Podcasts about Cerebral palsy

Zul Rodriguez: Cerebral Palsy, Highschool Drop Out, Teen Pregnancy, Motherhood, CHISME & MORE! Download Hily Dating App from the App Store or Google Play, or visit ⁠⁠⁠⁠⁠⁠https://hily.go.link/yDhNz⁠⁠⁠⁠⁠ •Don't forget to subscribe to the podcast for free wherever you're listening or by using this link: ⁠⁠⁠⁠⁠https://bit.ly/NochedePendejadasPodcast⁠⁠⁠⁠⁠ •If you like the show, telling a friend about it would be helpful! You can text, email, Tweet, or send this link to a friend: ⁠⁠⁠⁠⁠https://bit.ly/NochedePendejadasPodcast⁠⁠⁠⁠⁠ ⁠⁠⁠⁠⁠Follow Alannized on IG⁠⁠⁠⁠⁠ ⁠⁠⁠⁠⁠Follow Alannized on TikTok⁠⁠⁠⁠⁠ ⁠⁠⁠⁠⁠Follow Alannized on Twitter⁠⁠⁠⁠⁠  Learn more about your ad choices. Visit podcastchoices.com/adchoices

Why did Chad start running?What began as preparation for a Spartan Race became a complete transformation of his physical health, confidence, mindset, and sense of purpose.In this episode of Why Did You Start Running, Chad shares how a difficult period following COVID left him struggling with mobility, spasticity, self-doubt, and depression. Living with cerebral palsy, he found himself facing an important decision: continue down a path of inactivity or take a chance on himself and see what was possible.That decision led to his first 5K.Since then, Chad has logged more than 1,000 miles, completed dozens of races, earned a first-place age group finish, organized a charity virtual 5K, launched a scholarship program, and become a voice of encouragement within both the running and cerebral palsy communities.We also discuss the power of community, the mental health benefits of running, navigating grief, overcoming self-doubt, and how one small decision can create opportunities you never imagined.Whether you're a runner, someone living with a disability, or simply looking for a reminder of what's possible when you take a chance on yourself, this conversation is packed with inspiration and perspective.In This Episode• Why Chad signed up for a Spartan Race in 2022• Living with cerebral palsy and navigating physical challenges• How running helped improve mobility and confidence• The mental and emotional benefits of running• The importance of supportive communities• Running through grief and difficult life experiences• Finding purpose through helping others• Creating a scholarship program and charity 5K• Building confidence through personal growth• Why taking one chance on yourself can change everythingConnect With ChadInstagram: https://www.instagram.com/chadwillia1/Learn More About Cerebral Palsy PerspectiveWebsite: https://cerebralpalsyperspective.comIf this episode encouraged you, share it with someone who needs a reminder that progress doesn't require perfect circumstances. Sometimes the biggest transformations begin with a single decision to try.

In this special episode of The Cerebral Palsy Perspective Podcast, Chad Williams and Daryl Perry welcome Luke, the first recipient of the Doing Hard Things My Way Adaptive Athlete Scholarship.After reviewing hundreds of applications, Luke's story stood out because of his determination, leadership, athletic accomplishments, and commitment to helping others. A recent high school graduate from Alabama, Luke has spent the last four years competing in football and track while developing a passion for adaptive athletics and disability advocacy.During this conversation, Luke shares how he unexpectedly found his love for sports, what athletics taught him about teamwork and leadership, and how discovering adaptive sports opened new possibilities for his future. He also discusses his decision to pursue a career in physical therapy and his goal of helping other individuals with disabilities discover opportunities in adaptive athletics.The conversation highlights the power of community, the importance of creating opportunities for others, and what it means to truly do hard things your own way.In This Episode• Meet Luke, the first Doing Hard Things My Way scholarship recipient• How a friend's encouragement led him into athletics• Lessons learned through football and track and field• Why teamwork matters beyond sports• Discovering adaptive athletics and new opportunities• Attending the University of Alabama's adaptive athletics program• Pursuing a future career in physical therapy• Advocating for people with disabilities in sports• The impact of mentorship, support, and community• What it means to build a future centered around helping othersAbout The ScholarshipThe Doing Hard Things My Way Adaptive Athlete Scholarship was created to recognize adaptive athletes who demonstrate perseverance, determination, leadership, and a commitment to making a difference in the lives of others. Luke's story embodies those values and serves as an inspiration for athletes and advocates alike.Connect With Luke:https://www.instagram.com/luke__ramos_Connect With ChadInstagram: https://www.instagram.com/chadwillia1/Connect With DarylInstagram: https://www.instagram.com/daryltperryIf you enjoyed this episode, share it with someone who could benefit from hearing Luke's story. Conversations like these help create awareness, build community, and remind us of what's possible when we choose to keep moving forward.

ResearchWorks is heading to AACPDM 2026 in Philadelphia this year!We can't wait to see you there - it's a special 80th Annual Meeting for the American Academy for Cerebral Palsy and Developmental Medicine (AACPDM).Join with us as we speak with Dr Kristie Bjornson - live from EACD 2026 in Galway Ireland, the final episode that we recorded on our European tour! A preview of what to expect from this year's annual congress and a look at the host city, Philadelphia!Register here:https://www.aacpdm.org/events/2026/registration

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.

Helping Children Flourish: Parent-Informed Social Narratives to Support Readiness for Upper Limb Rehabilitation in Cerebral Palsy

Health-Related Quality of Life after Guided Growth Treatment for Hip Displacement in Young Children with Cerebral Palsy

Non-invasive Measurement of work of breathing in children and young adults with high level cerebral palsy.

Power mobility experience, meaning and outcomes for children with complex non-ambulant cerebral palsy: A scoping review

Implementing low-cost powered mobility devices in children with Cerebral Palsy: from concept to clinical practice  (workshop)

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.

Sometimes it's important to take a minute to appreciate and understand the power of being involved with Major League Baseball. Andrew Bailey certainly does. The Red Sox pitching coach sits down with Bradfo to discuss how he and his family have taken up the cause of raising and awareness and funds for the battle against Cerebral Palsy, a group of lifelong neurological disorders that affects a person's movement, muscle tone and posture. It's an issue near and dear to Bailey's heart, considering his daughter, Teddy, has been battling CP since birth. The conversation should strike a chord in understanding the power of baseball and those who use it to help others.

In this podcast, Sue Reid discusses her paper 'Causal subgroups and declining rates of cerebral palsy in Victoria, Australia'.   The paper is available here: https://doi.org/10.1111/dmcn.70298   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

Billy Horsburgh from Northeast Fife in Scotland, lives with Cerebral Palsy and glaucoma. Over the years, he was told due to the two conditions he would not qualify for a guide dog, so William set out to do something many doubted he could manage: raise a lively Jack Russell terrier puppy on his own. Now, his memoir My Perfect Companion: Because love is blind is finally out and Paulina Kuchorew spoke with the author to learn more.  Image shows the RNIB Connect Radio logo. On a white and black background ‘RNIB' written in bold black capital letters and underline with a bold pink line. Underneath the line: ‘Connect Radio' is written in black in a smaller font. 

Time toxicity and shared decision-making in cerebral palsyDavid B Frumberg, Paige T Church, Nathan RosenbergPMID: 41387091 DOI: 10.1111/dmcn.70123AbstractClinicians and families regularly enter into a process of shared decision-making. Seldom, if ever, however, is the critical question of time usage, or, more specifically, time-related burdens, accounted for when establishing goals and outcome measures. Time-related burdens are not included, for instance, as an outcome measure in cerebral palsy research-something which may have profound effects about which we are unaware. By contrast, in the field of oncology, time-related burdens, or, more technically, what has been termed time toxicity, has been increasingly studied. Building on that work, we seek to apply the concept of time toxicity to people with disabilities who interface with healthcare at great frequency.https://pubmed.ncbi.nlm.nih.gov/41387091/

Send us Fan MailCheck our the full viva in the Final Exam Coursehttps://anaesthesia.thinkific.com/courses/FinalExamFinal exam peper 2025.2 VIVA 4Viva StemYou are providing anaesthesia in the interventional radiology suite of your major hospital. On the list is a 22 year old woman who requires a CT-guided biopsy of a left renal mass that was discovered incidentally on abdominal imaging. The patient was admitted today for the procedure and is accompanied by her parents who are her legal guardians and carers. A postoperative bed has been booked for the patient.Medical HistorySevere cerebral palsy- spastic quadriplegia- moderate intellectual disabilityRecurrent aspiration pneumonia- severe gastro-oesophageal reflux- oropharyngeal dysphagia- gastrostomy feeding tube (feeds ceased for six hours)Anxiety- distress with medical proceduresEpilepsyMedications - Baclofen 10 mg tds - Levetiracetam 1000 mg bd- Pantoprazole 40 mg once dailyAllergies- Nil knownObservations- height 155 cm - estimated weight 40 kg estimated - (BMI approx. 16.6 kg/m2) - HR 90 bpm- BP 95/55 mmHg- SpO2 96% on room airPreoperative Investigations- Blood test results are normal- Blood Group and Hold has been conductedWhat are your specific considerations when planning anaesthesia care for this patient?---------Find us atInstagram: https://www.instagram.com/abcsofanaesthesia/Twitter: https://twitter.com/abcsofaWebsite: http://www.anaesthesiacollective.comPodcast: ABCs of AnaesthesiaPrimary Exam Podcast: Anaesthesia Coffee BreakFacebook Page: https://www.facebook.com/ABCsofAnaesthesiaFacebook Private Group: https://www.facebook.com/groups/2082807131964430---------Check out all of our online courses and zoom teaching sessions here!https://anaesthesia.thinkific.com/collectionshttps://www.anaesthesiacollective.com/courses/---------#Anesthesiology #Anesthesia #Anaesthetics #Anaesthetists #Residency #MedicalSchool #FOAMed #Nurse #Medical #Meded ---------Please support me at my patreonhttps://www.patreon.com/ABCsofA---------Any questions please email abcsofanaesthesia@gmail.com---------Disclaimer: The information contained in this video/audio/graphic is for medical practitioner education only. It is not and will not be relevant for the general public.Where applicable patients have given written informed consent to the use of their images in video/photography and aware that it will be published online and visible by medical practitioners and the general public.This contains general information about medical conditions and treatments. The information is not advice and should not be treated as such. The medical information is provided “as is” without any representations or warranties, express or implied. The presenter makes no representations or warranties in relation to the medical information on this video. You must not rely on the information as an alternative to assessing and managing your patient with your treating team and consultant. You should seek your own advice from your medical practitioner in relation to any of the topics discussed in this episode' Medical information can change rapidly, and the author/s make all reasonable attempts to provide accurate information at the time of filming. There is no guarantee that the information will be accurate at the time of viewingThe information provided is within the scope of a specialist anaesthetist (FANZCA) working in Australia.The information presented here does not represent the views of any hospital or ANZCA.These videos are solely for training and education of medical practitioners, and are not an advertisement. They were not sponsored and offer no discounts, gifts or other inducements. This disclaimer was created based on a Contractology template available at http://www.contractology.com.PerOral Endoscopic Myotomy Failed intubation | Final Exam Viva

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

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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!

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.

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.

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

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

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