Podcasts about cancer survivors

Skate, Paint, Heal: Rewiring Trauma into Flow with Brett Ashby Contemporary Performance Artist with 20+ Years of International Practice Creating Portrait Paintings While Rolling and Exploring Human Connection Brett Ashby is a multidisciplinary artist working in painting, photography, video, sculpture, and installation, grounded in formal training and over two decades of international practice. He innovatively merges movement-driven painting with live performance, notably painting while skateboarding, to dissolve fear, balance, and synchronicity into layered, expressive works. His distinctive, gestural style unites physicality with compositional discipline, making each artwork a dynamic record of being present. Ashby's art radiates energy, vulnerability, and deep human connection, inviting the viewer to feel the resonance of body, space, and collective experience.Linkshttps://www.brettashby.com/https://www.instagram.com/brettashbyartist@brettashbyartist Tagspodcast for creatives,creative podcast,podcast creator interviews,professional podcast,creative podcasts,podcast host interviews,creative podcast ideas,Artist,Cancer Survivor,Entrepreneur,Entrepreneurial Mindset,Mental Health,Music Producer,Painter,Performing Arts,Trauma Recovery,Visual ArtsSupport PEG by checking out our Sponsors:Download and use Newsly for free now from www.newsly.me or from the link in the description, and use promo code “GHOST” and receive a 1-month free premium subscription.The best tool for getting podcast guests:https://podmatch.com/signup/phantomelectricghostSubscribe to our Instagram for exclusive content:https://www.instagram.com/expansive_sound_experiments/Subscribe to our YouTube https://youtube.com/@phantomelectricghost?si=rEyT56WQvDsAoRprRSShttps://anchor.fm/s/3b31908/podcast/rssSubstackhttps://substack.com/@phantomelectricghost?utm_source=edit-profile-page

In 2020, Emily Mendenhall drove from Washington, DC to Okoboji, Iowa, a town of 800 that swells to 200,000 every summer, and walked into a pandemic that looked nothing like the one dominating national headlines. Inside gas stations and bars, masks marked you as an outsider. In one stop, a man told her family they would not be served if they kept theirs on. Her 6 year old daughter cried, confused. Mendenhall, a medical anthropologist at Georgetown University, did what she always does. She started asking questions. Over months, she interviewed neighbors, former classmates, and local officials, including her own brother in law who helped lead the local COVID response. The result became Unmasked, a case study in how community identity, economics, and politics shaped public health decisions in real time. That work led directly into her latest book, Invisible Illness: A History, from Hysteria to Long COVID, where she tracks a much older problem. Patients with chronic illness, especially women, often fail to meet medicine's demand for proof. Without a clear diagnosis, they lose access to care, insurance coverage, and legitimacy. Mendenhall argues that long COVID did not create this failure. It exposed it.This conversation centers on how healthcare systems reward certainty and punish complexity. Long COVID clinics send patients to 17 specialists without resolution. Insurance structures require diagnoses that many conditions cannot provide. Medical training still struggles to integrate trauma, mental health, and chronic disease into a coherent model of care.Mendenhall brings lived experience into the conversation. After COVID, she dealt with months of fatigue and escalating anxiety that altered her baseline health. She does not claim the label of long COVID, but she understands how quickly the system becomes harder to navigate once symptoms stop fitting clean categories. The stakes are not theoretical. In the United States, access to healthcare, disability benefits, and treatment still depends on whether a condition can be measured, coded, and reimbursed. For millions living with invisible illness, the burden of proof becomes the illness itself.RELATED LINKSEmily MendenhallInvisible Illness: A History, from Hysteria to Long COVIDScience PoliticsGeorgetown UniversityFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

A Christchurch cancer survivor who won a privacy case is furious that a company director has told her that two of his companies can't pay tribunal-ordered damages. The Human Rights Review Tribunal found Richard Brady's companies breached Cheryl Horrell's privacy, and ordered them to pay her more than $10,000. Mr Brady says the companies are broke, although another of his businesses has received more than $11 million in taxpayer funding. Keiller MacDuff reports.

Observed every June, National Cancer Survivors Month honors cancer survivors around the world, raises awareness about the challenges they face, and celebrates life after a cancer diagnosis.

Join us as Tim McDonald shares his inspiring journey through cancer, mental health challenges, and community advocacy. Discover practical tips for managing stress, the power of community, and how writing and podcasting can be therapeutic."We can't control what happens, only how we react."Chapters00:00 Facing the Diagnosis: A Journey Begins01:50 The Power of Community and Advocacy05:33 Mental Health and Survivor Guilt09:28 Finding Purpose Through Writing11:41 Practical Mental Health Strategies15:40 Advice for Navigating Tough Times"Pretending it's not there is not healthy."Other Takeaways*Mental health challenges during cancer treatment*The role of community and support groups in recovery*Writing and podcasting as therapeutic tools*Stress management techniques: walks, reflection, and perspective*The importance of control over reactions, not events*Building advocacy for chronic illness and mental healthSupport the showEnjoy the show and thank you for being here. Please subscribe to stay current and share with a friend who could use this episode.All questions for the host or guest: Email Danica at PodcastsByLanci@gmail.com.This show is brought to you by Living Proof TBI Coaching specializing in recovery for Traumatic Brain Injury Survivors, Families, and CaregiversCRISIS LINE: DIAL 988

She had a six-pack, a thriving ER career, and did everything right on the surface. Then she was diagnosed with cancer. The cause was not genetics. It was the lifestyle pattern most founders follow every day.Dr. Jennifer Ron is an ER physician turned Integrative Cancer Care specialist and cancer survivor. She breaks down which founder habits accelerate aging and the protocols that reset your health fast.00:00:00 Introduction00:02:05Q: What are the habits that founders have right now that are accelerating their aging?A: Dr. Jennifer Ron shares her story of being a fit ER doctor diagnosed with cancer. The four pillars: nutrition, exercise, stress management, and sleep.00:05:48Q: Did your lifestyle cause the cancer?A: Dr. Jennifer Ron says it was 100% stress and sleep deprivation, averaging four to six hours per night during shift work.00:08:18Q: How much of cancer is actually genetic versus lifestyle?A: Dr. Jennifer Ron explains genetics cause only 5-10% of cancers. The other 90% are epigenetic lifestyle factors founders can control.00:13:28Q: What do you say to the busy founder who thinks they don't have time for health?A: Dr. Jennifer Ron says founders are models for their team and recommends morning routines, meal prep, and hard time boundaries.00:22:18Q: Which is worse for you — sugar, alcohol, or processed foods?A: Dr. Jennifer Ron says ultra-processed foods are the absolute worst and should be cut first, even before sugar and alcohol.00:29:30Q: How does intermittent fasting work and what does it do?A: Dr. Jennifer Ron explains the 16:8 window, metabolic flexibility, and how fasting promotes gut health and immune function.00:37:10Q: Are oncologists teaching patients about nutrition and lifestyle?A: Dr. Jennifer Ron says most oncologists lack bandwidth. Integrative care fills the gap alongside conventional treatment.Subscribe to Founder Talk so you never miss an episode.

Most of the menopause conversation happening right now, on social media, in podcasts, in the press, is aimed at women going through a natural hormonal transition. But there is a population of women whose menopause arrived differently. Suddenly and surgically. In the middle of one of the most frightening experiences of their lives, a cancer diagnosis or a high-risk prevention decision. This episode is for those women. And for every woman who loves one of them. My mother was 50 years old, on hormone therapy, when her breast cancer was diagnosed. Nobody talked about menopause then, what her future would look like, how the diagnosis would affect her long-term health, or what her options were. It wasn't until I was in my mid-forties, two decades later, that my own doctor finally brought up perimenopause. My guest, Elana Silber, CEO of Sharsheret, a national nonprofit supporting women, men, and families facing breast and ovarian cancer. Elana has spent her career at the intersection of cancer, women's health, and community, and she brings both professional expertise and deep personal commitment to one of the most underreported conversations in the menopause space: what happens when cancer forces the conversation. In this episode, we cover: The difference between natural menopause and surgically or chemically induced menopause after cancer treatment What breast and ovarian cancer diagnosis means for a woman's hormonal health, immediately and long-term Navigating survivorship and menopause simultaneously, the symptoms, the decisions, and the silence around both Hereditary cancer risk and what women need to know before menopause arrives How Sharsheret supports women and families through diagnosis, treatment, and survivorship If this episode resonates with you, share it with the women in your life navigating cancer, survivorship, or a hereditary risk decision. This is a conversation that needs to reach further than it currently does. Medical Disclaimer: This podcast is for informational purposes only and does not constitute medical advice. Do not use this content to diagnose or treat any medical condition. Consult your physician for any medical concerns. This disclaimer applies to all guests featured on this podcast. Learn more about Sharsheret: Website: www.sharsheret.org IG: @sharsheretofficial Stay connected with JFW: Book your 60-minute Menopause Care Consultation: https://www.jillfooswellness.com/menopause-care-consult-page Follow on Instagram: @jillfooswellness Follow on Facebook: @jillfooswellness Follow on YouTube: @jillfooswellness Grab discounts on my favorite menopause wellness products: https://www.jillfooswellness.com/health-products Enjoy 20% savings and free shipping at Fullscript for your favorite supplements by leading brands: https://us.fullscript.com/welcome/jillfooswellness/store-start Subscribe to the JFW newsletter at www.jillfooswellness.com and receive your FREE Guide on How To Create Your Menopause Health Equation Ebook. Schedule your free 15-minute consultation here: https://calendly.com/jillfooswellness/15-minute-zoom-consultations If you're a Chicago-area midlife woman, check out the Chicago Menopause Collective, a nonprofit dedicated to navigating menopause locally with experts: https://chicagomenopausecollective.org

In a no holds barred interview, Martin Sweeney took us through diagnosis, treatment and beyond with prostate cancer. Hosted on Acast. See acast.com/privacy for more information.

This Men's Health Month, Navigating Cancer TOGETHER sits down with Clarence Jones, prostate cancer survivor and one of Minnesota's most trusted names in community health.Clarence Jones, MA, CHW, CPH, CPE, is the Executive Director and Community Health Strategist of the Hue-MAN Partnership, a founding member of the organization he helped build into one of Minnesota's most trusted voices in public health. He serves as an Adjunct Instructor of Medicine at Mayo Clinic, is a founding member of the Minnesota Fathers and Families Network, has served as the Mayor's Representative and co-chair of the Public Health Advisory Committee for the City of Minneapolis, and holds affiliations with the CTSI Executive Leadership team and the University of Minnesota's CEARCH initiative. He is also a fatherhood doula, the host of the Community Health Dialogue radio show on KMOJ 89.9 FM, and co-host of the Health Chatter podcast.In this warm, honest, and personal conversation, Clarence opens up about his own journey through prostate cancer, from watching his PSA numbers climb year after year and practicing watchful waiting, to eventually choosing surgery. He shares why the digital exam scares men, and why early detection is the greatest gift you can give your family.But Clarence's story doesn't stop at survival. He shares how his experience deepened his mission to make sure the men and families in his community have access to credible, culturally relevant, evidence-based health information. That's the heartbeat of everything Hue-MAN does.You'll also hear him talk about what he wants every man facing a cancer diagnosis to know right now.✨ Episode Highlights:00:04:38 The Moment He Knew: Clarence's Prostate Cancer Journey00:09:22 How to Invite Men into Health Conversations Without Lecturing Them00:14:44 What Young Men Need to Know About PSA Screening and Biopsies00:27:45 Fatherhood Doula: What That Means and Why Fathers Matter00:36:55 What 'Navigating Cancer TOGETHER' Really MeansTranscript: https://bit.ly/podscript184Connect & Engage with ClarenceWebsite: www.huemanpartnershipalliance.orgHealth Chatter Podcast: www.healthchatterpodcast.comKMOJ Community Health Dialogue: 89.9 KMOJ FM

When Claire Rumore was lifted into a hospital gurney to undergo her first biopsy, she stepped aside to use the restroom first. And while she was there, she heard a quiet internal voice ask her a question: Do you want to go back to the life you had before? Is that what you want? Without hesitation, her answer was no. What followed was one of the most unusual cancer journeys in modern medicine. Claire was 43 years old. She had stage four pancreatic cancer — a diagnosis that typically affects older men, and that her medical team never actually disclosed to her during treatment. She went through two major abdominal surgeries, dropped to 74 pounds, lost her menstrual cycle, lost her libido, and lost the person she had been. And then, slowly, over the course of eighteen months, she found her way back. Not to who she was- but to someone clearer, more embodied, and more deeply connected to her own desire than she had ever been before. In this episode, Dr. Jenni Skyler and Daniel Lebowitz sit down with Claire for a conversation about the emotional, relational, and erotic dimensions of cancer recovery that medicine almost never addresses. Claire is the founder of Cancer and Intimacy, an education platform built on a three-part framework she developed from her own experience and her work with patients, survivors, and their partners. The first lily pad is erotic grief, the deeply under addressed process of mourning what's been lost: The body you knew, the sexuality you had, the intimacy you can no longer access in the same way. Claire has written a free ebook on erotic grief and makes a compelling case that this experience is not exclusive to cancer. It's universal to anyone navigating major change. The second is libido listening. The slow, quiet, inward practice of reacquainting yourself with your own body's signals after illness or loss. Claire describes learning to feel pleasure in the sheets against her skin, in the air in the room, in the gentlest forms of touch, what she calls subtle sexuality. A term she coined to describe the low, soft, sensory orientation to desire that becomes the entry point back to conventional sexuality. Claire Rumore WebsiteSee omnystudio.com/listener for privacy information.

At 25, Jace Yawnick was building a career in health and wellness sales, chasing growth, status, and the usual young adult fantasy of getting somewhere fast. Then his body stopped cooperating. Fatigue turned into chemotherapy. The diagnosis was primary mediastinal B cell non Hodgkin lymphoma, and the rest of his life split into before and after. Now in remission, he talks about cancer the way people actually live it, not the way nonprofits package it. He gets into survivorship, mental health, young adult isolation, and the deadening absurdity of prior authorization. One of the sharpest parts of the conversation lands on a simple American insult disguised as policy: treatment innovation means very little when insurance can still deny the scan, the drug, or the next step. Jace has seen that firsthand, including during routine monitoring after active treatment. This episode tracks what happens when a young cancer patient becomes a public voice and refuses to play mascot. It covers oncology, insurance, remission, advocacy, and the long mental hangover that follows survival. It also names the part too many institutions dodge: the system works great right up until it doesn't, and when it fails, patients get handed the bill, the panic, and a camera if they want anyone to care. RELATED LINKSJace Beats CancerJace Yawnick on LinkedImConquer Cancer ArticleCURE Today ArticlePyure BrandsFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Dr. Karen Mustian is an energetic, passionate scientist, world traveler, yogi, scuba diver, and foodie whose life's work is dedicated to improving the quality of life of individuals affected by cancer. Through her research, leadership, and advocacy, she strives to help cancer patients and survivors not only live longer, but live better.Dr. Mustian is a Dean's Distinguished Professor in the Department of Surgery at the University of Rochester Medical Center and an internationally recognized leader in Cancer Survivorship, Integrative Oncology, Exercise Oncology, Geriatric Oncology, Behavioral Oncology, and Gender, Sexuality, and Women's Health.She serves as Associate Director for Population Science at the Wilmot Cancer Institute, Director of the University of Rochester Cancer Center NCI Community Oncology Research Program Clinical Trial Network and Founding Director of the PEAK Human Performance Research Laboratory at the University of Rochester Medical Center. She is also a Faculty Associate with the Susan B. Anthony Institute for Gender, Sexuality, and Women's Studies.At the national level, Dr. Mustian serves on the National Cancer Institute Cancer Advisory Board Working Group for Extramural Research Concepts and Programs and the National Cancer Institute Symptom Management and Quality of Life Steering Committee, where she helps shape the future of cancer research and supportive care. Dr. Mustian has secured more than $145 million in peer-reviewed research funding and ranks among the most highly NIH-funded researchers in the United States. She has authored more than 250 scientific publications and is widely recognized for her pioneering contributions to oncology research, supportive care, and clinical trial innovation.Her accomplishments have been honored with more than 45 national and international awards, including recognition as a Fulbright Scholar, recipient of the ASCO Walther Supportive Oncology Lifetime Achievement Award, and recipient of the Prime Minister's Yoga Award for her transformative impact on yoga research worldwide. Dr. Mustian is best known for advancing evidence-based, integrative approaches to cancer care. Through groundbreaking research on yoga, tai chi, mindfulness, and exercise, she has helped establish non-pharmacologic interventions as effective strategies for reducing treatment- related toxicities, improving symptom management, and enhancing the health and well-being ofcancer patients and survivors around the globe.Support the show

At 20 years old, newly arrived from Puerto Rico and trying to build a future in science, Benjamin Suarez Jimenez found himself sitting in front of two senior faculty members accused of plagiarism. He knew the material. He had done the work. His mistake came from failing to cite class notes during an exam because nobody had told him that was expected. In a matter of minutes, he watched what felt like his entire career flash before him.On this episode of Standard Deviation, host Oliver Bogler examines the hidden architecture of academic science through the experiences of Dr. Benjamin Suarez Jimenez, Assistant Professor at the University of Rochester and a neuroscientist studying PTSD, anxiety, trauma, and spatial cognition through virtual reality and video game environments.Benjamin traces his path from Puerto Rico to the mainland United States, through the NIH, Columbia University, and eventually to leading his own laboratory. Along the way, he encountered a series of barriers that had little to do with scientific ability and everything to do with access to unwritten rules. From academic gatekeeping to grant writing expectations, he learned that success in biomedical research often depends on knowledge that never appears in a textbook.Oliver explores how those invisible obstacles shape careers, influence research funding, and determine who gains access to opportunity. The conversation also examines the Justice, Equity, Diversity, and Inclusion Program at the Life Science Editors Foundation, which pairs scientists from underrepresented backgrounds with experienced scientific editors. Through that mentorship, Benjamin transformed a critical grant proposal into a successful pilot award that helped launch an NIH R01 application.The discussion extends beyond one scientist's experience. Benjamin describes helping a former mentee navigate dissertation roadblocks that threatened her graduation, illustrating how institutional bureaucracy can delay careers and discourage talented researchers. Together, they explore the hidden administrative burden, cultural barriers, and bias that many scientists carry alongside their research, and what happens when someone who receives support turns around and opens the door for others.RELATED LINKSLife Science Editors FoundationBenjamin Suarez Jimenez LabDr. Benjamin Suarez JimenezBenjamin Suarez JimenezFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

This Men's Health Month, Navigating Cancer TOGETHER sits down with Samuel "Sam" Simmons, a trauma-informed healing advocate with over 36 years of experience supporting men and their communities. Sam is the author of Just Sam: A Black Man's Journey to Healing, the visionary behind the 18th Annual Community Empowerment Through Black Men Healing Conference, co-host of Voices Radio Show on 89.9 KMOJ, and the 2024 NAMI Minnesota Professional of the Year. In this powerful conversation, Sam opens up about his own journey through trauma, addiction, and healing, and shares why telling the full truth is the first step toward freedom.✨ Episode Highlights:00:01:08 Meet Sam Simmons: 36 Years of Healing Work00:08:07 Growing Up Angry: Sam's Personal Trauma Story00:36:54 Male Trauma, Silence, and Why Men Don't Ask for Help00:52:25 The 18th Annual Black Men Healing Conference00:56:47 A Message for the Black Man Who Just Got a Cancer DiagnosisTranscript: https://bit.ly/podscript183Connect & Engage with Sam SimmonsWebsite: samuelsimmonsconsulting.comLinkedIn: https://www.linkedin.com/in/simmonsconsulting/18th Annual Community Empowerment Through Black Men Healing Conference: June 25 & 26 at St. Paul College — Register at brothershealing.comBook: https://a.co/d/03IvmBdM

Dr. Sarah Matt trained as a burn surgeon, working in a field where patients arrive with catastrophic injuries and survival depends on speed, skill, and resources. She left the bedside after confronting a limit that medicine does not like to admit. One physician can only see so many people in a day. The system surrounding those patients decides the rest. She moved into health technology, held leadership roles in startups, and built global infrastructure at Oracle to scale care across populations. Then she watched billions of dollars in digital health and AI initiatives stall out when they hit real clinical environments.This episode follows that pivot from surgeon to strategist and back into direct patient care in rural New York, where she now treats uninsured patients, migrant workers, and communities pushed to the margins. The conversation centers on a persistent failure across healthcare systems. Products get built for regulators, executives, and investors instead of the people who use them. The result shows up in failed adoption, broken workflows, prior authorization delays, and rising physician burnout.The discussion cuts through health policy language and lands on lived consequence. The system rewards speed over usability, scale over trust, and compliance over care. Patients absorb the fallout. Physicians carry the liability. The incentives remain intact.RELATED LINKSDr. Sarah MattThe Borderless Healthcare RevolutionThe Clinical RealistJessica FedererSovatoFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

What happens when the very product you've been recommending to clients your entire career ends up being the thing that saves your family? For Kat Naguiat-Madarang, that question is personal.In this episode, Kat takes us on a journey that spans three generations. From her grandfather, who founded one of the first insurance agencies in the Philippines in the 1950s, to her mother, who rebuilt her career from scratch after immigrating to Canada, to Kat herself, who was diagnosed with breast cancer in late 2024 and had to navigate surgery, recovery, and the emotional weight of facing a serious illness while running a business with her husband.Kat shares what it felt like to receive her diagnosis, the decisions she faced, and how her critical illness policy, set up by her mother years earlier, gave her something money can't manufacture on its own: choice. The choice to step back from work, to focus on recovery, and to take her kids to Japan.She also opens up about paying five critical illness claims that same year — four of them before her own diagnosis — and how living through cancer changed the way she shows up for clients going through the same thing.This one is equal parts raw and real. Kat's story is a reminder of why we do what we do.

Vancouver resident Myronie McKee was filming a commercial playing a breast cancer patient when she received her own diagnosis the very next day. At PeaceHealth Southwest Medical Center's National Cancer Survivors Day, she shared how surgery, radiation, and community transformed her outlook on survival. https://www.clarkcountytoday.com/people/peacehealth-celebrates-national-cancer-survivors-day/ #CancerSurvivors #NationalCancerSurvivorsDay #PeaceHealth #Vancouver #ClarkCounty #CancerCare #Survivorship #WashingtonState

Relay for Life Clare returns to Tim Smythe Park in Ennis on Saturday, 13th June 2026, for a day filled with music, entertainment, inspiring stories, and community spirit. The event celebrates cancer survivors, remembers loved ones lost to cancer, and raises vital funds to support those affected by the disease. To find out more, Alan Morrissey was joined by Natasha Bourke, Cancer Survivor and Committee member, and Olive Walsh, Teams Chair on the committee. Photo (c) Clare FM

Pippa Hudson speaks to Lindy James ahead of National Cancer Survivors’ Day. She’s a mother of two who has recently come through treatment for colon cancer. Lunch with Pippa Hudson is CapeTalk’s mid-afternoon show. This 2-hour respite from hard news encourages the audience to take the time to explore, taste, read, and reflect. The show - presented by former journalist, baker and water sports enthusiast Pippa Hudson - is unashamedly lifestyle driven. Popular features include a daily profile interview #OnTheCouch at 1:10 pm. Consumer issues are in the spotlight every Wednesday while the team also unpacks all things related to health, wealth & the environment. Thank you for listening to a podcast from Lunch with Pippa Hudson Listen live on Primedia+ weekdays between 13:00 and 15:00 (SA Time) to Lunch with Pippa Hudson broadcast on CapeTalk https://buff.ly/NnFM3Nk For more from the show, go to https://buff.ly/MdSlWEs or find all the catch-up podcasts here https://buff.ly/fDJWe69 Subscribe to the CapeTalk Daily and Weekly Newsletters https://buff.ly/sbvVZD5 Follow us on social media: CapeTalk on Facebook: https://www.facebook.com/CapeTalk CapeTalk on TikTok: https://www.tiktok.com/@capetalk CapeTalk on Instagram: https://www.instagram.com/ CapeTalk on X: https://x.com/CapeTalk CapeTalk on YouTube: https://www.youtube.com/@CapeTalk567 See omnystudio.com/listener for privacy information.

Leave a message and let us know what you liked about the episode!Survivor's guilt is a common and not often talked about emotional experience after cancer. Dr. Leah Sherman sits down with returning guest Natasha Ewa, licensed clinical social worker and founder of I Thrive Therapy and Wellness, for an honest conversation about what survivor's guilt actually looks like, why body image after cancer is so personal, and what healing can feel like on the other side.The conversation widens to cover grief over pre-cancer identity, hypervigilance, reconstruction decisions, and Natasha's documentation of her own DIEP flap experience and complications.Whether you're navigating survivorship yourself or supporting someone who is, this one meets you where you are.Visit the I Thrive Therapy and Wellness websiteFollow Natasha on InstagramSupport the showBecome a member of The Cancer Pod Community! Gain access to live Q&As, exclusive content, and so much more! Join us today on Buy Me a Coffee or on Patreon!Check out our website! Looking for more information? We have blogs, merch, and all of our episodes listed by season and category. Shop our favorite reads! We've joined with Bookshop.org to offer some of our fave books!Buy our merch! Whether it's a cozy hoody or a handy water bottle, we have something for everybody.Have a comment or suggestion? Email us at info (at) thecancerpod (dot) com Follow us wherever you browse. We're always @TheCancerPod:InstagramBlueskyFacebookLinkedInYouTubeTHANK YOU!!

In this special National Cancer Survivor Month episode of Navigating Cancer TOGETHER, host and 15-year cancer thriver Talaya Dendy brings together seven survivors at different stages of their journey to explore what survivorship truly means. From newly diagnosed to 20 years out, Vanessa, Shoni, Savio, Jerry, Ebonie, Christopher, and Heather share their challenges, unexpected blessings, and the raw, unfiltered truth about life after a cancer diagnosis. Together, they redefine what it means to truly live. Whether you are a survivor, a caregiver, or someone who loves a person carrying this story, this episode is for you.✨ Episode Highlights:00:00:37 What Does It Mean to Be a Cancer Survivor?00:02:26 The Growing Number of Survivors and Why It Matters00:04:09 The Physical, Emotional, and Financial Challenges of Survivorship00:09:00 Vanessa Berrueta | Breast Cancer Survivor | Adapting Like a Butterfly00:13:55 Shoni Brown | 10-Year Breast Cancer Survivor | Going Through It, Not Around It00:31:22 Savio Clemente | Non-Hodgkin's Lymphoma Survivor | Permission to Heal00:37:58 Jerry McCormick | Prostate Cancer Survivor | It's a Bump, Not a Pothole00:51:47 Ebonie Michelle | Bilateral Breast Cancer Survivor | Thrivership Over Survivorship01:03:04 Christopher Shaddock | Stage 4 Prostate Cancer Survivor | Big Boy Pants On01:14:01 Heather Von St. James | 20-Year Mesothelioma Survivor | Speaking for Those Who No Longer Can01:18:34 Closing | What If You Were Always Becoming This?Transcript: https://bit.ly/podscript182

Evelyn trifft Rose – dreifache Mama, Cancer Survivor, heute Elternberaterin mit klarem Fokus: Gewaltfreie Kommunikation im echten Leben. Rose hat eine Brustkrebserkrankung hinter sich, die alles auf den Kopf gestellt hat. In dieser Folge geht's aber vor allem darum, was sie daraus für sich mitgenommen hat – und wie sehr sich ihr Blick auf Kommunikation, Bedürfnisse, Beziehungen und Selbstfürsorge verändert hat. Rose sagt: Kinder machen nichts gegen uns, sondern für sich. Hinter jedem Verhalten steckt ein Bedürfnis. Wie schaffen wir es, alte Reiz-Reaktionsmuster loszulassen und so zu reagieren, wie wir es uns eigentlich für unsere Kids wünschen? Und was hat das Ganze mit unserer eigenen Kindheit zu tun? Es geht um Haltung statt perfekter Sätze, ums Nervensystem und um Mom Guilt. Plus: Warum das dritte Eis kein Bedürfnis ist, sondern ein Wunsch… Eine sehr persönliche und intensive Folge, die Mut in vielerlei Hinsicht macht! Viel Freude! Mehr zu Rose? Hier entlang: https://www.instagram.com/beziehungsvoll_elterncoach/ Du möchtest mehr über unsere Werbepartner erfahren? Hier findest du alle Infos & Rabatte: https://linktr.ee/AllemeineEltern Du möchtest Werbung in diesem Podcast schalten? Dann erfahre hier mehr über die Werbemöglichkeiten bei Seven.One Audio: https://www.seven.one/portfolio/sevenone-audio

    Early in Dr, Jessa Landmann's medical training, she discovered a need for attention given to those after they had received treatment for cancer.  The post-treatment phase can be difficult physically, mentally and emotionally.  Nutrition, what survivors eat, how much they eat and when they eat is where she starts in dealing with those going through the multi-layered challenges of post-treatment.  Dr. Landmann urges those in the post-treatment phase to be proactive and seek direction from healthcare professionals.   Dr. Landmann is by trade a naturopathic doctor.  At the forefront of her care for those who have been treated for cancer is what is known as complimentary therapies.  She says this is an "umbrella term" for everything from exercise to nutrition to acupuncture to mindfulness and meditation and herbal supplements.  When she encounters one in the post-treatment phase, the thing she sees most is fatigue.  Patients tell her the bulk of the treatment may be in the past, but they still feel exhausted.   She seeks to utilize the therapies in her toolbox to make post-treatment patients feel better physically, mentally and emotionally.  When there is improvement in all three areas, then she says survivors are more apt to as best as possible, return to the life they led before they were diagnosed.    Before her caring for survivors become more multi-faceted, Jessa starts by trying to improve their diet.  She says a lot of people experience eating problems during treatment, whether it is from nausea or a change in appetite or changes in taste or certain medications like steroids for example increase people's appetite, so maybe they are eating more than they usually do, maybe they gain some weight, or a lot of people want that comfort food, maybe they are not eating in the healthiest way.  That's when she takes a deep dive into the person's eating habits, making sure there is enough protein, enough fruits and vegetables, not a lot of processed food.  She also watches the time of day in which the person is eating.  For example, if someone eats late at night he or she can have more frequent night-time awakenings.  That might lead to poor sleep and fatigue during the day.  Dr. Jessa Landmann says the best thing a survivor can do is to look into ways in which they can improve the post-treatment phase of their cancer journey.  There is much more to optimized healing during this difficult time, but she says a great place to start is being proactive about diet and exercise and to try to do as many things as the survivor did before they were diagnosed.   Additional Resources:   Jessa's website: https://www.drjessalandmann.com   Jessa's Book: "Beyond Cancer Fatigue: A Path to Reclaiming Energy", available on Amazon, but Cancer Interviews listeners and viewers can take advantage of a 20 percent discount if they purchase the book on the Wiley Publishing website by entering the code BCF20 at checkout.            

In the late 1980s, a child exposed to fallout from the Chernobyl disaster lay in a hospital bed while doctors told his family there were no clear answers and no reliable path forward. Decades later, that same child, Yan Leyfman, walks into exam rooms as a hematology oncology fellow, expected to deliver clarity inside a system that still runs on delay, uncertainty, and institutional self preservation.This episode traces the throughline from early life shaped by radiation exposure and hospice level uncertainty to a career inside academic medicine, translational research, and oncology media. Yan built his identity around survival and usefulness, moving from patient to physician while carrying the memory of what it feels like to sit on the other side of the table. He helped launch MedNews Week during the COVID crisis to push back on misinformation and expand access to medical knowledge, stepping into a public role while still in training.The conversation stays grounded in the friction between personal narrative and system reality. Clinical training demands efficiency, hierarchy, and emotional distance. Cancer care demands time, clarity, and human connection. Those forces collide in real patient encounters where prior authorization delays, insurance barriers, and fragmented care pathways shape outcomes as much as any treatment protocol.Yan speaks openly about mentorship, belonging, and the drive to make meaning out of survival. The discussion pushes further into what the healthcare system actually rewards, what it quietly strips away, and how quickly empathy can erode under institutional pressure. The episode also examines the role of medical media, where education, industry influence, and narrative control often blur together.This is a conversation about identity under construction, about what happens when someone who remembers powerlessness steps into a role that carries authority, and about whether that memory can survive long enough to change anything.RELATED LINKSYan Leyfman on LinkedInYan Leyfman on InstagramSurviving ChernobylFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

What happens when the medical system tells you you're clear, but the hardest part of your recovery is actually just beginning? In this special roundtable episode, brought to you in partnership with Postcode Lottery, we explore the unseen side of living through and beyond cancer.Joining Jake in the studio are legendary solo sailor Dame Ellen MacArthur, Frank Fletcher (CEO of the Ellen MacArthur Cancer Trust), and Josh Rands, a young survivor who rebuilt his life after a rare cancer diagnosis at just 19. Together, they share a raw, open conversation about why true bravery isn't always something you choose, the reality of life when treatment structures suddenly fall away, and how reclaiming independence on the open sea can give young people their futures back. It's a powerful look at resilience, the daily grind of running a purpose-driven charity, and why finding a genuine sense of belonging is often the ultimate medicine.Postcode Lottery

Matthew Zachary is a brain cancer survivor, healthcare advocate, founder of Stupid Cancer and We the Patients, and host of Out of Patients. In April 2026, he returned to the stage at Merkin Hall near Lincoln Center for his first solo public piano concert in almost 22 years while launching his debut book, We the Patients: Understanding, Navigating, and Surviving America's Healthcare Nightmare.What unfolded became far larger than a concert.Over 2 hours, survivors, clinicians, advocates, nonprofit founders, journalists, pharmaceutical sponsors, and healthcare insiders gathered in one room to reflect on 30 years of survivorship, institutional failure, accidental advocacy, and the emotional afterlife of cancer. The evening moved through original piano performances, live chapter readings, and deeply personal conversations about infertility, disability, financial toxicity, insurance denials, grief, burnout, and what happens when patients spend decades navigating systems designed around transactions instead of continuity.Guests including Wendell Potter, Maimah Karmo, Craig Lustig, Shelly Fuld Nasso, Tamika Felder, and others reflected on how the modern cancer advocacy movement emerged largely because patients built parallel systems where healthcare infrastructure failed to meet human needs. The conversation explored how prior authorization, reimbursement incentives, administrative fragmentation, and institutional distrust continue shaping the patient experience across oncology and survivorship.The performance also marked a deeply personal milestone. After brain cancer compromised his left hand at age 21, Zachary spent 6 months rehabilitating both hands to return to public performance for the first time in over 2 decades. The result became part concert, part civic gathering, and part historical record of a generation of survivors who refused to disappear quietly.RELATED LINKSMZLIVE Official WebsiteMZLIVE YouTube VideoFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Episode 90 - With Susie Pearl - author, TEDx and SXSW speaker, cancer survivor and PR founder - about her remarkable Near Death Experience, years of sobriety and books on happiness and creativity with David Lynch.Disclaimer: Please note that all information and content on the UK Health Radio Network, all its radio broadcasts and podcasts are provided by the authors, producers, presenters and companies themselves and is only intended as additional information to your general knowledge. As a service to our listeners/readers our programs/content are for general information and entertainment only.  The UK Health Radio Network does not recommend, endorse, or object to the views, products or topics expressed or discussed by show hosts or their guests, authors and interviewees.  We suggest you always consult with your own professional – personal, medical, financial or legal advisor. So please do not delay or disregard any professional – personal, medical, financial or legal advice received due to something you have heard or read on the UK Health Radio Network.

In December 1996, a 37 year old pharmaceutical executive sat in a Borders bookstore reading medical textbooks on the floor, trying to understand a disease she had never heard of. Multiple myeloma carried a three year prognosis. Her daughter was 18 months old. Her father had just died of cancer. Within weeks, she pushed her doctors to say the quiet part clearly. This would likely end her life before her child entered kindergarten.Kathy Giusti refused to accept passive survival. She built a plan while the system offered fragments. She interviewed oncologists and fertility specialists at the same time. She pursued IVF to have a second child while preparing for treatment. She stayed employed to keep insurance coverage. Every decision carried financial, medical, and emotional risk.That same urgency exposed a deeper failure. Cancer research moved slowly. Academic centers guarded data. Clinical trials lacked coordination. Patients entered a system that demanded compliance without providing clarity. Giusti responded by building the Multiple Myeloma Research Foundation, not as a support group, but as an operating engine to accelerate drug development, fund research, and force collaboration across institutions.This episode tracks the tension between individual agency and systemic failure. Giusti describes how patients navigate diagnosis, insurance barriers, and fragmented care in real time. She explains how data, genomics, and clinical trials reshape cancer treatment while still leaving patients responsible for decisions they are not trained to make. She addresses disparities in access, the limits of early detection, and the reality that progress in oncology often depends on speed, funding, and alignment of incentives.The conversation moves between lived experience and structural critique. It names the cost of delay, the burden placed on patients to act as their own advocate, and the tradeoffs required to push a system forward that still protects itself first.⸻RELATED LINKSKathy GiustiMultiple Myeloma Research FoundationFatal to FearlessAmerican Society of Hematology⸻FEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Welcome back to When Words Fail, Music Speaks, the podcast that battles depression and heartache with the healing power of song. I'm your host, James Cox, and today we're honored to sit down with a true powerhouse of soul, strength, and the blues—Miss Freddie, the Pittsburgh‑born “Lady of the Blues.”From singing in church choirs as a child to surviving cancer twice, Miss Freddye's journey is a testament to resilience. By day she's a full‑time nurse and devoted mom, and by night she commands two dynamic ensembles: Roots of the Soul—her evolving blues‑rock‑R&B outfit—and Miss Freddye's Home Cooking Band, a genre‑bending crew that serves up everything from gospel to jazz, country, and classic rock.In this conversation we'll explore:The roots of the blues—Clarksdale vs. Memphis and the lore of Robert Johnson.What the title “Pittsburgh Lady of the Blues” means to her personally.How music helped her navigate two cancer battles and chronic stage fright.Her ever‑growing musical palate—from classical piano to heavy metal, jazz, and beyond.The behind‑the‑scenes struggles of a performer who still gets nervous at 15.A dream she's still chasing: mastering the bass guitar.And a handful of fun lightning‑round revelations—her favorite live song (“Slipping Away”), the biggest crowd she's ever played (Picklesburg), and a surprising future plan to open a barber shop.Stay tuned as we dive deep into Miss Freddye's story, her empowering anthem “Lady of the Blues,” and the heart‑fueled music that keeps her moving forward. Whether you're a blues devotee, a fellow survivor, or simply someone looking for a lift, this episode is a reminder that when words fall short, the music always speaks.Website:https://missfreddye.com

When Samuel Shepherd was diagnosed with a rare terminal blood cancer, doctors told him there was no treatment, no cure, and possibly very little time left. For many people, that would have been the end of the story. For Samuel, it became the beginning of an obsession. A physicist, engineer and inventor with decades of experience across biochemistry, environmental science and high-level government projects, Samuel turned all of his knowledge towards one goal: staying alive. What followed was years of relentless research, experimentation and a refusal to accept inevitability. This conversation is different from most episodes of Mid-Life Men. It's part survival story, part deep dive into inflammation, disease and the science behind Samuel's discovery of a naturally occurring molecule called 'astaxanthin' – and why he believes it changed everything for him. But beneath the science is something more human: what happens psychologically when you're told your life may be ending how fear can completely change shape why purpose matters when everything familiar falls away and what relentless determination really looks like in practice Whether you agree with Samuel's conclusions or not, this is a fascinating conversation about resilience, mortality, curiosity and refusing to give up when the odds look impossible.If you want to find independent research on astaxanthin, go to the National Institute of Health website or the National Center for Biotechnology Information. To find out more about ValAsta as a supplement, visit Valasta.net. 

Cubs for a Cure: Various cancer survivors share their stories (Hour 9) full 2627 Thu, 21 May 2026 23:50:41 +0000 9uZr3vGCZhFeX3EjIcAJ26oncueROkZM sports Best of 104.3 The Score sports Cubs for a Cure: Various cancer survivors share their stories (Hour 9) Best of 104.3 The Score Best of 104.3 The Score is a curated snapshot of the station at its best, delivering the standout moments Chicago sports fans don't want to miss. Featuring top interviews, expert commentary, and memorable segments from across the lineup, the podcast covers everything from Bears Sundays and Cubs summers to Bulls, Blackhawks, and White Sox headlines. Whether you're catching up or reliving the biggest conversations of the day, Best of 104.3 The Score brings the voices, stories, and debates that power Chicago sports talk into one easy listen. © 2026 Audacy, Inc. Sports https://player.amperwave

Lindsey Walker, founder of Walker + Associates Media Group, a global public relations and communications agency that helps entrepreneurs, creatives, and culture-shaping leaders build visibility and credibility that translates into real legacy.Through strategic media positioning, thought leadership, and high-impact visibility campaigns, Lindsey supports purpose-driven founders and brands to amplify their mission and grow with intention, not just secure press.Now, Lindsey's journey as a Stage IV cancer survivor while continuing to lead and scale her agency demonstrates what it truly means to build while healing, with faith, resilience, and clarity.And while guiding leaders through the messy middle of growth and alignment, she's redefining success by proving that impact, health, and legacy can be built together.Here's where to find more:Website: https://www.walkerassocmediagroup.comInstagram: https://www.instagram.com/lindseyawalker________________________________________________Welcome to The Unforget Yourself Show where we use the power of woo and the proof of science to help you identify your blind spots, and get over your own bullshit so that you can do the fucking thing you ACTUALLY want to do!We're Mark and Katie, the founders of Unforget Yourself and the creators of the Unforget Yourself System and on this podcast, we're here to share REAL conversations about what goes on inside the heart and minds of those brave and crazy enough to start their own business. From the accidental entrepreneur to the laser-focused CEO, we find out how they got to where they are today, not by hearing the go-to story of their success, but talking about how we all have our own BS to deal with and it's through facing ourselves that we find a way to do the fucking thing.Along the way, we hope to show you that YOU are the most important asset in your business (and your life - duh!). Being a business owner is tough! With vulnerability and humor, we get to the real story behind their success and show you that you're not alone._____________________Find all our links to all the things like the socials, how to work with us and how to apply to be on the podcast here:https://linktr.ee/unforgetyourself

At 19, Shlomit woke up unable to speak. The right side of her body went numb. An emergency room sent her home and called it stress. That moment did not end in a diagnosis that changed policy or triggered reform. It sent her into a decade long pursuit of understanding how the brain fails language and how the healthcare system fails patients who cannot advocate for themselves.Shlomit trained as a speech language pathologist and spent years inside acute care hospitals and ICUs, performing endoscopies and treating patients with brain injury, stroke, and dysphagia. She watched medical teams rotate in and out, deliver dense updates, and leave families nodding without comprehension. She stayed behind and translated. Every day, patients told her she was the only one who explained what was happening. That gap is not an accident. Hospital systems optimize for throughput, not understanding. Patients move through beds based on cost, not readiness. Discharge planning becomes a financial decision wrapped in clinical language. A stay under 48 hours can shift the insurance burden dramatically, leaving patients exposed to higher out of pocket costs. Shlomit left the system and built Patient Path NYC, a private patient advocacy service. She now spends 15 to 20 hours a week per client reading charts, coordinating care teams, and translating medical decisions into plain language. Her work sits in the uncomfortable space between healthcare policy and lived experience. Families pay out of pocket to understand their own care. Hospitals benefit from the clarity she provides while maintaining the same structural incentives that created the confusion.This conversation tracks the human cost of fragmented care, the economics behind discharge decisions, and the quiet reality that patients who cannot communicate clearly often lose control of their own outcomes.RELATED LINKSShlomit LibertyShlomit Liberty on LinkedInPatient Path NYCBoard Certified Patient AdvocateFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Dr. Jeanine Cook-Garard talks with Julie Stevens, who at 43 years old, was given a stage 4 colon cancer diagnosis—and only a 14% chance of survival.  She hosts the podcast MOJO Rising... How to Make Cancer Suck Less - and is the author of MOJO Healing... How to Build a Holistic Healing Strategy and Maximize Joy. Julie is also the founder of Vedalife, a health tech startup developing "Ginger," an AI-powered nutrition platform designed to help people optimize their health through comprehensive bio marker tracking and personalized insights.

Learn More about Peter at: https://www.linkedin.com/in/petertmclaughlin/ and his work at : https://blueskyhypnosis.com Follow him on Social Media: Twitter: https://x.com/PetMcLaughlin IG: https://www.instagram.com/thepetermclaughlin/ YT: https://www.youtube.com/@BlueSkyHypnosis Show Notes   

In 2020, developmental biologist Dr. Crystal Rogers drove the country roads outside Davis, California crying between grant rejections, wondering whether she was about to lose her lab, her career, and the scientific future she had spent years building. She had already done what academia tells young scientists to do. She earned the credentials. She landed a faculty position at UC Davis. She built a lab. Then the real test began.On this episode of Standard Deviation, Dr. Oliver Bogler examines the unspoken rules that determine which scientists survive academic research and which quietly disappear from it. The conversation follows Crystal Rogers and cancer biologist Dr. Michelle Mendoza as they collide with the “Hidden Curriculum” of biomedical science: the unwritten rhetoric, institutional signaling, and grant writing strategies that often decide who receives funding, tenure, and long term stability.Michelle Mendoza entered a tenure track position at the Huntsman Cancer Institute while raising 3 children, navigating a divorce, and trying to secure major NIH funding during COVID. What looked like objective scientific review turned out to depend heavily on persuasion, presentation, and insider fluency. Established researchers could promise massive research agendas based on reputation alone. Junior investigators faced a completely different standard.Oliver traces how the Life Science Editors Foundation and its JEDI program intervened by pairing scientists with former editors from journals including Cell and Nature. The work had little to do with commas or grammar. Editors challenged logic, structure, and scientific framing before grant reviewers could destroy an application in public.Both researchers eventually secured career defining grants. One realized she would keep her job and not have to move her family. The other celebrated by ordering a personalized “DEV BIO” license plate and driving through Davis blasting nineties hip hop and Beyoncé.The episode exposes how biomedical research funding rewards institutional fluency as much as scientific talent, and how hidden systems inside academic medicine continue shaping who gets to stay in science long enough to make discoveries.RELATED LINKSDr. Crystal Rogers LinkedInDr. Crystal Rogers Faculty PageDr. Crystal Rogers LabDr. Michelle Mendoza LinkedInDr. Michelle Mendoza Faculty PageHuntsman Cancer Institute Mendoza LabLife Science Editors FoundationFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

For his entire adult life, Olivier Duhaime has been no stranger to taking on hard challenges. Running his first marathon at just 18 years old proved a gateway into endurance sport that would see the Gatineau native tackle events from ironmans to ultramarathons and even a multi-day cross-province run from Quebec City to Ottawa. But when a shock cancer diagnosis in late 2021 put a pause to his endurance-sport lifestyle, it presented a test of perseverance unlike any he'd faced before. From training everyday to barely able to get out of bed, Olivier was faced with a mountain to climb that dwarfed even his longest trail ultras. But from a lifetime spent pushing his body to do the impossible he knew that at rock bottom there's nowhere to go but up, and after 51 rounds of chemotherapy and a bone marrow transplant, he emerged from a years-long battle cancer free.  Next week, Olivier will make his long-anticipated return to a marathon starting line close to home at the Tamarack Homes Ottawa International Marathon, where he'll be toeing the line in support the Ottawa Hospital Foundation whose care helped save his life.  Olivier joins The Shakeout Podcast to share his journey of recovery and his return to full the intensity marathon training,  and why this marathon carries extra importance as he raises awareness and funds for the future of the cause that gave him back his.  Support Olivier's Fundraising Efforts for the Ottawa Hospital Foundation Campaign to Create Tomorrow Subscribe to The Shakeout Podcast feed on Apple, Spotify, YouTube or wherever you find your podcasts. The Shakeout Podcast will be LIVE from The Tamarack Homes Ottawa Marathon Race Expo: Friday, May 22nd @ 4pm EST: Come by and check out our interview with some of Canada's top distance stars, plus a chance to win free gear! [This collaboration is part of an advertising campaign led by the Podpass agency for Altitude Sports] Shop now at Altitude Sports and enjoy up to 20% off your first order with the promo code “shakeout2026” Click here to order

In 2008, Katy Talento walked away from Capitol Hill and into a Catholic convent. Within a year, she walked out. Within another decade, she sat inside the White House shaping health policy. Somewhere in between, she got labeled “infertile” after a single cycle of testing and spent years believing it.That label stuck. The pain that came before it never got investigated. Doctors offered birth control and moved on. No one asked why her body was struggling. No one followed the thread.Talento built her career inside the very systems she now critiques. She worked on federal health policy, global disease programs, and later advised the Trump administration on healthcare reform. She helped advance price transparency rules in a system where hospitals can still list 457 different prices for the same service.Then she left.Now she builds employer health plans that bypass insurers, PBMs, and traditional networks. Her approach replaces insurance contracts with direct payment, nurse navigators, and cost sharing models that promise simplicity but raise hard questions about risk and protection.This conversation sits in that tension.Talento describes a healthcare system shaped by layered incentives, where insurers, hospitals, and intermediaries profit from complexity. She argues that employers hold the leverage to disrupt it. The host pushes on what happens when patients fall outside those structures, when contracts disappear, and when community based models fail.The episode moves through infertility, misdiagnosis, insurance design, and the mechanics of employer sponsored care. It tracks how policy decisions made in Washington ripple into exam rooms, billing departments, and family lives.It also confronts a harder truth.Even insiders who understand the system can still get caught in it.RELATED LINKSAllBetter HealthKaty TalentoThem Before UsAn Arm and a LegRelentless Health ValueFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Interview with Shalender Bhasin, MBBS, author of Testosterone Treatment in Prostate Cancer Survivors With Hypogonadism: A Randomized Clinical Trial, and Peter C. Albertsen, MD, author of Collaborating to Improve Quality of Life Among Prostate Cancer Survivors. Hosted by Eve Rittenberg, MD. Related Content: Testosterone Treatment in Prostate Cancer Survivors With Hypogonadism Collaborating to Improve Quality of Life Among Prostate Cancer Survivors

Interview with Shalender Bhasin, MBBS, author of Testosterone Treatment in Prostate Cancer Survivors With Hypogonadism: A Randomized Clinical Trial, and Peter C. Albertsen, MD, author of Collaborating to Improve Quality of Life Among Prostate Cancer Survivors. Hosted by Eve Rittenberg, MD. Related Content: Testosterone Treatment in Prostate Cancer Survivors With Hypogonadism Collaborating to Improve Quality of Life Among Prostate Cancer Survivors

Send us Fan MailSend us Fan MailIn this inspiring episode of Living the Dream with Curveball, we are joined by Jenn Greenhut Tollin, a remarkable survivor of stage four breast cancer who transformed her diagnosis into a powerful mission of love and positivity. After facing the harsh realities of her illness, Jenn created Zero Negativity, a brand that promotes positivity through unique accessories while supporting cancer research.Jenn shares her deeply personal journey, detailing the challenges she faced as a healthy yoga instructor suddenly confronted with a life-threatening diagnosis. She reflects on the emotional turmoil of infertility struggles and how it ultimately led her to embrace life in a new light. With a mindset shift that transformed her battle with cancer into a journey of gratitude, love, and trust, Jenn emphasizes the importance of viewing obstacles as opportunities for growth.Throughout the episode, Jenn discusses her innovative approach to healing, including the significance of self-love and the power of community support. She introduces her company, Zero Negativity, and its mission to empower cancer patients and caregivers alike. From chemo tote bags filled with comfort items to fundraising events, Jenn is dedicated to making a positive impact in the lives of others facing similar struggles.Join us for a heartfelt conversation filled with hope, resilience, and practical advice for anyone navigating the challenges of cancer or supporting a loved one through their journey.What You'll Learn in This Episode:- The transformative power of a positive mindset in the face of adversity- How Jenn turned her cancer diagnosis into a mission of love and support- The importance of community and self-love during difficult times- Insights into Jenn's company, Zero Negativity, and its initiatives- Tips for caregivers and patients on navigating the cancer journey togetherFor more information on Jenn Greenhut Tollin and her work, visit www.lovezeronegative.com and www.zeronegativefoundation.org.Support the show

In a wooded campground cabin in the early 2000s, 19 year old Ben Unger stood in the doorway and watched 20 naked men form a circle around a crying teenager. A counselor held up two tangerines and shouted, “These are your balls.” The exercise claimed to cure same sex attraction by forcing young men to “reclaim” their masculinity from overbearing mothers. Phones had been confiscated. Parents had paid thousands of dollars. Religion supplied the script. Pseudoscience supplied the props.Ben had grown up in an Orthodox Jewish community in Brooklyn and later studied in Israel to become a rabbi. When he admitted he felt attracted to men, rabbis told him to eat 7 figs a day, immerse in a ritual bath 5 times daily, or marry a woman and trust that “if there's friction, it works.” At 19, he entered conversion therapy through an organization called Jews Offering New Alternatives to Homosexuality, known as JONAH. He left with depression, religious trauma, and 6 months of silence toward the mother he had been taught to blame.Years later, represented by the Southern Poverty Law Center, Ben helped sue JONAH for consumer fraud in a landmark New Jersey case. The argument centered on evidence, not theology. Sexual orientation cannot be changed. The jury deliberated for 3 hours and ruled against the organization. The verdict helped reshape how states regulate conversion therapy and protect minors from psychological harm disguised as treatment.Today, Ben runs Buff Personal Training in New York City, a gym built on autonomy, mental health, and self respect. His story traces the arc from institutional control to self authorship. The conversation examines religion, LGBTQ rights, conversion therapy, consumer protection law, and the lasting cost of being told your identity is a disorder.RELATED LINKSBen Unger on LinkedInBen Unger on InstagramBUF Personal TrainingSouthern Poverty Law CenterJONAHFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

In this episode, I sit down with Roxy and her mom, Diana, to share a story that is both deeply emotional and incredibly hope-filled. Roxy was just four years old when her family discovered a lump that would quickly turn their world upside down. From diagnosis to treatment, and then facing a relapse scare, Diana shares what it was like to walk through fear, uncertainty, and the weight of life-altering decisions as a parent. But what unfolds in this conversation is something even more powerful—a story of faith, resilience, and the unwavering belief in healing. From Roxy's childlike confidence in her healing, to the intentional choices their family made to support her body, this episode is a reminder of the strength that can be found in both faith and action. LINKS: Join Thrive Through Cancer Community: https://biodynamicwellness.com/services Follow us on Instagram: @BiodynamicWellness Learn about our Thrive Through & Beyond Cancer Programs: biodynamicwellness.com/thrive-through-cancer and biodynamicwellness.com/thrive-beyond-cancer Follow Season on Instagram: @seasonjohnson Learn more: www.seasonjohnson.com Diana (Roxy's Mom) Instagram:  instagram.com/samkodiana

Kevin details his life challenges with cancer and what inspired him to become a life coach.

Mason Moore survived testicular cancer three times, with his first diagnosis in 2003, just two weeks before his wedding. He made the wedding as planned and became a vocal advocate for men's health and men taking responsibility for their health. The cancer returned in 2018 with a nodule in his right lung. And again, in 2019, in the same lung, Mason will share the details of these diagnoses, which were testicular cancer. He continues to give back to the cancer community as a testicular cancer survivor and is now seven years cancer-free. Send us Fan MailSupport the showFind us on Twitter,  Instagram,  Facebook  &  Linkedin. If you can please support our nonprofit through Patreon. 

Drew Flugstad-Clarke never planned to work in brain cancer. She planned to play Division I soccer at Georgetown. She planned to paint. She even tried investment banking, answering emails at 4am in a cubicle that never slept. Then in June 2022 her father, Jim, was diagnosed with glioblastoma at 57. He died 1 day shy of 7 months later, just before his 58th birthday. His symptoms began with emotion, not seizures. A steady HR executive suddenly cried. His golf game slipped. By the time he entered the hospital for a scan, he did not leave without surgery. A subway poster for a 5K became a lifeline. Drew showed up. She found a community. She later joined the American Brain Tumor Association as Community Manager for the Eastern Region. This conversation walks through anticipatory grief, caregiving in real time, strategic numbness, and what it costs to curate hope when the median survival clock is already ticking.RELATED LINKSDrew Clark Flukestad on LinkedInTopor StudiosAmerican Brain Tumor AssociationGeorgetown University Women's SoccerFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Want to Start or Grow a Successful Business? Schedule a FREE 13-Point Assessment with Clay Clark Today At: www.ThrivetimeShow.com   Join Clay Clark's Thrivetime Show Business Workshop!!! Learn Branding, Marketing, SEO, Sales, Workflow Design, Accounting & More. **Request Tickets & See Testimonials At: www.ThrivetimeShow.com  **Request Tickets Via Text At (918) 851-0102   See the Thousands of Success Stories and Millionaires That Clay Clark Has Helped to Produce HERE: https://www.thrivetimeshow.com/testimonials/ Download A Millionaire's Guide to Become Sustainably Rich: A Step-by-Step Guide to Become a Successful Money-Generating and Time-Freedom Creating Business HERE: www.ThrivetimeShow.com/Millionaire   See Thousands of Case Studies Today HERE: www.thrivetimeshow.com/does-it-work/  

Janine Durso spent 30 years inside pharmaceutical advertising shaping healthcare narratives before becoming a belief strategist and founder of The Believist. In November 2024, during a routine Zoom coaching session, she felt what she called a sharp, terrible pain in the right side of her head. Within hours she was in surgery for a ruptured brain aneurysm. She does not remember the ambulance, the ICU, or the first weeks that followed. She spent 5 weeks in intensive care, then 10 days relearning how to walk, calculate simple change, and manage basic cognition. Doctors later placed a stent and continue monitoring a second unruptured aneurysm.This episode traces the moment she told her husband something broke in my brain, the 14 days doctors called touch and go, and the slow mental rebuild that followed. It also examines insurance barriers that require 2 direct relatives with aneurysms before screening coverage, and why she now lobbies in Washington for change.RELATED LINKSJanine DursoThe BelievistBrain Aneurysm FoundationWhite Plains HospitalDr. Jared CooperFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Rebecca Benghiat holds a JD, passed the bar, and skipped corporate law to build mental health systems instead. She now serves as Chief of Staff and Head of Impact at Inner Foundation, where she helps direct capital toward emerging adults ages 18 to 30 and asks a hard question every day: Is this actually working?In this conversation, she dismantles the myth of easy fixes. She explains why mental health measurement resists clean metrics, why a PHQ 9 score starts a conversation but never finishes one, and why “scale” often flatters institutions more than it helps people. She breaks down how impact investing shapes care delivery, why schools need networked systems not slogans, and why friction might be developmentally necessary.The stakes are real. Vulnerable families navigate snake oil, glossy apps, and pay to play algorithms while carrying the burden of choice in crisis. Benghiat lives inside that complexity and refuses to simplify it.RELATED LINKSRebecca BenghiatInner FoundationAspen Ideas HealthThe Jed FoundationFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

At age 12, Dr. Chrystal Starbird stood by a pond after turning her mother in to the police. She watched tadpoles and fish move beneath the surface and found a strange kind of order. Science became her refuge long before it became her career. Years later, she built that refuge into a profession. She now serves as an Assistant Professor at the University of North Carolina, studies structural biology tied to cancer and Alzheimer's disease, and won Cell's first Rising Black Scientist Award in 2020. On paper, she fits the model of success. In practice, she had to fight for basic access at every stage.Conference travel required upfront cash she did not have. Networking favored pedigree over merit. Mentorship often depended on who knew your name in the room. Chrystal learned those rules, then chose to break them open for others.Oliver Bogler examines what Chrystal calls the advocacy tax. She has delivered over 70 invited talks. Nearly 40 percent focus on equity, mentorship, and policy. Academic reward systems do not count that labor toward tenure. She still does it.Through her leadership at the Life Science Editors Foundation, Chrystal helped build the JEDI program, which pairs underrepresented scientists with editors from journals like Cell and Nature. The program has supported over 100 awardees with more than 1,000 hours of mentorship. This episode exposes how biomedical science rewards output while ignoring the work required to make the system accessible. It also shows what happens when the people most affected refuse to step back.RELATED LINKSDr. Chrystal StarbirdStarbird LabLife Science Editors FoundationJEDI ProgramFEEDBACKLike this episode? Rate and review Out of Patients on your favorite podcast platform. For guest suggestions or sponsorship email podcasts@matthewzachary.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.