cray-cray on a man with cerebral palsy in West Hollywood.

Dr. Patricia Tan serves as Medical Director for Rusk Pediatrics Rehabilitation. Her Certification is from the American Board of Physical Medicine & Rehabilitation. She has been selected as a Fellow by the following organizations: American Academy of Physical Medicine and Rehabilitation; American Academy of Pediatrics; American Academy of Cerebral Palsy and Developmental Medicine; and the Association of Academic Physiatrists. Her medical degree is from the University of Santo Tomas in Manila, Philippines. Dr. Megan Conklin is Associate Director of Rusk Pediatric Therapy Services at NYU Langone. She works collaboratively with an interdisciplinary team across the spectrum of pediatric diagnoses from birth through the transition into adulthood. She has a Doctor of Physical Therapy degree, 20 years of clinical experience at NYU; and is certified as a clinical specialist in pediatric physical therapy by the American Board of Physical Therapy Specialties of the American Physical Therapy Association. Part 1 The discussion included the following topics: kinds of health problems and conditions treated; age range of patients; clinical guidelines and evidence-based treatment protocols used; holistic approaches to treatment; collaboration with families of patients; and composition of the health care team

Text Us!In this episode of Raising Disabled, we talk to Caroline about raising her daughter Briella who has Cerebral Palsy.  Caroline is the social media manager for our sponsors Altimate Medical and Zing Standers.  Follow Caroline on Instagram @briellaandme Please subscribe, leave a review, and follow us on social media to know about upcoming episodes and to participate in this podcast.Instagram - @raisingdisabledpodcastFacebook - Raising Disabled Podcast

What does it truly mean to face life's challenges with genuine joy? Meet Orly Koenig, a remarkable 10-year-old who transforms her daily struggles with cerebral palsy into opportunities for growth, laughter, and inspiration.Born two months premature, Orly candidly shares her journey—from her diagnosis and multiple surgeries to her everyday life navigating the world sometimes on foot, sometimes by wheelchair, and often on her beloved electric scooter. With wisdom that defies her years, she reveals her secret to maintaining positivity: "Sometimes you don't feel like a normal kid because it's hard. But in life, things can be hard—you just have to keep pushing through."Orly's approach to life's obstacles isn't about ignoring difficulties but reframing them through gratitude and purpose. Perhaps most touching is how Orly's joy becomes contagious. From distributing lollipops during hospital stays to volunteering at the gift shop while still a patient herself, she consistently turns personal hardship into opportunities to brighten others' lives. Her name "Orly," meaning "my light," perfectly captures her essence as someone who illuminates every room she enters.As we approach Rosh Hashanah, Orly's story reminds us that crowning Hashem as King isn't done through fear or sadness, but through celebration and recognition of blessings. Join us for this heartwarming conversation that will leave you looking at your own challenges with fresh eyes and perhaps, like Orly, finding unexpected joy along the way..........................................................................

What's it really like to live with a disability? - "Persistence: Living an Authentic Life with a Disability" by Linda DezenskiHow do you navigate a world that wasn't built with you in mind?What's it really like to live with a disability?Linda Dezenski pulls no punches in this raw and revealing memoir. Born with Cerebral Palsy, Linda takes us on a rollercoaster ride through the ups and downs of life with a body that doesn't always cooperate and a society that often misunderstands.But Persistence isn't just about struggles -it's a story of triumph. With humor and heart, Linda shares her lightbulb moment: disability doesn't define her, it's just part of the package. Join Linda as she learns to embrace her whole self and discovers her mission to help others do the same. Whether you have a disability or not, this book will change how you see the world and yourself.Linda Dezenski works for a city agency that provides services to people with Intellectual disabilities. She is passionate about civil rights for people with disabilities, particularly those pertaining to independent living. Linda earned two master's degrees from Bryn Mawr College's Graduate School of Social Work and Social Research. She was born with cerebral palsy. Linda has authored children's books and continues to educate and support those living with disabilities and their loved ones.https://www.amazon.com/Persistence-Living-Authentic-Life-Disability/dp/B0FMJ5QML2/ref=monarch_sidesheet_titlehttps://lindadezenski.com/http://www.ecpublishingllc.com    http://www.bluefunkbroadcasting.com/root/twia/91825ldec.mp3  

You don't survive ten years of podcasting without a few scars—and a hell of a lot of stories. In part one of this milestone episode, the guys sit down with Brock, a new intern with a fiery past—literally. From being wrongly accused of arson at age four to navigating life with cerebral palsy, Brock's journey is as hilarious as it is jaw-dropping. He unpacks what it means to live with PVL, how systemic failures nearly derailed his education, and why he wouldn't trade his disability for anything. Then in part two, the hosts turn the mics inward. Reflecting on a decade of Sickboy, they revisit the biggest lessons, most surprising moments, and the impact this show has had—not just on listeners, but on themselves. With equal parts heart and humour, this is the definitive Sickboy episode: raw, reflective, and wildly unforgettable.You can watch this entire episode over on YouTube: https://www.youtube.com/playlist?list=PL0EVgIbBQOxtKJ4qjAlfeutzZRfCGV8nbSickboy LIVE in Calgary!Follow Sickboy on Instagram, TikTok and Discord

You don't survive ten years of podcasting without a few scars—and a hell of a lot of stories. In part one of this milestone episode, the guys sit down with Brock, a new intern with a fiery past—literally. From being wrongly accused of arson at age four to navigating life with cerebral palsy, Brock's journey is as hilarious as it is jaw-dropping. He unpacks what it means to live with PVL, how systemic failures nearly derailed his education, and why he wouldn't trade his disability for anything. Then in part two, the hosts turn the mics inward. Reflecting on a decade of Sickboy, they revisit the biggest lessons, most surprising moments, and the impact this show has had—not just on listeners, but on themselves. With equal parts heart and humour, this is the definitive Sickboy episode: raw, reflective, and wildly unforgettable.You can watch this entire episode over on YouTube: https://www.youtube.com/playlist?list=PL0EVgIbBQOxtKJ4qjAlfeutzZRfCGV8nbSickboy LIVE in Calgary!Follow Sickboy on Instagram, TikTok and Discord

Episode Notes In E394, Andrew reviews the 2024 Disney movie "Out of My Mind" about a young girl with Cerebral Palsy who uses a wheelchair and can't speak. We talk about the way the movie portrays her disability, what it is like feeling ignored as a disabled teen + so much more. Enjoy! and watch on Disney Plus. Episode Sponsors Are you looking for attendant care when you need it at your convenience? Check out your team, on tap www.whimble.ca Get 15% off your next purchase of sex toys, books and DVDs by using Coupon code AFTERDARK at checkout when you shop at trans owned and operated sex shop Come As You Are www.comeasyouare.com Order Andrew's book Notes From a Queer Cripple and hire him to speak on it by e-mailing andrew@andrewgurza.com US: https://us.jkp.com/products/notes-from-a-queer-cripple Canada: https://www.ubcpress.ca/notes-from-a-queer-cripple This podcast is powered by Pinecast.

Cerebral palsy can affect bladder function in many different ways, often leading to challenges such as incontinence, urgency, or difficulties with emptying. In this episode, Madison Hughes and Dr. Sean Elliott discuss how cerebral palsy impacts the bladder, the common issues patients may face, and what families should know about treatment and management. 

Episode Notes On E393, Andrew sits down with mental health advocate and provider, Jose Rosario. We talk about his experience as someone with Cerebral Palsy, and what it means to provide mental health supports as a marginalized person. We talk about so much in this episode that is so important! Enjoy! Follow Jose and his work here: https://www.thephoenixempowered.org/ Support Palestine by donating to E-Sims for Gaza here: https://connecting-humanity.org/ Episode Sponsors Are you looking for attendant care when you need it at your convenience? Check out your team, on tap www.whimble.ca Get 15% off your next purchase of sex toys, books and DVDs by using Coupon code AFTERDARK at checkout when you shop at trans owned and operated sex shop Come As You Are www.comeasyouare.com Order Andrew's book Notes From a Queer Cripple and hire him to speak on it by e-mailing andrew@andrewgurza.com US: https://us.jkp.com/products/notes-from-a-queer-cripple Canada: https://www.ubcpress.ca/notes-from-a-queer-cripple This podcast is powered by Pinecast.

In this week's episode, Brain & Life Podcast hosts Dr. Daniel Correa and Dr. Katy Peters discuss some of their favorite articles in the most recent issue of Brain & Life Magazine. The dive into the effects of ultra-processed foods, helpful innovations like smartphone apps and specialized gyms, and the support sibling caregivers provide to their loved ones. If you would like to read these articles and more, check out the latest issue!   Brain & Life Articles Mentioned How Ultra-processed Foods Can Have a Negative Effect on Brain Health Smartphone Apps Can Help Manage Parkinson's, Migraines, Epilepsy, and More How Specialized Gyms Empower People with Neurologic Conditions Sibling Caregivers are Supporting Brothers and Sisters Through Chronic Conditions   Other Brain & Life Podcast Episodes on These Topics The Many Faces of Cerebral Palsy with Micah Fowler, Phoebe Rae Taylor, and Kelsey Cardona We Are Brave Together with Jessica Patay Cheryl Hile is Running Around the World with Multiple Sclerosis Exploring Longevity with Author Dan Buettner   We want to hear from you! Have a question or want to hear a topic featured on the Brain & Life Podcast? ·       Record a voicemail at 612-928-6206 ·       Email us at BLpodcast@brainandlife.org   Social Media:   Hosts: Dr. Daniel Correa @neurodrcorrea; Dr. Katy Peters @KatyPetersMDPhD

Police have taped off the car park of a council office building in Sittingbourne.Officers were called to Swale House on East Street last night while paramedics were also reportedly seen early this morning. Hear from reporter Joe Crossley who has also been there.Also in today's podcast, a Sittingbourne mum has told us how it took her having a 'breakdown' in an A&E ward to find out her daughter has a life-changing condition.Morgan Austin from Teynham gave birth to Matilda in January and was told her baby had reflux. She was eventually diagnosed with cerebral palsy and now needs extensive physiotherapy.Police have told the podcast they won't be arresting anyone for putting up flags in public places across Kent.You may have noticed Union Flags appearing on lamp posts in recent days while roundabouts and road markings have been spray painted to look like St George Crosses.A popular shop in Rochester has reopened two days after a suspected arson attack.The door and front of Get Ready Comics on the High Street was badly damaged when a floral arch outside was reportedly set alight early on Tuesday morning. Hear from the owner who has been chatting to us while a police investigation is underway.And in sport, Kent's Emma Raducanu says she's looking to build on progress every day as she continues her strong run at the US Open.She's through to the third round after beating Indonesian qualifier Janice Tjen.

Our preview of the upcoming AACPDM Conference in New Orleans USA.We look ahead at The American Academy for Cerebral Palsy and Developmental Medicine (AACPDM) Conference - the 79th Annual Meeting!“Celebrating Resilience” October 15-18, 2025, to be held in New Orleans, LA. We catch up with AACPDM First Vice President Dr Theresa Sukal-Moulton and Scientific Program Committee Co-Chair Dr Paige Church.You can still register at the link below!https://www.aacpdm.org/events/2025

In this week's episode of Judaism with Altitude, we sit down with David Last, author of the upcoming book Forged by Limitations. David was born with Cerebral Palsy, and instead of letting his challenges hold him back, he turned them into the very forces that shaped his strength, resilience, and faith.We dive into his journey of overcoming obstacles, reframing limitations, and discovering meaning in adversity. Along the way, David shares powerful lessons for anyone facing struggles—reminding us that resilience isn't about avoiding hardship, but learning how to grow from it.David's story of growing up with Cerebral PalsyHow challenges can become the very things that shape our characterThe mindset and daily habits that help him stay resilientWhat it was like to write Forged by LimitationsWho this book is for, and what David hopes readers will take awayHow his journey can inspire not just those with disabilities, but anyone searching for hope and courageForged by Limitations officially launches Sunday, August 24th with a special event.The book will be available for the public on Saturday, August 31st.

Report shows rapid declines in health of children and adolescents since 2007; N-acetylcysteine (NAC) for Parkinson's; Statins increase likelihood of hearing loss, tinnitus; Lithium orotate for Alzheimer's; Is tinnitus reversible? Novel implantable electrical vagus nerve stimulator approved for treatment of rheumatoid arthritis.

In this inspiring episode of The District 3 Podcast, Irvin sits down with JWOW to hear his remarkable journey of living — and thriving — with cerebral palsy. From excelling as a successful car salesman to breaking down barriers with his determination, JWOW shares how he turns challenges into motivation and inspires those around him. This conversation dives into his work ethic, positive mindset, and the life lessons he's learned along the way. An uplifting story that will leave you motivated and ready to tackle anything life throws your way.

An American golden boy. He was born in 1947, the early years of the baby boom, he was an honor student, an athlete and a student council member. But, somewhere along the way, things went sideways and by 2007, at age 60, Verle Dills became internationally famous as the man who spent years videotaping himself humping street signs - which sounds like an internet punchline, but the truth is much darker than that...What went so horribly wrong?EXCITING NEWS: THE KINDA MURDERY HOTLINE: (888) MURDERY that's (888) 687-3379 is LIVE!Sources:https://www.thesmokinggun.com/documents/crime/bubba-humps#lightbox-popup-1https://www.cracked.com/pictofacts-278-21-insane-true-sex-stories-you-thought-were-urban-legendshttps://jalopnik.com/south-dakota-man-arrested-for-sex-with-street-signs-285080https://mutcd.fhwa.dot.gov/services/publications/fhwaop02084/index.htmVarious articles from www.newspapers.com search term: "Verle Dills"Become a supporter of this podcast: https://www.spreaker.com/podcast/kinda-murdery--5496890/support.

Today I was joined by my good friend Ronan Sharkey. Ronan was born with Cerebral Palsy and given just 48 hours to live. As a kid, he was told he'd never ride a bike or play sports, and was pushed toward special education. But Ronan didn't let any of those labels stick. He fought through every barrier — physical, mental, and social — and today, he's out conquering some of the toughest trail ultramarathons in Ireland and Backyard Ultras. He's also a proud volunteer and regular runner with I.M.R.A., the Irish Mountain Running Association.This chat is all about grit, resilience, and refusing to let others define your limits. Ronan's journey is not just inspiring — it's a reminder that with the right mindset, you can go far beyond what anyone thought was possible.

On this week's episode of the podcast comedian Marshall Loether stopped by to talk getting into comedy, living with Cerebral Palsy, fatherhood, omlettes and more. Enjoy.

Evening Prayer (people with brain tumors _ cerebral palsy) Ephesians 3_16-21 #prayer #prayers #jesus #god #holyspirit #aimingforjesus #healing #eveningprayer #cerebralpalsy #brain #braintumor Thank you for listening, our heart's prayer is for you and I to walk daily with Jesus, our joy and peace aimingforjesus.com YouTube Channel https://www.youtube.com/@aimingforjesus5346 Instagram https://www.instagram.com/aiming_for_jesus/ Threads https://www.threads.com/@aiming_for_jesus X https://x.com/AimingForJesus Tik Tok https://www.tiktok.com/@aiming.for.jesus

Celeste Warren (she/her), Diversity & Inclusion Leader, Speaker, and Author, and I recap the latest 5 Things (good vibes in DEI) in just 15 minutes. This week, our conversation is about Denmark drafting women, Chicago Sky blocking trolls with national security tech, H-E-B delivering to flood zones, and more!Here are this week's good vibes:Denmark Drafts WomenChicago Sky Blocks TrollsAccessibility: Not Extra, It's CultureH-E-B Delivers More Than GroceriesSinners Streams in BASLGood Vibes to Go: Bernadette's GVTG: It's Disability Pride month. For some great vibes, check out the documentary Crip Camp on Netflix. It's about “a joyful disability revolution.” I loved it. Celeste's GVTG: Check out Celeste's new book, "Equity: It's Not a Dirty Word", everywhere you find books.Read the Stories.Connect with Celeste Warren.Subscribe to the 5 Things newsletter.Watch the show on YouTube. Join thousands of readers by subscribing to the 5 Things newsletter. Enjoy some good vibes in DEI every Saturday morning. https://5thingsdei.com/

Gretchen Bandoli, Ph.D., highlights four major research initiatives within her division focused on maternal and child health. The Center for Better Beginnings studies medication and vaccine safety during pregnancy and lactation through ongoing cohort studies. The Mommy's Milk Human Milk Research Biorepository collects breast milk samples to investigate postnatal exposures. The SOMI study links medical records and geolocated data for over 7 million California births to examine maternal-child health outcomes. Bandoli also leads a site for the Healthy Brain and Child Development Study, a national project following 7,500 mother-child pairs over the first ten years of life with neurodevelopmental assessments and biological sampling. All projects welcome collaboration and emphasize long-term outcomes. Series: "Motherhood Channel" [Health and Medicine] [Show ID: 40772]

Gretchen Bandoli, Ph.D., highlights four major research initiatives within her division focused on maternal and child health. The Center for Better Beginnings studies medication and vaccine safety during pregnancy and lactation through ongoing cohort studies. The Mommy's Milk Human Milk Research Biorepository collects breast milk samples to investigate postnatal exposures. The SOMI study links medical records and geolocated data for over 7 million California births to examine maternal-child health outcomes. Bandoli also leads a site for the Healthy Brain and Child Development Study, a national project following 7,500 mother-child pairs over the first ten years of life with neurodevelopmental assessments and biological sampling. All projects welcome collaboration and emphasize long-term outcomes. Series: "Motherhood Channel" [Health and Medicine] [Show ID: 40772]

Gretchen Bandoli, Ph.D., highlights four major research initiatives within her division focused on maternal and child health. The Center for Better Beginnings studies medication and vaccine safety during pregnancy and lactation through ongoing cohort studies. The Mommy's Milk Human Milk Research Biorepository collects breast milk samples to investigate postnatal exposures. The SOMI study links medical records and geolocated data for over 7 million California births to examine maternal-child health outcomes. Bandoli also leads a site for the Healthy Brain and Child Development Study, a national project following 7,500 mother-child pairs over the first ten years of life with neurodevelopmental assessments and biological sampling. All projects welcome collaboration and emphasize long-term outcomes. Series: "Motherhood Channel" [Health and Medicine] [Show ID: 40772]

In this episode of ListenABLE, registered psychologist Kellie Forrest shares her experiences living with cerebral palsy and working in mental health. As both a parent and a professional, Kellie provides insight into how internalised ableism, societal attitudes, and systemic gaps impact people with disability in day-to-day life. Kellie speaks candidly about parenting with a disability, navigating hospitals and schools, and the assumptions she’s encountered as a disabled parent. She reflects on how these experiences intersect with her work as a psychologist, where she supports neurodivergent clients and applies trauma-informed and behaviour support frameworks. The conversation dives into the complexity of the NDIS, including inconsistent access to support and difficulties with innovative treatments. Kellie also recounts her personal experience with a car accident and the barriers faced during the insurance claims process—especially when dealing with modified vehicles. Throughout the episode, Dylan and Angus explore how lived experience can shape professional practice, and why representation within psychology and healthcare matters. Want to contact Kellie? Reach out to her clinic: info@assessable.com.au Watch the Full Episode with Captions Here: https://youtu.be/Yul1SVSnomAGrab our first merch release at our website Session in Progress.https://fromyourpocket.com.au/work/listenable/merch Recorded, edited and produced by Angus' Podcast Company: www.sessioninprogress.com.auSee omnystudio.com/listener for privacy information.

Mother and son Lisa and Tyler Sexton discuss their amazing story of parenting a child with special needs and how - through God's work and faithfulness - Tyler was able to overcome limitations and pursue a medical degree. Receive the book No Such Thing as Can't and a free audio download of “Overcoming the Obstacles of Cerebral Palsy” for your donation of any amount! Plus, receive member-exclusive benefits when you make a recurring gift today. Your monthly support helps families thrive. Get More Episode Resources If you've listened to any of our podcasts, please give us your feedback.

Mother and son Lisa and Tyler Sexton discuss their amazing story of parenting a child with special needs and how - through God's work and faithfulness - Tyler was able to overcome limitations and pursue a medical degree. Receive the book No Such Thing as Can't and a free audio download of “Overcoming the Obstacles of Cerebral Palsy” for your donation of any amount! Plus, receive member-exclusive benefits when you make a recurring gift today. Your monthly support helps families thrive. Get More Episode Resources If you've listened to any of our podcasts, please give us your feedback.

Bonner Paddock was born with cerebral palsy — and went on to climb Mt. Kilimanjaro and complete an Ironman. His story is powerful proof that limits can be redefined.

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/

Hannah Diviney made history in 2022 when she became the first person with a disability to film a sex scene for Australian television. Then she went viral when she confronted both Lizzo and Beyonce over an ableist slur in their song lyrics.When Hannah was growing up, the only people she saw on TV who used a wheelchair like her were Paralympians or in Road Safety ads.Hannah spent a lot of her childhood feeling lonely and left out, though she was sure she wanted to be a writer when she grew up.She was still at pre-school when she realised that names on the front of books belonged to the people who had written them.It was also around this time when Hannah became aware that her body didn't work in the same way as her friends at childcare.Hannah has since started the Krazy Kosci Klimb, which supports young people with Cerebral Palsy to climb Australia's highest peak.Hannah always knew representation was important for young, disabled people like her to be reflected in pop culture and to belong.So she wrote to Disney, requesting they create their first princess who uses a wheelchair.That petition secured Hannah's first job in journalism with Mamamia — at the age of 15.She has since made history, becoming the first person with a disability to film a sex scene for Australian television.in 2022, Hannah went unexpectedly viral for confronting musician Lizzo about an ableist slur in her song lyrics.Several weeks later, Beyonce used the same slur, and Hannah realised she had to take on the biggest pop star in the world.Further informationHannah's collection of autobiographical essays, I'll Let Myself In is published by Allen & Unwin.This episode was produced by Alice Moldovan.Conversations' Executive Producer is Nicola Harrison.Find out more about the Conversations Live National Tour on the ABC website.

Eric Merola speaks to Max. HIs sone was treated for cerebral palsy, and Max was treated for Crohn's disease using fetal stem cells at EmCell in Kyiv, Ukraine.

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/

Patrick encourages men and women grappling with lust to focus on modesty, purity, and self-control in today’s world. He fields a deeply personal call about grief, the ache of unanswered prayers, and the daily effort to pursue virtue, offering compassion, practical wisdom, and the rock-solid hope found in Scripture and community. Sudden moments of humor and heartfelt support blend with advice on modest dress, addiction battles, and the sacred duty to lift up one another—whether that means praying for strangers or connecting a hurting listener with the Knights of Columbus. Laurie - I just wanted to encourage men in custody of eyes. The world, flesh and devil are trying to get us to forget who we are. Men, you are made for this. (01:41) Lisa - The Bible says ask and you shall receive. Did you have any words of comfort for those who don’t get their prayers answered? (06:12) Paul - I agree with you about lust addiction. Praying a daily Rosary and having custody of the eyes helps. I rely on the strength of my guardian angel. (14:07) Katie (email) – Women, please dress modestly. We can help the fight. (20:29) Robert - Custody of the eyes: I turn away and thank God for their beauty instead of ruminating on it. (21:20) Janet – It used to bother me a great deal when I saw women scantily clad. I confessed my anger. I am always praying for them when I see them, it really relieves me of anxiety and angst. (22:08) Ben - CS Lewis’ Screwtape Letters helped me mentally with lust. (24:47) Tom – I have Cerebral Palsy and am being mistreated where I live. How can I deal with this without falling into sin? (28:05) Maria – The friend of my grandson dresses very skimpy. I told him I didn’t like how she was dressed. My family was upset with me for saying this. (39:52) Lisette - My daughter received Voodoo dolls as gift (43:53)

Abbie Hills is a UK-based talent agent, producer, writer, and passionate disability advocate with cerebral palsy. Abbie founded The Dazey Hills Company in 2019 to promote diversity and inclusion in the entertainment industry, representing talent across the UK and Europe. Her writing has gained recognition with recent placements in film festivals, including the British Independent Film Festival, Lit Laughs, and the Palm Springs Diversity Screenplay Contest.  In addition to her writing, Abbie works as an Access Coordinator, supporting D/deaf, disabled, and neurodivergent talent in film and television productions. She also mentors aspiring talent, advocating for greater accessibility and representation in the entertainment industry. During this episode, you will hear Abbie talk about: Her experience growing up with cerebral palsy, which for her is an “invisible" disability How an MRI scan of her brain changed the way she viewed her disability How people have judged her because of her disability How cerebral palsy affects her day-to-day life What inspired her to become an actress, and how her disability affected her experience in the entertainment industry The need for community among adults with disabilities Her journey from being an actor who hid her disability to founding her own talent agency and working as an Access Coordinator To find out more about Abbie and her work, visit her personal website AbbieHills.uk and production company website TheDazeyHillsCompany.co.uk and follow her on Instagram @itsabbiehills. Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations. These episodes are for informational purposes only and do not substitute for professional medical advice. Consult a medical professional or healthcare provider if you are seeking medical advice, diagnoses, or treatment.*

Buy Zach's Books: https://www.amazon.com/stores/Zachary-Fenell/author/B006M49S6ACheck Out Zach's Blog: https://www.zacharyfenell.com/blog/Connect with Zach on Instagram: https://www.instagram.com/zacharyfenell/Email Zach: contact@zacharyfenell.comIn this replay from Zach's YouTube channel I sit down with my long-time friend Zachary Fenell to tackle a topic that every adult with cerebral palsy understands all too well, the art of falling. Zach asks the gritty questions and I pull back the curtain on what it is really like to hit the ground three to five times a month and still chase a fitness-first life. We talk about daily balance drills, why fatigue makes escalators feel like trap doors, and how taking a twenty second sit break can save an entire day of mobility. You will hear honest stories of tumbles that ended in laughter, hard lessons learned from near injuries, and the mindset shifts that turn embarrassment into self-assessment. We also share straight talk for family and friends who want to help yet never know when to jump in. If you live with CP, or love someone who does, this chat will give you practical tips, fresh perspective, and a reminder that the score is always you versus CP… and you can still win.Please share this episode with anyone you think would be interested in listening to it.Visit darylperrypodcast.com for links to the show page on each of the major podcast directories. From there, you can subscribe and share this pod.For comments, questions, topic ideas, possible collaborations please email daryl@yourlevelfitness.com

Defying the Odds — Vance Walker's Back-to-Back Ninja Warrior Victories This week on the Team Never Quit podcast, we welcome American Ninja Warrior legend Vance Walker, the first athlete in the show's history to win back-to-back million-dollar championships. At just 19 years old, Vance has become a beacon of perseverance, grit, and unstoppable belief. Born with spastic diplegia, a form of cerebral palsy that affected his ability to walk, Vance was told he may never walk without braces. But through years of determination and relentless training, he not only walked — he ran, jumped, climbed, and conquered Mount Midoriyama... twice. In this episode, Vance shares His journey from leg braces to Ninja Warrior champion, the mental and physical challenges of competing in two seasons back-to-back, and what it means to represent those born with disabilities on a national stage,  Whether you're chasing a personal dream or overcoming an obstacle of your own, this is an episode that will inspire you to keep climbing. In This Episode You Will Hear: • [My mom] She gave me the mindset I've had ever since then, which is “Whatever it takes.” (5:19) • At 17 months old I was diagnosed with cerebral Palsey and was told I might never be able to walk without braces on my legs. (5:37) • If you don't have hard things, you can't get stronger. (13:26) • I always wanted to be good at something, and there was always something that would keep me from being the best. And when I found Ninja, I was able to make my own scheduled, because Ninja Warrior is not a team sport. (15:39) • I can make my own path in this. I can train any way I want to. If there's an obstacle, there's not [just] one way to do it. (18:59) • Just like in life, you need a mentor. You need somebody who's done things before to be able to see how to do things. (29:39) • When was 12, I won my first national championship. (26:59) • I want to get into speaking and sharing my story because that's such as important part of this. (44:22) • When I was a kid in school, I was always different from the other kids. I never fit in with anybody. The only thing that kept me going was the mindset that my mom gave me. (44:57) • To become the best at something is already such an insane challenge, but I started from below everybody else. (45:30) • Any challenge, any obstacle – Never give up. (47:14) • The show is always the one thing I'm the best at. That's where I'm at home. (53:57) • I get that dismount, I hit the buzzer about a thousand times, and I just start bawling my eyes out, because I knew at that point no one was beating me on the rope. I did it. And I ended up winning a million dollars. (62:41) Support Vance   - https://youtube.com/@vancewalkerninjawarrior?si=WcAQTH4fhJbm7-cM   - https://www.instagram.com/vance_walker_anw?igsh=MWpseTcxeDR0NnRmbA== Support TNQ   - IG: team_neverquit , marcusluttrell , melanieluttrell , huntero13   -  https://www.patreon.com/teamneverquit Sponsors:   -  cargurus.com/TNQ    - armslist.com/TNQ   - partnersinbuilding.com - Navyfederal.org        -    - You can find Cremo's new line of antiperspirants and deodorants at Target or Target.com    - WARFARE IN THEATERS APRIL 11th Watch Trailer here: https://www.youtube.com/watch?v=JER0Fkyy3tw First Look Link: https://www.youtube.com/watch?v=-3DWuqiAUKg&t=3s    -   - PXGapparel.com/TNQ   - bruntworkwear.com/TNQ    - Selectquote.com/TNQ    - Groundnews.com/TNQ    - You can find Cremo's new line of antiperspirants and deodorants at Target or Target.com    - shipsticks.com/TNQ    - Robinhood.com/gold    - strawberry.me/TNQ    - stopboxusa.com {TNQ}    - ghostbed.com/TNQ [TNQ]   -  kalshi.com/TNQ   -  joinbilt.com/TNQ    - Tonal.com [TNQ]   - greenlight.com/TNQ   - PDSDebt.com/TNQ   - drinkAG1.com/TNQ   - Shadyrays.com [TNQ]   - qualialife.com/TNQ [TNQ]   - Hims.com/TNQ   - Shopify.com/TNQ   - Aura.com/TNQ   - Policygenius.com   - TAKELEAN.com [TNQ]   - usejoymode.com [TNQ]

In this episode of the Brain & Life Podcast, co-host Dr. Katy Peters is joined by actors Micah Fowler, Kelsey Cardona, and Phoebe Rae Taylor. Micah shares how his Cerebral Palsy (CP) diagnosis differs from the character who he played on ABC's Speechless and his sister Kelsey explains the benefits of this representation that she's seen in real-time. Phoebe Rae then explains how she got her role in Disney's Out of my Mind and how acting has inspired her for the future. Dr. Peters is then joined by Dr. Ann Tilton, a Professor of Neurology and Pediatrics at LSU Health New Orleans with more than 30 years of experience in the field. Dr. Tilton explains what CP is, how it can differ from person to person, and what advancements the community can look forward to.   Additional Resources What is Cerebral Palsy?  Biking Gives Freedom to a Teen with Cerebral Palsy Becky Dilworth Skied and Raised a Family Despite Cerebral Palsy   Other Brain & Life Podcast Episodes on Similar Topics Scoring Goals with CP Soccer's Shea Hammond Gavin McHugh is Building an Acting Career and a Community with Cerebral Palsy RJ Mitte on Living Confidently with Cerebral Palsy   We want to hear from you! Have a question or want to hear a topic featured on the Brain & Life Podcast? Record a voicemail at 612-928-6206 Email us at BLpodcast@brainandlife.org   Social Media: Guests: Micah Fowler @micahdfowler; Kelsey Cardona @thekelseycardona; Phoebe Rae Taylor @phoeberaetaylorx Hosts: Dr. Daniel Correa @neurodrcorrea; Dr. Katy Peters @KatyPetersMDPhD

Brittany Gilbert, an inspiring adult with cerebral palsy, helps us understand CP from a lived perspective, offering actionable insights on nurturing independence, building support networks, navigating social interactions, and fostering a positive

In this raw and real episode of Operation Pigmentation, Seth Money, Craig the Barber, and Real Rio open up and chop it up about life, loss, and unexpected stories. Rio gets vulnerable, sharing memories of his late cousin who battled Cerebral Palsy, and what that relationship meant to him. Meanwhile, Craig finally moves in—and it hasn't taken long for a few Ray Ray types to show up at his door. Seth recounts the hilarious moment Craig gave out his number (maybe too freely), and the crew dives into wild sidebars about Stefon Diggs, Cardi B, and those bizarre Suge Knight and grocery store rumors making the rounds.Tune in for laughs, real talk, and the kind of unfiltered honesty only this trio can deliver.Don't forget to rate, review, and subscribe—new episodes every week!See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

When the cost of survival outweighs the cost of death, something has gone deeply wrong. In this sobering and eye-opening episode, Mitch, living with cerebral palsy and chronic pain, shares his harrowing journey through a Canadian healthcare and social system that he argues is failing its disabled citizens. From the challenges of inadequate education and inaccessible post-secondary programs, to the emotional toll of societal stigma and the bureaucratic obstacles in pursuing intimacy, Mitch exposes the gaps that leave many disabled individuals isolated, under-resourced, and overlooked. He bravely discusses everything from systemic failures and addiction to sex work and survival strategies — reminding us how much dignity and independence are shaped by equity, not charity.You can watch this entire episode over on YouTube.Follow Sickboy on Instagram, TikTok and Discord!