Podcasts about transplants

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

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!

“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

Mark Anderson from Anderson's Seed and Garden discusses how to transplant vegetable plants into your garden without shocking them. He also discusses ways to get rid of insects and disease in your lawn and garden.

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 Burkhard talks with Dr. Amar Kelkar of the Dana-Farber Cancer Institute about the medical side of survivorship after bone marrow, stem cell, or CAR-T transplant. The conversation begins with the important shift from the urgent “save my life” phase to the longer “protect my health” phase. Dr. Kelkar explains that this transition often starts around the 100-day mark, though timing varies by transplant center, geographical region and patient needs. A major theme is the need to restart routine care that may have been paused during transplant. Dental care, dermatology, ophthalmology, and primary care all become important again. Dental visits are especially important because oral graft-versus-host disease (GVHD) can cause dry mouth, irritation, cavities, and other problems. Skin checks matter because transplant can increase the risk of skin cancers. Dr. Kelkar stresses annual dermatology visits, sun protection, SPF 50 or higher, protective clothing, and smart decisions about sun exposure. Fatigue is another central topic. Dr. Kelkar describes post-transplant fatigue as different from normal tiredness. It can feel deep, physical, and mental, and it may last for months or even years. He encourages patients to pace themselves, listen to their bodies, and build activity back slowly. Returning to work also needs to be individualized. Some patients work remotely during treatment, while others may need extended disability or a gradual return. The episode also covers immune recovery and repeat vaccinations. Dr. Kelkar explains that after transplant, the immune system has been reset, and many childhood vaccines need to be repeated. Most programs begin revaccination around six, nine, or 12 months, depending on immune suppression and other factors. He reassures listeners that many patients have fewer vaccine symptoms early on because their immune systems are still rebuilding. Dr. Kelkar also reviews long-term screening and prevention. Survivors need routine cancer screenings, including mammograms, colonoscopies, lung cancer screening when appropriate, skin exams, and monitoring for thyroid or other changes. Metabolic health is also important. Steroids can affect blood sugar, transplant can change body composition, and quick weight loss often includes muscle loss. Nutrition support and exercise programs can help, and Peggy notes that Blood Cancer United offers nutrition services for patients and caregivers. Blood Cancer United's nutrition program provides free one-on-one consultations with oncology dietitians by phone or email. Bone health, hormone changes, sexual health, and early aging are also discussed. Dr. Kelkar explains that steroids, menopause, testosterone changes, vitamin D deficiency, and time indoors can affect bones. Many centers use DEXA scans and vitamin D supplementation. He also encourages patients to bring up sexual health concerns, including menopause symptoms, low testosterone, pain with intercourse, ulcers, or fear about resuming intimacy. The episode closes with practical advice for everyday life. Food restrictions often loosen around 100 days, but patients should reintroduce foods slowly and carefully. Raw foods, alcohol, tobacco, and inhaled smoke should generally be avoided, especially during the first year. Dr. Kelkar also emphasizes mental health support, counseling, and honest conversations with the medical team. Survivorship is a bumpy road, but the goal is to help patients regain control and thrive. Blood Cancer United Nutrition Offerings: https://bloodcancerunited.org/blood-cancer-care/adults/food-nutrition Thanks to this season's sponsors, Incyte and Sanofi. (00:00) Intro (01:16) Moving from acute treatment to survivorship (02:17) Dental, dermatology, ophthalmology, and routine care (05:45) Fatigue after transplant versus normal tiredness (08:35) Pacing yourself and avoiding setbacks (10:26) Returning to work after transplant (12:24) Resetting the immune system and repeat vaccinations (16:07) Secondary malignancy prevention and cancer screenings (18:59) Sun protection and skin cancer prevention (20:23) Metabolic health, blood sugar, and weight management (23:58) Bone health, vitamin D, DEXA scans, and early aging (29:32) Sexual health and hormonal changes (32:43) Everyday living after transplant (36:07) Psychological and cognitive hurdles in survivorship (38:16) Pulmonary function tests and liver monitoring (40:42) Closing thoughts 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.

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.

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.

In this episode of Better Edge, Palak Shah, MD, the new chief of the Section of Heart Failure and medical director of the Heart Transplant Program at Northwestern Medicine Bluhm Cardiovascular Institute, shares how his career has been shaped by the transformation of advanced heart failure care, from LVADs to transplantation. Dr. Shah discusses his clinical training and research, his systems-based vision for delivering advanced heart failure and surgical care closer to patients' communities, and his commitment to equitable access, innovation and multidisciplinary collaboration. The conversation offers referring physicians insight into how Bluhm Cardiovascular Institute is shaping the next era of personalized, longitudinal heart failure care across a regional health system.

On the Q1 2026 earnings call for TransMedics, the CEO said something that stopped everyone in their tracks. Major transplant programs, he said, are going to Home Depot and buying YETI coolers to preserve human hearts before transplantation. None of those coolers are FDA-approved. None are validated for that purpose. That is the status quo TransMedics is trying to replace.This is CSI's update on TransMedics following their May 5th earnings report. TransMedics is not a semiconductor company — it sits in CSI's small bets basket, a collection of positions outside the core semiconductor thesis that Kasey follows closely. The company is building what it describes as the premier program for organ transplantation, combining a warm perfusion technology called the Organ Care System with its own aviation logistics network to dramatically improve the odds that a donated organ reaches its recipient in viable condition.The Q1 2026 numbers are solid. Revenue of $174 million, up 21% year over year, with 82% of organ transplants now covered by TransMedics' own logistics service. But the more interesting story is what comes next across four distinct growth catalysts.First, the CHOPS system — a new cold preservation device TransMedics just developed to serve the segment of the heart transplant market where cold storage is sufficient and warm perfusion is not required. Of 4,646 hearts transplanted in 2025, roughly 2,100 were preserved for less than four hours. That entire segment is currently going to Home Depot coolers. CHOPS is also the control arm TransMedics needed to run the ENHANCE Heart clinical trials — a clever solution to the problem of not being able to find a competitor willing to run head-to-head against their warm perfusion system.Second, European expansion — a logistics partnership with PAD Aviation in Germany and new infrastructure in Italy that could eventually double the total addressable market.Third, the kidney opportunity. Over 20,000 deceased kidney transplants happen annually in the United States. Between 8,000 and 9,000 kidneys are discarded every year due to prolonged ischemic times. TransMedics has designed a Gen 3.0 OCS platform for kidney transplantation, targeting 2027 for market entry.Fourth, the Gen 3.0 platform upgrade for liver, heart, and lung — parallel development tracks that modernize the core product across every organ.Kasey closes with something genuinely useful: an honest accounting of what could go right and what could go wrong, and why she continues to hold a small position.This episode was released to Semi Insider members several weeks before this public version. Members get Kasey and Nick's full research, live Q&A sessions, and analysis like this as it happens. Join at chipstockinvestor.com/membershipWhat we cover:— The CHOPS cold preservation system and why it exists— ENHANCE Heart trial — Part A and Part B explained— Will CHOPS cannibalize OCS warm perfusion revenue? The CEO's answer— Heart transplant market data — 2,131 hearts going to cold storage annually— European expansion — PAD Aviation and Italy buildout— The kidney opportunity — 20,000+ transplants, 8,000–9,000 discarded— OCS Gen 3.0 — kidney platform targeting 2027— Q1 2026 financials — $174M revenue, balance sheet, Summit Aviation debt— What could go right and what could go wrong for TMDX— CSI's current position and ongoing convictionDisclosure: Kasey and Nick hold a position in TransMedics. This content is for general information only and is not individual investment advice. All investing involves risk.chipstockinvestor.com

Season 20 of the Marrow Masters Podcast, produced by the National Bone Marrow Transplant LINK, focuses on thriving in survivorship post-transplant. You'll hear from patients, caregivers, doctors and social workers as they share their best tips and practices. Season 20 of the Marrow Masters Podcast is sponsored by Incyte and Sanofi. Look for Season 20 on May 27, 2026. And be sure not to miss an episode! Follow our show for free on Apple, Spotify, YouTube, or wherever you're listening right now. 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.

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

DAVID WEILL, M.D., is the former Director of the Center for Advanced Lung Disease and Lung and Heart-Lung Transplant Program at Stanford University Medical Center. He is currently the Principal of the Weill Consulting Group which focuses assisting hospitals in improving their transplant programs and developing new programs in the US and throughout the world. David's writing has appeared in the Wall Street Journal, USA Today, Newsweek, and The San Francisco Chronicle. In his new novel, "All That Really Matters," David explores the demands, challenges and complications of a fictional transplant surgeon. We discuss his 25 year career as a lung transplant surgeon and the behind-the-scenes world of medical ethics, corporate greed in medicine and the life and death decisions made in "the selection room," where it is decided who gets a transplant and who doesn't. www.davidweill.com

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

What if aging isn't a hundred separate problems but a single one — an energy crisis inside the tiny power plants of every cell? At 91, Dr. John G. Cramer is betting his own body on the answer.In this episode of Health Longevity Secrets, Robert Lufkin MD sits down with Dr. John G. Cramer — Emeritus Professor of Physics at the University of Washington and author of "How to Live Much Longer" — the oldest human on Earth to receive an experimental mitochondrial transplant. They unpack a unifying theory of aging built around damaged mitochondrial DNA, why replication errors (not just free radicals) drive most of the damage, and what it felt like to receive escalating doses of "Mitlets" — liposomes carrying fresh mitochondria harvested from young blood platelets — at a Texas right-to-try clinic.Buy Dr. Cramer's book "How to Live Much Longer": https://www.amazon.com/How-Live-Much-Longer-Cramer/dp/B0DV3ZW5T6 Cramer & Benson white paper (CBC): https://faculty.washington.edu/jcramer/Bio/CBC.pdf Mitrix Bio: https://mitrix.bio/CHAPTERS00:00 Cold open — "the oldest young human on the planet" 01:18 Meet Dr. John Cramer: physicist turned longevity pioneer at 91 03:45 Why a physicist became obsessed with aging 06:20 The unifying theory: aging as mitochondrial DNA damage 09:40 The 16,569 base pairs that run your life 13:05 Replication errors vs. free radicals — correcting Denham Harman 16:30 The damage doubling time: 12 years, then 3-4 19:50 David Sinclair's information theory of aging 23:15 James McCully and the birth of mitochondrial transplantation 27:00 "No negative results, only spectacular successes" 30:25 Mitrix Bio, Tom Benson, and the Mitlet platform 34:10 Inside Cramer's four Texas right-to-try sessions 38:30 Arm injection, belly fat, and the IV mainline that worked 42:15 What it actually feels like to receive young mitochondria 45:40 Haplogroup H2A1G1 and the Norwegian great-grandmother 48:20 The economics: scaling Mitlets to the world 51:05 Becoming the oldest young human — target age 129 54:30 What Cramer wants you to do tomorrow morning 57:00 Final reflections and where to find the bookKEY STUDIES & SOURCESCramer J.G. & Benson T. — Cellular Bioenergetic Crisis white paper: https://faculty.washington.edu/jcramer/Bio/CBC.pdfHarman D. (1972) — The biologic clock: the mitochondria?: ⭐ Enjoying the show? Please leave a 5-star review on Apple Podcasts — it takes 30 seconds and helps more people discover the science of health and longevity. Thank you!New episodes every Tuesday & Thursday. Subscribe so you don't miss one.Continue this conversation on Substack: https://robertlufkinmd.substack.comLies I Taught In Medical School — Free sample chapter: https://www.robertlufkinmd.com/lies/Web: https://www.robertlufkinmd.comYouTube: https://www.youtube.com/robertlufkinmdX: https://x.com/robertlufkinmdInstagram: https://www.instagram.com/robertlufkinmd/TikTok: https://www.tiktok.com/@robertlufkinLinkedIn: https://www.linkedin.com/in/robertlufkinmd/

This content has been developed for healthcare professionals only. Patients who seek health information should consult with their physician or relevant patient advocacy groups.For the full presentation, downloadable Practice Aids, slides, and complete CME/AAPA information, and to apply for credit, please visit us at PeerView.com/ZWS865. CME/AAPA credit will be available until April 23, 2027.An Immune Reset for AlloHCT Recipients: Updates on Engineered Cell Therapy for Improving Transplant Outcomes and Reducing GVHD In support of improving patient care, PVI, PeerView Institute for Medical Education, is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.SupportThis activity is supported by an educational grant from Orca Bio.Disclosure information is available at the beginning of the video presentation.

Normothermic machine perfusion (NMP) allows transplant teams to assess the function of donor kidneys that may have otherwise been declined. Jacqueline Garonzik Wang, M.D., Ph.D., explains how this pump-based assessment “wakes up” the donor kidney and provides real-time data to guide transplant decisions. With unused kidneys numbering in the thousands each year, it may help shorten wait times and allow earlier transplantation for some patients.

X: @JanJekielek @americasrt1776 @ileaderssummit @NatashaSrdoc @JoelAnandUSA @supertalk @JTitMVirginia Join America's Roundtable radio co-hosts Natasha Srdoc and Joel Anand Samy with Jan Jekielek, author of "Killed to Order: China's Organ Harvesting Industry and the True Nature of America's Biggest Adversary." Jan is Epoch Times senior editor, and host of American Thought Leaders. Jan's career has spanned academia, international human rights work, and now for almost two decades, media. He has interviewed nearly a thousand thought leaders on camera, and specializes in long-form discussions challenging the grand narratives of our time. He's also an award-winning documentary filmmaker, producing The Unseen Crisis, DeSantis: Florida vs. Lockdowns, and Finding Manny. About the Book: "Killed to Order: China's Organ Harvesting Industry and the True Nature of America's Biggest Adversary" A crime the Chinese regime can no longer deny—Forced Organ Harvesting. What if everything you need to understand about the Chinese Communist Party—and how the free world should respond to it—could be explained through this one issue? In this urgent and eye-opening book, journalist Jan Jekielek distills decades of investigations from reputable sources, combined with his own research and in-depth firsthand insight, into a compelling case for rethinking our approach to the CCP. Through the lens of grave human rights abuses—most disturbingly, the state-sanctioned harvesting of organs from prisoners of conscience—Jekielek exposes the inner workings of a regime built on deception, coercion, and control. Killed to Order: The Organ Harvesting Industry of China and the True Nature of America's Biggest Adversary reveals why continuing to misunderstand the CCP poses a growing threat to global freedom. americasrt.com https://ileaderssummit.org/ | https://jerusalemleaderssummit.com/ America's Roundtable on Apple Podcasts: https://podcasts.apple.com/us/podcast/americas-roundtable/id1518878472 X: @JanJekielek @ileaderssummit @americasrt1776 @NatashaSrdoc @JoelAnandUSA @supertalk @JTitMVirginia America's Roundtable is co-hosted by Natasha Srdoc and Joel Anand Samy, co-founders of International Leaders Summit and the Jerusalem Leaders Summit. America's Roundtable radio program focuses on America's economy, healthcare reform, rule of law, security and trade, and its strategic partnership with rule of law nations around the world. The radio program features high-ranking US administration officials, cabinet members, members of Congress, state government officials, distinguished diplomats, business and media leaders and influential thinkers from around the world. Tune into America's Roundtable Radio program from Washington, DC via live streaming on Saturday mornings via 68 radio stations at 7:30 A.M. (ET) on Lanser Broadcasting Corporation covering the Michigan and the Midwest market, and at 7:30 A.M. (CT) on SuperTalk Mississippi — SuperTalk.FM reaching listeners in every county within the State of Mississippi, and neighboring states in the South including Alabama, Arkansas, Louisiana and Tennessee. Tune into WTON in Central Virginia on Sunday mornings at 9:30 A.M. (ET). Listen to America's Roundtable on digital platforms including Apple Podcasts, Spotify, Amazon, Google and other key online platforms. Listen live, Saturdays at 7:30 A.M. (CT) on SuperTalk | https://www.supertalk.fm

Immigrant life in New York City looks glamorous from the outside, but what happens when you arrive in January with snow up to your knees, no work permit, and no roadmap for who you're supposed to become? In this episode, host Saadia sits down with Laura Peruchi, a Brazilian journalist, content creator, podcaster, and one of New York City's most trusted voices for immigrants navigating life in a new country. Laura is the host of Transplants, a podcast about women thriving in new roots abroad, and the writer behind The Tiny Apple, a newsletter about New York life told with radical honesty. Laura and Saadia get into the raw, unfiltered parts of immigrant life that don't make it onto Instagram: What it really feels like to go from financially independent to completely dependent on a dependent visa, and why Laura didn't talk about it until she got her green card The identity shift of switching your content from Portuguese to English, and how language changes your personality Why Laura started a podcast specifically for immigrant women, and why she says "men already have enough spotlight.” The in-between world of being a transplant: too Brazilian for America, too Americanized for Brazil Code-switching, insecurity, online hate, and the quiet courage of building something from scratch in a city that doesn't owe you anything Why is she learning French as a third language, just because she wanted to Community-building in East Harlem, and why a WhatsApp group about stolen packages became her unexpected found family Laura also opens up about something rarely discussed: the emotional weight immigrant spouses carry when they feel they "should be grateful" and how that guilt silently erodes self-worth and belonging. Whether you're a first-generation immigrant, a partner who followed someone to a new country, or simply someone who has ever felt like an outsider in a place you chose to call home, this conversation will feel like a long exhale.

Full Show Notes: bengreenfieldlife.com/fmt In this episode, you'll get to uncover one of the most intriguing developments in gut health—fecal microbiota transplants (FMTs). Joining me is Jason Klop, CEO of Novel Biome, who brings cutting-edge insight into how FMT is transforming from an obscure, hospital-based procedure into an accessible, precise, and surprisingly simple tool for optimizing your microbiome at home. We’ll break down how FMT is now being used for everything from irritable bowel issues to food sensitivities, and why the technology has advanced well beyond its origins. You'll also hear about the meticulous screening behind “super donors,” the science of oral FMT capsules, and the real-world results you can expect—including my own personal experience. Whether you’re looking to boost your gut health, support your immune system, or simply curious about the connection between your microbiome and overall vitality, this episode has what you need to stay on the cutting edge of holistic wellness. Jason Klop brings a clinical background in naturopathic medicine to his role as founder and CEO of Novel Biome, Canada's first licensed manufacturer of Fecal Microbiota Transplant (FMT) products. Having personally treated hundreds of patients with FMT in clinical practice, Jason saw a gap in the availability of safe, standardized microbiome restoration therapies and set out to build the infrastructure himself. Today, Novel Biome supplies FMT products to clinics, hospitals, and clinical trials around the world. Episode Sponsors: Take Ultra: Take Ultra is a clean, nicotine-free and caffeine-free pouch designed to deliver smooth, sustained energy and focus using clinically backed nootropics and adaptogens without the jitters, crashes, or sleep disruption. With flavors like their new Blue Razz, it’s a simple, effective way to stay sharp throughout the day. Visit takeultra.com and use code BENGREENFIELD for 15% off. Qualia Stem Cell: Qualia Stem Cell is a science-backed supplement designed to support your body’s natural repair system by enhancing stem cell function - helping you recover, renew, and maintain healthy tissues as you age. Taken just four days per month and formulated with premium, clinically supported ingredients, it’s an easy way to support long-term healing and vitality. Visit qualialife.com/boundless and use code BOUNDLESS for 15% off. Young Goose: Young Goose: To experience the transformative power of Young Goose's cutting-edge products, visit younggoose.com and use code BEN10 at checkout to enjoy a 10% discount on your first order. BlockBlueLight: BlockBlueLight: BlockBlueLight BioLights are the only lights extensively tested and recommended by building biologist Brian Hoyer as truly flicker-free, ultra-low EMF, and circadian-friendly, with three modes (day, evening, night) that support natural rhythms and optimize sleep quality. Get 10% off your first order at blockbluelight.com/Ben (discount autoapplied at checkout). See omnystudio.com/listener for privacy information.