Podcasts about Cerebral palsy

Roger Basick and Marina Santee tell us about Cerebral Palsy and how to be more helpful and considerate to those who live with this condition.https://spotlightenglish.com/uncategorized/i-am-not-drunk/Download our app for Android at http://bit.ly/spotlight-androidDownload our app for iOS at http://bit.ly/spotlight-appleFacebook: https://www.facebook.com/spotlightradioAre you learning English? Are you looking for a way to practice your English? Listen to Spotlight to learn about people and places all around the world. You can learn English words, and even practice English by writing a comment.Visit our website to follow along with the script: http://spotlightenglish.com

We welcome Lisa Kenyon, PT, DPT, PhD, PCS, and professor at Grand Valley State University, to this episode of Wheelchair Nerds, where we discuss all things on-time mobility. This conversation ranges from Lisa's wide-ranging experience in pediatric power mobility to stories about kids she's helped independently move to why she does it all. ***SHOW NOTES*** Andrina Sabet et al. article "ON Time Mobility: Advocating for Mobility Equity" (2022) - https://pubmed.ncbi.nlm.nih.gov/35943383/ Lisbeth Nilsson 2014 article about Assessment of Learning Powered Mobility Use tool - https://pubmed.ncbi.nlm.nih.gov/25357100/ Heather Feldner, Sam Logan, Bethany Sloane et al study on Ride-On Car usage - https://pmc.ncbi.nlm.nih.gov/articles/PMC7529107/ "Short-Term Powered Mobility Intervention Is Associated With Improvements in Development and Participation for Young Children With Cerebral Palsy: A Randomized Clinical Trial" - https://pubmed.ncbi.nlm.nih.gov/39450982/ "Powered Mobility Device Use and Developmental Change of Young Children with Cerebral Palsy" - https://pubmed.ncbi.nlm.nih.gov/37232636/ Wheelchair Skills program - Dalhousie University in Nova Scotia - https://wheelchairskillsprogram.ca/en/

Roger Basick and Marina Santee tell us about Cerebral Palsy and how to be more helpful and considerate to those who live with this condition.https://spotlightenglish.com/uncategorized/i-am-not-drunk/Download our app for Android at http://bit.ly/spotlight-androidDownload our app for iOS at http://bit.ly/spotlight-appleFacebook: https://www.facebook.com/spotlightradioAre you learning English? Are you looking for a way to practice your English? Listen to Spotlight to learn about people and places all around the world. You can learn English words, and even practice English by writing a comment.Visit our website to follow along with the script: http://spotlightenglish.com

SUPPORT STAN HERE: https://www.gofundme.com/f/help-stan-find-new-home-cover-disability-costs AND JOIN HIS PATREON HERE: https://patreon.com/Stanislavart Become an Official Member of the Dark Art Society! www.patreon.com/DarkArtSociety This week we have legendary dark artist Stanislav Krawczyk (AKA Stan Dark Art) back to the podcast to check in and try and help get him some financial support. For those unfamiliar with Stan, he has Cerebral Palsy and a degenerative eye condition and is currently being evicted from his home. He has had a very rough life and needs our help! We discuss his current living situation as well as his escape from Ukraine right as the Russian invasion was starting, spending years in a Ukrainian hospital as a child, difficulties gaining US citizenship and many other topics. Please help Stan if you can! Also, a quick art life update. Stan's links: GoFundMe: https://www.gofundme.com/f/help-stan-find-new-home-cover-disability-costs Patreon: https://www.patreon.com/c/Stanislavart/posts BigCartel: https://standarkart.bigcartel.com https://www.instagram.com/standarkart The Dark Art Society Podcast is produced by Chet Zar. Become an Official Member of the Dark Art Society: https://www.patreon.com/DarkArtSociety Chet's Patreon: https://www.patreon.com/ChetZar Our sponsors: https://beautifulbizarreartprize.art Entries are now open for the 2025 Beautiful Bizarre Art Prize! There is over $70,000 worth of cash and prizes, and you can enter from anywhere in the world. Better yet, you don't have to submit a physical artwork! All you need to do is submit an image of your favourite piece from your whole portfolio – it doesn't even matter if the work you enter has sold. The Beautiful Bizarre Art Prize has six award categories: the RAYMAR Painting award, Victoria Olt Gallery Drawing award, Yasha Young Projects Sculpture award, Photography award, Digital Art award, and the Catherine K Gyllerstrom Emerging Artist Award. There is a brand new jury panel this year so it's a brand new chance to win! As well as the whole host of cash and product prizes, winners will also be invited to exhibit in the Beautiful Bizarre Magazine exhibition at Haven Gallery in Northport, NY alongside 70 of the world's best contemporary representational artists in October 2025. Better yet - the Beautiful Bizarre Magazine team guarantee that they look at every single entry! This is a great way to get on their radar for future opportunities too. AND they also share many of the entries on their social media and in online blogs from now until entries close on 17th July. For more information and to enter, go to https://beautifulbizarreartprize.art That's https://beautifulbizarreartprize.art ----- The Skull Shoppe: https://www.SkullShoppe.com ----- Art n Glow: My affiliate link : https://www.artnglow.refr.cc/chetzar Get 10% off by using code ZAR The Dark Art Society Podcast is produced by Chet Zar. Become an Official Member of the Dark Art Society: https://www.patreon.com/DarkArtSociety Chet's Patreon: https://www.patreon.com/ChetZar The Dark Art Society Instagram: https://www.instagram.com/darkartsociety Official Dark Art Society Website: https://www.darkartsociety.com The Dark Art Society Podcast is now available in a variety of places, including the following platforms: SoundCloud: @darkartsociety iTunes: https://apple.co/2gMNUfM Stitcher: https://www.stitcher.com/s?fid=134626&refid=stpr Podbay: https://podbay.fm/show/1215146981 YouTube: https://www.youtube.com/channel/UCrQBJayd-dfarbUOFS5m7hQ https://DarkArtSociety.com Copyright Chet Zar LLC 2025

This fall, an additional $3.5 million will fund family support programs for NY residents with cerebral palsy and other developmental disabilities. Home Care Advisory Group can help residents apply for these life-changing services. To learn more, visit https://homecareadvisory.org/understanding-opwdd-services-for-special-needs Home Care Advisory Group City: New York Address: 99 Hudson Street #5th floor Website: https://homecareadvisory.org/ Phone: +1 212 540 2984 Email: info@homecareadvisory.org

In this episode Sylvia Owusu-Ansah, MD, FAAP, discusses her experience as a medical consultant on the hit television series The Pitt. Hosts David Hill, MD, FAAP, and Joanna Parga-Belinkie, MD, FAAP, also talk to Bhooma Aravamuthan, MD, DPhil, about standardizing the diagnosis of cerebral palsy. For resources go to aap.org/podcast.

In this episode of ListenABLE, hosts Dylan Alcott and Angus O'Loughlin speak with Peta Hooke, a podcaster and disability advocate living with Cerebral Palsy. As the creator and host of The I Can’t Stand Podcast, Peta brings a practical perspective to disability representation, drawing from her personal experiences and conversations within the disabled community. Peta discusses what it’s like to live independently with a physical disability, the ongoing role of support workers, and the reality of navigating healthcare systems that often lack accessibility. The conversation also covers the complexities of fertility treatment for disabled people, including access to IVF and the ableism that can shape medical experiences. "Unfortunately, I had massive issues, particularly around ableism. And it took 313 days to get approval". Peta shares her thoughts on parenting as a disabled person and why disability is simply one part of her life—not something to be overcome. In addition to her podcast work, Peta is an accessibility consultant and recently launched Eggs, a limited-series podcast focused on fertility and disability. Want to support Peta? Check our the links below! Instagram: https://www.instagram.com/petahooke/ The 'I Can't Stand Podcast': https://tr.ee/kcSeq-lNJ4 The 'Egg's Podcast': https://tr.ee/tnkRdoeiOZ Watch the Full Episode with Captions Here: https://youtu.be/J-kRHBrRimGrab 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.

In this podcast, Alexandra Kalkantzi & Lize Kleeren discuss their paper 'Daily-life executive functions and bimanual performance in children with unilateral cerebral palsy'.   The paper is available here: https://doi.org/10.1111/dmcn.16297   Follow DMCN on Podbean for more: https://dmcn.podbean.com/ ___ Watch DMCN Podcasts on YouTube: https://bit.ly/2ONCYiC __ DMCN Journal: Developmental Medicine & Child Neurology (DMCN) has defined the field of paediatric neurology and childhood-onset neurodisability for over 60 years. DMCN disseminates the latest clinical research results globally to enhance the care and improve the lives of disabled children and their families. DMCN Journal - https://onlinelibrary.wiley.com/journal/14698749 ___ Find us on Twitter! @mackeithpress - https://twitter.com/mackeithpress

In this podcast, Daniela Testani discusses her paper 'Predictors of community participation from preschool to school age in children with cerebral palsy'.   The paper is available here: https://doi.org/10.1111/dmcn.16322   Follow DMCN on Podbean for more: https://dmcn.podbean.com/ ___ Watch DMCN Podcasts on YouTube: https://bit.ly/2ONCYiC __ DMCN Journal: Developmental Medicine & Child Neurology (DMCN) has defined the field of paediatric neurology and childhood-onset neurodisability for over 60 years. DMCN disseminates the latest clinical research results globally to enhance the care and improve the lives of disabled children and their families. DMCN Journal - https://onlinelibrary.wiley.com/journal/14698749 ___ Find us on Twitter! @mackeithpress - https://twitter.com/mackeithpress

Today we have the honour and privilege of being joined by Mike Gibbs, Disability Advocate from Christchurch Canterbury on New Zealand's South Island (Te Waipounamu). He's here to share his story with Cerebral Palsy (CP).Learn more about Mike's work via the link below:Official Website:mikegibbs.nzIf you would like to reach out feel free to send an email to: atelierfuralle@gmail.com. You can also leave a review of the podcast and follow this show on:Instagram:https://instagram.com/atelierfuralle?igshid=OGQ5ZDc2ODk2ZA%3D%3D&utm_source=qr⁠⁠Facebook:⁠⁠https://www.facebook.com/profile.php?id=61551850785306⁠⁠Feel free to join the "JD Dragon Disability Rights Podcast" Facebook Group:https://www.facebook.com/share/g/12Eit9sBPuR/?mibextid=wwXIfrSnapchat:https://t.snapchat.com/FVWn1jmTDiscord ServerJD DragonX (formerly known as Twitter):@JDDragonPodcast

Our guest this week is Jim Littlefield-Dalmares of Louisville, KY who is Director of Market Development at BNI Middle Tennessee, author, podcast host, founder of Seeing Ability and perhaps most importantly, father of two including a child with Cerebral Palsy. Jim and his wife, LeAnn, have been married for 27 years and are the proud parents of two: Peter (21) and Sophia (25) who was born very prematurely, diagnosed early on with Spina Bifida and who has Cerberal Palsy.  Professionally, Jim is the Director of Market Development at BNI of Middle Tennessee.  He is also author of the book: Seeing Ability: Finding Your Path In Parenting A Child With Special Needs and host of the Seeing Ability Podcast.  More recently, Jim has also created the Seeing Ability Foundation.We'll hear Jim's life story and all about the Seeing Ability book, podcast and foudnation all on this episode of the SFN.Dad to Dad Podcast.Show Notes - Phone – (502) 528-0894Email – jimld858@aol.comLinkedIn –  https://www.linkedin.com/in/jimld/Website – https://seeingability.com/Book – Seeing Ability: Finding Your Path In Parenting A Child With Special Needs - https://tinyurl.com/2fpfw4vpPodcast - https://seeingability.com/podcast/Register for the 6th Annual SFN Dads Virthual Conference on May 10, 2025: https://us02web.zoom.us/meeting/register/TLkN_ViJTTqnaK-M8pHPNA After registering, you will receive a confirmation email containing information about joining the meeting.Special 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/  

In this podcast, Owais A. Khan discusses his paper 'Assessment of cortical activity, functional connectivity, and neuroplasticity in cerebral palsy using functional near-infrared spectroscopy: A scoping review'.   The paper is available here: https://doi.org/10.1111/dmcn.16238   Follow DMCN on Podbean for more: https://dmcn.podbean.com/ ___ Watch DMCN Podcasts on YouTube: https://bit.ly/2ONCYiC __ DMCN Journal: Developmental Medicine & Child Neurology (DMCN) has defined the field of paediatric neurology and childhood-onset neurodisability for over 60 years. DMCN disseminates the latest clinical research results globally to enhance the care and improve the lives of disabled children and their families. DMCN Journal - https://onlinelibrary.wiley.com/journal/14698749 ___ Find us on Twitter! @mackeithpress - https://twitter.com/mackeithpress

Brace yourself! This week, we're learning about cerebral palsy from Dr. Matthew MacCarthy, who is both a pediatric physical medicine and rehabilitation (PM&R) specialist at Prisma Health in South Carolina AND a person with cerebral palsy. We're talking NICU, Botox, and puberty, so get ready to stretch your knowledge with a thoughtful approach to CP diagnosis and management.

Show Links:Join the Daily Email: https://yourlevelfitness.com/daily-emailExplore the YLF Blog: https://yourlevelfitness.com/blogJoin The YLF Experience: https://app.moonclerk.com/pay/5t93iox9udm3Episode Description:In this episode, I open up about sharing more of my day-to-day fitness journey with cerebral palsy. From daily walk-in videos to clips of my workouts, I'm documenting my progress in a way that not only tracks physical change, but also reflects the work I've done around body image and self-confidence.I talk about how difficult it used to be to show my full body on camera, let alone share how I walk. I've been leaning into this discomfort and using content as a way to tell my story—not to fit in, but to stand out. I also get into something new I've been doing: writing messages on coffee cups as part of my “Caffeine with Compassion” project. What started as a deeply personal struggle with handwriting as a kid has turned into something I now proudly share.This episode is a reminder that the things we've hidden away can become the things that make us most powerful. By sharing them, we take back control and connect with others who may be going through the same thing.Please share this episode with anyone you think would be interested in listening to it.Visit https://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

Episode Notes On E386, Andrew sits down with Erica Carson-Sami, founder of CARCO Disability Strategies as they talk about disability entrepreneurship, Cerebral Palsy (the best of the Palsies) and a whole lot more. Enjoy! You can follow and support Erica and CARCO Disability Strategies by heading over to carcodisability.ca 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 Come to Andrew's Virtual Book Launch for Notes From A Queer Cripple on May 22, 2025 from 6-8 p.m. EST time. FREE TIX here: www.andrewgurza.com Pre-order Andrew's book Notes From a Queer Cripple US: https://us.jkp.com/products/notes-from-a-queer-cripple Canada: https://www.ubcpress.ca/notes-from-a-queer-cripple UK: https://uk.jkp.com/products/notes-from-a-queer-cripple?_pos=4&_psq=notes&_ss=e&_v=1.0 Support us on Patreon: www.patreon.com/disabilityafterdark This podcast is powered by Pinecast.

In this episode of Once Upon a Gene, I'm joined again by rare mom and powerhouse advocate Gay Grossman. Gay works at GeneDx—home to one of the largest clinical genomic databases—and she's here to share two exciting updates that could change everything for rare families and patient advocacy orgs. We talk about: GeneDx's new commitment to the cerebral palsy community and why every CP diagnosis deserves a genetic test How families can access exome and genome testing through telehealth The launch of the Discover Snapshot, a tool designed to help rare orgs find, understand, and grow their communities using real genomic data We also dive into why many CP, autism, and epilepsy diagnoses are just the beginning—and how getting to the root cause can open doors to treatments, clinical trials, and life-changing connection.

Hey Friends~  Sometimes it is helpful to hear success stories!  We know that raising kids is a marathon not a sprint, and that means that success stories occur millions of times while raising our kids.  Sometimes- when challenges are significant, we need to dig even deeper to find wins along the way.   Today's guest tells her story of raising a child with Cerebral Palsy.  She learned to celebrate along the way, listen to the therapists, and follow the lead of her heart as well as listen to her son.  In doing so, they found success!  Non -verbal to verbal to even speaking on a podcast!   Remember parents, life is a journey.  Always remember to celebrate!  The little wins are important - and they add up!  I know you will feel so encouraged and enlightened by this conversation. Grab a cup of coffee and relax if you are able.   CORRECTION!!  In the show I said Marsh earned a PhD.  I was wrong.  She earned a DPT (Doctorate of Physical Therapy) Thank you, Marsh, for calling this mistake to my attention!  And Readers, please join me in congratulating Marsh!   Always cheering you on!  Dinalynn CONTACT the Host, Dinalynn:  hello@thelanguageofplay.com   ABOUT THE GUEST:   Marsh Naidoo is a physical therapist and parent to Kellan a 12 year old teen with cerebral palsy. She founded a nonprofit digital platform to empower, connect and educate parents raising children with disabilities. She hosts Raising Kellan Podcast and two self-published books. CONTACT THE GUEST:   Www.raisingkellan@gmail.com Raising Kellan Podcast  https://open.spotify.com/show/1BwWELnlV4wWlsE35JBA0X For Kellan's episode 113 : https://open.spotify.com/show/1BwWELnlV4wWlsE35JBA0X Episode 2 on the Raising Kellan Podcast: What parents need to know when language and speech development is delayed!  Angie Brasher , SLP  https://podcasts.apple.com/us/podcast/episode-2-what-parents-need-to-know-when-language-and/id1480164076?i=1000458440281   YOUR NEXT STEPS: FREEBIES:    Sign up for the Newsletter:  https://dinalynnr.systeme.io/newsletter-optin 5 Ways To Get Your Kids To Listen Better: https://dinalynnr.systeme.io/7ca5ce43-d436ea91 21 Days of Encouragement:  https://dinalynnr.systeme.io/1-21signup To discuss how we can work together:  https://calendly.com/hello-play/strategy-session   Love this podcast?  Leave a Review:  https://lovethepodcast.com/play Follow & subscribe in 1-Click: https://followthepodcast.com/play Leave a Voice Message:  https://castfeedback.com/play   For Workshops, Speaking Events, or Partnerships:  https://calendly.com/hello-play/discovery-session ** For Speaking Engagements, Workshops, or Parent Coaching (virtual or live), contact me at hello@thelanguageofplay.com   IF YOU LIKED THIS EPISODE, YOU WILL WANT TO LISTEN TO THESE EPISODES: 160 Michael Hingston: Develop Your Child's Gifts! Whether Or Not A Disability Is Present 197 Michelle Choiary: Our Speech Therapist Became Family. Help for Complex Kids 199 Krista Melanson: Do I Wait or Get Help? My child's speech is “different.”

Dive into Friends Like Us as host Marina Franklin talks with veteran comedians Ralph Harris, Keith Robinson, and Charles Walden. They share stories, laughs, and insights on what keeps them thriving in the industry.  Keith Robinson: Born and raised in South Philadelphia, Keith Robinson, is considered a comic's comic. He has captivated audiences around the world with his straightforward humor. He was a regular on Comedy Central's Tough Crowd; and the co-host of The Wanda Sykes Show (Fox), His first hour special; 2014's Kevin Hart Presents: Back of the Bus Funny can still be streamed on Amazon Prime, Peacock and Tubi. Keith has been featured in films such as Trainwreck and King of Staten Island. After two strokes, and an extended hospital stay, during COVID, Keith marched right back to the stage to create his latest and most personal work yet, Different Strokes; his second hour special, picked up and to be released in 2024 by Netflix. Keith is currently working on several projects, including, feature films, television and tours. Charles Walden: Celebrity standup comedian and actor Charles Walden has been doing what he loves for over 30 years and that's entertaining his audience. Stricken by Cerebral Palsy from birth Charles doesn't allow his condition to limit or stop him from living his best life. Between gigs Charles has been employed by the State of Philadelphia for over fifteen (15) years. He enjoys traveling the world making people laugh.  Charles Walden was raised in the rough and tough inner city of Philadelphia and had to struggle and survive like any other kid in the inner city. He got No breaks just because he had Cerebral Palsy. He was not babied at all by family, friends, or the community. He had to put his pants on one leg at a time like every other boy or man. He had to overcome many obstacles. There was a lot of mental and physical pain he endured from living and growing up in the inner city of Philadelphia. The death of his mother crushed him, but he kept going. She was his rock. Many years have passed since her death and the pain never goes away but he keeps going. Charles' greatest pleasure is when he's on stage performing as he gives his audiences the most inspirational laughing good time they've had in a long while.  Charles Walden is not embarrassed or ashamed of his Cerebral Palsy and has incorporated his condition in a unique way into his standup comedy show.  Charles is proud to say stand up comedy has giving him the opportunity to perform on some iconic TV shows and stages such as BETs Comic View, Martin Lawrence 1st Amendment and even Def Comedy Jam's All-Star Season, to name a few.  Charles is a requested favorite to perform at  colleges, universities, comedy clubs, churches and military bases across the Country. Ralph Harris - From humble beginnings in North Philadelphia to the bright lights of Hollywood, Ralph Harris has been living the dream as a successful comedian and actor, in a career that spans over thirty-five years, and remains in full swing. Labeled by his peers as one of today's legendary comedic talents, with a resume that includes notable acting experience. Harris also served as host of the Culinary Competition, My Momma Throws Down on the TVOne network. He also made his feature film debut in the Golden Globe hit DREAMGIRLS, starring one of his comedy idols Eddie Murphy, Beyonce´, Jamie Foxx and Oscar winner Jennifer Hudson. Harris kicks off the movie as the Detroit MC that helps Jamie hook up with the Dreamettes. Not one to slow down, Harris continued his film career momentum, immediately landing his second feature role in the film Evan Almighty starring Steve Carell and Wanda Sykes. Harris' jump to the big screen comes after years of successful television work, including appearances on Seinfeld, The Parent ‘Hood, Nick Freno, Living Single and In Living Color. No stranger to late night TV, Harris has been featured on The Tonight Show and Late Night with Conan O'Brien, and Arsenio. Harris, is best known for his starring role in the ABC sitcom On Our Own which aired during the immensely popular TGIF block on Friday nights, the show has also aired in syndication on TVOne. You can catch Harris on TV and the Web, in either of his previously recorded specials – Comedy Central Presents and the widely popular HBO Comedy Half-Hour, also on all major streaming music platforms, on his previously recorded album titled HICKEY HEAD. When he's not filming, Harris continues to tour the world and the sea, literally! Performing to sold-out audiences as a comedian, his first career and love. Harris' comedy is character driven, a throwback to many of the greats including his other comedy idols Pryor, Cosby, Redd Foxx, Jonathan Winters and the list goes on. Born and raised in Philadelphia… Ralph spends what little time he's not on the road performing, at home in Los Angeles. Always hosted by Marina Franklin - One Hour Comedy Special: Single Black Female ( Amazon Prime, CW Network), TBS's The Last O.G, Last Week Tonight with John Oliver, Hysterical on FX, The Movie Trainwreck, Louie Season V, The Jim Gaffigan Show, Conan O'Brien, Stephen Colbert, HBO's Crashing, and The Breaks with Michelle Wolf. Writer for HBO's 'Divorce' and the new Tracy Morgan show on Paramount Plus: 'Crutch'.         

Marina Franklin host comedy giants on Friends Like Us! Tune in as Ralph Harris, Charles Walden, and Keith Robinson share stories about their journey, friendship, and the comedic landscape today. It's a laughter-packed episode with comedy legends! Keith Robinson: Born and raised in South Philadelphia, Keith Robinson, is considered a comic's comic. He has captivated audiences around the world with his straightforward humor. He was a regular on Comedy Central's Tough Crowd; and the co-host of The Wanda Sykes Show (Fox), His first hour special; 2014's Kevin Hart Presents: Back of the Bus Funny can still be streamed on Amazon Prime, Peacock and Tubi. Keith has been featured in films such as Trainwreck and King of Staten Island. After two strokes, and an extended hospital stay, during COVID, Keith marched right back to the stage to create his latest and most personal work yet, Different Strokes; his second hour special, picked up and to be released in 2024 by Netflix. Keith is currently working on several projects, including, feature films, television and tours. Charles Walden: Celebrity standup comedian and actor Charles Walden has been doing what he loves for over 30 years and that's entertaining his audience. Stricken by Cerebral Palsy from birth Charles doesn't allow his condition to limit or stop him from living his best life. Between gigs Charles has been employed by the State of Philadelphia for over fifteen (15) years. He enjoys traveling the world making people laugh.  Charles Walden was raised in the rough and tough inner city of Philadelphia and had to struggle and survive like any other kid in the inner city. He got No breaks just because he had Cerebral Palsy. He was not babied at all by family, friends, or the community. He had to put his pants on one leg at a time like every other boy or man. He had to overcome many obstacles. There was a lot of mental and physical pain he endured from living and growing up in the inner city of Philadelphia. The death of his mother crushed him, but he kept going. She was his rock. Many years have passed since her death and the pain never goes away but he keeps going. Charles' greatest pleasure is when he's on stage performing as he gives his audiences the most inspirational laughing good time they've had in a long while.  Charles Walden is not embarrassed or ashamed of his Cerebral Palsy and has incorporated his condition in a unique way into his standup comedy show.  Charles is proud to say stand up comedy has giving him the opportunity to perform on some iconic TV shows and stages such as BETs Comic View, Martin Lawrence 1st Amendment and even Def Comedy Jam's All-Star Season, to name a few.  Charles is a requested favorite to perform at  colleges, universities, comedy clubs, churches and military bases across the Country. Ralph Harris - From humble beginnings in North Philadelphia to the bright lights of Hollywood, Ralph Harris has been living the dream as a successful comedian and actor, in a career that spans over thirty-five years, and remains in full swing. Labeled by his peers as one of today's legendary comedic talents, with a resume that includes notable acting experience. Harris also served as host of the Culinary Competition, My Momma Throws Down on the TVOne network. He also made his feature film debut in the Golden Globe hit DREAMGIRLS, starring one of his comedy idols Eddie Murphy, Beyonce´, Jamie Foxx and Oscar winner Jennifer Hudson. Harris kicks off the movie as the Detroit MC that helps Jamie hook up with the Dreamettes. Not one to slow down, Harris continued his film career momentum, immediately landing his second feature role in the film Evan Almighty starring Steve Carell and Wanda Sykes. Harris' jump to the big screen comes after years of successful television work, including appearances on Seinfeld, The Parent ‘Hood, Nick Freno, Living Single and In Living Color. No stranger to late night TV, Harris has been featured on The Tonight Show and Late Night with Conan O'Brien, and Arsenio. Harris, is best known for his starring role in the ABC sitcom On Our Own which aired during the immensely popular TGIF block on Friday nights, the show has also aired in syndication on TVOne. You can catch Harris on TV and the Web, in either of his previously recorded specials – Comedy Central Presents and the widely popular HBO Comedy Half-Hour, also on all major streaming music platforms, on his previously recorded album titled HICKEY HEAD. When he's not filming, Harris continues to tour the world and the sea, literally! Performing to sold-out audiences as a comedian, his first career and love. Harris' comedy is character driven, a throwback to many of the greats including his other comedy idols Pryor, Cosby, Redd Foxx, Jonathan Winters and the list goes on. Born and raised in Philadelphia… Ralph spends what little time he's not on the road performing, at home in Los Angeles. Always hosted by Marina Franklin - One Hour Comedy Special: Single Black Female ( Amazon Prime, CW Network), TBS's The Last O.G, Last Week Tonight with John Oliver, Hysterical on FX, The Movie Trainwreck, Louie Season V, The Jim Gaffigan Show, Conan O'Brien, Stephen Colbert, HBO's Crashing, and The Breaks with Michelle Wolf. Writer for HBO's 'Divorce' and the new Tracy Morgan show on Paramount Plus: 'Crutch'.       

In this uplifting episode of the Radio Coffee House, host Clint Armitage introduces us to Trenton, a remarkable young man whose journey with cerebral palsy serves as a powerful testament to faith and resilience. Through Trenton's inspiring story, we explore how a positive outlook can redefine limitations and illuminate the path of purpose. The episode features a heartfelt clip from the Tim Tebow Foundation, showcasing Trenton's unwavering belief that “God is able.” Despite the challenges posed by his disability, Trenton's perspective on life is nothing short of extraordinary. He shares how his struggles have shaped him into a beacon of hope for others, emphasizing the importance of relying on God and surrounding oneself with supportive, godly individuals. Clint reflects on Trenton's favorite scripture, Philippians 4:13, which reminds us that strength comes from Christ, regardless of our circumstances. He dives deep into the context of this verse, discussing the Apostle Paul's message of contentment and gratitude in all situations. Clint draws parallels between Trenton's life and the teachings of Paul, illustrating how a shift in focus from earthly concerns to heavenly perspectives can transform our responses to life's challenges. Listeners are encouraged to adopt a mindset of gratitude and to seek out the good in every situation, just as Trenton does. This episode serves as a powerful reminder that our outlook can change everything, and that with faith, we can overcome obstacles and inspire those around us. Tune in to this episode of the Radio Coffee House to be inspired by Trenton's journey and to discover how embracing a positive, faith-filled perspective can lead to a more fulfilling life. -----

This podcast will discuss Care for Children and Youth with Cerebral Palsy (GMFCS levels III to V). This podcast was created by Juliette Eshleman a medical student at the University of Calgary with the help of Dr. Scott McLeod, a Clinical Associate Professor at the Cumming School of Medicine in the department of pediatrics, and a Child Health & Wellness Researcher for the Alberta Children's Hospital Research Institute.. This PedsCases podcast focuses on an overview of care for children and youth with cerebral palsy, with a specific focus on those who are within the Gross Motor Function Classification System (GMFCS) levels III to V

Send a text or comment!MY NEW NORM Pocast- S5 E11Guest: Steve KramerEpisode: Against All OddsHost: Barry Scott YoungShow Notes:In this episode, you'll hear from Steve Kramer. Steve is a walking miracle. He was born two-and-a half months premature with Cerebral Palsy. The doctors did not have much hope for him…but God had other plans. Steve has seen God's faithfulness as he has been a radio disc jockey, TV news anchor/reporter, pastor, missionary and motivational speaker.  He feels his most important role in life is to be a godly husband and father to his kids.Steve and Julie met while Steve was speaking at a church in Oregon and they got married in 2005. Julie has a background in ministry and missions as well. She served at a women's shelter and orphanage in Mexico before meeting Steve.Steve and his family are headed back to the The Netherlands sometime this year as full time missionaries!Resources:-Main Website:www.stevekramer.org-Fixed Mindset vs Growth Mindset Notes-Growth Mindset:Those who have a growth mindset believe that their abilities can be developed through hard work and dedication, which can lead to increased motivation and a willingness to take on new challenges.These are the key elements of a growth mindset:1.  Intelligence can be developed. A fixed mindset might say intelligence is static.2.  Embrace challenges. ...3. Persist in the face of setbacks. ...4.  See effort as a path to mastery. ...5. Learn from criticism. ...5 ½. Find inspiration in the success of others.Fixed Mindset:Those with a fixed mindset tend to view their abilities as being set in stone, which can lead to a fear of failure or a reluctance to take on challenges.People with a fixed mindset believe individual traits cannot change, no matter how much effort you put in, and are more likely to:1. Believe intelligence and talent are static.2. Avoid challenges to avoid failure.3. Ignore feedback from others.4. Feel threatened by the success of others.5. Hide flaws so as not to be judged by others.This has been a presentation of the BEARANOOGA PRODUCTIONS group!MY NEW NORM Podcast-Email: mynewnorm@email.comCommunity / MERCH: www.mynewnorm.shopFaceBook: @mynewnormInstagram: @mynewnorm_podcastmynewnorm.buzzsprout.com/ / YouTube.com/@mynewnorm

Send us a textCord Blood Treatment for Children With Cerebral Palsy: Individual Participant Data Meta-Analysis.Finch-Edmondson M, Paton MCB, Webb A, Reza Ashrafi M, Blatch-Williams RK, Cox CS Jr, Crompton K, Griffin AR, Kim M, Kosmach S, Kurtzberg J, Nouri M, Ri Suh M, Sun J, Zarrabi M, Novak I.Pediatrics. 2025 Apr 11:e2024068999. doi: 10.1542/peds.2024-068999. Online ahead of print.PMID: 40210215As always, feel free to send us questions, comments, or suggestions to our email: nicupodcast@gmail.com. You can also contact the show through Instagram or Twitter, @nicupodcast. Or contact Ben and Daphna directly via their Twitter profiles: @drnicu and @doctordaphnamd. The papers discussed in today's episode are listed and timestamped on the webpage linked below. Enjoy!

Send us a textFunisitis increases the risk of death or cerebral palsy in extremely preterm infants.Jain VG, Parikh NA, Rysavy MA, Shukla VV, Saha S, Hintz S, Jobe A, Carlo WA, Ambalavanan N; Eunice Kennedy Shriver NICHD Neonatal Research Network.Am J Obstet Gynecol. 2025 As always, feel free to send us questions, comments, or suggestions to our email: nicupodcast@gmail.com. You can also contact the show through Instagram or Twitter, @nicupodcast. Or contact Ben and Daphna directly via their Twitter profiles: @drnicu and @doctordaphnamd. The papers discussed in today's episode are listed and timestamped on the webpage linked below. Enjoy!

Speaking on the Canadian (Can lit) literary scene and on April/May's The Festival of Literary Diversity (FOLD) specifically, Canadian author and accessibility advocate Amanda Leduc says: It's impossible to have something that's 100 percent accessible all the time. We're always working towards a more accessible world, working towards making those adjustments, bit by bit by bit. And that's where I think having a sense of humility about this and an openness and willingness to learn and to change and grow, for all of us, is really important. This week on Outlook we're talking with Amanda and learning more about Cerebral Palsy and her own experience with the neurological condition causing everything from muscle weakness to fatigue to pain. Leduc tells us about her time getting her Masters at St. Andrew's University in Scotland and something she calls “a monument to exclusion” when it comes to the inaccessibility of heritage buildings and old cities. From the built environment of capital Edinburgh to the natural environment of Canada's winters, Amanda is speaking to us on the show about her own accessibility needs plus considering other's accessibility considerations after being bullied for a visible limp in childhood to her practice of valuing rest and energy preservation (recharging and rejuvenating) in order to be at her most creatively as a writer. For Amanda Leduc, it's about reimagining what storytelling can mean. Check out more on Amanda's work by visiting her website: https://amandaleduc.com Leduc tells us about her previous role as the Festival's Communications and Development Coordinator, about the origins of FOLD for filling a void in Canada's literary and festival spaces as far as diversity and representation are concerned, and about some of the events being offered (both virtual and in-person) such as the Friday night Literary Cabaret and the Sunday High Tea and her involvement in some panels from April 27th to May 4th. And so as The FOLD celebrates its tenth year here in 2025, we're talking bringing people of all experiences and perspectives into the fold with creativity and innovative opportunities for diversity, just as we do every week on Outlook On Radio Western. For more on FOLD go to: https://thefoldcanada.org

Our guest this week is Eli Pierce of Aurora, CO who is a customer service representative at Silk Trade, a UK based software company.  Eli is the father of four children, including one who is a spastic quadriplegic with cerebral palsy and epilepsy.  Eli, and his wife, Cassidy, have been married for 5 years and he is the proud father of four children: Evelyn (14), Elias (11), adopted daughter Annabelle (6) and Ettison (13) who is spastic quadriplegic with Cerebral Palsy and epilepsy. For many years, Eli was a single dad with full custody of his three children from his first marriage.  Eli's an overcomer dad.  He's overcome a challenging upbringing, a challenging first marriage and the ongoing challenges of fathering four children, including one with profound disability.  Eli's commitment to his family is second to none and he serves as a great role model to those within and outside the disability community.  More recently Eli has joined the Denver SFN Mastermind Group and is thriving. Learn this and more on the current episode of the SFN Dad to Dad Podcast.Show LinksPhone – (719) 639-1782Email – elishapierce88@gmail.comLinkedIn –  https://www.linkedin.com/in/elishapierce/Developmental Pathways in Denver https://www.dpcolo.orgColorado Springs Resource Exchange  https://www.tre.orgChildren's of Hospital Colorado https://www.childrenscolorado.orgRegister for the 6th Annual SFN Dads Virthual Conference on May 10, 2025: https://us02web.zoom.us/meeting/register/TLkN_ViJTTqnaK-M8pHPNA After registering, you will receive a confirmation email containing information about joining the meeting.Special 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/  

Pop culture guru, OG to the podcast game, and Glee superfan DJ Bob Runkel is bringing his unique brand of fun to the pod! As a wheelchair user with Cerebral Palsy, DJ Bob reflects on what it meant to him to see a main character like Artie on-screen and shares his thoughts on Kevin playing the role. Bob reveals the episode that inspired him to work hard in physical therapy so he could walk across the stage at his high school graduation, the fun story of crossing paths with Kevin during his NLT days, and the hard-hitting questions and pop culture references that blow Jenna and Kevin away! For fun clips and more inside scoop, don't forget to follow us on Instagram @andthatswhatyoureallymissedpod! See omnystudio.com/listener for privacy information.

Grove Bags: Mission to Protect Terpenes, Science Behind Grove, Preserving Purity with TerpLocFor this special episode of FSOTD, we want you to forget everything you think you know about packaging and storing the plant post-harvest, including your current perception of a “mylar bag.”Blackleaf is joined in the studio by Jack of Grove Bags, to do the ultimate scientific deep dive into what needs to happen to the plant after it's been harvested, cured, and trimmed, the exact water activity levels of the ideal nug, what defines quality bud beyond smell and appearance, what “gradual slope” means, and most importantly, how to create the most advanced and effective Passive Modified Atmospheric Packaging.Founded in Cleveland in 2016, Grove Bags is a company that specializes in

A disabled teenager is dead in Idaho after police shot him nine times through a fence in his own backyard. Drew Nelson reports.See omnystudio.com/listener for privacy information.

In this episode, NYC Special Education Lawyer Adam Dayan speaks with the inspiring Jessica Salonus, a mother of a child with cerebral palsy and a passionate special education lawyer for children with disabilities. Jessica opens up about her journey raising a child with special needs and her professional experience fighting for the rights of children who require special education services. The episode wraps up with a heartwarming conversation between Adam and Jessica's son, Grey. Don't miss this empowering discussion on resilience, determination, and advocacy.

Stephen and Richard Smith and Dr Chaffee (12 minutes into the video) discuss various aspects of nutrition, focusing on the carnivore diet and its implications for health. They explore hormonal health, the impact of diet on autoimmune conditions, blood pressure, and the role of specific nutrients like B12. The discussion also touches on the effects of alcohol consumption and the myths surrounding cholesterol. Dr. Anthony Chafee joins to provide insights on GLPs and the importance of dietary choices in managing health conditions.Chapters00:00 Introduction to Nutrition and Health05:41 Understanding Hormones and Diet10:47 Blood Pressure Insights13:01 The Role of GLPs in Diet14:47 Cerebral Palsy and Dietary Impact25:32 Cancer and Nutrition28:00 Community Engagement and Resources29:03 Understanding B12 Levels and Their Importance35:05 The Impact of Alcohol on Performance40:02 Challenging LDL Cholesterol Myths49:12 The Flaws in Cholesterol Research51:26 Addressing Motor Neuron Disease with Diet

This week, the SLPs talk all about selective feeding and inter-professional collaboration with Joy Hack.Joy is a registered occupational therapist, certified by the National Board for Certification in Occupational Therapy. She is also licensed with the North Carolina Board of Occupational Therapy. Joy grew up in Chicago, Illinois, but obtained her undergraduate degree in Health and Human Physiology with a minor in Spanish at the University of Iowa. Joy has always been passionate about working with children of all abilities. Growing up, her family took in foster children, providing her first-hand experiences with pediatric mental health and the benefits of occupational therapy. She is devoted to treating not only the child, but the entire family unit in order to facilitate a child's success and opportunity to thrive. Joy volunteered in the neonatal intensive care unit throughout her undergraduate degree as a developmental care volunteer and mentor. She went on to pursue her Master's degree in occupational therapy at the University of Wisconsin-Milwaukee. Throughout graduate school, she worked full time as a respite caregiver to a child with Down Syndrome and young man with Cerebral Palsy. Joy has a pug named Elvis Presley, whom she loves dearly, and enjoys playing tennis, spending time outdoors, and drawing. Joy believes in a holistic and family-centered approach to facilitate a child's development and independence. ........................................⭐️ Help us grow by subscribing and rating our podcast on any platform (don't forget to leave a 5 ⭐️ review)❤️ ⁠Support our podcast⁠

“Hello I'm Rosie, I'm disabled, I'm here, I'm proud of it listen to us make us in the conversation because we are not ever going to go away!”.On this episode of ListenABLE, Angus O'Loughlin is joined by the unstoppable Rosie Jones — comedian, writer, actor, and all-round legend. With her razor-sharp wit and deliciously dark humour, Rosie doesn’t just take up space in the comedy world — she owns it. She spills on everything from growing up with cerebral palsy to tackling the stand-up circuit with jokes that hit harder than a British winter. Along the way, we get into her comedy and writing credits (Sex Education, thank you very much), her kids’ books that actually get it right when it comes to disability (The Amazing ED Eckhart series), and why being trolled online won’t stop her from saying exactly what she thinks. Rosie’s not here to be your inspiration — she’s here to make you laugh, and maybe rethink a few things. This episode is a mix of sharp observations, real talk about ableism, and plenty of “did she just say that?” moments. It’s bold, smart, and totally Rosie.Want to support Rosie? Check our the links below! Melbourne Comedy Festival: https://www.comedyfestival.com.au/browse-shows/rosie-jones/ Website: https://rosiejonescomedy.com/ Instagram: https://www.instagram.com/josierones/ Documentary 'Am I a R*tard?': https://tv.apple.com/gb/show/rosie-jones-am-i-a-rtard/umc.cmc.26vz2vwf2t4fdzp7e4djyeqmy Watch the Full Episode with Captions Here: https://youtu.be/ULvMJw4FRtcGrab 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.

An Upper Hutt man with cerebral palsy says his specialist has been unable to diagnose the cause of his debilitating foot pain because he can't order the diagnostic scans he needs. Ruth Hill reports.

In this powerful and educational episode of Goddess on the Rise, I'm joined by my incredible friend Erin Noon Kay-CEO & Founder of Claiming Disability. We dive deep into the realities of living with a disability, the state of DEI (Diversity, Equity, and Inclusion) in the U.S. right now, and the urgent need for true representation and accessibility.This conversation is filled with truth, lived experience, and real talk-especially around how society views disability, the barriers that still exist, and how we can all do better when it comes to allyship and advocacy.Here's a little more about Erin in her own words:Erin Noon Kay is the CEO & Founder of Claiming Disability. Erin identifies a "fierce disabled entrepreneurial woman," with Cerebral Palsy. She uses a walker and wheelchair occasionally, but she believes it's "OK" to look disabled and is working hard to bring representation for disability in film and everyday culture through media projects and disability related content. She believes "disabled," is NOT is a bad word, but a badge of honor, a beautiful community, a culture. She has worked in the non-profit, governmental, and business sector for over 10 years.Now, Claiming Disability, is connected to over 35k disability advocates from around the world, including Jim Lebrecht and Nicole Newnham, the Directors/Executive Producers of Crip Camp. A groundbreaking summer camp galvanizes a group of teens with disabilities to help build a movement, forging a new path toward greater equality.Tune in to learn, unlearn, and walk away more empowered to be part of the change.To support Erin or follow her journey check out her link tre,e https://linktr.ee/claiming_disability

A Cerebral Palsy diagnosis can bring a wave of emotions—especially for families who have already been through the NICU. In honor of Cerebral Palsy Awareness Month, this episode is dedicated to helping NICU parents feel more informed, supported, and empowered as they navigate the possibility or reality of CP.In this episode, we'll talk through the different types of Cerebral Palsy, what can cause it, and why certain babies—especially those born prematurely or with conditions like IVH, PVL, or HIE—may be at higher risk. We'll also discuss why the diagnosis can take time, the early signs parents might notice, and how healthcare providers typically confirm a CP diagnosis. From there, we'll explore treatment options, therapy approaches, and supportive services that can help improve quality of life and promote progress over time.Equally important, we'll talk about the emotional toll a diagnosis can bring and the importance of prioritizing your own well-being as a parent. With the right support systems in place, children with CP can grow, thrive, reach milestones, and live joyful lives—and you deserve to feel supported along that journey too.If you're looking for clarity, encouragement, and practical tools for advocating for your child, this episode was made with you in mind. Be sure to check the show notes for a free downloadable PDF filled with trusted resources to support your family.You are not alone in this—there is strength in knowledge, healing in connection, and so much hope ahead.Dr. Brown's Medical: https://www.drbrownsmedical.com Our NICU Roadmap: A Comprehensive NICU Journal: https://empoweringnicuparents.com/nicujournal/ NICU Mama Hats: https://empoweringnicuparents.com/hats/ NICU Milestone Cards: https://empoweringnicuparents.com/nicuproducts/ Newborn Holiday Cards: https://empoweringnicuparents.com/shop/ Empowering NICU Parents Show Notes: https://empoweringnicuparents.com/shownotes/ Episode 67 Show Notes: https://empoweringnicuparents.com/episode67 Empowering NICU Parents Instagram: https://www.instagram.com/empoweringnicuparents/ Empowering NICU Parents FB Group: https://www.facebook.com/groups/empoweringnicuparents Pinterest Page: https://pin.it/36MJjmH

3/29/20251. Seven Minute Summary2. Intraoperative Hypotension as a Modifiable Risk Factor. Spine. Jan 15, 20252. Surgical Apgar Score in Scoliosis Surgery for Patients with Cerebral Palsy. Spine. Jan 15, 2025

Retired microbiologist and now activist and writer Lily Collison shares her story as a mother of three and how her personal experiences with her son Tommy transformed her life, turning her into a healthcare advocate inspiring her to write six volumes of books to help guide families through the diagnosis and treatment of children with disabilities,

03-26-25 - PHX PD Officers Suspended Following Excessive Force Take Down Of Deaf Man w/Cerebral PalsySee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Holmberg's Morning Sickness - Wednesday March 26, 2025 Learn more about your ad choices. Visit podcastchoices.com/adchoices

“It wasn't any kind of strength within myself that helped me get through the NICU. It was the strength they had—they gave it to me.”- Savannah O'Malley We extend our sincere gratitude to our sponsor for this episode, Gebauer PainEase®. We are pleased to provide more information about this product, and we invite you to learn more by visiting their website. What happens when your birth plan is shattered in an instant? For Savannah, the unexpected arrival of her micropreemie twins at just 24 weeks turned her world upside down. One of her sons faced significant medical challenges, including brain bleeds and a cerebral palsy diagnosis, while the other grew without complications. Through it all, Savannah found healing in advocacy, art, and the power of sharing her story. In this moving episode, we explore: ✅ The emotional and medical complexities of delivering micro-preemie twins ✅ How a cerebral palsy diagnosis reshaped their family's journey ✅ The silent struggle of maternal mental health after a traumatic birth ✅ Why peer support and storytelling matter in healing and advocacy ✅ How Savannah's Cards of Hope project is making a difference for other NICU moms Savannah's story is a testament to resilience, love, and the incredible strength of mothers navigating complex medical journeys. Whether you're a NICU parent, a healthcare professional, or someone seeking inspiration, this episode will leave you feeling empowered.   Timestamps & Key Topics ⏱️ [00:00] – Episode Intro Welcome to today's episode featuring Savannah O'Malley The importance of sharing NICU and maternal mental health stories ⏱️ [01:00] – Meet Savannah Mom to three, including twin micro-preemies Advocate for maternal mental health and children with disabilities ⏱️ [03:00] – The Unexpected Arrival: 24-Week Twins How Savannah's pregnancy took a sudden turn Navigating a traumatic birth and immediate NICU admission ⏱️ [09:00] – The Medical Rollercoaster Begins Brain bleeds, heart complications, and emergency surgeries Balancing hope with overwhelming medical challenges ⏱️ [13:00] – A Life-Changing Diagnosis: Cerebral Palsy & Hydrocephalus How Lachlan's brain injury shaped their early intervention journey The emotions of receiving a CP diagnosis and shifting expectations ⏱️ [24:00] – Maternal Mental Health: The Hidden Battle Why Savannah struggled with PTSD and anxiety  The moment a medical professional finally validated her trauma Why maternal mental health screenings should extend beyond the NICU ⏱️ [30:00] – The Power of Peer Support Finding community in other NICU and disability moms How social media became a lifeline for connection and hope ⏱️ [38:00] – Turning Pain into Purpose: Cards of Hope How Savannah combined her love for art with her advocacy Sending free, uplifting artwork to mothers of traumatic births How small acts of kindness can have a profound impact ⏱️ [44:00] – Lessons from Motherhood & Advocacy Why Savannah wouldn't change a thing about her son's journey The importance of celebrating progress, not just milestones How caregivers can find strength in their child's resilience ⏱️ [50:00] – Where to Find Savannah & How to Support Cards of Hope How you can receive or gift a Card of Hope Why sharing your story can be the start of healing Resources & Links

In this episode of That Chronic Thing, I sit down with Kim to discuss her experiences navigating life with Cerebral Palsy, Celiac Disease, and Lupus. From the exhausting hoops disabled people have to jump through—like prioritizing health while risking financial aid—to the long and winding road of diagnosing chronic illness, Kim shares her journey with honesty and humor.But it's not all medical talk! We also chat about her college experience at Disney, her adventures in live streaming, and the ways she finds joy in the midst of it all.Stay in Touch with Kim→ Kim's Instagram

03-26-25 - PHX PD Officers Suspended Following Excessive Force Take Down Of Deaf Man w/Cerebral PalsySee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Geri's Jewels and Gems Bookhttps://a.co/d/eLFLnKm  Show CreditsHost/Producer: Steve KmetkoAll things technical: Justin ZangerleExecutive Producer: Jim LichtensteinMusic by: Brian SanyshynTranscription: Mushtaq Hussain https://stillherehollywood.comhttp://patreon.com/stillherehollywoodSuggest Guests at: stillherehollywood@gmail.comAdvertise on Still Here Hollywood: jim@stillherenetwork.comPublicist: Maggie Perlich: maggie@numbertwelvemarketing.com

Spastic Chatter Time! In this episode, I chat with Hunter (@hunter_moore.123) all about his body building journey!Watch the episode here: https://youtu.be/5yBbUi2JumwYou can also listen to this episode on your favorite podcast platform by searching Spastic Chatter.Want to be featured on Spastic Chatter? Leave a comment and/or fill out the form by clicking this link --- https://forms.gle/7gDx7V6R4PDmvbdQA#CerebralPalsy #Disabled #Disability #SpasticChatter #BodyBuilding #Weightlifting  #fyp #foryou

This episode is brought to you by Faulkner University. www.faulkner.edu Preorder "The Adventures of Ben and Travis and The Joy Rider" here: https://www.benandtravis.com/store/p/joyrider Get $5 off your off your Pre order by using code "CPMONTH25" at checkout. Ben, Travis and Will discuss "National Cerebral Palsy Awareness Month" and the Joy Rider himself, Bradley Dupree. Bradley will turn 50 on Friday March 14th. The guys discuss the lessons that Bradley and others with special needs have taught us throughout our lives. The guys share some thoughts about "The Adventures of Ben and Travis and the Joy Rider". The show wraps up with some good Bradley stories. Links mentioned in this episode: Get our free ebook "28 Days of Focused Living" here: https://www.benandtravis.com https://www.facebook.com/groups/benandtravis Reframing Hope Book: https://www.benandtravis.com/books For extra content and material you can use for your family or ministry go to https://www.patreon.com/benandtravis Represent the show: https://www.benandtravis.com/store The Friday ReFresh: https://podcasts.apple.com/us/podcast/the-friday-refresh/id1611969995 Good Old Fashioned Dislike Podcast: https://podcasts.apple.com/us/podcast/good-old-fashioned-dislike/id1643163790 Co-Producers: Justin B., Doris C., Rhonda F., Scott K., Mary H. This podcast is hosted by ZenCast.fm

In this Complex Care Journal Club podcast episode, Dr. Cristina Sarmiento discusses a qualitative study exploring experiences of young adults with cerebral palsy and their caregivers with transition to adult care. She describes the major barriers and facilitators to transition, challenges and opportunities related to conducting the study, implications for practice, and next steps from this work. SPEAKER Cristina Sarmiento, MD Assistant Professor University of Colorado Anschutz Medical Campus HOST Emily J. Goodwin, MD Clinical Associate Professor of Pediatrics University of Missouri Kansas City School of Medicine Pediatrician, General Academic Pediatrics Beacon Program Children's Mercy Kansas City DATE Initial publication date: March 10, 2025. ARTICLE REFERENCED Sarmiento CA, Wyrwa JM, Glaros C, Holliman BD, Brenner LA. Experiences of young adults with cerebral palsy in pediatric care transitioning to adult care. Dev Med Child Neurol. 2025 Jan;67(1):99-110. doi: 10.1111/dmcn.15907. Epub 2024 Mar 24. PMID: 38523396.‌ TRANSCRIPT https://cdn.bfldr.com/D6LGWP8S/as/63kfcjrfv57nh4t8qbrhrvj/March_CCJCP_Sarmiento_transcript_Final_3-5‌ Clinicians across healthcare professions, advocates, researchers, and patients/families are all encouraged to engage and provide feedback! You can recommend an article for discussion using this form: forms.gle/Bdxb86Sw5qq1uFhW6 Please visit: http://www.openpediatrics.org OPENPediatrics™ is an interactive digital learning platform for healthcare clinicians sponsored by Boston Children's Hospital and in collaboration with the World Federation of Pediatric Intensive and Critical Care Societies. It is designed to promote the exchange of knowledge between healthcare providers around the world caring for critically ill children in all resource settings. The content includes internationally recognized experts teaching the full range of topics on the care of critically ill children. All content is peer-reviewed and open-access thus at no expense to the user. For further information on how to enroll, please email: openpediatrics@childrens.harvard.edu CITATION Sarmiento, C, Goodwin EJ. Let's Talk about Transition: Experiences of Young Adults with Cerebral Palsy and their Caregivers. 3/2025. OPENPediatrics. Online Podcast.

Cerebral Palsy is a term that most people recognize, but most don't really understand that entails. Chelsea has dealt with the realities of cerebral palsy her whole life, and is more than happy to share her experience with us! From unfortunate misconceptions, to the horror stories of mistreatment... Those who deal with cerebral palsy deserve the recognition and acknowledgement that they deserve. The more we learn and understand about this disability, the more we are able to support those who may need it. Follow Rebecca: @rrogersworld To watch the podcast on YouTube:  https://bit.ly/RebeccaRogersYouTube Don't forget to subscribe to the podcast for free wherever you're listening or by using this link:  https://bit.ly/WouldYouBelievePodcast If you like the show, telling a friend about it would be amazing! You can text, email, Tweet, or send this link to a friend:  https://bit.ly/WouldYouBelievePodcast Learn more about your ad choices. Visit podcastchoices.com/adchoices

In this episode of the Brain & Life Podcast, co-host Dr. Katy Peters is joined by Shea Hammond, athlete and founder of CP Soccer. Shea shares about his personal experience growing up with Cerebral Palsy (CP) and how staying active and working with a physical therapist has helped him continue to reach his goals. He also discusses CP Soccer's mission, to build a nationwide soccer league for kids who are affected by cerebral palsy, stroke or traumatic brain injury, and what's next for the organization. Dr. Peters is then joined by Dr. Mauricio Delgado, professor of neurology at UT Southwestern Medical Center, former president of the American Academy for Cerebral Palsy and Developmental Medicine and co-founder member of the Mexican Academy for Cerebral Palsy and Neurodevelopmental Disabilities. Dr. Delgado explains how CP is diagnosed and treated, and what the future for those affected and their caregivers looks like.   Additional Resources CP Soccer Biking Gives Freedom to a Teen with Cerebral Palsy How Parents Advocate for Their Children with Rare Diseases   Other Brain & Life Podcast Episodes RJ Mitte on Living Confidently with Cerebral Palsy Gavin McHugh is Building an Acting Career and a Community with Cerebral Palsy Josh Blue Uses Humor to Ease the Stigma Around 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: Shea Hammond @shea_hammond; Dr. Mauricio Delgado @utswmedcenter Hosts: Dr. Daniel Correa @neurodrcorrea; Dr. Katy Peters @KatyPetersMDPhD

The first episode of our new call-in show is here, and we have two callers who seemed to be totally unrelated: a new rancher in Texas, and a Swiftie with Cerebral Palsy in New York. But (get your red string and your tinfoil hat) everything is connected! Especially us.  That's easy to forget when we're constantly pushed to see each other as the enemy, and something we need to remember now more than ever.  For full episodes, the full back catalog and a listener community, you can join us here. Want to be on the show? Call or text 612.568.4441 or email thanks@feelingsand.co Learn more about your ad choices. Visit megaphone.fm/adchoices