Podcasts about Cerebral palsy

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]

*Can Music Defy Disability? Brandon Mendenhall's Mind Over Matter

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.

Send a textMeet Melbourne-based podcaster and disability advocate Peta Hooke. She is the host of 'The I Can't Stand Podcast', and in 2025, she released a short podcast series called 'Eggs', where she chronicles her real-life experience navigating IVF and fertility with a Cerebral Palsy. On Have the Nerve, Susan and Peta talk a bit more about that podcast and the reception, medical equity and they discuss how our lifelong disabilities have shaped what gratitude means to them. Information in this episodeThe I Can't Stand Podcast https://www.icantstandpodcast.com/Eggs - The I Can't Stand Podcast https://omny.fm/shows/the-i-cant-stand-podcast/playlistsAs a Disabled Woman, My Abortion Wasn't Questioned, but My Pregnancy Was - Article by Nicole Lee (April 27, 2020 Women with Disabilities Australia) https://oursite.wwda.org.au/stories/as-a-disabled-woman-my-abortion-wasnt-questioned-but-my-pregnancy-wasI Just Needed a Mammogram - Article by Asha Prasad (January 16, 2026 Spinal Cord Injuries Australia) https://scia.org.au/resource-hub/i-just-needed-a-mammogram/Woman who uses wheelchair turned away from mammogram appointment - Article by Nas Campanella (July 9, 2025, Australian Broadcasting Corporation)  https://www.abc.net.au/news/2025-07-09/woman-wheelchair-turned-away-from-mammogram/105464036CreditsThis episode has been written, produced and edited by Susan Wood. Logo art by Cobie Ann Moore.Spinal Cord Injuries Australia is a for-purpose organisation that supports people with a spinal cord injury and other neurological conditions. For more information about our supports and services, visit our Resource Hub at https://scia.org.au/resource-hub/.

In this podcast, Julia Hanes, Joel Ewert & Dynai Eilig discuss their paper 'Parasports for cerebral palsy: Thinking and ‘prescribing' beyond the Paralympics'. The paper is available here: https://doi.org/10.1111/dmcn.70115 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

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.

Following a meeting with the COCT, Browyn Brookes, a young lady living with Cerebral Palsy, joined Clarence Ford on air for an update into her case. Views and News with Clarence Ford is the mid-morning show on CapeTalk. This 3-hour long programme shares and reflects a broad array of perspectives. It is inspirational, passionate and positive. Host Clarence Ford’s gentle curiosity and dapper demeanour leave listeners feeling motivated and empowered. Known for his love of jazz and golf, Clarrie covers a range of themes including relationships, heritage and philosophy. Popular segments include Barbs’ Wire at 9:30am (Mon-Thurs) and The Naked Scientist at 9:30 on Fridays. Thank you for listening to a podcast from Views & News with Clarence Ford Listen live on Primedia+ weekdays between 09:00 and 12:00 (SA Time) to Views and News with Clarence Ford broadcast on CapeTalk https://buff.ly/NnFM3Nk For more from the show go to https://buff.ly/erjiQj2 or find all the catch-up podcasts here https://buff.ly/BdpaXRn Subscribe to the CapeTalk Daily and Weekly Newsletters https://buff.ly/sbvVZD5 Follow us on social media: CapeTalk on Facebook: https://www.facebook.com/CapeTalk CapeTalk on TikTok: https://www.tiktok.com/@capetalk CapeTalk on Instagram: https://www.instagram.com/ CapeTalk on X: https://x.com/CapeTalk CapeTalk on YouTube: https://www.youtube.com/@CapeTalk567See omnystudio.com/listener for privacy information.

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

A young lady Bronwyn Brookes reached out to us after she applied for a post in the Expanded Public Works Programme last year, she uploaded all the relevant information & went for an interview, she was told she got the job but when the time came for her to report for duty EWP told her the job had already started and they hired another person. Bronwyn has Cerebral Palsy & feels this could be the reason she was passed over for the EPWP jobs, She joins us live in studio to tell her story Views and News with Clarence Ford is the mid-morning show on CapeTalk. This 3-hour long programme shares and reflects a broad array of perspectives. It is inspirational, passionate and positive. Host Clarence Ford’s gentle curiosity and dapper demeanour leave listeners feeling motivated and empowered. Known for his love of jazz and golf, Clarrie covers a range of themes including relationships, heritage and philosophy. Popular segments include Barbs’ Wire at 9:30am (Mon-Thurs) and The Naked Scientist at 9:30 on Fridays. Thank you for listening to a podcast from Views & News with Clarence Ford Listen live on Primedia+ weekdays between 09:00 and 12:00 (SA Time) to Views and News with Clarence Ford broadcast on CapeTalk https://buff.ly/NnFM3Nk For more from the show go to https://buff.ly/erjiQj2 or find all the catch-up podcasts here https://buff.ly/BdpaXRn Subscribe to the CapeTalk Daily and Weekly Newsletters https://buff.ly/sbvVZD5 Follow us on social media: CapeTalk on Facebook: https://www.facebook.com/CapeTalk CapeTalk on TikTok: https://www.tiktok.com/@capetalk CapeTalk on Instagram: https://www.instagram.com/ CapeTalk on X: https://x.com/CapeTalk CapeTalk on YouTube: https://www.youtube.com/@CapeTalk567See omnystudio.com/listener for privacy information.

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.

In this episode of Life Beyond The Mic, Shawna and LaLa talk about why they're stepping away from one-size-fits-all, textbook medicine and embracing a more holistic, individualized approach to healthcare, all while preparing for the snowstorm of the century.  They open up about medical gaslighting, being dismissed by doctors, and the importance of doing your own research, bringing case studies to appointments, and getting second (and third) opinions. Both share moments when doctors didn't listen, and how they were right all along.  LaLa discusses the devastating reality of medical negligence and how her colon ruptured after five doctors failed to take her symptoms seriously.Shawna also shares a major update: after 36 years of unanswered questions, she recently met with a genetics doctor who may finally have answers related to her Cerebral Palsy and other long-standing health issues that have gone unexplained for decades.  This episode is a reminder that patient advocacy saves lives, holistic health looks at the whole person, and you are allowed to push for answers, even when the system makes it hard.

Los artículos que se tratan en el episodio de hoy están listados aquí: The neonatal SOFA score in very preterm neonates with early-onset sepsis. Tagerman M, Sahni R, Polin R. Pediatr Res. 2025 Oct 9. doi: 10.1038/s41390-025-04068-z. Online ahead of print.PMID: 41068313Systemic Postnatal Corticosteroids, Bronchopulmonary Dysplasia, and Survival Free of Cerebral Palsy. Doyle LW, Mainzer R, Cheong JLY. JAMA Pediatr. 2025 Jan 1;179(1):65-72.doi: 10.1001/jamapediatrics.2024.4575.PMID: 39556404 Bienvenidos a La Incubadora: una conversación sobre neonatología y medicina basada en evidencia. Nuestros episodios ofrecen la dosis ideal (en mg/kg) de los más recientes avances para el neonato y para las increíbles personas que forman parte de la medicina neonatal.Soy tu host, Maria Flores Cordova, MD.Este podcast está presentado por los médicos neonatólogos Dani de Luis Rosell, Elena Itriago, Carolina Michel y Juliana Castellanos.No dudes en enviarnos preguntas, comentarios o sugerencias a nuestro correo electrónico: nicupodcast@gmail.comSíguenos en nuestras redes:Twitter: @incubadorapodInstagram: @laincubadorapodcastCreado originalmente por Ben Courchia MD y Daphna Yasova Barbeau MD http://www.the-incubator.org  Bienvenidos a La Incubadora: una conversación sobre neonatología y medicina basada en evidencia. Nuestros episodios ofrecen la dosis ideal (en mg/kg) de los más recientes avances para el neonato y para las increíbles personas que forman parte de la medicina neonatal. Soy tu host, Maria Flores Cordova, MD. Este podcast está presentado por los médicos neonatólogos Dani de Luis Rosell, Elena Itriago, Carolina Michel y Juliana Castellanos. No dudes en enviarnos preguntas, comentarios o sugerencias a nuestro correo electrónico: nicupodcast@gmail.comSíguenos en nuestras redes:Twitter: @incubadorapodInstagram: @laincubadorapodcast Creado originalmente por Ben Courchia MD y Daphna Yasova Barbeau MD http://www.the-incubator.org

In this podcast, Nihad A. Almasri discusses her paper 'Common data elements of cerebral palsy registries in Arabic-speaking countries: A scoping review'.   The paper is available here: https://doi.org/10.1111/dmcn.70059   Follow DMCN on Podbean for more: https://dmcn.podbean.com/ ___ Watch DMCN Podcasts on YouTube: https://bit.ly/2ONCYiC __ DMCN Journal: Developmental Medicine & Child Neurology (DMCN) has defined the field of paediatric neurology and childhood-onset neurodisability for over 60 years. DMCN disseminates the latest clinical research results globally to enhance the care and improve the lives of disabled children and their families. DMCN Journal - https://onlinelibrary.wiley.com/journal/14698749 ___ Find us on Twitter! @mackeithpress - https://twitter.com/mackeithpress

In this podcast, Nihad A. Almasri discusses her paper 'Common data elements of cerebral palsy registries in Arabic-speaking countries: A scoping review'.   The paper is available here: https://doi.org/10.1111/dmcn.70059   Follow DMCN on Podbean for more: https://dmcn.podbean.com/ ___ Watch DMCN Podcasts on YouTube: https://bit.ly/2ONCYiC __ DMCN Journal: Developmental Medicine & Child Neurology (DMCN) has defined the field of paediatric neurology and childhood-onset neurodisability for over 60 years. DMCN disseminates the latest clinical research results globally to enhance the care and improve the lives of disabled children and their families. DMCN Journal - https://onlinelibrary.wiley.com/journal/14698749 ___ Find us on Twitter! @mackeithpress - https://twitter.com/mackeithpress

In this podcast, David Frumberg, Paige Church & Nathan Rosenberg discuss their paper 'Time toxicity and shared decision-making in cerebral palsy'. The paper is available here: https://doi.org/10.1111/dmcn.70123 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

Stand-Up On The Spot! Featuring completely improvised sets from Tina Friml, Chris "Comedian CP" Powell, Daniel Van Kirk, Rafe Williams & Jeremiah Watkins. No material. Comedians create Stand-Up On The Spot off audience suggestions. Everything is covered from weird dm's to Bruce Springsteen, conspiracy theories, high school sports, and more! Jeremiah Watkins you know from Trailer Tales, Dr. Phil Live, his special DADDY, and as the host and creator of Stand-Up On The Spot. Tina Friml has appeared on Tonight Show and has gone viral with her unique sense of humor and wit with her Cerebral Palsy. CP has appeared on Empire, The Detroiters and Keep Your Distance with Kevonstage. Daniel Van Kirk has a special you can watch on youtube called Rose Gold and can be heard on Bob's Burgers. Rafe Williams has a new special on Don't Tell and another special on Youtube called Young Grandpa. Follow the Comedians! Jeremiah Watkins  @jeremiahwatkins   @TrailerTalesPod   @standupots  https://www.instagram.com/jeremiahstandup Tina Friml  @tinafriml  https://www.instagram.com/tinafriml CP  @ComedianCP  https://www.instagram.com/comediancp Daniel Van Kirk  @DanielVanKirkComedy  https://www.instagram.com/danielvankirk Rafe Williams  @RafeWilliams  https://www.instagram.com/iamrafewilliams Stand-Up On The Spot https://www.instagram.com/standupots  @standupots  Sponsored by: Blue Chew Get 10% off your first month of BlueChew Gold w/ code SPOT @ http://BlueChew.com/ Sponsored by: HelloFresh Get 10 free meals + a free Zwilling knife at http://HelloFresh.com/standup10FM Sponsored by: Mint Mobile Get premium wireless for $15/month on a 3, 6, or 12 month plan at http://MintMobile.com/STANDUP Interested in sponsoring the show? Email standupots@gmail.com for inquiries #1HourSpecial #StandupComedy #TinaFriml #ComedianCP #JeremiahWatkins #DanielVanKirk #RafeWilliams SOTS St. Louis: Tina Friml, CP, Daniel Van Kirk, Rafe Williams & Jeremiah Watkins | Ep 89 Learn more about your ad choices. Visit podcastchoices.com/adchoices

Send us a textBrent and Kyle's story is rooted in life-shaping experiences that led them to become who they are today.Kyle was born with cerebral palsy, leaving him with full cognitive ability but very limited physical mobility. He lives life in a wheelchair and requires assistance with daily tasks like eating. Brent is Kyle's older brother, and they grew up in a household where their family never accepted limitations on what was possible for Kyle.Today, Brent acts as Kyle's legs so Kyle can compete in some of the world's most challenging endurance events — including the IRONMAN World Championship (140.6 miles) and the Boston Marathon among several others. Not only are they completing these races as a push-assist duo, they've also raised millions through The Kyle Pease Foundation to give other individuals with disabilities the chance to experience their own finish-line moments. Their efforts also support inclusive employment opportunities for people with disabilities who, like Kyle, deserve meaningful roles and visibility.We had a great conversation and you will love this inspiring episode! Thanks guys!Website: https://kylepeasefoundation.orgInstagram: https://www.instagram.com/thekylepeasefoundation/ LinkedIn: https://www.linkedin.com/company/kyle-pease-foundation/posts/?feedView=all FaceBook: https://www.facebook.com/TheKylePeaseFoundationYouTube: https://www.youtube.com/channel/UCNfzbm0kpTagaHRwMptuV9QSupport the show

Dan McDermott got in touch with the show because of his daughter Eve. Eve has had Cerebral Palsy since she was 9 weeks old, and her family are fighting to give her the treatment to help her walk.Dan joins Andrea to discuss Eve's life, and the fundraising effort they are making.If you would like to donate, you can visit https://www.idonate.ie/fundraiser/SupportEvesDreamtoWalk

As an elite young soccer player, Nick Mayhugh excelled on the field but always struggled to overcome some physical limitations that he didn't understand. In spite of that, Nick was on track to play soccer at the highest levels. Until the grand mal seizure he suffered at 14, led him to a series of tests which uncovered that Nick had been born with cerebral palsy and would therefore never play soccer again. Nick shares his story on this episode, how he eventually allowed the news to fuel him into playing D1 College soccer. Nick then played on the U.S. Paralympic soccer team, before become a Paralympic sprinter, winning 3 gold medals and 1 silver at the Tokyo Paralympics. Nick's story is one of grit, determination, and inspiration and you don't want to miss this episode.

Our guest this week is Mike Kinner of Colorado Springs, CO who is the founder of Air-O-Sport and father of three including a son with microcephaly.Mike and his wife, Stephanie, have been married for 12 years and are the proud parents of three children: daughters; Elieyanah (1) and McKenzie (9) as well as son, Samuel (6) who has microcephaly, which is linked to several disorders, including; epilepsy, cerebral palsy, being deaf, visually impaired and non-verbal.Mike is the founder of Air-O-Sport, a unique fast-paced, non-contact team game where players pass and throw a lightweight ring through the air to score points by hitting targets or completing passes in a defined zone. It blends elements of basketball, ultimate frisbee, and handball, emphasizing agility, teamwork, and quick decision-making.We learn about the Kinner family, their love for Samuel and the energy they bring to life, all on this episode of the SFN Dad to Dad Podcast.Show Notes - Phone – (719) 243-9111Email – mike@playairosport.comLinkedIn –  https://www.linkedin.com/in/mikekinner/Website - https://playairosport.com/Special Fathers Network –SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 800+ SFN Mentor Fathers, who are raising kids with special needs, have said: “I wish there was something like this when we first received our child's diagnosis. I felt so isolated.  There was no one within my family, at work, at church or within my friend group who understood or could relate to what I was going through.”SFN Mentor Fathers share their experiences with younger dads closer to the beginning of their journey raising a child with the same or similar special needs. The SFN Mentor Fathers do NOT offer legal or medical advice, that is what lawyers and doctors do. They simply share their experiences and how they have made the most of challenging situations.Check out the 21CD YouTube Channel with dozens of videos on topics relevant to dads raising children with special needs - https://www.youtube.com/channel/UCzDFCvQimWNEb158ll6Q4cA/videosPlease support the SFN. Click here to donate: https://21stcenturydads.org/donate/Special Fathers Network: https://21stcenturydads.org/  SFN Mastermind Group - https://21stcenturydads.org/sfn-mastermind-group/Special thanks to SFN Mentor Father, SFN Mastermind Group dad and 21CD board member Shane Madden for creating the SFN jingle on the front and back end of the podcast.. 

All riders have bodies and some have Complex bodies. Our guest Stephanie shares her story of riding with Cerebral Palsy and how working with her body instead of against it she is able to meet her riding goals. We talk about different tack options as well as how having a positive outlook makes all the difference in the world! This month's rider's tip and homework tackles crookedness and leaning on the horse's back. Let Solange help you tackle your “bad foot” once and for all! Listen in....Horses in the Morning Stable Riding with Solange Episode 3846:Host: Solange of Stable RidingSponsor: Stable RidingGuest: Stephanie C.Time Stamps:01:00 - Intro to topic08:14 - Stephanie 31:15 - Joy and Judgement32:29 - Rider Tip

All riders have bodies and some have Complex bodies. Our guest Stephanie shares her story of riding with Cerebral Palsy and how working with her body instead of against it she is able to meet her riding goals. We talk about different tack options as well as how having a positive outlook makes all the difference in the world! This month's rider's tip and homework tackles crookedness and leaning on the horse's back. Let Solange help you tackle your “bad foot” once and for all! Listen in....Horses in the Morning Stable Riding with Solange Episode 3846:Host: Solange of Stable RidingSponsor: Stable RidingGuest: Stephanie C.Time Stamps:01:00 - Intro to topic08:14 - Stephanie 31:15 - Joy and Judgement32:29 - Rider Tip

Our guest this week is Nick Massie of Los Angeles, CA, a film industry veteran and father of an adult son who is an actor with Cerebral Palsy. Nick and his wife, Michelle, have been married for 29 years and are the proud parents of Cole (28), an actor and member of the Screen Actors Guild, who also has cerebral palsy. Cole was featured in the highly acclaimed movie The Paper Bag Plan, which debuted in 2024.  It's a well told story and Cole gave a heartfelt performance as Billy, a young man with Cerebral Palsy.  The screen play was written and the film was directed by Anthony Lucero.  We also learn about the impact that various organization's have had on Cole's development, including: Canine Companions, Shane's Inspiration, United CP and Ronald McDonald House.  It's an uplifting father-son interview with a cameo appearance from Michelle, all on this episode of the SFN Dad To Dad Podcast. Show Notes - Phone – (323) 620-3903Email – nickmassie04@gmail.comPaper Bag Plan YouTube -  https://www.youtube.com/watch?v=GFRKK3wIQ3ECole Massie's Web Page: http://www.colemassie.comSpecial Fathers Network -SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 800+ SFN Mentor Fathers, who are raising kids with special needs, have said: "I wish there was something like this when we first received our child's diagnosis. I felt so isolated.  There was no one within my family, at work, at church or within my friend group who understood or could relate to what I was going through."SFN Mentor Fathers share their experiences with younger dads closer to the beginning of their journey raising a child with the same or similar special needs. The SFN Mentor Fathers do NOT offer legal or medical advice, that is what lawyers and doctors do. They simply share their experiences and how they have made the most of challenging situations.Check out the 21CD YouTube Channel with dozens of videos on topics relevant to dads raising children with special needs - https://www.youtube.com/channel/UCzDFCvQimWNEb158ll6Q4cA/videosPlease support the SFN. Click here to donate: https://21stcenturydads.org/donate/Special Fathers Network: https://21stcenturydads.org/  SFN Mastermind Group - https://21stcenturydads.org/sfn-mastermind-group/Special thanks to SFN Mentor Father, SFN Mastermind Group dad and 21CD board member Shane Madden for creating the SFN jingle on the front and back end of the podcast.. 

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

Welcome to the return of the "True Tales By Disability Advocates" podcast! In Episode 24, hosts MsBoye, Jennifer McKinney, and Adam Griebel hear multiple stories from Tanya Winters about "Maurice," the arm of her friend Susie Angel that has its own personality. This episode was recorded in September of 2024, and it will be the last episode hosted by Ms Boye due to her unfortunate passing. In Ms Boye's final episode she, Jennifer, and Adam discuss with Tanya about remembering our friends who have passed, learning to love your own body, and how important dance can be in expressing your disability.LinksArt Spark DanceBody Shift CollectiveDanceAbility InternationalClick here to listen with the full transcriptFor more details about our programs go to Art Spark Texas, True Tales Podcast Page.

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.

Send us a message!In this episode we will be covering Facebook Live Questions 11/17-11/23/25  from Dana's free Facebook Group Registered Dietitian Exam Study Group with Dana RD!Get the free RD Exam Prep Masterclass here. test out the recorded classes with the Free Trial.  Looking for additional tutoring service? Visit my website! Shop all recorded courses at https://danajfryernutritiontutoring.teachable.comJoin the RD Exam Prep Mastery Program for access to the Situational Practice Questions,  Key Topics Review, Vocab Classes, Wed 8pest Group tutoring , study guides and a new trouble area video each week!Need a Crash Course before your exam? Check out the 4 part Pre-Exam Crash Course: Key Topics Review.

Have you ever been told you couldn't do something? That's what happened to today's guest, Shelbi Davenport. Years ago, Shelbi was told she wouldn't be able to attend college due to her disability. However, she didn't take "NO" for an answer. Shelbi Davenport is a disability advocate, podcaster, and speaker. After many struggles and victories, Shelbi graduated from Texas A&M. Being awarded the first Peer-to-Peer Training certification in Texas on February 5th, 2017, was one of her greatest achievements. Shelbi's passion is to change lives by teaching individuals with disabilities to advocate for themselves and dream big. Shelbi played a big role in advocating for HB 2081 (a bill that would allow Universities to receive more funding for post-secondary programs), which passed not too long ago. Shelbi is currently attending school to get her Master's Degree in Mental Health.You can check out her Shelbi Show on Facebook or Spotify. Check out her website at http://betterlivespcp.com.Her mom's book, "Thanks For Telling Her No" can be purchased here.Send us a textTEDx Talk, Disrupt HR Talk

This special episode brings you inside the 79th Annual Meeting of the American Academy of Cerebral Palsy and Developmental Medicine (AACPDM), held in New Orleans, October 15–18, 2025. Join host Tyler McDonald from the University of South Alabama as he attends his first AACPDM meeting and highlights the moments, conversations, and clinical insights most relevant to pediatric orthopedic surgeons. Hosted, recorded, and produced by Tyler McDonald. Intro music by A. A. Aalto. Additional royalty-free music provided by Pixabay. Link to Jon David's diagnostic matrix for gait analysis: https://journals.lww.com/jbjsjournal/pages/articleviewer.aspx?year=2003&issue=11000&article=00028&type=Citation

Cerebral Palsy- it takes courage to remain postitive about life with CP.  It takes courage to fight cancer.  What the hell does it take to struggle through both of them simultaneously?  We asked Brian Now, who did just that.  Join us for an inspiring conversation.  ESSENTIAL LINKS: https://okboomer.libsyn.com/site YouTube: https://www.youtube.com/watch?v=0ANJjEbjvP0&list=PLkRx0bBfd2KyT7PSb2RVQcGhZyPCvTarp Facebook page:  https://www.facebook.com/TTaudioworks/?modal=admin_todo_tour Website:  https://tommytones.webnode.com/ Email:  ttaudioworks@gmail.com

In this essential episode of the Gritty Nurse podcast, host Amie Archibald-Varley engages in a critical discussion with Amy Coupal, CEO of the Ontario Caregiver Organization (OCO), about the vital role of caregivers in Ontario. This conversation illuminates the significant challenges faced by these essential, yet often overlooked, members of the healthcare team. Listeners will gain insight into the dynamics of caregiving and the crucial support available through the OCO. Key Takeaways for Listeners: Caregiver Recognition: Understand why caregivers must be recognized as essential members of the healthcare team in Ontario. Tailored Support: Learn about the need for tailored support and resources specifically designed for diverse caregiving communities. Burnout Prevention: Discover the importance of organizations implementing caregiver-friendly policies to prevent caregiver burnout and improve their experience. Political Awareness: The episode stresses the significance of political awareness and advocacy to drive systemic change for caregivers.

Orion is a 12-year-old with spastic diplegic cerebral palsy and is evaluated for gait abnormalities. The therapist observes excessive hip flexion, knee flexion, and ankle dorsiflexion throughout the gait cycle. Which of the following gait patterns BEST describes these findings?A) Crouch gaitB) Scissoring gaitC) Ataxic gaitD) Steppage gaitTEXT OUR TEAM:(727) 732-4573

In this special Complex Care Journal Club podcast episode, host Dr. Kilby Mann interviews presenters of posters and oral abstracts relevant to the care of children with medical complexity at the American Academy for Cerebral Palsy and Developmental Medicine (AACPDM) 79th Annual Meeting, October 15-18, 2025, in New Orleans, Louisiana. Speakers describe their study findings and implications for practice. Dr. Francisco Valencia also discusses the role of the Complex Care Committee and the profound impact of mentorship in the field of complex care. SPEAKERS Laura Brunton, PT, PhD, Associate Professor, School of Physical Therapy, Western University, London, Ontario, Canada Caitlin Cassidy, MD, Associate Professor, Department of Physical Medicine and the Department of Rehabilitation and Pediatrics, Western University, London, Ontario, Canada Susan Gibb, MBBS, FRACP, Medical Lead, Complex Care Hub, Royal Children's Hospital, Melbourne, Australia Francisco Valencia, MD, Pediatric Orthopedic Surgeon, Children's Clinics For Rehabilitative Services, Tucson, Arizona Simran Prakash, BA, Medical Student, University of Miami Miller School of Medicine Karen Pratt, BA, MSc, PhD Candidate, Western University School of Health Sciences, London, Ontario, Canada Claire Wallace, PhD, Pediatric Psychologist, Ranken Jordan Pediatric Bridge Hospital, Maryland Heights, Missouri Esther Yap, BPharm, MD, Physician, Royal Children's Hospital, Melbourne, Australia HOST Kilby Mann, MD, Assistant Professor, Pediatric Rehabilitation Medicine, Children's Hospital Colorado DATE Initial publication date: November 11, 2025. RESOURCES REFERENCED - American Academy for Cerebral Palsy and Developmental Medicine (AACPDM) 29th Annual Meeting, October 15-18, 2025, New Orleans, LA. https://www.aacpdm.org/events/2025/program - American Academy for Cerebral Palsy and Developmental Medicine (AACPDM), www.aacpdm.org/ - AACPDM Complex Care Committee (www.aacpdm.org/about-us/committees/complex-care) TRANSCRIPT https://cdn.bfldr.com/D6LGWP8S/as/bgmft56r8ksk85qxbthvzs/CCJCP_AACPDM_Transcript_11-4-25‌ Clinicians across healthcare professions, advocates, researchers, and patients/families are all encouraged to engage and provide feedback! You can recommend an article for discussion using this form: https://forms.gle/Bdxb86Sw5qq1uFhW6. Please visit: http://www.openpediatrics.org OPENPediatrics™ is an interactive digital learning platform for healthcare clinicians sponsored by Boston Children's Hospital and in collaboration with the World Federation of Pediatric Intensive and Critical Care Societies. It is designed to promote the exchange of knowledge between healthcare providers around the world caring for critically ill children in all resource settings. The content includes internationally recognized experts teaching the full range of topics on the care of critically ill children. All content is peer-reviewed and open-access thus at no expense to the user. For further information on how to enroll, please email: openpediatrics@childrens.harvard.edu CITATION Valencia F, Brunton L, Cassidy C, Gibb S, Prakash S, Pratt K, Wallace C, Yap E, Mann K. Practice-Changing Research in Complex Care at the AACPDM Annual Meeting 2025. 11/2025. OPENPediatrics. Online Podcast.‌ https://soundcloud.com/openpediatrics/practice-changing-research-in-complex-care-at-the-aacpdm-annual-meeting-2025.

Episode Notes In E402, Andrew does another in the Popcorn & Power Chair series as they review the Netflix film 37 Seconds. It's about Yuma, a 23 year old manga artist with Cerebral Palsy trying to find herself, her sexuality and her independence. Listen to find out why Andrew liked this film, but how it could have been deeper too. Enjoy! Episode Sponsors Do you wanna turn b*tt stuff up a notch. Go to bvibe.com and use code AFTERDARK to receive 20% off orders of $100 (including bundles, discounted items and more). Disability content creation doesn't have to be hard. Follow @seated.perspectives on Instagram to learn how to make content creation a gentle, easy, accessible experience. 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.

Dylan Dreyer joins in on the fun and makes her Jenna & Friends debut. Also, Danny Murphy and Evan Real from the page six podcast "Virtual Reali-Tea" pop in to breakdown the latest Hollywood headlines. Plus, actor Jay Ellis stops by to discuss his new series "All Her Fault" coming out on Peacock and stays back to play an edition of "Don't Look Back." And, Drew University student and rising golf star, Cassie Sengul shares her inspiring story rising up to the challenges  of the sport while dealing with cerebral palsy. Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

About the Episode Join us for an inspiring conversation with Allison Hernandez as she shares her journey of raising a child with cerebral palsy. From the unexpected diagnosis to navigating daily challenges, Allison opens up about the strength and resilience she's found through faith and community. Discover how her experiences have reshaped her beliefs and brought unexpected blessings into her life. This episode is a story of love, support, and the power of community in overcoming life's hurdles. About Allison Allison is a single full time working mom. She works a highly demanding job and manages her home, which includes her and her child, and numerous caregivers. Related Links Hey Friend Moment of Reflection I really love how open and honest Allison was about her faith — how the challenges she faced before Roxie led her to walk away for a time, but through her journey as Roxie's mom, she found her way back to God. She realized just how much she depended on Him. Take a moment to think about where you are on your faith journey. Are you feeling angry with God? Does He seem distant or far away? Or maybe He feels close and present right now. Wherever you are, invite Him into that space. Ask God to show you His heart — for you, and for your child.

The tremendous Athena Stevens gives an interview and chats with Ben and Nico about telling stories on the stage and the page.Send us a text Support the show

This week Sebastian Trzcinski-Clément from Canonical joins Noah and Steve to talk about Ubuntu Summit 25.10. -- During The Show -- 00:50 Intro Steve's TV Falling asleep to TV LG OLED 55A1 06:05 Sebastian Trzcinski-Clément What was out there Ubuntu CDs Working for Google Promotion Committees Putting on a Conference Abdula Developer Library Google to Canonical Ubuntu Summit Dreamworks MoonRay Microsoft & WSL Thinking Fast and Slow Reach out to people The Canonical Office 39:32 News Wire Peazip 10.7 - peazip.github.io (https://peazip.github.io/changelog.html) Calibre 8.13 - calibre-ebook.com (https://calibre-ebook.com/whats-new) Squid Proxy 7.2 - github.com (https://github.com/squid-cache/squid/releases) Less 685 - greenwoodsoftware.com (https://www.greenwoodsoftware.com/less) Digikam 8.8 - digikam.org (https://www.digikam.org/news/2025-10-19-8.8.0_release_announcement) Gnome 49.1 - gnome.org (https://discourse.gnome.org/t/gnome-49-1-released/31977) Thunderbird 144 - thunderbird.net (https://www.thunderbird.net/en-US/thunderbird/144.0/releasenotes) Firefox 144 - firefox.com (https://www.firefox.com/en-US/firefox/144.0/releasenotes) Zorin OS 18 - zorin.com (https://blog.zorin.com/2025/10/14/zorin-os-18-has-arrived) Tails 7.1 - torproject.org (https://blog.torproject.org/new-release-tails-7_1) Q3 Malware Index - eweek.com (https://www.eweek.com/news/open-source-malware-2025) LinkPro Root Kit - thehackernews.com (https://thehackernews.com/2025/10/linkpro-linux-rootkit-uses-ebpf-to-hide.html) Operation Zero Disco - cyberpress.org (https://cyberpress.org/cisco-snmp-vulnerability-exploited) F5 Hacked - thehackernews.com (https://thehackernews.com/2025/10/f5-breach-exposes-big-ip-source-code.html) EdenSpark - gamingonlinux.com (https://www.gamingonlinux.com/2025/10/gaijin-announced-edenspark-an-open-source-ai-assisted-platform-for-making-games) Project CodeGuard - siliconangle.com (https://siliconangle.com/2025/10/16/cisco-unveils-project-codeguard-open-source-framework-secure-ai-written-software) Coral in SL2610 SoCs - cnx-software.com (https://www.cnx-software.com/2025/10/17/google-open-source-coral-npu-synaptics-sl2610-edge-ai-socs) AI and Cerebral Palsy - globenewswire.com (https://www.globenewswire.com/news-release/2025/10/16/3168076/0/en/Open-Source-AI-Tool-by-Yandex-Detects-Signs-of-Infant-Cerebral-Palsy-With-Over-90-Accuracy.html) Mysql 9.5.0 - mysql.com (https://dev.mysql.com/doc/relnotes/mysql/9.5/en/news-9-5-0.html) SuperTuxKart 1.5 - supertuxkart.net (https://supertuxkart.net/Main_Page.html) KDE Plasma 6.5 - kde.org (https://kde.org/announcements/plasma/6/6.5.0) Fedora 43 - phoronix.com (https://www.phoronix.com/news/Fedora-43-Release-Day) Zorin saw 300,000 Downloads - reddit.com (https://www.reddit.com/r/linux/comments/1oih2hv/zorin_os_18_has_already_hit_over_300000_downloads) Qilin Malware - trendmicro.com (https://www.trendmicro.com/en_us/research/25/j/agenda-ransomware-deploys-linux-variant-on-windows-systems.html) Lightricks LTX-2 - prnewswire.com (https://www.prnewswire.com/news-releases/lightricks-releases-ltx-2-the-first-complete-open-source-ai-video-foundation-model-302593012.html) MiniMax-M2 - venturebeat.com (https://venturebeat.com/ai/minimax-m2-is-the-new-king-of-open-source-llms-especially-for-agentic-tool) IBM Mellea - app.daily.dev (https://app.daily.dev/posts/ibm-s-mellea-tackles-open-source-ai-s-hidden-weakness-xqmwbepaq) 90% of Games Run on Linux - tomshardware.com (https://www.tomshardware.com/software/linux/nearly-90-percent-of-windows-games-now-run-on-linux-latest-data-shows-as-windows-10-dies-gaming-on-linux-is-more-viable-than-ever) boilingsteam.com (https://boilingsteam.com/windows-games-compatibility-on-linux-is-at-a-all-time-high) 42:55 F5 Breach Claims Nation State Level Attack Effect of Breach Disclosure laws If you can get the info off your system, do so F5 Competitors MetalLB (https://github.com/metallb/metallb) HA Proxy (https://www.haproxy.org/) theregister.com (https://www.theregister.com/2025/10/15/highly_sophisticated_government_hackers_breached/) 51:05 Proxmox Backup Server DHCP? - David Tiny From the community Proxmox Virtual Enviornment Proxmox Backup Server Use the tailscale IP or DNS Name Proxmox docs (https://forum.proxmox.com/threads/changing-network-to-manage-backups.104771/) -- The Extra Credit Section -- For links to the articles and material referenced in this week's episode check out this week's page from our podcast dashboard! This Episode's Podcast Dashboard (http://podcast.asknoahshow.com/464) Phone Systems for Ask Noah provided by Voxtelesys (http://www.voxtelesys.com/asknoah) Join us in our dedicated chatroom #GeekLab:linuxdelta.com on Matrix (https://element.linuxdelta.com/#/room/#geeklab:linuxdelta.com) -- Stay In Touch -- Find all the resources for this show on the Ask Noah Dashboard Ask Noah Dashboard (http://www.asknoahshow.com) Need more help than a radio show can offer? Altispeed provides commercial IT services and they're excited to offer you a great deal for listening to the Ask Noah Show. Call today and ask about the discount for listeners of the Ask Noah Show! Altispeed Technologies (http://www.altispeed.com/) Contact Noah live [at] asknoahshow.com -- Twitter -- Noah - Kernellinux (https://twitter.com/kernellinux) Ask Noah Show (https://twitter.com/asknoahshow) Altispeed Technologies (https://twitter.com/altispeed) Special Guest: Sebastian Trzcinski-Clément.

Athena Stevens is an Olivier Award-nominated actor, playwright, and author. Her first book, 'What's Done Cannot Be Undone', was published with Harper Collins in June 2025 and is available now. In this episode, Athena joins Ben and Nico in writing for the prompt "Vintage".Send us a text Support the show

To celebrate the 400th episode of the SFN Dad To Dad Podcast, David Hirsch, founder of 21st Century Dads Foundation and host of the SFN Dad To Dad Podcast offers his heartfelt thanks to all those who have been involved with and supported 21CD & SFN.  He reflects on:addressing the issue of father absence in society,his journey as a fatherhood advocate,starting the Illinois Fatherhood Initiative, making an appearance on the Oprah Winfrey Show, starting the 21st Century Dads Foundation, Dads Honor Ride 2015 from Santa Monica to Chicago, 2,325 miles in 21 days, giving a TEDx Talk entitled: Why We Need To Break The Cycle Of Father Absence, writing the book: A Father's Journey To Break The Cycle Of Father Absence, Dads Honor Ride 2016 from Boston to Chicago, 1,400 miles in 21 days, Creating the C2EFA (Cycle To End Father Absence) indoor riding events, Dads Honor Ride 2017 Around Lake Michigan, 958 miles in 9 days, creating the Special Fathers Network Mentoring Program, starting the SFN Dad To Dad Podcast, recording 24 bi-weekly Zoom calls on various topicscreating the 21CD YouTube channel,holding annual SFN Dads Virtual Conferences, creating the SFN audiobook series, creating the weekly virtual SFN Mastermind Group experience, andholding annual SFN Mastermind Group weekend retreatsSpecial thanks to all the individuals, businesses, and foundations that have financially supported 21CD, the growing list of partners and affiliates, all the individuals who have volunteered, especially the 21CD board of directors: Tom Costello, Rich Gathro, Gary Grube, Chris Hunter, Shane Madden, Wayne Messmer, Brian Page and John Shouse.  Special thanks to Shane Madden for creating the SFN fathers jingle at teh beginning and end of this episode.  And last but not least, Tom Couch of Couch Media, who has produced the past 398 episodes of the SFN Dad To Dad Podcast. Show Notes –   Email - david@21stCenturyDads.orgEmail - tcouch2501@gmail.comWebsite - https://21stcenturydads.org/  TEDx Talk -  https://www.youtube.com/watch?v=7CDeMgmeb94Special Fathers Network - SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 500+ SFN Mentor Fathers, who are raising kids with special needs, have said: "I wish there was something like this when we first received our child's diagnosis. I felt so isolated. There was no one within my family, at work, at church or within my friend group who understood or could relate to what I was going through."SFN Mentor Fathers share their experiences with younger dads closer to the beginning of their journey raising a child with the same or similar special needs. The SFN Mentor Fathers do NOT offer legal or medical advice, that is what lawyers and doctors do. They simply share their experiences and how they have made the most of challenging situations.21CD YouTube Channel: https://www.youtube.com/@21stcenturydads58/videosClick Here to donate: https://21stcenturydads.org/donate/Special Fathers Network: https://21stcenturydads.org/SFN Dads Mastermind Group - https://21stcenturydads.org/sfn-mastermind-group/

The Unseen Sibling: Rebecca Robinson's Journey Through Love, Loss, and HopeRebecca Robinson grew up in a home marked by both deep love and quiet sacrifice. Her older sister, Kara, was born with severe Cerebral Palsy. From the beginning, Kara required round-the-clock care, medical equipment, and endless patience — needs her parents met with unwavering devotion and compassion. Their home was filled with the tenderness of a family bound together by something far stronger than circumstance: love.But amid the visible weight her parents carried, Rebecca faced an invisible burden of her own. As the younger sibling, she often felt the pressure to be “the easy one.” She learned not to complain, not to need too much, and not to add stress to her already overwhelmed parents. This quiet phenomenon, known as Glass Child Syndrome, left Rebecca feeling transparent.“I didn't want to be a burden,” she shared in a recent episode of the Cedarville Stories podcast. “My parents were doing everything they could for Kara. I just didn't want to take up more space.”Now a 2025 graduate of Cedarville University, Rebecca has taken her story and transformed it into a gift for others. Her children's book, Penelope Panda's Peculiar Family, gives voice to the complex emotions that siblings of children with disabilities often experience — grief, love, confusion, and resilience. With warmth and whimsy, it helps families talk about what often goes unsaid.Rebecca's heart for ministry doesn't stop at home. Her book is being translated into Japanese to address a culture where disabilities often remain hidden in silence. She hopes it will open doors for compassion, healing, and Gospel conversations.Though Kara has since passed, Rebecca holds fast to her faith. “She's with Christ now,” she says. “And while my past shaped me, my identity is in the hope of what's to come.”From the quiet corners of her childhood to the global impact of her words, Rebecca's story is one of grace woven through pain — a light shining through even the most delicate glass.https://share.transistor.fm/s/4fb72e3ehttps://youtu.be/StvgyN4CC2U

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

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

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

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

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

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

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

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