Podcasts about Cerebral palsy

Episode Notes On E430, Andrew talks with Dr Dan Rosenfeld, award winning physchologist, stand up comic and author to talk about Cerebral Palsy; his experiences growing up with it, how they differ from mine, and so much more. We talk about his new book, The Confidence Equation: Three Keys to Unleashing Self-Confidence as an Introvert, plus a whole lot more. Enjoy! You can follow Dr. Dan here: @dr.dan.phd Episode sponsors: Episode Sponsors  Buy the new novella Descent here 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 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 Support the show with a donation: https://patreon.com/disabilityafterdark This podcast is powered by Pinecast. This podcast is powered by Pinecast.

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

Brenna and Joe check out Sharon Draper's Out Of My Mind (2010) about Melody, a non-verbal girl with Cerebral Palsy who wants to be able to communicate more than anything.Unlike so many other books about disability, however, this isn't a book about how Melody changes the world...and it's better for it!Plus: exceptional Middle Grade fiction; resisting the temptation of a fantasy ending; and garbage children and systemic barriers.Wanna connect with the show? Follow us on Instagram and BlueSky @HKHSPod or use the hashtag #HKHSPod:> Brenna: @brennacgray> Joe: @bstolemyremote (Instagram) or @joelipsett (BlueSky)Have a mail bag question? Email us at hkhspod@gmail.com Theme music: Rewind Kid "Rhythm Revolution" Hosted on Acast. See acast.com/privacy for more information.

When looking into tethered oral tissues, it is easy to focus entirely on visual structural appearance. However, judging a restriction by looks alone frequently misses the true clinical picture. Real progress happens when healthcare providers shift the diagnostic paradigm away from what a tie looks like and focus entirely on how it affects dynamic function over a patient's lifespan.In this episode, Hallie sits down with Dr. Richard Baxter, DMD, MS, FAAPD, a board-certified pediatric dentist, founder of the Alabama Tongue-Tie Center, and lead author of the bestselling book Tongue-Tied. Dr. Baxter shares his personal and professional insights into the complexities of identifying oral restrictions, moving past basic anatomical definitions to explore how a tiny string under the tongue can alter systemic, long-term health.About the Guest: Dr. Richard BaxterDr. Richard Baxter is a board-certified pediatric dentist, a Fellow of the American Academy of Pediatric Dentistry (AAPD), a Diplomate of the American Board of Laser Surgery, and the founder of the Alabama Tongue-Tie Center. As an internationally recognized speaker and creator of the Tongue-Tied Academy, he has dedicated his career to educating healthcare providers and parents on the structural and functional impacts of oral restrictions. Having experienced a tongue-tie himself and treated his three daughters as infants, his dedication to the field is deeply personal. He resides in Birmingham, Alabama, with his family.Key Topics & TakeawaysSymptoms Over Appearance: Why a visual exam never tells the full story and why diagnostic protocols must prioritize symptom functional profiles over pure aesthetics.Groundbreaking Research in Complex Profiles: Dr. Baxter shares fascinating insights from recent research surrounding oral restrictions and their structural correlations to cerebral palsy.Buccal and Lip Ties Exploded: Clarifying the distinct functional impacts of cheek and lip restrictions, and how they play a role in infant feeding dynamics.The Interdisciplinary Standard: Best practices for post-operative care, follow-up timelines, and maintaining clear, collaborative communication lines across the therapy team.Soundbites"Common does not mean normal." "Digestion starts in the mouth.""Untie the shoelaces for proper function."Timestamps00:00:00 – Intro Hook: The Shoelace Analogy breakdown.00:01:03 – Guest Welcome: Dr. Richard Baxter joins the show.00:02:43 – Clinical Debate: Treating oral restrictions based on symptoms vs. appearance.00:06:51 – Collaborative Care: How a therapist should present a concise, one-page case review to a doctor.00:09:13 – The Post-Op Rule: Why myofunctional therapy is essential (The knee surgery comparison).00:11:51 – Clinical Truths: Why "common" does not mean "normal" when tracking snoring or mouth-breathing.00:13:08 – Complex Case Study: Dr. Baxter's landmark research on tongue-tie releases in children with Cerebral Palsy.00:20:27 – Digestion & The Nervous System: How poor swallowing mechanics trigger chronic fight-or-flight states.00:26:49 – Emerging Research: Survey insights on identifying and treating Buccal (cheek) ties globally.00:32:24 – The Bed-Wetting Link: The surprising connection between airway stress, heart peptides, and nocturnal polyuria.00:48:28 – Reclaiming "No-Man's Land": Why releasing ties between 6 months and 4 years old is critical for core brain development.Links & ResourcesRead the Best Selling Book: Tongue-Tied by Dr. Richard BaxterExplore Clinical Resources: Visit TongueTie.comWatch and Learn: Tune into Dr. Baxter's YouTube ChannelWORTH A LISTEN: CONTINUE YOUR JOURNEYEpisode 200: Functional Impact: When A Tongue Tie Is ACTUALLY A Tongue TieEP 348: Tongue Ties, Sleep Apnea & More: The Patient-Centered Approach to Airway DentistrySTAY CONNECTED & GROW YOUR PRACTICEJoin the conversation: Get behind-the-scenes insights, clinical pearls, and real conversations over on Substack. Hosted on Acast. See acast.com/privacy for more information.

Today on The Front, a beautiful story about courage and love: a young boy with a powerful will to love, a mother’s devotion and the doctors and nurses in our public hospitals who make magic every single day. Read more about this story at theaustralian.com.au and see the video by subscribing to our YouTube channel. Inside the cutting-edge surgery that will change Oscar’s life for good This episode of The Front is presented by Claire Harvey, produced by Kristen Amiet and edited by Tiffany Dimmack. Our team includes Lia Tsamoglou, Joshua Burton and Jasper Leak, who also composed our music. See omnystudio.com/listener for privacy information.

What happens when the person keeping you alive is also the person roasting your life choices the hardest? If you're new to the show, Brock is our brilliant, hilarious resident intern who navigates life with Cerebral Palsy. But this week, we're turning the spotlight on the real hero of his life. His long-term care worker (and for sure NOT his wife) Katherine, joins the fellas to talk about the chaotic, beautiful, and hilariously messy reality of being a Personal Support Worker (PSW). From catastrophic bladder blunders involving white pants and aggressive speed bumps, to asking the highly inappropriate boundary questions everyone else is too polite to touch, this episode is a raw look at what happens when your medical partner feels less like a sterile clinician and more like a cranky old spouse. But again… Not his spouse. Follow Sickboy: Instagram: https://www.instagram.com/sickboypodcastTiktok: https://www.tiktok.com/@sickboypodcastDiscord: https://discord.gg/expeUDN

What happens when the person keeping you alive is also the person roasting your life choices the hardest? If you're new to the show, Brock is our brilliant, hilarious resident intern who navigates life with Cerebral Palsy. But this week, we're turning the spotlight on the real hero of his life. His long-term care worker (and for sure NOT his wife) Katherine, joins the fellas to talk about the chaotic, beautiful, and hilariously messy reality of being a Personal Support Worker (PSW). From catastrophic bladder blunders involving white pants and aggressive speed bumps, to asking the highly inappropriate boundary questions everyone else is too polite to touch, this episode is a raw look at what happens when your medical partner feels less like a sterile clinician and more like a cranky old spouse. But again… Not his spouse. Follow Sickboy: Instagram: https://www.instagram.com/sickboypodcastTiktok: https://www.tiktok.com/@sickboypodcastDiscord: https://discord.gg/expeUDN

In this podcast, Kanishka Badun discusses her paper 'Cognition in adults with cerebral palsy: A systematic review'.   The paper is available here: https://doi.org/10.1111/dmcn.70280   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

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Jerzy Gregorek (@TheHappyBody) is a 4x World Weightlifting Champion, co-founder of UCLA's weightlifting team, and co-creator, with his wife Aniela, of the Happy Body program. You can watch the documentary Prisoner No More, directed by Jeff Wolfe and produced by WolfePrideProductions.com, for free here: tim.blog/hardchoices. To fill out the form on Cerebral Palsy Research Project, visit tim.blog/cp.This episode is brought to you by:Matic the intelligent robot vacuum and mop that navigates obstacles and needs no babysitting: MaticRobots.com/TimOur Place's Titanium Always Pan® Pro using nonstick technology that's coating-free and made without PFAS, otherwise known as “forever chemicals”: FromOurPlace.com/TimTimestamps[00:00:00] Start.[00:01:29] The transformation I've been chasing for a decade.[00:02:39] When an unstoppable coach meets an immovable cerebral palsy diagnosis.[00:04:35] Three pounds to 170: the bench press that woke a brain up.[00:07:17] Navigating autism and building the basics of communication that sustain higher education.[00:10:41] Treadmills exhaust, athletes progress: why physical therapy stalled where coaching took off.[00:19:00] Lethargy, sleeping in the car, and the quiet power of resting energy.[00:20:22] The 16-inch box that opened the bathroom door — and everything after.[00:24:26] Micro-progressions, certificates, ceremonies, and writing history onto a blank brain.[00:29:16] Parental dedication and appreciation.[00:31:54] The adulthood gambit: quit piano, quit training — if you can stick an 18-inch jump.[00:35:14] License plates as the gateway drug from counting to math five hours a day.[00:40:04] Jerzy's coaching style doesn't court approval.[00:42:42] Genghis Khan vs. Admiral Yi Sun-Sin vs. Jerzy vs. Tae Jin.[00:46:35] In search of the science behind such transformations: 25 patients, five years, and a method built to be replicated (interested researchers, visit tim.blog/cp).[01:05:39] Hard choices, easy life — and the call to find your starting point.*For show notes and past guests on The Tim Ferriss Show, please visit tim.blog/podcast.For deals from sponsors of The Tim Ferriss Show, please visit tim.blog/podcast-sponsorsSign up for Tim's email newsletter (5-Bullet Friday) at tim.blog/friday.For transcripts of episodes, go to tim.blog/transcripts.Discover Tim's books: tim.blog/books.Follow Tim:Twitter: twitter.com/tferriss Instagram: instagram.com/timferrissYouTube: youtube.com/timferrissFacebook: facebook.com/timferriss LinkedIn: linkedin.com/in/timferrissSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

In this episode of the Scrum.org Community podcast, Dave West sits down with Dave Dame, Senior Director of Human-Centered Design at Microsoft, to explore the lessons behind his new book, “Leading with Imperfect Feet.”Dame shares his journey of leadership through the lens of imperfection, emphasizing the value of vulnerability, humility, and learning from mistakes. Drawing on personal experiences, including overcoming the challenges of Cerebral Palsy to walk on the beach, he illustrates how embracing imperfection can empower leaders and their teams.The conversation dives deep into inclusive design, human factors, cognitive science, and user research, showing how thoughtful, human-centered approaches create better products and more effective teams. Dame discusses how organizations can balance efficiency with creativity and human connection, and why continuous learning and adaptive leadership are essential in today's fast-changing work environment.Whether you're a product leader, designer, or someone striving to lead with empathy, this episode offers practical insights and inspiring stories on how embracing imperfection can drive innovation, inclusivity, and authentic leadership.Leading with Imperfect Feet is now available for pre-order and will be published in June!

In this podcast, Hana Alazem discusses her paper 'Socioeconomic status, environmental factors, and motor function in children with cerebral palsy'. The paper is available here: https://doi.org/10.1111/dmcn.70243 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 the episode, I continued my conversation with Mikael Avatar about his story about being born with Cerebral Palsy. How despite him having Cerebral palsy he has lived a phenomenal life. How he has achieved multiple Special Olympic records. How has traveled for Switzerland to Thailand, and way people have treated him with his disability? How despite his disability, he found love, and got married? We talk about the way people with disabilities are treated worldwide as far as pre-judgement based on society standards. He discusses his journey of living with his disability and overcoming obstacles and stereotypes that come with it. His story is very interesting that I wanted millions of people should hear. His achievements, coaching others with disabilities, traveling, been married, and living normally dispite his disabilities. His story should inspire any parents raising children with disabilities, and adults with disabilities can do anything dispite their disabilities. What happens when you label someone can cause damage to their self-esteem, self-worth, self-value, confidence, and believing in themsleves. How they can do anything despite their disabilities? How you should never let your children be based on their disabilities?Become a supporter of this podcast: https://www.spreaker.com/podcast/a-happier-you-leads-to-a-healthier-you--5161886/support.

Longitudinal decline in upper-limb range of motion in adults with cerebral palsyErika Cloodt, Jenny Hedberg-Graff, Anna Lindgren, Marianne Arner, Evgenia Manousaki, Katina Pettersson, Elisabet Rodby-BousquetAbstractAim: To analyse longitudinal changes in passive range of motion (ROM) in the upper limb in adults with cerebral palsy (CP).Method: Passive ROM for shoulder abduction and flexion, supination, and elbow and wrist extension was analysed in a longitudinal cohort of adults aged 16 to 76 years from the Swedish CP registry. Individual ROM trajectories and mean ROM curves were calculated using the Manual Ability Classification System (MACS). A mixed-effects model was used to examine changes over 3 to 13 years 7 months.Results: In total, 1395 adults with CP were analysed (769 males, 626 females; median age 26 years). A continuous decline in shoulder ROM, supination, and wrist extension was observed across all MACS levels. Decline rates differed between MACS levels for shoulder flexion, elbow extension, and wrist extension, with steeper declines at higher MACS levels (levels IV and V). Adults classified in lower MACS levels (I and II) had greater initial ROM and slower declines compared to adults classified in higher MACS levels.Interpretation: Upper-limb ROM continuously declined in adults with CP, particularly at higher MACS levels. The varied decline rates highlight the need for tailored interventions and systematic follow-up to maintain ROM and functional ability, especially among individuals at higher risk.

Welcome to Mysteries to Die For.I am TG Wolff and am here with Jack, my piano player and producer. This is a podcast where we combine storytelling with original music to put you in the heart of a mystery. All stories are structured to challenge you to beat the detective to the solution. Jack and I perform these live, front to back, no breaks, no fakes, no retakes.In the world's most dangerous working environments it can seem like everything is out to kill you. The equipment you use. The materials you work with. The very air you breathe. Stored energy is a coiled viper waiting for the right moment to lash out. Owners, manufacturers, contractors, and beyond have developed safety protocols to combat STCKY, that is, Stuff That Can Kill You. Gravity, Motion, Mechanical, Electrical, Pressure, Sound, Radiation, Biological, Chemical, Temperature. This season is all about the means of murder as authors put our STCKY detective skills to the test. This is Season 9, Stuff That Can Kill You.This is Episode 9, where Magnetic is our STCKY means of death. This is Magnetically Ever After by Karina BartowDELIBERATIONMinka's family celebration has turned into a tragedy. She could use our help to catch Aunt Dahlia's killer, give the family some closure, and hopefully keep Cassidy and Graham together. Here are the suspects in the order we met them:Graham, the drunk, already married groomSerenity, the college bestie doubling as wedding plannerLaurel, the college bestie and RNEdie, the cousin selling magnetic blingABOUT Karina BartowKarina Bartow hails from Northern Ohio. Though born with Cerebral Palsy, she's never allowed her disability to define her. Rather, she's used her experiences to breathe life into characters who have physical limitations, but like her, are determined not to let them stand in the way of the life they want. Her works include the four installments of The Unde(a)feated Detective Series, as well as Forgetting My Way Back to You, Wrong Line, Right Connection, and Undeveloped Memories. She may only be able to type with one hand, but she writes with her whole heart!Website: www.KarinaBartow.com Facebook: https://www.facebook.com/karinabartowauthor/Instagram: https://www.instagram.com/karina.bartow/WRAP UPThat wraps this episode of Mysteries to Die For. Support our show by subscribing, telling a mystery lover about us, and giving us a five-star review. Check out our website m2d4podcast.com for links to this season's authors.Mysteries to Die For is hosted by TG Wolff and Jack Wolff. Magnetically Ever After was written by Karina Bartow. Music and production are by Jack Wolff. Episode art is by TG Wolff. Join us next week for a Toe Tag, which is the first chapter from a fresh release in the mystery, crime, or thriller genre. Then come back in two weeks for our next original story where mechanical is our STCKY means of murder. It's Finely Ground Karma by Jason Little

Chris Whitaker has spent his life navigating systems that weren't built with him in mind … and then choosing to change them.   Born six weeks prematurely with cerebral palsy, Chris grew up learning how to operate in a world that often underestimated him. That early experience only served to sharpen his ambition. From university rowing squads to national-level sport, and later into leadership roles across the charity and disability sectors, he developed a perspective grounded in both lived experience and performance.   Today, as founder of Purple Advantage, Chris works with organisations to rethink how they approach disability, employment, and inclusion. His focus is on closing the disability employment gap, unlocking overlooked talent, and helping leaders move beyond uncertainty into confident, human conversations.   We explore the moments that shaped Chris's identity, his competitive drive, and his approach to leadership … including the role his wife, a Paralympian, played in helping him fully embrace his own story.   This is a perspective formed through experience, challenge, and reflection, and it invites a different way of seeing the people around us. The Unlock Moment is hosted by Dr Gary Crotaz, PhD — executive coach, speaker and award-winning author. Downloaded in over 120 countries. Sign up to The Unlock Moment newsletter at https://tinyurl.com/ywhdaazp Find out more at https://garycrotaz.com and https://theunlockmoment.com Also discover his other podcasts, The Box of Keys and Unlock Your Leadership. Follow, subscribe and leave a review wherever you get your podcasts — and connect with Dr Gary on LinkedIn for more leadership insights. Part of The Unlock Moment podcast family.

Cerebral Palsy Athlete Competes in First Strength Competition | Savannah HinegardnerSavannah Hinegardner joins Wheel With It to share her inspiring journey living with cerebral palsy and competing in her first strength competition.Savannah explains how personal training became the best therapy she's ever experienced — both physically and mentally — and how she's using strength training to advocate for the disability community.Because Savannah communicates using an AAC device, this unique conversation highlights accessibility, determination, and breaking barriers.

What do you do when you're born with a brain-body communication glitch?. If you're Dr. Dan, you don't just "manage". You go out and collect a PhD, a Paralympic gold medal in table tennis, and a career as a dating coach just to keep things interesting. This week, the fellas sit down with the legendary Dr. Dan to talk about life with Spastic Quadriplegic Cerebral Palsy. Dan gets real about the "Super Crip" pressure to be ten times better than everyone else just to be seen as equal. But the real meat is in the mindset. As a psychologist and author of The Confidence Equation, Dan breaks down the "veil of misperception," the toxic trap of Instagram comparisons, and why your self-doubt is actually just a bunch of external voices living rent-free in your head. You can find more of Dr. Dan on Instagram: @dr.dan.phdFollow Sickboy: Instagram: https://www.instagram.com/sickboypodcastTiktok: https://www.tiktok.com/@sickboypodcastDiscord: https://discord.gg/expeUDN

What do you do when you're born with a brain-body communication glitch?. If you're Dr. Dan, you don't just "manage". You go out and collect a PhD, a Paralympic gold medal in table tennis, and a career as a dating coach just to keep things interesting. This week, the fellas sit down with the legendary Dr. Dan to talk about life with Spastic Quadriplegic Cerebral Palsy. Dan gets real about the "Super Crip" pressure to be ten times better than everyone else just to be seen as equal. But the real meat is in the mindset. As a psychologist and author of The Confidence Equation, Dan breaks down the "veil of misperception," the toxic trap of Instagram comparisons, and why your self-doubt is actually just a bunch of external voices living rent-free in your head. You can find more of Dr. Dan on Instagram: @dr.dan.phdFollow Sickboy: Instagram: https://www.instagram.com/sickboypodcastTiktok: https://www.tiktok.com/@sickboypodcastDiscord: https://discord.gg/expeUDN

An Auckland University researcher is using virtual reality, 3D printing, and real-time data to design and create leg braces for children with cerebral palsy, that are more comfortable. Cerebral palsy affects 1 in 500 New Zealand children, and 7000 New Zealanders currently live with cerebral palsy. It generally appears in very early childhood as the result of brain damage that occurs before or during a baby's birth, and the main symptoms are related to movement and posture. About half of children with cerebral palsy need ankle-foot braces to help them walk and prevent muscle tightening, but they can be bulky and uncomfortable. Sara Chami worked as a clinical orthotist in Tehran fitting braces for children. And also studied prosthetics. She's now with Auckland University's Bioengineering Institute and researching if the braces can be built better.

What happens to patients with disabilities when the government signals their lives don't matter, and what does that mean for the doctors fighting alongside them? Ashna Shome, a pediatrics resident with cerebral palsy, joins the show to discuss her KevinMD article, "The impact of policy cuts on ableism in health care." She explains how proposed Medicaid cuts, the rollback of physical access requirements for federal buildings, and harmful rhetoric around autism and vaccines are compounding to create a more hostile environment for the one in four U.S. adults living with disabilities. You will hear how anti-vax discourse tacitly suggests that developmental disabilities are worse than death, why she now relies almost exclusively on the American Academy of Pediatrics as a trusted source of health information, and how her own experience navigating medicine with cerebral palsy has shaped her advocacy. Shome also makes a compelling case for physician unionization as a tool for disability justice, arguing that the artificial barrier between doctor and patient must be dismantled. If you care about disability rights, health equity, or the future of physician advocacy, this conversation demands your attention. Partner with me on the KevinMD platform. With over three million monthly readers and half a million social media followers, I give you direct access to the doctors and patients who matter most. Whether you need a sponsored article, email campaign, video interview, or a spot right here on the podcast, I offer the trusted space your brand deserves to be heard. Let's work together to tell your story. PARTNER WITH KEVINMD → https://kevinmd.com/influencer SUBSCRIBE TO THE PODCAST → https://www.kevinmd.com/podcast RECOMMENDED BY KEVINMD → https://www.kevinmd.com/recommended

Episode 244 of the Transition Drill Podcast explores the power of working backwards from a goal for veterans and first responders navigating the complexities of career shifts. You'll hear retired Navy Commander and helicopter pilot Jeremy Vellon on overcoming the friction of being an outsider, and what it takes to build a successful post-service life by finding your people.Jeremy's journey started in Brooklyn, inspired by a trip to the movies with his father to see Top Gun. That moment sparked a lifelong commitment to naval aviation. His father didn't just offer support; he laid out a clear roadmap of the grades, athletic milestones, and leadership skills required to reach the Naval Academy. Jeremy took that advice to heart, spending his youth working backwards from that singular objective despite being younger and smaller than his peers.Throughout his twenty-year career in the Navy, Jeremy leaned into the discipline of setting preconditions for success. Set to deploy on September 19, 2011, his unit was one of the first to go active after 9/11; deploying immediately to Afghanistan. He faced the harsh realities of service, including the loss of friends, which grounded his professional outlook in the gravity of the mission. This mindset of service and sacrifice was a family legacy, shared with his father who served during the Vietnam era.After retiring in 2018, Jeremy transitioned into a new chapter that prioritized his family and individual growth. Building on his military experience and his MBA from the University of Michigan, he embarked on a new Human Resources career, with a stop at Amazon, he was building his own HR Consulting company. But while he was focused on his career, he was not focused on himself. Then one day he struggled physically to get out of bed. With his wife's prompting and the need to help care for his son, who has Cerebral Palsy, he realized he needed to put focus back on his personal fitness. That caused a new career pivot, and he and his wife are now owners of a Burn Bootcamp Fitness center. CONNECT WITH THE PODCAST:Instagram: https://www.instagram.com/paulpantani/WEBSITE: https://www.transitiondrillpodcast.comLinkedIn: https://www.linkedin.com/in/paulpantani/SIGN-UP FOR THE NEWSLETTER:https://transitiondrillpodcast.com/home#aboutQUESTIONS OR COMMENTS:paul@transitiondrillpodcast.comSPONSORS:GRND CollectiveGet 15% off your purchaseLink: https://thegrndcollective.com/Promo Code: TRANSITION15Blue Line RoastingGet 10% off your purchaseLink: https://bluelineroasting.comPromocode: Transition10Frontline OpticsGet 10% off your purchaseLink: https://frontlineoptics.comPromocode: Transition10

Text Us!In this episode of Raising Disabled, we talked to Stacy Faulkner about raising her daughter Addy with Cerebral Palsy and their adoption journey.  You can learn more about Stacy by following their story on Facebook.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

You could already be leading by example and you don't even know it yet! -------- Thank you for listening! Your support of Joni and Friends helps make this show possible.     Joni and Friends envisions a world where every person with a disability finds hope, dignity, and their place in the body of Christ. Become part of the global movement today at www.joniandfriends.org   Find more encouragement on Instagram, TikTok, Facebook, and YouTube.

Recap and review the top pearls from episodes #120: Muscular Dystrophy, #141: Cerebral Palsy from Birth to Adolescence & #126: Trisomy 21 with a few members of our production team! It's Fables from the Cribside! (FFTC), our series providing a rapid review of recent Cribsiders episodes for your spaced learning.

Nik dreams of a red racing bike. His friend, Josh wants to help, but he has doubts of his own. Together, they learn what it means to believe in yourself, lean on your friends and never give up. Nik is witty, determined and full of life--even when his body doesn't move the way he wants it to With help from his best friend, Josh and a new friend, Matt--a former football captain, now in a wheelchair--Nik proves that a "Champion" isn't someone who never falls. It's someone who gets back up, time and time again.Together, these boys start a paper-shredding business, train for Special Olympics and rewrite what it means to be strong. this isn't a story about "overcoming a disability". It's a story about building community, dreaming big and discovering the superpowers we all carry inside. At its core, The Making of Champions is a celebration of resilience. Nik's journey--from navigating schoolyard prejudices to competing in special Olympics.Beth Watter grew up in the Ozark Mountains of Missouri. She moved to Illinois at sixteen to live with her father. After graduating High School, she married her high school sweetheart, Klaus. Their third son, Nik was born with a heart defect, After heart surgery, complications caused him to have Cerebral Palsy. After helping him to get through school and become an Eagle Scout. Beth decided to take writing classes from the East Coast. After being a Boy Scout Leader and working with boys with disabilities, she decided to write books to encourage families and kids to dream big and be courageous.https://www.amazon.com/Making-Champions-Beth-Watter/dp/1966477694https://elisabethwatter.com/https://www.ecpublishingllc.com/http://www.bluefunkbroadcasting.com/root/twia/4226bwec.mp3   

GuestJames (Jim) Reuter, President and Chief Executive Officer First interstate Bank FIBKCompany NameFirst Interstate BancSystem, Inc.Websitehttp://www.fibk.comTicker $FIBKCompany Biohttps://fibk.com/overview/default.aspxJim's BioJames A. Reuter has been President and Chief Executive Officer of the Company and First Interstate Bank as well as a member of the Board of Directors since November 2024. Mr. Reuter leads with expertise drawn from more than 37 years in the banking industry. Prior to joining First Interstate Bank, Mr. Reuter was the President and Chief Executive Officer of FirstBank Holding Company of Colorado from 2017 to 2024. Mr. Reuter started his banking career at FirstBank in 1987 and, prior to CEO, served as the bank's Chief Operating Officer, overseeing many of the bank's divisions including: loan/mortgage operations; information technology (IT); digital banking; payments; business banking; contact center; online account/loan acquisition; marketing; and treasury management. Mr. Reuter has been actively involved in the industry, serving on the Board of Directors of the American Bankers Association (ABA), ABA Government Relations Committee, ABA Payments Systems Advisory Council, and the ABA Venture Investment Committee. He also served on The Clearing House Real Time Payments Business Committee, the Board of Directors for the Mid-Size Bank Coalition of America, the Federal Reserve Bank Faster Payments Task Force Steering Committee, and the Colorado Bankers Association. In addition to industry-related work, Mr. Reuter has served on the boards of numerous nonprofits including: the American Cancer Society of Colorado's CEOs Against Cancer; Women's Foundation of Colorado; Special Olympics of Colorado; Ability Connection Colorado; Blind Institute of Technology; and Cerebral Palsy of Colorado. Mr. Reuter currently serves as Chair of the First Interstate BancSystem Foundation Board of Directors. Mr. Reuter earned a Bachelor of Arts degree in Finance from Luther College in Decorah, Iowa, and attended the Graduate School of Banking at the University of Wisconsin.

In this moving episode, Ryan Cadres joins the Crown Refs Podcast in honor of Cerebral Palsy Awareness Month to share his powerful journey through officiating, leadership, and life. A 27-year official, current president of IAABO Board 54 in Massachusetts, and longtime varsity girls basketball referee, Ryan opens up about what it has meant to navigate the officiating world while living with cerebral palsy. He speaks candidly about confidence, courage, trust, and the emotional weight of being seen as “different” before ever blowing the opening whistle. Ryan reflects on the hardships he's faced — from insensitive comments and whispered judgments to moments of real pain and doubt — while also showing how officiating has become one of the greatest therapeutic outlets in his life, a place where he feels strong, capable, and fully himself.The conversation is filled with meaningful takeaways far beyond basketball. Ryan shares how he adapts mechanics and movement to fit his body, why trust from assigners and partners has meant so much throughout his journey, and how he has turned his story into a mission to advocate for others with disabilities. He also discusses his annual awareness efforts each March, the fundraising he's done for United Cerebral Palsy, and the message behind his growing platform: there is a major difference between being disabled and being unable. This episode is about far more than officiating — it's about resilience, perspective, humanity, and the reminder to be kinder, more thoughtful, and more understanding toward every person we encounter. Ryan's story will challenge you, inspire you, and leave you with a deeper appreciation for courage, both on and off the court.To Support Ryan's missionhttps://www.customink.com/s/2026-cerebral-palsy-awareness-month⛺️ Register for the Crown Refs Skill Development Camphttps://stan.store/crownrefs/p/crown-refs-skill-development-camp-tmq5jdse

Text Us!In this episode of Raising Disabled, Deonna and Rhandyl raise the voice of Logan Knowles.  Logan opens up about his birth story and Cerebral Palsy diagnosis.  He shares the challenges of learning to walk as a child and reaching independence by age eleven.  He tells us about how sports—especially skiing—transformed his life and confidence while living with cerebral palsy. Logan also talks about his experience training for and completing the NYC Marathon and his passion for speaking and nonprofit work to inspire others. You can learn more about Logan by visiting his website https://loganknowles.fit and on Instagram @logan_knowles14.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

In this week's episode, in honor of Cerebral Palsy Awareness Month, we're hosting a powerful roundtable conversation sharing real, honest stories from NICU moms navigating this diagnosis with their NICU miracles. Melissa, Vilma, Andrea, and Aisha together share about what it's like to hear the words Cerebral Palsy for the first time, why it can feel so heavy, and how that understanding shifts over time. We unpack the reality that CP is a spectrum and that no two children and no two journeys look the same.In this episode, you'll hear:How each of them processed the diagnosis and learned to hold both grief and joy at the same timeThe importance of early intervention, advocacy, and letting your child lead the wayWhat it looks like to navigate therapies, school systems, and support servicesThe emotional realities of motherhood, relationships, and life after the NICUMore than anything, this conversation highlights the power of community and how reaching out, finding support, and walking alongside other moms can be essential on our healing journeys.As we recognize Cerebral Palsy Awareness Month, we hope this episode brings greater understanding, compassion, and hope. Your child's unique story is still unfolding, and you are not alone!To get connected with DNM: Website | Private Facebook Group | InstagramThis podcast episode is not an attempt to practice medicine or provide medical advice. All information, content, and material on this website is for informational purposes only and is not intended to be a substitute for professional medical or mental health advice, diagnosis or treatment.To get connected with NICU Alumni: WebsiteSupport the show

For a long time, I shared pieces of my story online, but never the full picture.In this episode of The Daryl Perry Podcast, I finally sit down and share my experience growing up and living with cerebral palsy, how it influenced the way I view fitness, how it shaped my mindset, and why it ultimately led me to create Your Level Fitness.Living with cerebral palsy has impacted how I move, how I train, and how I approach my health. But more importantly, it shaped how I think about identity, self acceptance, and building a life around what is possible instead of focusing on limitations.This conversation is not just about cerebral palsy. It is about perspective. It is about learning to trust yourself, adapting to challenges, and building confidence in your own path even when it looks different from everyone else's.If you have ever struggled with self doubt, physical limitations, or feeling like you do not fit the traditional mold of the fitness industry, this episode will resonate with you.Your journey does not need to look like anyone else's. You simply need to find your level.• What it was like growing up with cerebral palsy• How cerebral palsy influenced my relationship with fitness• Why the fitness industry often misses the mark for people with physical differences• How mindset and self acceptance play a major role in long term health• The origin story behind the Your Level Fitness philosophyYour Level Fitness Links:Find Your Levelhttps://yourlevelfitness.com/find-your-levelCerebral Palsy Guidehttps://yourlevelfitness.com/cerebral-palsy-guideThe Your Level Fitness Frameworkhttps://yourlevelfitness.com/frameworkJournal Prompt Emailshttps://yourlevelfitness.com/journal-prompt-emailsShop Your Level Fitnesshttps://shopylf.comInstagramhttps://instagram.com/daryltperryFacebookhttps://facebook.com/daryltperryYour Level Fitness Instagramhttps://instagram.com/yourlevelfitnessThe Daryl Perry Podcast is about personal growth, mindset, mental health, and building a life that reflects who you truly are.Through honest conversations and personal stories, Daryl shares lessons about confidence, self trust, emotional awareness, and living with intention.

We continue the conversation with Precious and Marquis Potts as they give us a peak into their life's journey with Cerebral Palsy.

We continue to celebrate the Women, but we also celebrated and gained awareness into Cerebral Palsy. Precious and Marquis Potts gives us a peak into their world. We learned about an amazing woman who never questioned God, but only asked God for direction and strength.

Send a textNeste episódio especial, em que comemoramos nosso quinquagésimo JOurnal Club, iniciamos a apresentação de 50 Estudos que mudaram a Neonatologia. Este especial foi inspirado no livro "50 Studies Every Neonatologist Should Know". Neste primeiro especial, apresentamos 4 estudos que mostram como Interventionções aplicadas antes de nascer moldaram a rotina do período anteparto na Neonatologia. Vem com a gente celebrar esse episódio especial que marca o nosso Journal Club 50!Artigos apresentados: 1.     A controlled trial of antepartum glucocorticoid treatment for prevention of the respiratory distress syndrome in premature infants - https://pubmed.ncbi.nlm.nih.gov/4561295/2.     Prevention of early-onset neonatal group B streptococcal disease with selective intrapartum chemoprophylaxis - https://pubmed.ncbi.nlm.nih.gov/3520319/3.     Reduction of maternal-infant transmission of human immunodeficiency vírus type 1 with zidovudine treatment - https://pubmed.ncbi.nlm.nih.gov/7935654/4.     A randomized, controlled trial of magnesium sulfate for the prevention of Cerebral Palsy - https://www.nejm.org/doi/full/10.1056/NEJMoa0801187 Não esqueça: você pode ter acesso aos artigos do nosso Journal Club no nosso site: https://www.the-incubator.org/podcast-1 Lembrando que o Podcast está no Instagram, @incubadora.podcast, onde a gente posta as figuras e tabelas de alguns artigos. Se estiver gostando do nosso Podcast, por favor dedique um pouquinho do seu tempo para deixar sua avaliação no seu aplicativo favorito e compartilhe com seus colegas. Isso é importante para a gente poder continuar produzindo os episódios. O nosso objetivo é democratizar a informação. Se quiser entrar em contato, nos mandar sugestões, comentários, críticas e elogios, manda um e-mail pra gente: incubadora@the-incubator.org

In this episode, we review the high-yield topic of ⁠⁠Cerebral Palsy⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ ⁠from the Neurology section at ⁠⁠⁠⁠Medbullets.com⁠⁠⁠⁠⁠⁠Follow⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ Medbullets⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ on social media:Facebook: www.facebook.com/medbulletsInstagram: www.instagram.com/medbulletsofficialTwitter: www.twitter.com/medbulletsLinkedin: https://www.linkedin.com/company/medbullets

Welcome to Season 2 of the Orthobullets Podcast.Today's show is CoinFlips, where expert speakers discuss grey zone decisions in orthopedic surgery. This episode will feature doctors Jesse Otero, Charles Lawrie, Alexander Sah, & Conrad Ivie. They will discuss the case titled ⁠⁠"Dysplastic Hip in 20M with Cerebral Palsy.⁠"⁠⁠Follow ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Orthobullets⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ on Social Media:⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Facebook⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Instagram⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Twitter⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠LinkedIn⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠YouTube

Join Rory Mitchell as he interviews Brent and Kyle Pease to explore their inspiring journey in inclusive sports, community building, and the power of brotherhood. Discover how their foundation is transforming lives through endurance racing and fostering inclusion for people with disabilities. Speak on what true inclusion means for you. The purpose of The Kyle Pease Foundation (KPF) is to create awareness and raise funds to promote success for persons with disabilities by assisting them to meet their individual needs through sports and beyond.Programs include scholarship opportunities, purchasing of medical equipment or adaptive sports equipment for others, or contributing to other organizations that provide similar assistance to disabled persons, as well as participating in educational campaigns to create awareness about Cerebral Palsy and other disabilities. KPF will provide these services directly to individuals and partner with other non-profit organizations to achieve these goals.Direct benefits will be limited to persons with disabilities who need adaptive sports equipment, mobility devices, or medical care. The Kyle Pease Foundation, in turn, promotes success for young persons with disabilities by assisting them to meet their individual needs through sports and competition. Programs include scholarship opportunities, purchasing adaptive sports equipment, and participating in educational campaigns around Cerebral PalsyKey Topics:Inclusion in sports and community events Brotherhood and communication in high-pressure situations The founding and mission of the Kyle Pease Foundation Overcoming challenges with cerebral palsy through sportsThe importance of curiosity and empathy in supporting othersCONTACT BRENT & KYLE PEASEINSTAGRAM:https://www.instagram.com/thekylepeasefoundation/ WEBSITE: https://kylepeasefoundation.orgKYLE PEASE INSTAGRAM: https://www.instagram.com/kpzydaironman/?hl=enBRENT PEASE INSTAGRAM: https://www.instagram.com/bpeas9/?hl=en

I spent time this week in a musical improv class, and it was a masterclass in one thing: staying on the beat. In improv, if your mind wanders for even a second, you're out of sync with the whole team. It made me think about a request my son made when he was little for my "phone-free attention." That request stuck with me because giving someone our undivided focus is the most basic act of leadership we can offer. In this micro-lesson, I'm exploring why inclusion isn't a grand gesture—it's the radical, simple act of being fully present. Takeaways: The Gift of Presence: Why undivided attention is a non-negotiable leadership skill. Mental Leftovers: How to stop dragging the energy of your last "scene" into your next meeting. Tactical Grounding: Why staying in the moment sometimes requires tools like compartmentalizing (or even fidget toys). Your Challenge: Where are you finding it hard to stay on the beat today, and what's one thing you can do to tune back in? Good Vibes to Go: Watch the documentary Come See Me in the Good Light on Apple TV. It's about poet Andrea Gibson navigating their terminal diagnosis. It sounds dark but it's actually joyful, love-filled, and even funny. Connect with Me The Newsletter: This week in the newsletter, I wrote about prime-time disability leadership in Major League Baseball coverage, funding the first Inuit-led university, and more! Subscribe to the 5 Things Newsletter here.  Work with Me: Let's talk. Watch 5 Things on YouTube. Join thousands of readers by subscribing to the 5 Things newsletter. Enjoy some good vibes every Saturday morning. https://5thingsdei.com/

We catch up with Rachel Byrne - Executive Director at the Cerebral Palsy Foundation. We have the chance to discuss the topic of Scaling Australian clinical breakthroughs into a global CP roadmap.From Australian Advances to a Global Roadmap for Cerebral PalsyA continuing series from the Oceania 2026 Conference, live from Hobart, Tasmania, Australia.

We catch up with Dr Fiona Russo! We're discussing her paper: Four Layers Deep: Co-Designing a Community-Led Online Navigation Program for Families of Young Children with Cerebral Palsy.A continuing series from Oceania Conference 2026 - live from Hobart, Tasmania, Australia.

It's officially Day 1 of the Oceania 2026 Conference - live from Hobart Tasmania, Australia!We catch up with Dr Hayley Smithers Sheedy and Chrissie Macdonald to discuss their paper: Cerebral palsy: temporal trends in birth prevalence in Australia (1995-2018) and epidemiology of people with CP GMFCS IV and V

We catch up with one of our favourites, Dr Michelle Jackman!We get to discuss her paper: Early conversations about cerebral palsy: A message from families to health professionalsAll a part of our Oceania 2026 Conference series from Hobart, Tasmania, Australia!

Born with cerebral palsy, she has risen above challenges all her life and inspired countless people; friends, family, even total strangers along the way. On this episode of the Supercast, we invite you to listen closely as Oquirrh Hills Middle School Para-Educator Aubrey Allen talks about earning a bachelor's and master's degree in recreational therapy, leading her to a career in the classroom and as a Unified Sports coach. Amber doesn't let her disorder, which impacts movement, muscle tone, and speech, get in the way of making her dreams come true, and in the process, supporting others with special needs around her. Listen to Aubrey's powerful message, watch on YouTube or read along with subtitles in the transcript below. Audio Transcription Kathy Taylor: Aubrey is amazing. She is helping us with warm-ups. She's helping us design activities to do during our practice time, but not just for sports, because she helps with academics. Aubrey Allen: Students are the best part of my job. Anthony Godfrey: The students are always the best part of our job. [music] Anthony Godfrey: Hello and welcome to the Supercast. I'm your host, Superintendent Anthony Godfrey. Born with cerebral palsy, she has risen above challenges all her life and inspired countless people, friends, family, and even total strangers along the way. On this episode of the Supercast, we invite you to listen closely as Oquirrh Hills Middle School para-educator, Aubrey Allen, talks about earning a bachelor's and master's degree in recreational therapy, leading her to a career as a classroom aide and as a Unified Sports coach. Aubrey doesn't let her disorder, which impacts movement, muscle tone, and speech, get in the way of making her dreams come true and, in the process, supporting others with special needs around her. You won't want to miss Aubrey's powerful message. Subtitles and a transcript for this podcast are available on our website. [music] Anthony Godfrey: We are here at Oquirrh Hills Middle School talking with Aubrey Allen. Aubrey, thank you for taking time to talk with us. Aubrey Allen: Thank you so much. I'm excited. Anthony Godfrey: I'm really happy to meet you and talk with you. I think I've met you before, but it's been a little while since we've talked. Aubrey Allen: Yeah. Anthony Godfrey: Tell me about your job here at Oquirrh Hills Middle School. Aubrey Allen: I am a para-educator and one of our special educators. I'm here at Oquirrh Hills, and I love it. Anthony Godfrey: You love being the aide here in the class, the para-professional. Aubrey Allen: Yeah. Yeah. Anthony Godfrey: What do you love most about this job? Aubrey Allen: I love being able to work with and support the kids. The students are definitely the best part of my job. Anthony Godfrey: The students are always the best part of our jobs. Aubrey Allen: Yeah. Anthony Godfrey: That's wonderful. Who's your favorite student? I'm just kidding. I'm not making you say or answer that question. Now you are a highly qualified individual. Tell me about your degrees and the work that you do outside of Oquirrh Hills. Aubrey Allen: Yeah, though I have a bachelor's degree in math, my master's degree is recreational therapy, and now I'm a certified recreational therapist. I also manage a nonprofit called Adaptive Arena, and we offer free adaptive sports and activities for people of all abilities. I love working there, too. Anthony Godfrey: Now I understand that you also are an advocate for those with disabilities on social media. Aubrey Allen: Yeah, yeah. I started a social media platform for the video about my day-to-day life just to try to make others aware of what life can be like having a disability. Anthony Godfrey: For those listening, tell them about your disability. Aubrey Allen: I have cerebral palsy, and I have a moderate case of it. It affects the way I talk. The end is just how my body moves and how my muscles work. Anthony Godfrey: I've heard you're a big inspiration to those around you here at the school. What do you think about that? Aubrey Allen: I just try to be positive and uplift everyone. I think having my disability has given me a lot of pushback. There are a lot of things in life that are challenging for everyone, and you can either let them know who you are or try your best to write about your challenges and just be happy and positive. Anthony Godfrey: You're a great example of rising above your challenges, and I'm sure that your students really look to you for that positivity. I've only met you a couple of times, but you've been extremely positive. You light up, you're so friendly both times, and you really stand out that way. So I appreciate the positivity and the positivity you're bringing into the lives of the students and the people you work with. Aubrey Allen: That means so much to me. I really do try my best to overcome my challenges. Anthony Godfrey: So tell me more about what happens at the Adaptive Arena. Aubrey Allen: Yeah, it's more like a rec center for people with disabilities. We offer different activities. We have a cheer program and a wheelchair basketball program, and the cool thing about us is we let everyone play. So if somebody in a wheelchair has a brother who is not in a wheelchair, we put the brother in a wheelchair, too, and now they can play wheelchair basketball, or whatever together, and families really like that because typically kids with disabilities can't play on the same team as their siblings otherwise. So I just love that we can do well with different types of families and kids with all different abilities. Anthony Godfrey: So it really is inclusive. Anyone can participate. Aubrey Allen: Yeah. Yeah. Anthony Godfrey: And if you are playing with others who are in a wheelchair and you don't need a wheelchair, you're going to get a wheelchair. Aubrey Allen: Yes, yes. Anthony Godfrey: That seems fair. Now what is your favorite sport? I won't make you tell me who your favorite student is, but what's your favorite sport? Aubrey Allen: I think my favorite is wheelchair basketball because everyone gets so into it. Anthony Godfrey: Yeah, it's fast-paced. Aubrey Allen: Yeah, we do wheelchair basketball every Saturday morning, and we just have a blast. Anthony Godfrey: So it's your favorite and everyone else's also. [music] Anthony Godfrey: Stay with us when we come back. More with Aubrey Allen and her colleagues. [music] Male Voice: Never miss an episode of the Supercast by liking and subscribing on your favorite podcasting platform. Find transcripts for this episode and others at supercast.jordandistrict.org. [music] Female Voice: They are out on the job in the rain, sleet, snow, ice, and in the sunshine, as Jordan School District students navigate their way to and from school every day. We are truly grateful for our city crossing guards, always vigilant and looking out for students to ensure everyone's safety. Because they work so hard protecting our kids, let's give those crossing guards a hand. If you're driving near or around schools, slow down, pay attention, watch for students and staff, and follow instructions from the school crossing guards and know our cities are always looking to hire crossing guards. If you like kids and need some flexible hours, contact your local city and apply to be a crossing guard today. Together, let's make this a safe and successful school year. Anthony Godfrey: What advice do you have for folks about how to make sure that people with disabilities in their lives feel included and noticed and a part of things? Aubrey Allen: Yes, that's a great question. I remember when I was growing up and it was so easy to feel invisible because I had a disability. The people that stood out to me the most and that had the most impact on my life are the people who treated me like they were just anybody else and not only that, but they were comfortable talking to me and asking what I needed and if they should be aware of anything. So I think that is very important. Individual people do know that people with disabilities, they often times know they just want to be treated and included like everyone else. Anthony Godfrey: I love that. Just treat them like you treat everyone else. And I love that you said the people that have had an impact on your life are the ones who said, "How can I help you?" And just treated you like everyone else, asked you questions, and talked with you. Aubrey Allen: Yeah. Anthony Godfrey: Let's talk with some of the folks that you work with. Introduce yourself. Kathy Taylor: Hi, I'm Kathy Taylor and I am the teacher of the classroom that Aubrey is working in right now and we love Aubrey. She brings so much to our class. Anthony Godfrey: Tell me what it's like getting to work with Aubrey day in and day out. Kathy Taylor: Well, she's always positive. Anthony Godfrey: That's obvious. That's obvious. Kathy Taylor: Even when sometimes it doesn't feel like it's a positive day. Some days are up and some days are down, but Aubrey is always up. Aubrey's expertise with the recreational therapy has been great. We are a Unified Sports school meaning . . . Anthony Godfrey: You're a premier Unified Sports school. You're an award-winning Unified Sports school. Talk about that. Kathy Taylor: So Unified Sports is a program with Special Olympics where we are participating in team sports with our students that have disabilities and with their peers. Peers and our students with disabilities all play on the same team. And for us, that's a huge deal because a lot of times our students are not on teams. Or parents, they go and watch a lot of sibling games, or they watch a lot of their friends play sports. But a lot of our kids don't play sports on their own. So this gives them the opportunity to be on a team, to get that camaraderie, feel like what competition is like, feel experience at the tournament. And Aubrey has brought so much to that. She is our coach basically. I don't know if you've gone through all the trainings yet. I'm still working on those, too. But our official coaches, hands down Aubrey is amazing in that capacity with the sports. She is helping us with warm-ups. She's helping us design activities to do during our practice times that will help us work on specific skills. And she's able to adapt things for the kids that aren't able to do what everybody else does, and they can still interact with their peers. So it's been amazing having Aubrey, but not just for sports because she helps with academics. She goes to classes with kids. She helps us with their personal care. She does it all. She does it all, and she does it with grace, and she does it with humor, and she is a pleasure to work with. Anthony Godfrey: I would think it's pretty hard to be negative around Aubrey or be down on yourself. She doesn't let that happen. The incandescence keeps everyone from getting off the path, I guess. Kathy Taylor: She's very positive and the kids have responded really well to her. They really enjoy her. Anthony Godfrey: Let's talk with the principal. Introduce yourself and tell us about Aubrey. You contacted me and let me know that we really ought to come talk with her. Lisa Jackson: I did. I did. I'm Lisa Jackson, Oquirrh Hills principal. When we interviewed Aubrey, after Aubrey left the room, we all looked at each other and said, "How can we make this work because she needs to be part of our team here at Oquirrh Hills.” When we called for her references at the Adaptive Arena, they said the same thing, “She's amazing. Everything she does. She's just highly qualified. She's kind. She's motivated.” I interact with Aubrey in the halls a lot because she's walking these kids to and from class, and she understands what they need. She's receptive to their needs. And I think the coolest thing about it is just having our kiddos who do have disabilities, who have some struggles, being able to see just what they can accomplish in life and how successful they can be. And I think seeing Aubrey every day and seeing how successful she is just gives them motivation to follow in her footsteps and do some of the things she's done. Anthony Godfrey: You're not very convincing when you say you can't do it and Aubrey's in the room and she's bringing the energy and demonstrating that “yes, you can. You absolutely can.” Lisa Jackson: You can do it with a smile. Anthony Godfrey: Right. Lisa Jackson: Right. It might be hard, but you can do it. I think she also inspires all of the kids, though. Like, I feel like they didn't necessarily know, even our peer tutors didn't know what to expect when you meet Aubrey and you're not sure, you've never met Aubrey before. You're not sure. A lot of people don't have experience with somebody that has cerebral palsy. And so it's been great. I think it's an inspiration to them, too, because you're knowledgeable. You're educated. You're well spoken. And when you say they need to do something, you mean business. So, like, it's, you know, there's a level of respect that Aubrey has earned among all the kids and the adults, really. Anthony Godfrey: I'm inspired hearing about what you do and meeting you again. What do you like to do when you're not at the Adaptive Arena or here at school? Aubrey Allen: Oh, man. I spent a lot of time with my family. I have two younger brothers who I helped raise because there's a big age gap between them. There are things that my family and I work out every day. So I'm at the gym a lot. I feel like and then I like to hike and bike and just be outside. Anthony Godfrey: You're very active sounds like. Aubrey Allen: Yeah. Anthony Godrey: I sit in a lot of meetings. I do email. But, you know, I try to get as much pleasure from that as I can. [laughing] Anthony Godfrey: Well, it's a real pleasure meeting you. Thank you for everything you're doing, for inspiring me, the people that you work with and the students that you serve. You're awesome. Thank you. Aubrey Allen: Thank you for your time and opportunity. Anthony Godfrey: Thank you. And thank you both for talking with us. [music] Anthony Godfrey: Thanks for joining us on another episode of the Supercast. Remember, “Education is the most important thing you will do today!” We'll see you out there. [music]

Choose joy with a Romans 12 attitude! -------- Thank you for listening! Your support of Joni and Friends helps make this show possible.     Joni and Friends envisions a world where every person with a disability finds hope, dignity, and their place in the body of Christ. Become part of the global movement today at www.joniandfriends.org   Find more encouragement on Instagram, TikTok, Facebook, and YouTube.

00:00 - Intro 00:00:51 - Will has cerebral palsy: what it actually looks like day to day 00:02:57 - Growing up with CP, how Will started lifting, and what early training looked like 00:15:08 - Gym confidence, feeling judged, and pushing past the "new guy" phase 00:19:11 - Exercise selection: why barbell squats are tough (and what he does instead) 00:33:24 - Machines, imbalances, and unilateral work 00:38:20 - Should you compete? Dieting realities and expectations 00:40:50 - Bulking: eating enough, high protein, and making it work in real life 00:54:49 - Advice for lifters with disabilities

This episode covers cerebral palsy.Written notes can be found at https://zerotofinals.com/paediatrics/neurology/cerebralpalsy/Questions can be found at https://members.zerotofinals.com/Books can be found at https://zerotofinals.com/books/The audio in the episode was expertly edited by Harry Watchman.

Join Sandra for one of the most unique and inspiring interviews in the history of We Don't Die Radio. Rosemary Musachio was born with cerebral palsy and is non-verbal, meaning she has never spoken a word in the traditional sense. But that hasn't stopped her from meeting the Pope, riding in a motorcycle sidecar, hang-gliding at 5,000 feet, or training to become an evidential medium. Using a head-pointer and voice synthesis technology, Rosemary shares her incredible journey from a fearful child to a fearless woman. She opens up about the loss of her soulmate, Mylan, and the undeniable sign he sent her from the afterlife—physically moving her locked wheelchair across the room! She also discusses her training as a medium (using a word board to convey messages), her philosophy on overcoming limitations, and shares breathtaking poetry from her new book, Soul of a Rose. In this episode: * The Tech: How Rosemary communicates using a head-pointer and synthesizer. * The Daredevil: Why she chooses "insanity" (hang-gliding!) over safety. * The Afterlife Sign: The true story of a locked wheelchair moving on its own. * Mediumship: How a non-verbal person delivers messages from Spirit. * Poetry: Rosemary reads her moving poem "Uncaged Spirit." Get Rosemary's Book "Soul of a Rose": Amazon: https://amzn.to/4t9HWWa Visit Rosemary's Website: https://www.remcreativeconsulting.com/ *Connect with Sandra Champlain: * Website (Free book by joining the 'Insiders Club, Free empowering Sunday Gatherings with medium demonstration, Mediumship Classes & more): http://wedontdie.com *Patreon (Early access, PDF of over 800 episodes & more): Visit https://www.patreon.com/wedontdieradio  *Don't miss Sandra's #1 "Best of all things afterlife related" Podcast 'Shades of the Afterlife' at https://shadesoftheafterlife.com

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

Alex was itching to ask her partner Ben whether he'd be up for having kids one day — a question that felt scary and extra complicated because she has Cerebral Palsy. To muster some courage, she turned to an unexpected ally: a tiny stuffed lamb that can see the future. ⭐️ This episode originally ran on August 16, 2017 and is a favorite from the archives. We hope you enjoy, and we'll be back next week with a brand new episode. … • Join LST+ for community and access to You Know What, another show in the Longest Shortest universe! • Follow us on Instagram • Sign up for our newsletter, where we recommend other parenting + reproductive health media • Buy books by LST guests (your purchase supports the show!) • Website: longestshortesttime.com Learn more about your ad choices. Visit megaphone.fm/adchoices

Empowering Journeys: Embracing Life with Cerebral Palsy – Featuring Jason Moyle Host Tony Mantor welcomes Jason Moyle, an inspiring individual living with cerebral palsy. Jason shares his life story, from his premature birth and early diagnosis to his challenges growing up and facing bullying. Despite these obstacles, Jason has turned his experiences into opportunities to uplift others. He discusses his various roles at Civil Furland, CHBN Radio, and his passion for comedy writing. The conversation delves into his personal struggles, coping mechanisms, and the importance of empathy and understanding for people with disabilities. Tune in for an emotional and motivating episode that underscores the power of perseverance and community. Meet Jason Moyle: A Story of Courage and Determination Jason's Early Life and Diagnosis Challenges and Triumphs in School Living with Cerebral Palsy: Daily Life and Community Involvement Overcoming Physical and Emotional Challenges Future Outlook and Final Thoughts Conclusion and Call to Action INTRO/OUTRO: Music T.Wild Mantor Music BMI The content on Why Not Me: Embracing Autism amd Mental Health Worldwide, including discussions on mental health, autism, and related topics, is provided for informational and entertainment purposes only. The views and opinions expressed by guests are their own and do not reflect those of the podcast, its hosts, or affiliates.Why Not Me is not a medical or mental health professional and does not endorse or verify the accuracy, efficacy, safety of any treatments, programs, or advice discussed.Listeners should consult qualified healthcare professionals, such as licensed therapists, psychologists, or physicians, before making decisions about mental health or autism- related care.Reliance on this podcast's contents is at the listener's own risk. Why Not Me is not liable for any outcomes, financial or otherwise, resulting from actions taken based on the information provided. Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.