Podcasts about transplants

As Norway's crown princess, Mette-Marit, convalesces from lung transplant surgery, we bring together patients and doctors to share their experiences of this major life-saving procedure. Since the 1980s, lung transplantations have become increasingly routine, but as every operation relies on suitable donor organs becoming available, the timing is always uncertain.“Everything was so quick, everything was so scary,” says Aimee Morrison, who received her new lungs last year, only months after being told she had a chronic degenerative condition, “You don't really get an opportunity to think about what's happening … 10-12 hr surgery, unknown results, what's going to happen afterwards…” As we hear, Aimee's story was particularly dramatic as only a week before her operation she had given birth to her daughter. Lung transplant patients require life-long aftercare from physicians like Dr Vicky Gerovasili, as their condition will always eventually deteriorate. “That can be very emotionally stressful,” she says,”but it's also very rewarding because we are becoming part of their life and their family. I sign off patients to go scuba diving, travel the world and that's fantastic to see.”

In this episode, worker-owner Monica Ponce of Love is Love Cooperative Farm talks about the logistics of selling transplants to other growers.   Subscribe for more content on sustainable farming, market farming tips, and business insights!   Get market farming tools, seeds, and supplies at Modern Grower. Follow Modern Grower:  Instagram  Instagram Listen to other podcasts on the Modern Grower Podcast Network:  Carrot Cashflow  Farm Small Farm Smart  Farm Small Farm Smart Daily  The Growing Microgreens Podcast  The Urban Farmer Podcast  The Rookie Farmer Podcast  In Search of Soil Podcast Check out Diego's books:  Sell Everything You Grow on Amazon   Ready Farmer One on Amazon **** Modern Grower and Diego Footer participate in the Amazon Services LLC. Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to Amazon.com.

How do you ask someone to donate a kidney?   For many people living with kidney failure, this can be one of the most difficult and emotional conversations they will ever face. Fear of rejection, concerns about damaging relationships, feelings of guilt and uncertainty about where to begin can prevent people from exploring living kidney donation as an option.   In this episode of Diary of a Kidney Warrior Podcast, host Dee Moore is joined by Jen Lumsdaine, Lead Nurse for Living Donation.   Jen previously worked as a Living Donor Transplant Coordinator in Edinburgh, completed a PhD examining the quality-of-life impact of living kidney donation for donors and recipients, and has worked to improve equitable access to living donor transplantation across Scotland.   Together they discuss:  

It's our FIRST Father's Day and Jamie and Sophie are feeling emotional! Sophie gives her honest verdict on Jamie's parenting skills, and Jamie opens his very first Father's Day presents from Ziggy. We're not crying… you are.

After a 31-year career in banking, a diagnosis of chronic kidney disease in 2013 changed the course of Jean Sime's life. She began in-center hemodialysis in 2015 and, in 2019, received a life-saving kidney transplant from a living donor who was once a stranger.  Following a career transition in 2022, She entered the publishing industry and has since become a passionate advocate for organ donation and kidney health. Jean is the co-author of three award-winning books—Because of Organ Donation, Howl is Thankful for Kidney Donation, and Voices-19, and serves as a motivational speaker, mentor, and advocate for dialysis patients and transplant recipients. She is a proud member of Team Liberty for the Transplant Games of America, where 2026 marks her third participation. For more information on kidney donation and support, reach out to Kent at Kidney Solutions or call him directly at 830-285-2140. Host: Kent Bressler Producer: Jason Nunez Remember to keep breathing, and thank you for listening to Kent's Kidney Stories!

On today's podcast David, Jason and Natalie sit down with Ilya to talk about his new hair transplant, how much it cost and whether David might be getting the same procedure. And David gets upset with John about a gardening mishap, Natalie causes some drama by posting some Tiktoks and Jason has two incredible fan interactions. Also, the World Cup hits LA, getting 3 million followers in one day, and a $3000 pickleball bet. Listen to Jason's latest pod here: https://open.spotify.com/episode/7gvykgb1GcVutpd8E0ZhUC?si=3b0bcbccda524e72 Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

The Transplant Games of America are taking place in Denver this weekend, bringing together transplant recipients, living donors, and donor families for an Olympic-style event. This celebration of life is a unique opportunity for people who have overcome incredible challenges to come together and compete in various activities, including pickleball, swimming, and corn hole. The Transplant Games are more than just a fun event - they're a chance for people to connect with others who understand their experiences. The games feature different divisions for recipients, living donors, and donor families, allowing participants to compete against others with similar abilities. This inclusive approach ensures that everyone can participate and enjoy the experience. One of the highlights of the Transplant Games is the Murph Challenge, a military-style obstacle course that pushes participants to their limits. This event is a unique experience for transplant recipients, living donors, and the general public to come together and challenge themselves physically. The games also offer a chance for people to share their stories and connect with others who have gone through similar experiences. If you're interested in learning more about the Transplant Games of America or want to get involved, tune in to this episode to hear from Aimee Adelmann, a two-time kidney transplant recipient and team manager of the Transplant Games. She shares her inspiring story and provides details on how to participate or spectate at the event.See omnystudio.com/listener for privacy information.

Send us Fan MailIT's Therapy Thursday!!A doctor once told Tim McDonald he had three years to live. Tim didn't accept that as the end of the story, and he didn't try to “positive-think” his way out of reality either. He got curious, asked harder questions, tracked what his body was doing during chemo, and kept building a plan that matched his goals. What unfolds is a raw, practical conversation about stage 4 colorectal cancer, the shock of diagnosis, and what treatment is really like when fatigue, nausea, neuropathy, and scanxiety become part of the calendar. Tim shares how online patient communities helped him discover an option no one had brought to him early on: liver transplant for select colorectal cancer patients with liver-only metastases. We dig into what the living donor search feels like, why the waiting can be more emotionally draining than chemo, and how hope changes when you finally see a path off lifelong treatment. We also talk about the part people don't prepare you for: survivorship mental health, grief, and the strange weight of losing friends you met through advocacy and support spaces. Along the way, we pull out clear self-advocacy lessons you can use right now, whether you're facing cancer or any chronic illness: get multiple opinions until you believe what you hear, find specialists who know the nuances, and remember you're allowed to choose your care team. If this conversation helps you, subscribe, share it with someone who needs hope, and leave a review. What's one question you want to ask your doctor after listening?Tim McDonald is a stage IV colorectal cancer survivor, patient advocate, podcast host, and author. After being diagnosed with metastatic colorectal cancer in 2020, Tim transformed one of the most difficult seasons of his life into a mission of hope, support, and advocacy. Drawing from his experiences navigating fear, uncertainty, mental health challenges, and survivorship, he now mentors patients, advances cancer research initiatives, and helps others find purpose through adversity. Tim serves as a Research Advocate with Fight Colorectal Cancer, leads the Florida chapter of Man Up To Cancer, hosts the Advocacy at Work podcast, and is the author of From Patient to Advocate: Turning Survivorship into Impact.https://advocacyatwork.comhttps://manuprocancer.orghttps://COLONTOWN.orghttps://FightCRC.orghttps://www.patientadvocate.org/ (formerly PAN Foundation) From Patient to Advocate: Turning Survivorship Into Impact — Available on Amazon Support the showHost Candace PatriceCo-host Janet Halevisit the website at https://www.essentialmotivation.com/Instagram instagram.com/essentialmotivationllcvisit Janet's website https://haleempowermentllc.com/To be a guest on our show email me at candacefleming@essentialmotivation.comIn the subject line put EMH Guest Suicide Prevention Lifeline 988Music by Lukrembo: https://soundcloud.com/lukremboProvided by Knowledge Base: https://bit.ly/2BdvqzN

The signs were'nt significant initally, however, his first ever blood tests revealed leukaemia at a fairly advance stage, which ultimately meant a bone marrow transplant that saved Cian Brennan's life. Hosted on Acast. See acast.com/privacy for more information.

Jason talks with NMDP Patient Navigator Leanna Cooper about the process of a transplant, why the action isn't the most stressful part, and more!

Episode Title: Connected by Hope: How Sister Keli and Stephanie Bates Found Friendship Through Transplant Episode Description: What happens when two people who have walked through illness, uncertainty, and waiting find each other on the other side of survival? In this heartfelt episode of This Thing Called Life, host Andi Johnson welcomes Sister Keli and Stephanie Bates, whose connection began through transplant but became something much deeper—a sisterhood built on understanding, resilience, and hope. Together, they share their individual journeys through kidney disease, dialysis, setbacks, and ultimately transplantation. Through moments of heartbreak, perseverance, and unexpected friendship, Stephanie and Sister Keli reflect on what it means to keep showing up, trust the process, and find purpose in giving back. Their stories are a powerful reminder that healing doesn't happen alone—and sometimes the people who understand us best are the ones who have walked a similar road. Episode Highlights Host Andi Johnson welcomes Stephanie Bates and Sister Keli, two women whose lives became connected through their shared transplant journeys and commitment to supporting others. Stephanie reflects on how her health journey began after a traumatic cesarean delivery in 1999 that caused damage to her kidney. Years later, after noticing swelling in her leg, Stephanie sought medical care and was diagnosed with stage three kidney disease, beginning a long season of monitoring and treatment. From 2003 to 2013, she managed her condition through regular nephrology care before eventually beginning dialysis as her disease progressed. Stephanie shares the difficult but determined process of becoming transplant eligible, including being encouraged to lose weight in order to qualify. Through dedication and support, she achieved her health goals and was officially added to the transplant list in 2018. In 2019, Stephanie received her first kidney transplant, but unexpected complications during the COVID era eventually led her to undergo a second transplant in 2024. Sister Keli shares her own experience of learning her kidneys had progressed into end-stage renal disease (ESRD) and initially struggling to fully accept the seriousness of the diagnosis. She reflects on a turning point when conversations and encouragement from people around her helped her recognize the urgency of beginning treatment. Sister Keli started with peritoneal dialysis, later transitioning to hemodialysis after complications and challenges with treatment. Her journey included major life changes—including divorce and the eventual loss of a limb due to complications connected to inadequate dialysis treatment. Despite those setbacks, she remained committed to her health and continued pursuing transplant eligibility. Stephanie and Sister Keli describe meeting through a community connection event and immediately sensing a familiar understanding between them. What started as an invitation to volunteer quickly developed into a meaningful friendship rooted in shared experience. Both women speak openly about how transplant and dialysis journeys can feel isolating—and how finding someone who truly understands can change everything. They reflect on the emotional complexity of receiving a transplant call: excitement, disbelief, fear, gratitude, and awareness that another family experienced loss. The conversation highlights the emotional and physical realities of transplant while emphasizing the importance of hope, advocacy, and community support. Stephanie and Sister Keli encourage listeners to stay committed to treatment plans, ask questions, lean on others, and remember that healing often happens in connection with community. Key Takeaways: 1. Healing Is More Than Medical—It's Relational Recovery isn't only about procedures and appointments. Community, connection, and shared understanding can become powerful parts of the healing journey. 2. Small Decisions Can Create New Possibilities From staying committed to dialysis to making lifestyle changes for transplant eligibility, each step forward can open the door to life-changing opportunities. 3. Hope and Gratitude Can Coexist With Hardship Transplant journeys carry both joy and grief. Receiving a second chance at life often comes with deep appreciation for donors and renewed purpose moving forward. Tweetable Quotes “You have to be in a certain BMI to receive a transplant. The doctor connected me with weight loss people, we got a weight loss plan together, and I dropped that weight. Then less than six months after I dropped that weight, I was listed.” Stephanie Bates “I feel like the Lord started sending people to talk to me. You get a call from somebody that you haven't heard from in a while, and they have a message for you. And so these people over the weekend started talking to me, and I said, "Oh no,”  I said, "This is serious.” And so I reported, and they put me on peritoneal dialysis.” Sister Keli “This is why I'm here now, speaking out to people and letting them know, take your treatments seriously, don't cut off your treatments, don't skip your treatments, because the after effect of that? Sometimes you can't even come back from it.” Sister Keli “I'm like, something is familiar about her. And then I come to find her birthdays around my birthday, we just were familiar and able to link, but more than that, she understood where I had been, and I understood where she had been, and that was something I didn't have with any of my other friends.” Sister Keli “It (bond they share) creates a sense of like, “So there is someone who knows exactly what I'm going through.” Now our stories are not entirely the same. We've been through the same types of situations, the waiting process, “Is the kidney ever coming in?”, all the procedures, and all the testing. It feels daunting, it feels overwhelming.” Stephanie Bates Resources: Donatelifeky.org https://getoffthelist.org/ https://www.networkforhope.org/ https://www.networkforhope.org/about-us/ https://www.networkforhope.org/stories-of-hope/ https://www.facebook.com/NetworkForHopeOPO https://www.youtube.com/@NetworkforHope. https://aopo.org/ RegisterMe.org/NetworkforHope

Earlier this month, Alan Morrissey was joined by Kevin Haugh, to chat about the upcoming 2026 European Transplant Games.  Kevin, a former school principal and accomplished athlete from Carrigaholt and Doonaha, was one of two Clare athletes who are part of a 25-strong Team Ireland that is travel to Arnhem in the Netherlands for the Games.  The European Transplant Games get underway from this Sunday, the 21st of June, running until Saturday, the 27th of June.  The other Clare member of Team Ireland is Marie O'Connor, an experienced Transplant Games competitor  Marie, who hails from Lahinch, had to undergo two life-saving kidney transplants in 1996 and 1998 following a viral infection. Image (c) European Transplant Games

In episode 160, "When a Hope Transplant Is Needed," Dr. B dives into the lifeline that hope truly is. Just as breath sustains life, hope sustains the soul-but when hope falters, we sometimes need a transplant. Dr. B uses vivid metaphors to show how, in the darkest moments, hope can be revived, restored, and transplanted back into us. If you've ever felt like you were at the end of your rope, this episode will guide you to breathe again and receive a fresh infusion of hope. Tune in and let hope flow back into your life!The HOPE Zone...where there's HOPE for every situation!

Topics for tonight's show in the order we cover them:-Transplant tips-Pot sizes, when and why.-Plastic vs fabric pots, or something else?-How to help plant recover from shock-Pruning/deleaf/defoliate, none, light or heavy/when-Ph-ing water or not?-Testing water - why , what matters?-Water temperature, dissolved oxygen-Foliar feeding benefits/challenges/drawbacks?-Trim talk, wet v dry, scissors with or without spring, bent tip or straight tipsThis week host @Jackgreenstalk (aka @Jack_Greenstalk on X/instagram backup account) [or contact via email: JackGreenstalk47@gmail.com] is joined by @spartangrown on instagram or X f.k.a. Twitter at https://x.com/grown43626 or email spartangrown@gmail.com for contacting spartan outside social media, any alternate profiles on other social medias using spartan's name, and photos are not actually spartan grown be aware, we are also joined by Guest Caveman Seeds!.... This week we missed TheAmericanOne on youtube aka @theamericanone_with_achenes on instagram who's amy aces can be found at amyaces.com , Rust Brandon of @fulcrop.sciences / fulcrop.ceo regained @Rust.Brandon instagram page, and products can be found at bokashiearthworks.com , and @NoahtheeGrowa on instagram , Matthew Gates aka @SynchAngel on instagram and twitter @Zenthanol on youtube who offers IPM direct chat for $1 a month on patreon.com/zenthanol , @drmjcoco from cocoforcannabis.com as well as youtube where he tests and reviews grow lights and has grow tutorials and @drmjcoco on instagram and @ATG Acres Aaron The Grower aka @atgacres his products can be found at atgacres.com view his instagram to find out details about drops!

Tara Gregory, MD, Colorado Blood Cancer Institute, Denver, CO and Jay Spiegel, MD, Sylvester Comprehensive Cancer Center, Miami, FL Recorded on May 28, 2026 Tara Gregory, MD President Colorado Blood Cancer Institute Denver, CO Jay Spiegel, MD Assistant Professor Division of Transplant and Cellular Therapy University of Miami Sylvester Comprehensive Cancer Center Miami, FL In this episode, Dr. Tara Gregory from the Colorado Blood Cancer Institute, and Dr. Jay Spiegel from the Sylvester Comprehensive Cancer Center discuss the evolving role of CAR T-cell therapy in lymphoma and myeloma. They provide a practical overview of CAR-T, including currently approved indications, importance of early referral, patient selection considerations, and strategies for engaging patients in treatment discussions. The conversation also covers key aspects of toxicity management and post-treatment monitoring, while addressing current limitations of CAR-T therapy and future directions that may further expand its role in patient care. Tune in today for this exciting episode! Blood Cancer United Resources: Blood Cancer United Accredited and Non-Accredited Healthcare Professional Education Blood Cancer United Resources for Patients This episode is supported by Bristol Myers Squibb, Johnson & Johnson & Legend Biotech, and Kite, a Gilead Company.

“Take in your final breath before your first new one.”  Those were the words Jillian heard before her double lung transplant—words that would mark the end of one life chapter and the beginning of another. Jillian is 34 years old, living with cystic fibrosis, and a double lung transplant recipient. Her story is one of resilience, loss, hope, and purpose. From being diagnosed at birth to navigating adulthood, Jillian has faced more than most, but she continues to show up for her life and for others in the cystic fibrosis community. Jillian shares what it was like growing up with CF, supported by family and shaped by early connections within the community. She reflects on how advocates like Emily Schaller and the Rock CF Foundation influenced her outlook and helped her feel less alone. We also talk about her college years, what it meant to pursue independence while managing a complex disease, and how life shifted as her health declined into end-stage lung failure. Jillian walks us through the transplant process, not just medically, but emotionally—the fear, the uncertainty, and the strength it takes to keep going. One of the most profound parts of Jillian's story is the loss of her twin brother. She opens up about that grief and how it continues to shape her perspective, her resilience, and her compassion for others. Throughout it all, Jillian emphasizes the importance of support systems and mental health—especially during the transplant journey. No one goes through something like this alone, and her story is a reminder of how critical connection and care truly are. Today, Jillian looks toward the future with hope. She shares her dreams of building a family, continuing her advocacy work, and expanding the impact of the nonprofit she founded, Jillian's Jay Walkers Organization. Her story is not just about survival—it's about living with intention, honoring loss, and creating something meaningful from it all.

We have an extraordinary guest to give the weekend forecast! Listen to Weather Kid EJ and the Transplant Olympics!See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

We have an extraordinary guest to give the weekend forecast! Listen to Weather Kid EJ and the Transplant Olympics!See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Two recent studies have shown remarkable advances in HIV cure research: (1) a Norwegian man who achieved long-term HIV remission after a stem cell transplant from his brother and (2) a Phase 1 trial testing CAR-T cell therapy. On this episode, Antonio Urbina, MD, Medical Director for CEI's HIV Primary Care and Prevention Center of Excellence, dives into these studies and puts them into clinical context, including how to discuss cure research with patients. Related Content: CEI Line: 1-866-637-2342  https://ceitraining.org/ Clinicaltrials.gov

On this episode of VIE Speaks: Conversations with Heart & Soul podcast, host Lisa Marie Burwell, VIE's CEO/editor-in-chief, spoke with David Weill, renowned transplant pulmonologist, author, and former director of the Lung and Heart-Lung Transplant Program at Stanford University Medical Center.Over the course of his remarkable career, Dr. Weill has witnessed the profound intersection of life, loss, hope, and healing through the world of organ transplantation. From leading one of the nation's premier transplant programs to advocating for advancements in pulmonary and transplant care, his work has transformed countless lives while offering a unique perspective on what it means to care for patients during their most vulnerable moments.We also discuss his three books, Exhale, Tell Me I Belong, and All That Really Matters. He shares the process of writing and how it became a way to process the emotional realities of what he was experiencing. This episode offers a thoughtful and moving conversation about resilience, purpose, and the stories that connect us all.You can find all three books on Amazon as well as on Audiobook! And to learn more about David visit his website: davidweill.com

In this episode of Better Edge, Transplant Hepatologist Laura Lulik, MD moderates a panel discussion about the Northwestern Medicine Liver Transplant Tumor Clinic. The conversation covers advances in imaging, systemic therapies and innovative procedures, as well as the clinic's multidisciplinary approach.The panel includes: • Daniel Borja, MD, transplant surgeon• Aparna Kalyan, MD, medical oncologist • Robert Lewandowski, MD, interventional radiologist• Amira Borhani, MD, abdominal radiologist

Send us Fan MailCan you perform Hair transplants on textured hair? Celestine Gitau specialises in cosmetic chemistry and trichology. After a career as a certified nurse, in 2017 she went on to be a hair transplant technician. She works with brands to help to develop products & technologies.Celestine enjoys performing her trichology consultations, and helping people throug their journey. She has now performed over 500 hair transplants, and is an expert in working on afro textured hair.We discuss the unique differences & challenges that this can present, and the specialist experience necessary to extract and place the follicular units successfully, along with advising patients on the best process for them, and aftercare procedures.Connect with Celestine:InstagramLinkedIn Hair & Scalp Salon Specialist course Support the showConnect with Hair therapy:FacebookInstagramTwitterClubhouse- @Hair.TherapyHair Therapy WebsiteDonate towards the podcast Start your own podcastHair & Scalp Salon Specialist Course ~ Book now to become an expert! 

In this powerful episode of Diary of a Kidney Warrior Podcast, host Dee Moore is joined by Rebecca Griffiths, who shares her extraordinary journey through kidney failure, dialysis, kidney transplantation and transplant loss.   Rebecca's story is one of resilience, determination and hope. After gaining approximately 25kg of fluid in a matter of days and requiring emergency treatment to drain fluid from around her heart, she found herself facing kidney failure without the support of a renal team. What followed was a life-changing journey that included dialysis, a kidney transplant, the devastating loss of that transplant and the challenge of starting again.   In this episode, Rebecca discusses:  

Hour 3 of this Freedom Friday has Jon being joined by Max Rymer, Kathryn Johnson, and AK Kamara to talk about the Save America Act, an AI teddy bear for children, and eyebrow transplants. See omnystudio.com/listener for privacy information.

Later this month, Team Ireland will travel to Arnhem in the Netherlands for the 2026 European Transplant Games, a celebration of sport, resilience, and the gift of life.   Among the 25 athletes representing Ireland are two from County Clare, including Kevin Haugh from Carrigaholt and Doonaha.   A former school principal and accomplished athlete, Kevin has overcome tremendous health challenges and now proudly competes on the international stage, honouring the generosity of organ donors and raising awareness of the life-changing impact of transplantation.   Kevin joined Alan Morrissey to tell us more about his remarkable journey and his preparations for the Games.  Image (c) European Transplant Games

Amy Waterman, PhD, joins host Karandeep Singh, MD, to discuss how AI can improve kidney transplant care through earlier interventions, personalized patient support, and better access to transplantation across the patient journey.

Amy Waterman, PhD, joins host Karandeep Singh, MD, to discuss how AI can improve kidney transplant care through earlier interventions, personalized patient support, and better access to transplantation across the patient journey.

Grab my

Most people cannot imagine life on dialysis for even a year"Vanessa Evans has lived it for nearly three decades. Diagnosed at 12, she has seen it all: transplant, loss, in-center care, and home hemodialysis. But her story is not what you would expect. In this episode, she shares with Lori what really changed everything"and why she is now helping other people who have kidney failure choose a dialysis treament that works for them.

EP 148: The Gift of Life: Inside Pediatric Transplants with Dr. Mo Saying “yes” to organ, eye, and tissue donation can change everything. In this episode of This Thing Called Life, Dr. Monique “Dr. Mo” Goldschmidt from Cincinnati Children's Hospital Medical Center shares her passion for pediatric transplantation and the journey that brought her to Cincinnati. She reflects on the emotional connections she builds with her young patients and their families, and the extraordinary collaboration among care teams that makes successful outcomes possible. This episode is a moving reminder of the power of compassion, teamwork, and the gift of life.   Resources: Donatelifeky.org https://getoffthelist.org/ https://www.networkforhope.org/ https://www.networkforhope.org/about-us/ https://www.networkforhope.org/stories-of-hope/ https://www.facebook.com/NetworkForHopeOPO https://www.youtube.com/@NetworkforHope. https://aopo.org/ RegisterMe.org/NetworkforHope

In this episode of the OutThere Colorado Podcast, Spencer and Seth chat about a historic amphitheater you've never heard of, the data behind transplants and what surprised us both the most when moving to Colorado, a trail that leads to dinosaur tracks, a footrace series you've gotta check out, and more.

This Skeptical Sunday, Jessica Wynn explains how dialysis became a $50B industry where under 40% of patients survive five painful years of dependence.Welcome to Skeptical Sunday, a special edition of The Jordan Harbinger Show where Jordan and a guest break down a topic that you may have never thought about, open things up, and debunk common misconceptions. This time around, we're joined by writer and researcher Jessica Wynn!Full show notes and resources can be found here: jordanharbinger.com/1336On This Week's Skeptical Sunday:Dialysis is a life-sustaining external filtration system for the roughly 800,000 Americans in kidney failure — but it's grueling. Most patients endure three to five hours per session, three times a week, indefinitely, and fewer than 40% survive beyond five years.The financial structure is staggering. Dialysis is a $50 billion-a-year US industry, with Medicare spending about $36 billion annually — roughly 7% of its entire budget for under 1% of the population. Two companies, DaVita and Fresenius, control about 70% of all clinics.The system rewards permanence over cure. Since 1972, Medicare has covered kidney failure for everyone regardless of age, creating guaranteed, indefinite revenue. Transplants and home dialysis are cheaper and better for patients, yet under-incentivized because they cost providers customers.The human and safety toll is severe. Infections cause 36% of dialysis deaths, sepsis mortality runs 100 to 300 times higher than average, and understaffing worsens outcomes. Many patients lose their jobs, mobility, and social lives — some choose to stop treatment entirely.The hopeful part: much kidney disease is preventable or delayable, and you have real power here. Manage diabetes and hypertension aggressively, get your kidneys checked with a simple blood and urine test, and see a nephrologist early — catching it sooner can dramatically slow progression.Connect with Jordan on Twitter, Instagram, and YouTube. If you have something you'd like us to tackle here on Skeptical Sunday, drop Jordan a line at jordan@jordanharbinger.com and let him know!Connect with Jessica Wynn at Instagram (and Instagram!), and subscribe to her newsletters: Between the Lines and Where the Shadows Linger!And if you're still game to support us, please leave a review here — even one sentence helps! Sign up for Six-Minute Networking — our free networking and relationship development mini course — at jordanharbinger.com/course!Subscribe to our once-a-week Wee Bit Wiser newsletter today and start filling your Wednesdays with wisdom!Do you even Reddit, bro? Join us at r/JordanHarbinger!This Episode Is Brought To You By Our Fine Sponsors: Lufthansa Allegris: Go to Lufthansa.com and search for "Allegris" to learn moreCookUnity: 50% off first week: cookunity.com/jordan or code JORDANRevolve Man: 15% off: revolve.com/jordan, code JordanMarathon Rewards: Sign up today: marathonrewards.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Learn, Understand and Master the LANGUAGE of WOMEN

Ecclesiastes: Heart Transplant with Pastor Jason Eddy www.betheljanesville.org

When she was 4 months old on November 14th of 2023, Kalia Arrayan was diagnosed with High Risk B Cell Acute Lymphoblastic Leukemia. This diagnosis came as a complete shock to her parents Heather and Casey who did not see any clear symptoms before a routine checkup showed a lump on her spleen. Kalia went through a very difficult treatment process for the next 8 months before she underwent a Bone Marrow Transplant with her 11 year old brother being her donor. Kalia has been doing much better over the past nearly two years as she approaches her 3rd birthday.

Senator McConnell and Congressman Guthrie announce millions in funding for upgrades to a Kentucky county's water system, Congressman McGarvey proposes guaranteeing income for young adults, dozens paddle the Ohio River to highlight its recreational opportunities and restoration needs, and meet two Kentuckians participating in the Transplant Games of America.

What do you do when your own immune system decides to treat your organs like an all-you-can-eat buffet and drops eight separate medical diagnoses on your lap? This week, the brilliant and unapologetically defiant Jennifer Park joins the fellas to tier-rank her massive collection of interlocking illnesses. From competitive pro bodybuilding while navigating liver cirrhosis, to sneaking a giant wooden shower brush into high-level executive meetings just to fight off a systemic itch that literally feels like bugs under her skin, Jennifer is the ultimate biological overachiever. She gets hilariously raw about surviving a catastrophic colostomy bag explosion inside a crowded university bathroom, flying down to Texas for experimental exosome treatments, and the verbal smackdown she gave a snarky transplant surgeon who tried to flex a god complex on her.Follow Sickboy: Instagram: https://www.instagram.com/sickboypodcastTiktok: https://www.tiktok.com/@sickboypodcastDiscord: https://discord.gg/expeUDN

In this MMF Rewind, we're bringing back an important conversation with Lynda Lee Smith—one that shines a light on the ongoing challenges transplant families face and the critical role of research in improving outcomes.Lynda Lee Smith, CEO of Enduring Hearts, is featured on the Moving Medicine Forward Podcast to discuss the mission and impact of the nation's only nonprofit dedicated to funding pediatric heart transplant research. In this conversation, Lynda addresses the challenges transplant families face and how research is improving outcomes and quality of life. Listen now and consider donating to Enduring Hearts here.00:55 The mission behind the only organization dedicated exclusively to pediatric heart transplant research.01:19 How Lynda found Enduring Hearts and its mission-driven work.02:45 The personal story that exposed a major research gap in pediatric heart transplantation.03:50 Why heart transplants are lifesaving, but not a cure.04:22 More on home blood tests and their role in reducing invasive biopsies and improving quality of life.05:39 Why Enduring Hearts focuses on making one transplant last a lifetime.07:06 How Enduring Hearts supports bold research ideas before larger funders step in.09:40 The unique challenges teenagers face after transplant and how research helps. 12:05 Addressing the financial, emotional, and logistical burdens families face.15:21 Programs that connect families navigating life after pediatric transplant.15:49 Enduring Hearts' innovative approach to engaging a new generation through gaming.18:04 The move toward DNA informed, individualized treatment plans.19:19 What real success looks like for pediatric heart transplant patients.21:08 Stories of resilience, progress, and hope for the future.

What do you do when your own immune system decides to treat your organs like an all-you-can-eat buffet and drops eight separate medical diagnoses on your lap? This week, the brilliant and unapologetically defiant Jennifer Park joins the fellas to tier-rank her massive collection of interlocking illnesses. From competitive pro bodybuilding while navigating liver cirrhosis, to sneaking a giant wooden shower brush into high-level executive meetings just to fight off a systemic itch that literally feels like bugs under her skin, Jennifer is the ultimate biological overachiever. She gets hilariously raw about surviving a catastrophic colostomy bag explosion inside a crowded university bathroom, flying down to Texas for experimental exosome treatments, and the verbal smackdown she gave a snarky transplant surgeon who tried to flex a god complex on her.Follow Sickboy: Instagram: https://www.instagram.com/sickboypodcastTiktok: https://www.tiktok.com/@sickboypodcastDiscord: https://discord.gg/expeUDN

Today, Peggy talks with Daniel Gaylor, LCSW, OSW-C, ACHP-SW, and a social work supervisor at Moffitt Cancer Center, about what happens after patients and caregivers get through the intense treatment period and begin asking, “Now what?” Daniel explains that recovery does not mean life snaps back to normal. Survivorship brings fear, relief, hope, uncertainty, and exhaustion all at once. Those reactions are normal, and they deserve to be named. Daniel explains why post-traumatic stress disorder (PTSD) can show up after transplant. A transplant is not a routine treatment. It can involve long hospital stays, isolation, major physical side effects, and real fears about survival. When patients return for follow up visits, they may be brought back emotionally to those difficult hospital days. This can make survivorship feel complicated, even when the transplant was successful. Another key theme is slowly letting go. Patients may feel afraid to go out, socialize, eat in a restaurant, drive, or return to activities they once enjoyed. Daniel encourages survivors to start small and to be fair to the situation. It is easy to imagine the worst case. But it also helps to keep yourself honest - say out loud what could happen if things go well. The episode also addresses the “strain of worry.” Daniel describes signs of anxiety and depression, including sleep problems, racing thoughts, trouble concentrating, irritability, sadness, appetite changes, and not wanting to do things that usually bring joy. He reminds listeners that difficult days do not mean failure. Survivors should be able to say, “Today is not my best day,” and ask for help. Peggy and Daniel also talk about toxic positivity. While loved ones often mean well, phrases like “you're lucky to be alive” can minimize a survivor's fear or pain. Daniel encourages honest communication. Patients can thank loved ones for their support while also explaining what would help more. Social connection is another major part of healing. Daniel urges survivors and caregivers to increase connection and reduce isolation. A quick text, a short call, a support group, or a shared conversation can make a real difference. Peggy highlights programs where survivors can meet others who understand graft versus host disease (GVHD) and transplant recovery. Daniel closes with the idea of building a “tool belt.” Each person needs practical coping tools, whether that is a friend, music, journaling, counseling, mindfulness, a book, or a favorite place to reset. Caregivers need their own tool belts too. Transplant affects the whole support system, and survivorship works best when people communicate, ask for help, and remember they are not meant to do this alone. Links: Elephants and Tea: https://elephantsandtea.org/ BMT InfoNet: https://bmtinfonet.org/ Blood Cancer United: https://bloodcancerunited.org/ Thanks to this season's sponsors, Incyte and Sanofi. (00:00) Intro (01:01) Normalizing emotional reactions during recovery (04:22) PTSD after transplant and why it matters (08:59) Slowly letting go after transplant (13:12) Facing the worst case and choosing to move forward (13:53) The strain of worry and mental health red flags (19:31) Toxic positivity and the power of validation (20:26) How to talk with loved ones who are trying to help (22:39) Social health, connection, and friendship (26:43) Support groups, GVHD, and feeling understood (28:07) Building a survivorship "tool belt" (33:08) Why transplant never fully “stops” (36:39) A patient story about resilience and asking for help National Bone Marrow Transplant Link - (800) LINK-BMT, or (800) 546-5268.nbmtLINK Website: https://www.nbmtlink.org/Check out our valued nbmtLINK resource books, some for sale, some free as downloadable, https://www.nbmtlink.org/shop/nbmtLINK Facebook Page: https://www.facebook.com/nbmtLINKFollow the nbmtLINK on Instagram! https://www.instagram.com/nbmtlink/The nbmtLINK YouTube Page can be found by clicking here.This content is provided for informational purposes only and is not intended to substitute for professional medical advice, diagnosis, or treatment. It is crucial to consult directly with a qualified healthcare professional regarding any medical conditions, treatment options, or other health concerns.The views and opinions expressed by the speakers are their own and do not necessarily reflect the official policy or position of the nbmtLINK. Unless otherwise stated in an official policy, the nbmtLINK does not endorse any specific treatments, products, or services mentioned by the speakers. Reliance on any information provided is solely at your own risk.The Marrow Masters Podcast is produced by JAG Podcast Productions: https://jagpodcastproductions.com/ Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

In this episode of Marrow Masters, we talk with Adam Claxton, a British acute myeloid leukemia (AML) survivor who was diagnosed in 2024 and received a transplant in December 2024. He shares what early survivorship really feels like, especially the part no one prepares you for. Once treatment slows down, there is a gap between being a patient and figuring out who you are in the world again. Adam explains that around the 100 day mark, he felt dropped out of the system and forced to ask where he fit, what had changed, and who he was becoming after transplant. We also discuss graft versus host disease (GVHD) and how Adam reframes it. He calls it the price he pays for leukemic protection. That shift in perspective helps him see chronic GVHD not only as a complication, but also as evidence that the donor cells are doing their job. He is honest that it can be difficult physically and mentally, but he chooses to view it as part of survival and a sign that his body is being protected. A major focus of the conversation is mindset. Adam talks about mindset as something we have to work on daily, just like updating a device. He believes our thoughts shape how we feel, behave, and respond, and that mental habits matter just as much as physical recovery. He also opens up about relapse, calling it an even harder battle than the initial diagnosis. What helps him move through it is staying connected to his reasons for going on, including his family, his purpose, and his desire to help more people with his voice and experience. The episode also looks at faith over fear. Adam says both fear and faith still take you through the day, so he would rather choose the path that gives him hope. That same thinking connects to what he calls the reset after transplant. He realized he could not simply return to the same life, work, and identity he had before cancer. His priorities had changed, and so had his sense of purpose. Instead of trying to recover the old version of himself, he began building a new one. On a practical level, Adam shares advice about routines, mindfulness, exercise, social media boundaries, and finding joy again in simple things. One of his best suggestions is to go back to the things you loved doing around age 12, because those activities often reconnect you with peace, play, and presence. He also speaks warmly about the importance of support, especially from his wife and children, while reminding us that caregivers carry their own emotional burden too. By the end, Adam leaves listeners with a clear message. Survivors need to be kinder to themselves, own their stories, and start sharing what they have learned. His closing affirmation says it best: we can, we will, we must. More: Adam's Book, Daddy's Magic Blood, on Amazon: https://www.amazon.com/Daddys-Magic-Blood-story-healing/dp/B0GLGXHGW6 Thanks to this season's sponsors, Incyte and Sanofi. (00:00) Intro (01:52) The gap after treatment and early survivorship (03:52) Why survivorship can feel harder than treatment (07:24) Mindset and daily mental conditioning (10:23) Handling relapse and staying connected to purpose (13:20) Faith over fear (15:31) The post transplant identity reset (23:19) Social media, support, and emotional boundaries (26:50) The role of family and caregiver support (29:12) What survivors need more of (32:28) Final affirmation: We can, we will, we must National Bone Marrow Transplant Link - (800) LINK-BMT, or (800) 546-5268.nbmtLINK Website: https://www.nbmtlink.org/Check out our valued nbmtLINK resource books, some for sale, some free as downloadable, https://www.nbmtlink.org/shop/nbmtLINK Facebook Page: https://www.facebook.com/nbmtLINKFollow the nbmtLINK on Instagram! https://www.instagram.com/nbmtlink/The nbmtLINK YouTube Page can be found by clicking here.This content is provided for informational purposes only and is not intended to substitute for professional medical advice, diagnosis, or treatment. It is crucial to consult directly with a qualified healthcare professional regarding any medical conditions, treatment options, or other health concerns.The views and opinions expressed by the speakers are their own and do not necessarily reflect the official policy or position of the nbmtLINK. Unless otherwise stated in an official policy, the nbmtLINK does not endorse any specific treatments, products, or services mentioned by the speakers. Reliance on any information provided is solely at your own risk.The Marrow Masters Podcast is produced by JAG Podcast Productions: https://jagpodcastproductions.com/ Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Send us Fan MailWhat happens when a hair transplant doesn't go to plan? Dom is a 32 year old electrician, who lives in a van in Scotland.He shares his story about his hair loss journey, including dealing with the side effects of medication, disappointing hair transplant results, and why it's important to consider all your options and get lots of expert advice before making a decision.Dom shares how his confidence was low, so he looked to hair transplants as a way to resolve this. When it didn't give him the result he wanted, it made him reflect on his motivation for his decision.Dom now wears a hair system, and is very open about this on his social media. He says he is much happier now and shares his experience to help others.Connect with Dom:InstagramTikTokYoutube Hair & Scalp Salon Specialist course Support the showConnect with Hair therapy:FacebookInstagramTwitterClubhouse- @Hair.TherapyHair Therapy WebsiteDonate towards the podcast Start your own podcastHair & Scalp Salon Specialist Course ~ Book now to become an expert! Polytar Medicated Shampoo

Welcome to another episode of Diary of a Kidney Warrior Podcast. In this powerful Kidney Warrior Story episode, host Dee Moore is joined by Johanna, who shares her lifelong journey living with Chronic Kidney Disease (CKD). Diagnosed as a young child after years of unexplained symptoms, Johanna opens up about growing up with kidney disease, navigating dialysis, experiencing transplant loss, and undergoing multiple kidney transplants. She speaks honestly about the physical and emotional realities of living with CKD for decades, including the uncertainty that comes with transplantation and the challenges of returning to dialysis. Johanna also shares the impact kidney disease has had on her mental wellbeing, family life, pregnancy, identity, and future plans. Throughout the conversation, she highlights the importance of resilience, support, advocacy, and finding joy in life despite the ongoing challenges of chronic illness. This episode is an honest and deeply moving insight into the realities of long-term kidney disease and the strength it takes to keep moving forward through every stage of the journey. In this episode, Johanna discusses: Being diagnosed with kidney disease as a child Growing up with CKD The symptoms that led to diagnosis Starting dialysis Receiving her first kidney transplant The emotional impact of transplant loss Returning to dialysis Undergoing further kidney transplants Pregnancy after transplantation The uncertainty of living with CKD Mental health and emotional resilience Finding hope whilst living with chronic illness If you are living with kidney disease, supporting someone who is, or want to better understand the realities of CKD, this episode is not to be missed.

Show notes at pharmacyjoe.com/episode1132 In this episode, I’ll discuss a case report of the effects of ketamine on the clearance of tacrolimus and sirolimus.

After a QUICK five years since his last appearance on the show, Punchline's Steve Soboslai sits in this week to discuss the writing and recording of the band's fan favorite 2004 single “Heart Transplant.” Written from a real place of young heartbreak, the song has remained a live set constant decades after it was penned on the band's first full US tour. Produced by Sean O'Keefe, the recording has stood the test of time, capturing an energy and enthusiasm of a band feeling the moment. Tune in for a fun and honest look back at what fans of the band would consider the ultimate Punchline classic track. Check out all things Punchline (including the new album Somewhere To Land) at punchlinemusic.com. Chris DeMakes A Podcast is brought to you by DistroKid, the ultimate partner for taking your music to the next level. Get 30% off your first YEAR with DistroKid by signing up at ⁠http://distrokid.com/vip/demakes For bonus episode of The After Party podcast, an extensive back catalog of past After Party episodes, early ad-free releases of new episodes of Chris DeMakes A Podcast, full video versions of episodes, and MUCH more, head to the Patreon at ⁠http://www.ChrisDeMakes.com Follow Chris DeMakes A Podcast on Instagram: ⁠https://www.instagram.com/chrisdemakesapodcast/⁠ Join the Chris DeMakes A Podcast community on Facebook: ⁠https://www.facebook.com/groups/2643961642526928/⁠ Learn more about your ad choices. Visit megaphone.fm/adchoices

President Trump is on the way back to the U.S., following a summit in Beijing with Chinese President Xi Jinping, with key decisions on trade deals, sanctions, and Taiwan still to come. Reporters Eamon Javers and Eunice Yoon have been covereing the details of the trip – and its impact on the ongoing conflict in Iran. Dr. Mehmet Oz is focused on potential entitlement fraud as administrator of the Centers for Medicare and Medicaid.  He describes his landmark career as a heart surgeon, with former patient Roger Altman of Evercore.   Eamon Javers - 2:44  Dr. Mehmet Oz - 16:02  Roger Altman - 26:49  Eunice Yoon - 48:15    In this episode: Dr. Mehmet Oz, @DrOzCMS Eamon Javers, @eamonjavers Eunice Yoon, @onlyyoontv Joe Kernen, @JoeSquawk Andrew Ross Sorkin, @andrewrsorkin Katie Kramer, @Kramer_Katie Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

We're going to jail.

It might sound like a wacky treatment, but recently, the fecal microbiota transplant has emerged as an effective way to help reshape our gut microbiomes. There are a lot of ideas on how to use this emerging therapy, so to help us sort through the misinformation, we are joined by author and general surgeon, Dr. James Kinross. Before that, Sam digs into a bizarre question: why do humans have chins? And later, a new study reveals how heroic beavers are when it comes to combatting climate change. Link to Show Notes HERE Follow Curiosity Weekly on your favorite podcast app to get smarter with Dr. Samantha Yammine — for free! Still curious? Get science shows, nature documentaries, and more real-life entertainment on discovery+! Go to https://discoveryplus.com/curiosity to start your 7-day free trial. Terms apply. Hosted on Acast. See acast.com/privacy for more information.

LIVE SHOW IN Houston Texas June 7th at 7pm! Buy Tickets here: https://www.eventbrite.com/e/bueno-bueno-in-houston-texas-tickets-1988053420297   Call Us To Be On The Show! https://docs.google.com/forms/d/e/1FAIpQLSdV8WNMg69TLL4nYttVh_mKAoLRYzRtnCT226InJqh3ixQR5g/viewform   Watch Andy's Movie Reviews Here! https://youtube.com/@AndyCanchola?si=3r8Dzx7PmA_BukHu   Do you need to fix your hairline? Use our linker $800 off! https://lp.elithair.com/?ref=1824410002291914768&utm_source=Influencer&utm_medium=referral&utm_campaign=Bueno%20Friends   More Content & Channel Perks With Youtube Memberships! https://www.youtube.com/channel/UCcgSueiSghRsBLNuvK8MOQg/join   Join our Run Club! https://strava.app.link/r3ZRAqsd80b   Want to send us a gift? PO BOX 311145 Fontana, Ca 92331   Follow Us! https://linktr.ee/buenobuenopdc   Saul V Gomez Instagram -  https://www.instagram.com/saulvgomez/ Tik Tok - https://www.tiktok.com/@saulvgomez     Hans Esquivel Instagram - https://www.instagram.com/hans_esquivel/ Tik Tok - https://www.tiktok.com/Hanss444   Rexx Instagram - https://www.instagram.com/rexxb/ Tik Tok - https://www.tiktok.com/@rexx.b1 YouTube - https://www.youtube.com/@UCgf2SoAEsK4EDGWRxfcSJ1w   Time Stamps   00:00:00 - Intro 00:11:00 - Hans hair Transplant update 00:15:00 - bad bunny half time complaints 00:21:00 - World Cup 2026 00:24:00 - history class 00:32:00 - UFO files released 00:35:00 - Little brother has DBS 00:48:00 - Our parents crossing the border 01:00:00 - Hans is not a man anymore 01:06:00 - Todd the fisherman 01:13:00 - Peter the Dolphin 01:25:00 - Octopus Teacher 01:28:03 - YM shoutouts

A high-functioning HCC tumor board can turn complex transplant decisions into coordinated treatment plans that account for liver reserve, tumor biology, and evolving biomarkers. In this episode of the BackTable Podcast 2026 HCC Creator Weekend™, abdominal transplant surgeon Dr. Ari Cohen (Ochsner Health) and transplant hepatologist Dr. Neil Mehta (UCSF) join host Dr. Kavi Krishnasamy to map out strategies for effective multidisciplinary treatment and transplantation planning in HCC. --- Get the BackTable apphttps://www.backtable.com/app --- This podcast is supported by an educational grant from Sirtex and Boston Scientific. --- Timestamps 00:00 - Introduction00:51 - Starting a Tumor Board06:39 - Building Referral Streams09:03 - Academic and Community Practice Integration14:31 - Treatment Selection Criteria20:38 - Modern HCC Biomarkers25:24 - Role of ctDNA and Biopsy29:37 - Bridging Therapy on Transplant Waitlist32:34 - Downstaging Strategy and Risks39:25 - Final Thoughts and Closing Remarks --- More about this episode The physicians discuss what it takes to build a robust tumor board, from fostering hospital buy-in to engaging leaders across specialties and utilizing virtual formats for consistent participation. The conversation explores clinical decision-making, emphasizing the integration of AFP-L3 and DCP biomarkers alongside AFP to better understand tumor biology and predict post-transplant recurrence. Dr. Mehta and Dr. Cohen also share their patient selection criteria, discussing how bilirubin, liver disease etiology, and INR influence decisions. While radiographic guidance remains central to HCC management, they highlight the growing potential of reliable ctDNA analysis and other biomarkers. The specialists conclude by emphasizing that an integrated, communicative tumor board is the most effective way to navigate the nuances of liver reserve and HCC biology to achieve the best possible patient outcomes. --- Resources Sustained AFP-L3 or DCP expression is associated with progression risk and inferior outcomes in unresectable hepatocellular carcinoma.https://doi.org/10.1007/s10238-025-01877-8 --- BackTable Vascular & Interventional (VI) is the go-to podcast for interventional radiologists, vascular surgeons, and interventional cardiologists. Download the free BackTable app to get early access to new episodes, cases, and courses curated by physicians in your specialty. ► https://www.backtable.com/app