Podcasts about diagnosed

From Casual Drinking to Liver Failure: Jacob's Story of Alcoholic Cirrhosis, Sobriety, and Second Chances In this episode of the Sober Motivation Podcast, Jacob shares his powerful journey from a normal upbringing and moderate drinking to developing alcoholic liver cirrhosis after a slow, 10-year descent into alcohol dependency. Growing up in Wisconsin with a loving family, sports, and strong values, Jacob never saw alcohol as dangerous. Drinking started socially and casually — a beer here, wine at dinner, fun with friends. But as stress increased through marriage, business responsibilities, and parenting, alcohol quietly shifted from celebration to coping. In 2023, Jacob was hospitalized with severe abdominal swelling (ascites), jaundice, and ultimately diagnosed with alcoholic liver cirrhosis. Doctors gave him a grim prognosis and discussed palliative care. But this is not a tragedy story. It's about what Jacob is doing with his second chance.  ----------- Support the Show: https://buymeacoffee.com/sobermotivation Join the Sober Motivation Community: https://sobermotivation.mn.co/ Jacob in Instagram: https://www.instagram.com/feel_sober_good/

Discover what's possible when self-esteem saves lives. Are you looking for tools and to help your neurodivergent teen feel supported in this important phase in life? Whether that's your case or you're curious about behavioral parenting strategies, you'll want to listen to this episode with Jheri South.  Jheri South is a behavioral coach and the mother of seven neurodivergent children, five being on the autism spectrum. Diagnosed with ADHD herself at age 40, Jheri specializes in coaching teens and parents to navigate ADHD, autism, anxiety, and parenting with mindset, strategy, and community. This episode is part two of our conversation, and we discuss: Common struggles for parents of neurodivergent teens The importance of being consistent as parents How to help autistic teens build confidence and self-esteem How Jheri successfully helped an autistic teen to stop cutting herself Tips to set realistic expectations for autistic adolescents To learn more about Jheri South and her work, please visit: IG @msjherisouth ----more---- We appreciate your time. If you enjoy this podcast and you'd like to support our mission, please take just a few seconds to share it with one person who you think will find value in it too. Follow us on Instagram: @autismpodcast Join our community on Mighty Networks: Global Autism Community Subscribe to our YouTube channel: Global Autism Project We would love to hear your feedback about the show. Please fill out this short survey to let us know your thoughts: Listener Survey 

On this Make A Difference Minute, Coleman Drew talks about the timeline surrounding his upcoming transplant. Diagnosed with cystic fibrosis at just two years old, Coleman has spent his life managing daily treatments and health challenges. Now, as transplant becomes the next step in his journey, he shares what the process looks like, what happens next, and how he and his family are preparing. This is a powerful glimpse into the reality behind the word “transplant.” If you would like to support Coleman and his family with transplant-related expenses, visit: cota.org/cotaforcolemansfight Sponsor: Singing River Dentistry SingingRiverDentistry.com

What if a cancer diagnosis didn't mean surrender—but transformation?In this powerful episode of Integrative Cancer Solutions, Dr. K sits down with bestselling author, philanthropist, and lifelong learner Glenn Sturm, who has lived—and thrived—through nearly two decades of continuous chemotherapy. Diagnosed with a rare, incurable lymphoma and given just years to live, Glenn shares how integrative, multidisciplinary cancer care helped him defy the odds and reclaim his life.This conversation explores why silo-based oncology fails patients, how true integrative cancer care dramatically improves survival and quality of life, and why mindset, communication, movement, and purpose are as critical as chemotherapy itself. Glenn also shares deeply human stories—from surgery rooms to chemo suites—that reveal how gratitude, laughter, and patient empowerment can become some of the most powerful medicines available.Key Takeaways:0:00 Introduction4:10 Why Glenn refused to let cancer define him9:30 Integrative cancer care vs silo-based oncology15:20 Building a multidisciplinary cancer care team21:45 Cancer fatigue, chemo brain, and overlooked root causes29:10 Medication interactions and why patients must stay vigilant36:40 How mindset, purpose, and joy influence survival44:30 Why patients—not doctors—must be the quarterbacks of careResources Mentioned:Cancer Set Me Free - https://glennsturm.com/store/Cancer-Set-Me-Free-p711698418Medical Disclaimer: This content is for educational purposes only and is not intended to diagnose, treat, cure, or replace professional medical advice. Always consult your physician or qualified healthcare provider regarding any medical condition or treatment decisions. -----------------------------------------------A Better Way to Treat Cancer: A Comprehensive Guide to Understanding, Preventing and Most Effectively Treating Our Biggest Health ThreatGrab my book here: https://www.amazon.com/dp/B0CM1KKD9X?ref_=pe_3052080_397514860 Unleashing 10X Power: A Revolutionary Approach to Conquering CancerGet it here: https://store.thekarlfeldtcenter.com/products/unleashing-10x-powerPrice: $24.99100% Off Discount Code: CANCERPODCAST1Healing Within: Unraveling the Emotional Roots of CancerGet it here: https://store.thekarlfeldtcenter.com/products/healing-withinPrice: $24.99100% Off Discount Code: CANCERPODCAST2-----------------------------------------------Integrative Cancer Solutions was created to instill hope and empowerment. Other people have been where you are right now and have already done the research for you. Listen to their stories and journeys and apply what they learned to achieve similar outcomes as they have, cancer remission and an even more fullness of life than before the diagnosis. Guests will discuss what therapies, supplements, and practitioners they relied on to beat cancer. Once diagnosed, time is of the essence. This podcast will dramatically reduce your learning curve as you search for your own solution to cancer. To learn more about the cutting-edge integrative cancer therapies Dr. Karlfeldt offer at his center, please visit www.TheKarlfeldtCenter.com

Pain has a way of demanding your attention, but it doesn't get to decide who you become. Lyndsay Soprano's life has been shaped by layers of trauma, abuse, chronic illness, and a diagnosis of Complex Regional Pain Syndrome, one of the most painful conditions known. Yet instead of letting pain define her, Lyndsay made a conscious decision to give it purpose. This episode explores what it means to reclaim your power when your body hurts, your past weighs heavy, and healing feels overwhelming. Through honesty, humor, and radical gratitude, Lyndsay shares how facing trauma head-on, questioning broken systems, and choosing presence over despair changed everything. Her story is not about fixing pain,  it's about learning how to live fully in spite of it. Guest Bio Lyndsay Soprano is the founder and host of The Pain Game Podcast and a bold advocate in the chronic pain and trauma recovery space. Diagnosed with Complex Regional Pain Syndrome (CRPS) in 2017, Lyndsay is also a survivor of sexual, emotional, and physical abuse, infertility, depression, anxiety, and divorce. After years of misdiagnosis and failed treatments, she chose a trauma-informed, integrative approach to healing and turned her lived experience into a platform that helps others feel seen, understood, and less alone. Her guiding belief is simple but uncompromising: the only way out is through.   You'll hear About How early trauma quietly shaped Lyndsay's coping mechanisms Living with CRPS and navigating life in constant physical pain The moment she chose gratitude over despair Why Western medicine alone failed her — and what she did differently Turning pain into purpose through conversation, advocacy, and voice   Chapters 00:00 Welcome and Episode Introduction 02:00 Lyndsay's Early Trauma and Childhood Coping 05:00 Uncovering Repressed Memories and Their Impact 08:00 Living With CRPS and Daily Pain Decisions 12:00 Gratitude as a Survival Skill 15:30 The Night Everything Had to Change 18:30 Reclaiming Power From Medication and Misdiagnosis 22:30 Functional and Integrative Healing Approaches 26:30 Advocacy, Self-Trust, and Taking Control of Care 30:00 Why Pain Does Not Get to Define Identity 33:30 Creating The Pain Game Podcast 37:30 Writing, Forgiveness, and Letting Go 41:00 Lyndsay's Message to Anyone Feeling Hopeless 45:00 Chuck's Closing Reflections Chuck's Challenge This week, notice where pain or frustration is trying to take your power. Pause before reacting. Ask yourself how you can meet that moment with curiosity, compassion, or gratitude instead. Even small shifts can change the entire direction of a day. Connect with Lyndsay Soprano Website: thepaingamepodcast.com Email: talktoher@thepaingamepodcast.com Connect with Chuck Check out the website: https://www.thecompassionateconnection.com/ Linked In: https://www.linkedin.com/in/chuck-thuss-a9aa044/ Follow on Instagram: @warriorsunmasked Join the Warriors Unmasked community by subscribing to the show. Together, we're breaking stigmas and shining a light on mental health, one story at a time

What do you do when doctors give you five years to live… and you're still here more than twenty years later? In this moving episode of Contagious Influencers of America, nine-time Emmy winner David Sams interviews singer-songwriter and worship leader Tim Timmons. Diagnosed with incurable cancer in 2001 and given just five years, Tim's story deepened into one of profound faith, surrender, and hope. Now, over two decades later, his journey is portrayed by Milo Ventimiglia (Gilmore Girls, This is Us) in "I Can Only Imagine 2," tied to MercyMe's iconic song that has impacted millions "Even If." Tim shares openly about: Living with cancer while embracing both grief and hope Shifting from "working for God" to simply joining Jesus His daily grounding practice (the X he writes on his wrist each morning) Co-writing "Even If" with MercyMe's Bart Millard Watching his life and pain depicted on the big screen The heart of his new book, Waking Up Again: A Journey of Grief and Gratitude This isn't about pretending life is easy—it's about waking up again to presence, purpose, and a faith that holds joy and sorrow together. If you're facing uncertainty, loss, or a heavy season, this conversation will meet you with real hope. I Can Only Imagine 2 opens in theaters this Friday! "Waking Up Again" is available now wherever books are sold. Listen today—and share with someone who needs encouragement. Click here for tickets:  I Can Only Imagine 2 | Only In Theaters February 20 #PodcastInterview #FaithAndHope #WakingUpAgain #ICanOnlyImagine2 #EvenIf #GriefAndGratitude #TimTimmons #MercyMe #DavidSams #KeepTheFaith

On this episode of Walk and Roll Live – Disability Stories, Doug Vincent sits down with Ty Gipson, entrepreneur, motivational speaker, and resilience advocate whose life has been shaped by extraordinary medical and personal challenges. Diagnosed with Type 1 juvenile diabetes at a young age, Ty's journey includes multiple life-saving organ transplants, years of uncertainty, and moments where giving up might have seemed easier than pushing forward. Instead, Ty adopted what he calls a “No Options” mindset — a belief that when quitting isn't an option, purpose takes over. In this powerful conversation, Ty shares how his health challenges shaped his outlook on life, leadership, and service, how entrepreneurship gave him a sense of control and creativity, and how gratitude, faith, and community helped him thrive beyond survival. Together, Doug and Ty explore disability, chronic illness, resilience, and the power of choosing hope when the path forward is unclear. This episode is a must-watch for anyone navigating disability, chronic illness, major life transitions, or searching for inspiration to keep moving forward — no matter the odds. Walk and Roll Live 

Morgan Harper Nichols (All Along You Were Blooming) joins The Art of Kindness with Robert Peterpaul in a previously-released episode (2024) from our library, discussing: kindness through artistic spaces, the thoughtfulness of kindness, the kindness of memes and much more. ⁠Morgan Harper Nichols⁠ is an artist, writer, and creator based in Georgia. Diagnosed with autism, ADHD, and sensory processing disorder, Morgan's work often explores themes of embracing life's narrative and creating room to breathe. She began creating art and poetry in response to social media messages she received in 2017, and since then, her practice has expanded to include digital art, collage, coding, and 3D environments. Morgan is the creator of the app Storyteller and the online shop Garden24. Her WSJ bestselling book, All Along You Were Blooming, is one of several published works, and she currently serves as Vice President on the board of TWLOHA, a mental health organization. Morgan is passionate about the intersection of art, storytelling, and health, and her long-term goal is to teach and develop resources that explore how we create and interact with narratives in our lives. L Morgan Lee's "Reaching for Help from Drowning" Fundraiser: ⁠https://www.gofundme.com/f/reaching-for-help-from-drowning⁠ Follow Morgan: ⁠@morganharpernichols⁠ Follow us: ⁠@artofkindnesspod⁠ / ⁠@robpeterpaul⁠ ⁠youtube.com/@artofkindnesspodcast⁠ ⁠Support the show⁠! (https://www.buymeacoffee.com/theaok) Got kindness tips or stories? Want to just say hi? Please email us: artofkindnesspodcast@gmail.com Music: "Awake" by Ricky Alvarez & "Sunshine" by Lemon Music Studio. Learn more about your ad choices. Visit megaphone.fm/adchoices

When a story resonates across generations, it's usually because it touches something deeply human. Tim Timmons has that kind of story. He's the focus of I Can Only Imagine 2, a movie focusing on redemption, relationships, and the impact of people who choose to show up when it matters most. In this episode of the All Pro Dad Podcast, host Ted Lowe is joined by Tim to talk about the movie and his role as a dad.Why This MattersThe on-screen lessons from the movie can be implemented in your home today.   Who is Tim Timmons?·      Christian singer, songwriter, and worship leader known for joyful, authentic storytelling·      Best known for hit songs like “Cast My Cares” and “All About You”·      Built a strong following through music that blends faith, humor, and real-life honesty·      Passionate advocate for intentional faith, family, and meaningful connection·      Diagnosed with terminal cancer of unknown origin in 2000. Doctors told him he had just five years to liveWhy Intentional Fatherhood Matters: In the film, Tim's character (played by Milo Ventimiglia) embodies themes of perseverance, grace, and transformation. These aren't just cinematic ideas; they're the building blocks of healthy families. Every dad, at some point, faces moments when he has to decide whether to disengage or lean in, react or respond with wisdom, or drift or lead with intention.Tim Timmons's voice—both in the film and beyond it—invites dads to rethink what influence really looks like. It's not about control; it's about connection. It's not about having all the answers; it's about being willing to walk alongside your kids as they grow.Quotable MomentTim told Ted this powerful line: “I get drunk on worry all the time. I get drunk on worrying about my finances all the time. I get drunk on scarcity going, “I'm not going to have enough.” I get drunk on trying to work for God all the time. And I want to be more sober this year than I was last year.”Enjoy this conversation and the movie, which hits theaters on February 20, 2026. I Can Only Imagine 2 is based on the heartfelt true story behind the hit single “Even If.” The aim is to “Inspire the next chapter of faith, family, and finding God in the fire.”Important Episode Timestamps 00:00:42 – 01:39 | How Hard SeasonWe love feedback, but can't reply without your email address. Message us your thoughts and contact info!Connect with Us: Ted Lowe on LinkedIn Bobby Lewis on LinkedIn BJ Foster on LinkedIn Subscribe on Apple Podcasts Get All Pro Dad merch! EXTRAS: Follow us: Instagram | Facebook | X (Twitter)Join 200,000+ other dads by subscribing to the All Pro Dad Play of the Day. Get daily fatherhood ideas, insight, and inspiration straight to your inbox.This episode's blog can also be viewed here on AllProDad.com. Like the All Pro Dad gear and mugs? Get your own in the All Pro Dad store.Get great content for moms at iMOM.com

Sam Stockill is a Community Relationship Manager with The Leprosy Mission. On today's programme he tells tragically true stories that explain the challenges faced by the charity that's been working for the last 150 years to eradicate this treatable disease that continues to wreck lives. And there's music - plus a thought for the start of Lent, and another packed notice board.

In this episode of the Clinical Research Coach, I sit down with Ella Balasa, a cystic fibrosis patient advocate whose lived experience is shaping how our industry understands trust, transparency, and meaningful patient engagement.Diagnosed in infancy with cystic fibrosis, a progressive genetic lung disease, Ella has spent her life navigating hospital systems, breakthrough therapies, and clinical trials — not as an abstract participant, but as someone whose health and future depend on research progress. Along the way, she has become a powerful voice for improving how industry partners with patients.In this conversation, Ella shares what sponsors, sites, and biotech leaders often overlook:* Patient experience is never one-size-fits-all — even within the same diagnosis.* Patients learn about trials through trusted networks, not just databases or digital ads.* Transparency builds confidence and drives long-term participation in research.* Dropout affects more than timelines — it influences trust and future enrollment decisions.* Technology should support patients, but never replace human connection.Ella's perspective challenges us to think beyond enrollment metrics and toward something deeper: relational trust. Because sustainable progress in clinical research depends on listening to patients as individuals, partners, and experts in their own lives.To learn more about Ella:Https:/ellabalasa.com

Noah May joins Rich Bennett for one of the most honest conversations yet about mental health, resilience, and survival.Diagnosed with clinical depression at 14 and anxiety at 18, Noah shares how his symptoms escalated into severe nausea, dramatic weight loss, and daily fear that left him physically shaken. As a member of the Class of 2020, he also faced the emotional toll of graduating during the COVID pandemic, followed by six months of long COVID symptoms.But this story is not about defeat. It's about breakthrough.Noah opens up about finally finding the right medication, rebuilding his confidence, earning a journalism degree from Auburn University, and launching the Lethal Venom Podcast to help others speak their truth.If you or someone you know struggles with anxiety or depression, this episode offers hope, perspective, and encouragement to never fight alone.Send a textVote for us here 10% off All MembershipsRuntime: 2/10/2026 until 2/28/2026Code: CRBPodcast This discount is valid only for memberships purchased February 10, 2026 until February 28, 2026. It cannot be applied retroactively to previous purchases and may not be combined with any other discount or promotion. All memberships purchased are nonrefundable.Maryland PickersFamily Owned & Operated - Maryland Pickers Junk Removal & Hauling - Serving Harford & Baltimore CouDisclaimer: This post contains affiliate links. If you make a purchase, I may receive a commission at no extra cost to you.Support the showRate & Review on Apple Podcasts Follow the Conversations with Rich Bennett podcast on Social Media:Facebook – Conversations with Rich Bennett Facebook Group (Join the conversation) – Conversations with Rich Bennett podcast group | FacebookTwitter – Conversations with Rich Bennett Instagram – @conversationswithrichbennettTikTok – CWRB (@conversationsrichbennett) | TikTok Sponsors, Affiliates, and ways we pay the bills:Hosted on BuzzsproutSquadCast Subscribe by Email

Most dyslexic professionals grow up believing they're behind. Coach Willie Blake knows that story from the inside. Diagnosed in first grade, he spent years trying to hide, trying to catch up, and trying to be someone he wasn't. Eventually, he made a different choice — if he was going to live with dyslexia, he was going to lead with it.Today, Willie is the go‑to high‑performance coach for dyslexic entrepreneurs, creators, and career professionals who are ready to trade self‑doubt for confidence and overthinking for clarity. Through simple, practical frameworks like the 2% Rule and the GPS Goal Method, he helps people take real action even when they've felt “behind” their whole life.In this conversation, Willie brings the same mix of heart, humor, and lived experience that's made him a dynamic speaker on 500+ stages and the host of Light Beyond Limits. We talk about identity, momentum, and what actually helps dyslexic minds move forward. If you've ever felt different, stuck, or underestimated — this one will hit home.Willie Blake's Sites:Website: Willie Blake's WebsiteFacebook: https://www.facebook.com/WillieBlake.Light/YouTube Channel: https://www.youtube.com/@DyslexicAchieversHubInstagram: https://www.instagram.com/willieblake_light/LinkedIn: https://www.linkedin.com/in/willieblake-light/TikTok: https://www.tiktok.com/@willieblake_lightOTR Sites:Podcast Website: https://bobadleman.wixsite.com/otrmentalhealthPublic Square Community Ko-Fi.com/otrachieving Mail: OvertheRainbowbob@gmail.comFacebook: https://www.facebook.com/otrachievingmentalhealhfrInstagram: https://www.instagram.com/over_the_rainbow_achievingX: https://twitter.com/overtherain1bowYouTube Channel: https://www.youtube.com/channel/UChEYTddPDUaiZbFliit1r5QLinkedIn: https://www.linkedin.com/in/robert-adleman/This podcast uses the following third-party services for analysis: Podder - https://www.podderapp.com/privacy-policyPodtrac - https://analytics.podtrac.com/privacy-policy-gdrp

Listener note: We want to let listeners know that this episode includes discussion of trauma, suicidal ideation, and mental health crisis. Please listen in a way that feels supportive for you.In this episode, Catherine Asta is joined by Brian Haines for a deeply reflective conversation about the often-unseen mental health crises faced by late-diagnosed autistic adults, accumulated trauma, and the life-changing power of creativity - offering hope for anyone feeling unheard or misunderstood.Diagnosed as autistic at 61, Brian shares how his NHS diagnosis brought clarity to a lifetime of feeling “peculiar,” marginalised, and out of step with the social world. What followed was not relief, but a period of profound unravelling - burnout, mental health crisis, and standing, as he describes it, at the edge of the abyss.From that darkness, poetry emerged.Brian speaks openly about how writing became his emotional scaffolding when formal therapeutic support fell short - a way to structure overwhelming thoughts, process rage and loneliness, and give voice to what had long been hidden behind the mask. For someone who struggles with the spontaneity of social communication, poetry offers rhythm, certainty, and a space where his words can finally be heard, at his pace.Together they explore masking, marginalisation, suicidal ideation, autistic burnout, and the vulnerability of sharing creative work in a world that has not always felt safe. Brian reflects on isolation and the “crevasse” of autistic loneliness, and how creative expression - through poems such as Behind the Mask - has slowly built belonging, connection, and community.Brian also shares practical, gentle steps on how to begin your own creative journey, or support someone you care for, and why simply creating for yourself is enough to start. It's a powerful episode about voice, survival, and the courage to step out from behind the mask - a reminder that creativity can become both scaffold and bridge to belonging.Autism CentralSubscribe to our FREE newsletterExplore our FREE support - 1:1 sessions, group coaching, online events and resourcesConnect with Brian Instagram: @autistically61YouTube: ⁠https://m.youtube.com/@brianhaines7922⁠Connect with Catherine WebsiteInstagram Book

Ever notice how the most meaningful connections seem to happen "by accident"? They're not accidents. They're collisions you can engineer. James Eder—entrepreneur, coach, and author of The Collision Code—reveals the exact framework for creating serendipitous moments that change your business and life. His story: Built Student Beans to 200+ employees. Diagnosed with a heart condition. Told he might need a transplant. Instead of slowing down, he wrote a book, donating 100% of royalties to charity, and created a coaching practice serving entrepreneurs worldwide. The Collision Code breaks down to three elements: Permission - Give yourself permission to start conversations (or blame this podcast for making you do it) Confidence - Built through practice, not preparation Context - Create conversation starters through what you wear, carry, or say In our conversation on Get Yourself Optimized, James shares how he met his longest-running client (8+ years, £20,000+ engagement) by asking a stranger on the street, "Are you looking for a job?" because the man had a resume in his hand. Real connections. Real results. Real impact. The show notes, including the transcript and checklist to this episode, are at getyourselfoptimized.com/552.

Discover what's possible when understanding leads to acceptance. Have you ever wondered how ADHD and autism can affect family dynamics? Whether you're part of a neurodiverse family or know someone who is, you'll want to listen to this episode with Jheri South.  Jheri South is a behavioral coach and the mother of seven neurodivergent children, five being on the autism spectrum. Diagnosed with ADHD at age 40, Jheri specializes in coaching teens and parents to navigate ADHD, autism, parenting, and anxiety with mindset, strategy, and community. This episode is part one of our conversation, and we discuss: Jheri's journey of understanding her ADHD How her experience with her own neurodivergent children  shapes her coaching approach The importance of education and awareness in fighting the stigma surrounding autism and ADHD How societal misconceptions can make it hard for parents to accept their children's diagnoses Overlapping characteristics of ADHD and autism Why ADHD and Autism are underdiagnosed in females Mental health and suicidal ideation among neurodivergent adolescents To learn more about Jheri South and her work, please visit: IG @msjherisouth ----more---- We appreciate your time. If you enjoy this podcast and you'd like to support our mission, please take just a few seconds to share it with one person who you think will find value in it too. Follow us on Instagram: @autismpodcast Join our community on Mighty Networks: Global Autism Community Subscribe to our YouTube channel: Global Autism Project We would love to hear your feedback about the show. Please fill out this short survey to let us know your thoughts: Listener Survey

Tired of ADHD strategies that don't work? Here's what actually does. FREE training here: https://programs.tracyotsuka.com/signup_____Many neurodivergent women are not struggling because they lack ability. They struggle because the systems around them were never designed for how their brains actually work.In this episode, Tracy talks with Stephanie Ray, a neurodivergent lawyer, coach, and founder of Growthset Coaching. Diagnosed with ADHD in her early 30s, Stephanie spent years succeeding on the surface while quietly struggling with memorization, rigid study methods, and performance pressure in law school and legal practice.Once she understood how her brain learns best, she stopped forcing traditional systems and built visual, movement-based, and story-driven approaches that actually worked. Tracy and Stephanie break down why standard study advice often fails ADHD learners and what makes information stick instead.They also cover imposter syndrome, accommodations, time blindness, and task initiation, along with practical strategies for studying, exam prep, and managing demanding careers. If you feel smart but still behind, this episode will help you see why and what to change.Resources: Website: https://www.growthsetcoaching.com Linkedin: https://www.linkedin.com/in/stephanie-didomizio-ray-esq-75157347 Send a Message: Your Name | Email | Message If this podcast helps you understand your ADHD brain, Shift helps you train it. Practice mindset work in just 10 minutes a day. Learn more at tracyotsuka.com/shift Instead of Struggling to figure out what to do next? ADHD isn't a productivity problem. It's an identity problem. That's why most strategies don't stick—they weren't designed for how your brain actually works. Your ADHD Brain is A-OK Academy is different. It's a patented, science-backed coaching program that helps you stop fighting your brain and start building a life that fits.

Last week in Part 1, I shared the story of being diagnosed with metastatic (stage 4) breast cancer at just 26 years old — the shock, fear, and life-altering moment that changed everything.In Part 2, I talk about what came next.After living with metastatic disease for 27 years, my perspective on life, time, fear, and what truly matters has shifted in ways I never expected.This episode is about:• learning to live fully inside uncertainty• letting go of waiting for life to feel safe• naming the hard stuff without being consumed by it• and discovering meaning alongside ongoing treatmentIt's not about staying positive.It's about staying present.If you're living with cancer, loving someone who is, or navigating a season of life that feels uncertain or heavy, I hope this conversation reminds you that life can still be meaningful — even here.Available Now!

A baby boy was born in a Carl’s Jr. parking lot after his parents didn’t make it to the hospital on time. AND Diagnosed with bone cancer, a young soldier reunites with the dog he loved overseas. To see videos and photos referenced in this episode, visit GodUpdates! https://www.godtube.com/blog/born-at-carls-jr.html https://www.godtube.com/blog/soldier-reunites-with-dog.html Discover more Christian podcasts at lifeaudio.com and inquire about advertising opportunities at lifeaudio.com/contact-us.

On this episode I talk about Ross The Boss from the Dictators and Manowar (among others) being diagnosed with ALS, also known as Lou Gehrig's Disease. Also on the show, emails about some new music and Alice Cooper. We do a Listening With Butler on the new Roger Taylor song. Music by: The Dictators Manowar Alice Cooper The Outfit Joyce Manor Donate to the show – Rock and Roll Geek Friends And Family Membership Donate on Venmo Dan Gerawan. -$50 Tim Schall – $50 John Morgan – $25 Richard Fusey – $20 Gregg Brofer – $20 Blake Johnston – $20 Richard Fusey – $16.66 Todd Cunningham – $10 Steven Cohen – $5 Bruce McMillan – $3 (Venmo donation id is @Michael-Butler-11) PATREON DONORS Joe Pawlak – $16.66 Kirk Crawford – $12.77 Patrick Shanahan – $10 Cole Thornton – $9.99 Brian Springer – $8 Jon Scott – $8 Michael Stitik – $8 Michael Street – $7.50 Dave Slusher – $5.55 Robert Harvey – $5 Chiaki Hinohara – $5 MedakiMetal on Instagram Jamie Jefford – $5 Erik Klein – $5 Paul Smith – $5 Justin Lefkowitz – $5 Steve Trice – $5 James Shapiro – $5 Martin Clawley – $5 Nadi Itani – $5 Eric Stowell – $4 Mike Hellyer – 4 pounds Mark Mazzel – $3 Dan McBride – $3 Adrian Boschan – $2 Amelia Bowen – $2 RnR Pleeb – $1.42 3Legs4wheels – $1 Arne Stach – $1 Paypal Donors Michael Cranston – $100 Richard Strom – $20 Dave Franco – $20 Steven Laperriere – $20 William Bealle – $10 Bradley Lisko – $10 Ralph Miller – $10 Jason Separd – $10 School of Podcasting – $10 Jeff and Cheri Thieleke – $10 Peter Spark – $5 John Ofenloch – $5 Jayce Lesniewski – $5 Christopher Del Grande – $5 Andrew Howe – $5 Benjamin Mueller – $5 Jon Tennis – $5 Gregg Long – $5 Rachel Rosenberg – $5 Deborah Dreyfus – $2 Brian Grattidge – $2 Kai Matsuda – $2 William Moffett – $2 Lasse Satvethagen – $2 Chad Kifffmeyer – $2 Dave Alexander – $2 Adam Bruscha – $2 Adam Croft – $2The post Ross The Boss Diagnosed With ALS first appeared on The Rock and Roll Geek Show.

Dr Judith Mohring is a Cambridge educated psychiatrist who specialises in ADHD. She's here to guide you through the 5 stages of processing a late ADHD diagnosis. Chapters: 00:00 Trailer  03:33 The hardest part of a late ADHD diagnosis  04:34 Grief 06:44 Resentment  13:38 Relief  15:08 Unmasking realisations  18:49 Complex diagnosis emotions  20:27 Tiimo advert  21:29 Late diagnosis regression  23:53 How to unlearn ‘normal' 37:21 Personal growth after a diagnosis  39:19 Most popular audience questions  42:49 Judith's ADHD item Visit Dr Judith Mohring's website

Zandra Rhodes is a true British original, as integral to the creative iconography of British culture as Bowie, Ab Fab and the Spice Girls; an independent fashion designer who kick-started her career as a student on the Pop Art scene with David Hockney in London the 1960s; who built a successful global fashion empire in the 70s and 80s beloved by Jackie Kennedy, Freddie Mercury, Diana Ross, Princess Diana and Cher; and who, in the face of dwindling popularity in the 90s when her exuberant prints were no match for the grunge and minimalism trends of the era, pivoted to launch the Fashion and Textile Museum and designing costumes for the opera. The through line to all of this has been her innovative use of sketch and pattern as a founding block of her design; a love of travel and a delight in absorbing the world around her into her work; and her deep-rooted friendships with the likes of artists Andrew Logan, David Sassoon and Duggie Fields. Diagnosed with cancer in 2020, the electric-pink haired  Dame Zandra has defied the grim diagnosis and remains as exuberant and erudite as ever, quick to throw out a throaty chuckle and share a salty anecdote with her trademark gregariousness. As The Holburne Musuem in Bath, England, stages a retrospective of her famous prints, the 85-year old takes a moment out of her jam-packed schedule to talk to Danielle Radojcin about just what it is that makes her keep on keeping on…

Maithili Shah was told by one surgeon that her then 6 month old Agastya who was diagnosed with Medulloblastoma in July of 2023, would most likely not survive 4 more months. Thankfully, Matihili and her husband made a change in surgeon's, Agastya's Brain Tumor was totally resected, and now, over 2 1/2 years later , Agastya is doing well physically as he continues to make progress from this Pediatric Brain Cancer. 

Getting diagnosed with cancer make you more likely to commit crimes HR 4 full 2515 Mon, 09 Feb 2026 19:26:26 +0000 cMwSro49s1OvOYnyDvwoDOjtRln1EKoj news MIDDAY with JAYME & WIER news Getting diagnosed with cancer make you more likely to commit crimes HR 4 From local news & politics, to what's trending, sports & personal stories...MIDDAY with JAYME & WIER will get you through the middle of your day! © 2025 Audacy, Inc. News False https://player.amper

In this episode of It Takes Balls, Brian Carlson shares his powerful and rare experience of being diagnosed with testicular cancer twice, nearly a decade apart — first with an aggressive non-seminoma germ cell tumor, and later with seminoma affecting his remaining testicle. Diagnosed in his mid-20s the first time, Brian walks through how subtle pain led to rapid imaging, orchiectomy, and three cycles of BEP chemotherapy, followed by years of surveillance and recovery.Brian then speaks on the physical and mental toll of treatment, including the realities of chemotherapy side effects, trauma-related memory gaps, hearing loss, and long-term survivorship challenges. Brian opens up about navigating work, marriage, and mental health during treatment, as well as the shock of discovering a second testicular cancer diagnosis years later — this time during a period of major life upheaval that included separation, a new job, and relocation.Brian also offers an honest look at life after bilateral orchiectomy, including the challenges of low testosterone, delays in testosterone replacement therapy, mood changes, and learning to advocate for himself medically. He explains how testosterone replacement ultimately may have helped normalize tumor markers. The episode closes with Brian's reflections on survivorship, the importance of community, and why speaking openly about testicular cancer, men's mental health, and self-advocacy can make a life-saving difference.Provide your feedback on the podcast:https://www.testicularcancerawarenessfoundation.org/itbsurveyJoin The Ball Room:https://www.testicularcancerawarenessfoundation.org/theballroomWant to be a guest? Apply here:https://www.testicularcancerawarenessfoundation.org/it-takes-balls-submissionsFollow Testicular Cancer Awareness Foundation:⁠https://www.testescancer.orghttps://www.x.com/testescancer⁠⁠https://www.instagram.com/testescancerhttps://www.facebook.com/tca.orgFollow Steven Crocker:https://www.instagram.com/stevencrockerhttps://www.facebook.com/steven.crocker2Connect with Brian:https://www.instagram.com/briangetsbackupTheme song: No Time Like Now - Tom Willner www.tomwillner.com

In this episode of The Heart of Innovation, cohosts Kym McNicholas and Dr. John Phillips feature multiple patients courageously sharing their lived experiences with Peripheral Artery Disease, including rare and often misunderstood cases that challenge what patients are told is "possible." Pamela's story highlights a critical gap in PAD care. After being told by a large hospital system that amputation was inevitable, she reached out to the Global PAD Association's Leg Saver Hotline. Through patient advocacy and care coordination, the underlying contributors to her disease were identified, including the role climate played in worsening her symptoms. Her decision to relocate to a warmer environment helped stabilize her condition and avoid limb loss, proving that earlier intervention and individualized care matter. Francine's journey offers another rare perspective. Diagnosed at just 48 despite being a runner, personal trainer, and fitness instructor, she was found to have a full occlusion in her left leg and intermittent blockages in her right. After undergoing a femoral-popliteal bypass, multiple stents, and angioplasty procedures, Francine transformed her lifestyle through the Dean Ornish program and a low-fat vegan diet. She has since completed four half marathons and continues teaching group fitness, yoga, and Reiki. Theresa's story exposes how often PAD is dismissed, even when the warning signs are clear. With a family history of PAD, Theresa recognized the symptoms early. At 46, she sought help after developing walking pain, only to be told repeatedly that it was a back problem and that she was "too young" to have PAD. A Doppler study was performed but interpreted as normal. For five years, as her symptoms worsened and her walking distance shrank to less than ten metres, she continued to advocate for herself before finally insisting on a vascular referral. Within minutes of meeting a vascular consultant, Theresa was diagnosed with severe PAD. Imaging revealed a 100 percent blockage in her right leg and 80 percent in her left. Angioplasty provided temporary relief, but restenosis occurred quickly. A second procedure resulted in arterial injury, requiring placement of a 30-centimetre stent in her right thigh. Despite ongoing pain, Theresa developed remarkable collateral circulation, so robust that it complicated intervention attempts. Today, she remains closely monitored by a responsive vascular specialist and manages her condition with vigilance, pacing, and rest. She also notes a meaningful improvement in walking pain after starting Wegovy, an observation she continues to discuss with her care team. Equally important, Theresa speaks candidly about the emotional toll of PAD. A special education teacher who loves to travel, she feared the disease would take away the life she loved, as it had for her father. After a period of isolation, she made a conscious decision that PAD would be part of her story, but not the author of it. She now works full time, travels when she can, adapts when needed, and lives by a powerful truth: she controls PAD, not the other way around. Together, these stories reinforce a message too many patients never hear in time: Leg pain, cramping, and difficulty walking are not normal aging. They are warnings.

Both of this week's stories come from Chan Zuckerberg Initiative's Rare As One Project grantees, who share their deeply personal experiences with rare diseases and illustrate how research is so essential in the search for better treatments and cures. (For more stories like these, you can also check out our previous episode The Story Collider produced with Rare As One in 2019, 2021, 2023, and 2024, as well as our Rare Disease playlist.)Part 1: After multiple relapses, Carlos Guerrero-Anderson takes a chance on an experimental treatment for his rare cancer. Part 2: Angie Weaver holds onto an unshakable belief that her daughter, who has a rare SCN2A disorder, will beat the odds. Carlos Guerrero-Anderson is an executive leader and patient advocate committed to amplifying the voices of Hairy Cell Leukemia and rare disease communities. Diagnosed with a rare blood cancer at age 25, Carlos transformed his personal journey into a lifelong mission to advance equity and create inclusive spaces for patients and families. He currently serves as the Director of Multicultural Engagement & Insights at the Hairy Cell Leukemia Foundation, supporting patients through education, outreach to underrepresented communities, data analysis, program promotion, and the sharing of diverse patient stories. With over 20 years of experience in healthcare insights and data-driven communications, Carlos combines strategic expertise with a lived perspective to create and lead culturally responsive programs that strengthen trust, amplify patient voices, and deliver measurable impact across diverse communities. He is an active member of several national patient advocacy groups, and his work has been featured at national conferences, most recently at the NORD Rare Disease Summit 2025. Carlos believes that storytelling is one of the most powerful tools for breaking barriers, building trust, and ensuring that no patient has to fight alone. Angie Weaver is the Director of Philanthropy and Development for the FamilieSCN2A Foundation, whose mission is to accelerate research, build community, and advocate to improve the lives of those affected by SCN2A-related disorders around the world. After her daughter Amelia was diagnosed with SCN2A, Angie became a passionate advocate for rare disease families—sharing her story to advance research, policy change, and awareness. She lives in northern Minnesota with her husband, Josh, and their youngest daughter, Penelope.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Send me a DM here (it doesn't let me respond), OR email me: imagineabetterworld2020@gmail.comToday I'm thrilled to have back on the show for a second time: MK ULTRA and Project Stargate survivor and whistleblower, targeted individual, filmmaker, podcaster, musician, athlete and former Virginia Tech all-American running back, entrepreneur, mental health advocate, and hometown hero from the Blue Ridge Mountains of VA: Tommy Edwards aka: Touchdown Tommy!A little bit about Tommy if you are new here, if you missed his debut on ‘The Imagination', or if you need a quick recap: Born in February 1974 in Radford, Virginia - a historic town cradled by one of the world's oldest rivers - Tommy entered a world shadowed by grief yet illuminated by legacy. His father, Ken Edwards, a Virginia Tech Hall of Famer who wore jersey #33 and was drafted by the Buffalo Bills, carried the weight of family tragedies that shaped a dynasty of determination. Tommy, inheriting that same number and spirit, would become a beacon for thousands.As a boy, Tommy faced challenges - dyslexia, feeling like an outsider, family struggles - but he discovered fire on the field. At Radford High School, he exploded as a consensus All-American running back and first-team All-State linebacker. In his junior and senior years alone, he rushed for nearly 4,000 yards and scored an astonishing 57 touchdowns - a record that still echoes through the valleys. Recruited by powerhouses, he chose Virginia Tech in 1992, following his father's footsteps.In 1993, as a redshirt freshman, Touchdown Tommy burst onto the national stage. He scored 10 touchdowns (including four in a single game against Pittsburgh), led the nation in scoring for six weeks, and helped propel the Hokies to a top-15 finish and a bowl victory. He and his father became the first father-son duo in NCAA history to score rushing touchdowns in bowl games - a legacy of grit and glory. Headlines screamed his name; fans chanted "Touchdown Tommy"; the program ascended from mediocrity to dominance, setting the foundation for future championships.Tommy's story deepened into a profound journey of awakening. Repressed memories surfaced of childhood encounters with Project Stargate, MK ULTRA, and lifelong targeting as a gifted "star child." He endured gangstalking, electronic harassment, false hospitalizations, and a terrifying SWAT standoff - yet he emerged stronger, speaking truth against corruption, exploitation in sports, and hidden programs. Diagnosed with advanced CTE symptoms (brain scans showing severe damage that should have left him institutionalized), he battles daily with severe symptomology, but his spirit remains unshakeable. CONNECT WITH TOMMY:YouTube: @tommyedwards7062Twitter: https://twitter.com/TommyEdwardsTo1Instagram: https://www.instagram.com/touchdowntommyedwards/Facebook: https://www.facebook.com/tommytouchdowntommyedwardsSnapchat: t_edwards7802Cashapp: $DrGonzobingbongCONNECT WITH EMMA:YouTube: https://www.youtube.com/@imaginationpodcastofficialRumble: https://rumble.com/c/TheImaginationPodcastEMAIL: imagineabetterworld2020@gmail.com OR standbysurvivors@protonmail.comMy Substack: https://emmakatherine.substack.com/BUY ME A COFFEE: https://www.buymeacoffee.com/theimaginationVESupport the show

“Eating people is like eating pears.”Dorángel Vargas—known in Venezuela as El Comegente (“The People Eater”)—is one of the most disturbing figures in modern true crime. A homeless man living beneath bridges in the Andean state of Táchira, Vargas confessed to killing and eating multiple men during the late 1990s.But this episode of The A-Z Of Psychopaths asks a question that most true crime podcasts avoid:Was Dorángel Vargas actually a psychopath? Diagnosed with paranoid schizophrenia, Vargas presents a serious challenge to simplistic labels. Using the Hare Psychopathy Checklist (PCL-R) as a clinical framework, this episode examines his behaviour, motives, and mental state—carefully distinguishing psychopathy from severe mental illness.This is not a sensational account of cannibalism. It is a forensic and psychological analysis of where diagnosis, responsibility, and danger intersect—and why misclassifying offenders matters. Hosted by Simon Ford, The A-Z of Psychopaths explores one case per episode, questioning myths around serial killers, violence, and psychopathy through evidence-based analysis.Listener discretion advised.Become a supporter of this podcast: https://www.spreaker.com/podcast/psycho-killer-shocking-true-crime-stories--5005712/support.

On this episode of the Project Purple Podcast, host Dino Verrelli sits down with Andy Lyons, a commercial photographer from the heart of the Midwest, Iowa, as he shares his deeply personal journey with familial pancreatic cancer. With a family history spanning three generations, affecting countless family members, including his grandmother, mother, and brother, Andy has long felt the shadow of this disease. Diagnosed in 2021 after over two decades of proactive screenings, including ultrasound endoscopies and genetic testing through research studies in Chicago and Pittsburgh, Andy was fortunate to catch his pancreatic cancer early. He reflects on the importance of vigilance and early detection, and how his experience demonstrates the power of knowledge, community, and persistence in managing a disease often considered a death sentence, even when it runs in your family. Andy shares the emotional and practical aspects of his journey: robotic surgery at UPMC, chemotherapy, the support of caregivers and his community, and the mental resilience that comes from maintaining humor, positivity, and hope. He emphasizes the importance of asking questions, connecting with other patients, and taking control of your health, summarized in the motto: “knowledge is power.” Through his story, Andy shows that pancreatic cancer is scary, but it's not invincible. He talks about the strength found in numbers, the hope that comes from proactive care, and even the symbolic meaning of a survivor tattoo and a healing blanket passed among friends as a gesture of solidarity. You can reach Andy at andyboylyons@gmail.com. Subscribe to the Project Purple Podcast for more stories from the pancreatic cancer community. To learn more or support Project Purple's mission of a world without pancreatic cancer, visit projectpurple.org.

In this powerful testimony, a man raised in comfort confronts eternity, loss, and a call that redirects his life from law to ministry. Through brushes with death, miraculous healing, grief, and unexpected restoration, he reveals how Jesus met him at every crossroads and shaped his “yes.” This is a story of surrender, suffering, and hope that invites you to consider what God might do if you give Him your own yes.Thank you for watching and supporting our ministry. Our entire mission consists of continuing to record and share these incredible testimonies, but we can't do it without your help. Please consider donating to support this crowd-funded project: https://www.missiondelafe.org/give Listen on Podcast Spotify Podcast ⇨ https://spoti.fi/3RBKdq3Apple Podcast ⇨ https://apple.co/3evzCuuConnect with ushttps://www.facebook.com/delafetestimonieshttps://www.instagram.com/delafetestimonies/Connect With Dr. Stephen PowersWebsite ⇨ https://freedomjax.org/ Credits:Testimony by Stephen PowersDirected by Darvin RamirezInterviewed by Eric VillatoroEdited By Josh Gayle & Darvin RamirezAudio Mixed by Paul Nicholas Testimony Recorded In Jacksonville, FL00:00 Introduction00:30 Knowing I Was Made for More04:09 Giving My Life to Jesus07:32 Leaving Law School to Pursue Ministry Full Time11:43 God Uses Me to Heal the Sick13:40 My First Wife is Diagnosed with Cancer15:36 Preaching the Gospel in Various Places 20:49 Losing My First Wife to Cancer24:44 Meeting and Marrying My Current Wife29:36 Give Jesus Your Yes!32:13 Prayer33:45 Who is Jesus to You?34:56 Final WordsDelafé Testimonies is a global evangelistic project with the mission of creating the world's largest archive of Jesus testimonies until His return.Stephen Powers Testimony

Stacy Scarcella, a former corporate executive, transitioned to a creative entrepreneur after 13 years in fashion, advertising, and technology. Diagnosed with Marfan Syndrome at 25, she faced significant challenges, including legal blindness and potential infertility. Despite a grim prognosis, Stacy pursued self-care, research, and adaptive activities like Zumba and yoga. She emphasized the importance of self-advocacy and resilience. Stacy also works in mental health advocacy, particularly for adolescents, highlighting the need for early intervention and support. Her journey underscores the value of creativity, freedom, and positivity in overcoming health challenges. For the transcript and full story go to: https://www.drmanonbolliger.com/stacy-scarcella    Highlights from today's episode include:  Be your own health advocate and move one step at a time: When she was diagnosed with Marfan Syndrome at 25 with a very grim prognosis, Stacy chose not to stay stuck in fear. She did her own research, sought multiple opinions, adjusted her lifestyle, and focused on "What can I do right now and one minute forward?" rather than catastrophizing the future. Create freedom and possibility by redefining your path: Leaving a "boxed-in" corporate career, Stacy built Plaid Pony Productions around freedom: choosing diverse projects, not being tied to one creative partner, and continually pivoting (Zumba, yoga, events, mental health advocacy). Her core mindset  Bedside manner and medical 'fashion' can shape a patient's fate:  Manon highlights how the way a diagnosis is delivered can deeply harm or help a patient. She compares it to her own experience of being told she "needed" a C‑section because of narrow hips, only to safely have a home vaginal birth after seeking many opinions. She stresses that practitioners must be conscious of their language and the current "fashion" in medicine, because patients often meet a diagnosis first as doom and gloom, with very little visible information about alternatives, self-care, and hopeful possibilities.   ABOUT STACY SCARSELLA: For more than two decades, Stacy Scarsella has built a career defined by vision, resilience, and reinvention. A former corporate executive turned creative entrepreneur, Stacy spent over 15 years climbing the ranks in fashion, advertising, and technology working with industry giants such as Armani, Macy's, Talbots, TJX Companies, and Bose. Her career trajectory pointed toward becoming a CMO, but the demands of corporate life, constant travel, long hours, and lack of fulfillment sparked a personal reckoning. In 2015, following a season marked by profound loss and transformation, Stacy traded boardrooms for the beaches of Los Angeles, where a moment of clarity reshaped her entire future. That clarity became Plaid Pony Productions, a full-service production company known for its storytelling integrity, cinematic creativity, and world-class brand activations. From major commercial campaigns to experiential events, Stacy leads her team in producing standout work for global names including Disney, AT&T, and other Fortune 500 companies. Known for her strategic foresight and innate ability to forecast industry shifts, she's built a business that blends artistry with operational precision delivering results that can't be replicated by automation or artificial intelligence. But Stacy's story runs deeper than her professional accomplishments. Diagnosed with Marfan Syndrome at 25 and told she might never have children or live past 40, she defied every prediction. Today, at 43, she's a mother of two, a mentor, and a passionate advocate for mental health awareness and suicide prevention causes close to her heart following the loss of her best friend. Her philosophy, "Why not?", defines her approach to both business and life: embracing creativity, curiosity, and courage in the face of uncertainty. Beyond the studio, Stacy is a creative force in every sense an artist, yoga enthusiast, avid gardener, and dual citizen of Italy who finds joy in simple rituals like family dinners and dancing in the kitchen. Through speaking, consulting, and community initiatives, she now helps others humanize their brands in the age of AI, teaching entrepreneurs how to connect authentically and lead with purpose. Her work, both on and off the set, is a testament to her greatest belief: that success is not about control it's about creating a life that feels deeply alive. Core purpose/passion: My philosophy is: "Why not?", and it defines my approach to both business and life: embracing creativity, curiosity, and courage in the face of uncertainty. –  Facebook  |  Website | LinkedIn | Instagram - Stacy | Instagram - PladPony ABOUT MANON BOLLIGER, RBHT, FCAH: As a retired Naturopath 1992-2021, I saw an average of 150 patients per week and have helped people ranging from rural farmers in Nova Scotia to stressed out CEOs in Toronto to tri-athletes here in Vancouver. My resolve to educate, empower and engage people to take charge of their own health is evident in my best-selling books:  'What Patients Don't Say if Doctors Don't Ask: The Mindful Patient-Doctor Relationship' and 'A Healer in Every Household: Simple Solutions for Stress'. and What if Your Body is Smarter than You Think?  I am the Founder & CEO of The Bowen College Inc. which teaches BowenFirst™ Therapy and holds transformational workshops to achieve these goals. So, when I share with you that LISTENing to Your body is a game changer in the healing process, I am speaking from expertise and direct experience". Mission: A Healer in Every Household! For more great information to go to her weekly blog:  http://bowencollege.com/blog.  For tips on health & healing go to: https://www.drmanonbolliger.com/tips Follow: Manon Bolliger website  | Linktr.ee | Rumble | Gettr  | Facebook | Instagram | YouTube | Twitter | LinkedIn | Follow: Bowen College Inc. | Facebook | Instagram  | LinkedIn | YouTube | Twitter | Rumble | Locals ABOUT THE HEALERS CAFE: Manon's show is the #1 show for medical practitioners and holistic healers to have heart to heart conversations about their day to day lives. Subscribe and review on your favourite platform: iTunes | Google Play | Spotify | Libsyn | iHeartRadio | Gaana | The Healers Cafe | Radio.com | Medioq | Audacy |   Follow The Healers Café on FB: https://www.facebook.com/thehealerscafe   Remember to subscribe if you like our videos. Click the bell if you want to be one of the first people notified of a new release. * De-Registered, revoked & retired naturopathic physician after 30 years of practice in healthcare. Now resourceful & resolved to share with you all the tools to take care of your health & vitality!  

At 26 years old, I was diagnosed with metastatic (stage 4) breast cancer — a moment that changed everything in an instant.In Part 1 of my story, I share what led up to my diagnosis, the shock of hearing the words “stage four,” and what those early days of fear, uncertainty, and life-altering decisions were really like.This isn't a clinical cancer story.It's the human side — the emotions, the questions, the grief, and the beginning of learning how to live inside a life I never planned for.If you're newly diagnosed, supporting someone you love, or walking through something that feels overwhelming, this episode is for you.Part 2 will dive into how those early experiences shaped the way I live fully with metastatic disease today.Available Now!

In this inspiring and deeply human episode of Talking Wit' Kevin & Son Kevin sits down with Dr. Deep I. Shah pediatric dentist, educator, entrepreneur, and survivor whose life journey proves that healing can become a mission and compassion can change destinies.Diagnosed with acute lymphoblastic leukemia as a child, Dr. Deep's early experiences with fear, care, and resilience planted the seeds for a lifelong calling. Today, as Founder & CEO of Sidekick Smiles Pediatric Dentistry, he helps children feel safe, empowered, and confident — reminding them that they are the superheroes of their own story.With heart, humility, and purpose, Dr. Deep shares how adversity shaped his leadership, why emotional safety is essential in healthcare, and how standing beside others not above them creates lasting impact. This conversation blends storytelling, service, and faith-driven insight into a powerful reminder that purpose is often born in the places that once tried to break us.This episode invites parents, educators, leaders, and caregivers to rethink success, redefine strength, and lead with empathy.

New research from the Canadian Medical Association Journal has found that more people aged 14-20 are being diagnosed with psychotic disorders, including schizophrenia, than previous generations. We talk to study co-author Dr. Marco Solmi about his findings, and some of the possible reasons behind it. Plus, psychiatrist Dr. Oyedeji Ayonrinde on why early intervention matters, and why cannabis use can't be ignored as a potential factor in this rise.

I never thought heart disease would be part of my story. At 42, in the best shape of my life, I was diagnosed with mitral valve prolapse and severe regurgitation. What started as a strange episode during a workout turned into months of fear, waiting, uncertainty, and eventually heart surgery. This is Part 1 of My Heart Story. In this episode of Anatomy of a Leader, I share what it was really like to be diagnosed with a heart condition at 42 — from early symptoms and medical tests to the emotional impact of living with uncertainty while raising young children and running a business. This is the beginning of a deeper series about fear, vulnerability, healing, and what happens when your body forces you to slow down and listen.This is not medical advice. This is my real story — shared in the hope that it helps someone feel less alone, recognise symptoms earlier, or feel brave enough to get checked.In this episode I talk about: – Mitral valve prolapse diagnosis – Heart palpitations and symptoms – ECG and echocardiogram experience – Waiting for cardiology appointments – Anxiety and fear after diagnosis – Exercising with a heart condition – Women's heart health being underdiagnosed – Why “being strong” can make illness lonelier00:00 Thought Heart Disease Was an Old Man's Problem00:51 I Was Physically Fit & Healthy01:20 The Workout That Changed Everything01:56 Why I Nearly Ignored The Symptoms03:14 Going To The GP03:45 ECG Referral & Experience06:11 Echo Referral & Experience 09:03 Hearing “Mitral Valve Prolapse”09:50 Waiting, Fear & Not Knowing13:00 Anxiety vs Heart Condition13:23 Tachycardia, A&E & Health System14:21 Symptoms of Mitral Valve Prolapse 16:12 Exercise Regularly & Monitor17:49 Exercising With A Heart Condition18:39 Loss Of Control & Trust20:38 Women's Heart Health Being Missed23:10 What I Wish I'd Known25:15 If You're Ignoring Symptoms — Please ListenFollow Maria Hvorostovsky:IG: https://www.instagram.com/anatomyofaleader/IG: https://www.instagram.com/mariahvorostovsky/LinkedIn: https://www.linkedin.com/in/mariahvo/TikTok: https://www.tiktok.com/@mariahvorostovsky/Website: https://www.anatomyofaleader.com/Artwork and video by https://www.londonbeautyphotographer.com/If you're living with a heart condition, supporting someone who is, or ignoring symptoms because life feels too busy — this episode is for you.

4 year old Ava Blazis woke up on the morning of March 11th 2023 with a very unusual pain in her abdomen which continued to get worse as the day wore on. Her mother Angela brought her to UMass Memorial Medical Center and 3 days later on March 14th, she was diagnosed with Acute Lymphoblastic Leukemia. Angela and Ava then spent the next 65 days at Boston Children's Hospital while Ava was undergoing treatment. Meanwhile Angela's sister Johanna Annuziata got busy with helping to look after Ava's brother Michael, and also helping to start Team Ava, an unofficial Non-Profit, which has already raised over $300,000 to help in the cause of Pediatric Cancer. Ava is now 7 years old and is doing well physically as she has been in remission since May of 2025. 

Daelyn James, is someone who understands the power of owning your story. Diagnosed with cystic fibrosis at just four years old, she remembers what it felt like to go from a carefree childhood to one filled with treatments, doctor visits, and a reality she wasn't ready to face. For a long time, Daelyn kept her CF hidden because she was worried it would change how people saw her or limit what she could do.But in high school, everything shifted. Daelyn made the brave decision to stop running from her diagnosis and start embracing it as part of who she is. And that choice changed her life.Now 25, she proudly lives with CF and uses her experiences to raise awareness, connect with others, and offer hope. Her message is simple but powerful: even in the hardest moments, there is strength, there is goodness, and there is always a way forward.I'm so excited for you to hear her story.To connect with Daelyn visit her on IG: https://www.instagram.com/daelyn_j/To connect with Somer Love her IG is Love to Breath: https://www.instagram.com/lovetobreathe/ Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

In this beautifully hopeful episode, Wren, the creator of the Living Our Breast Lives Podcast, is joined by the incredible Metastatic Breast Cancer Thriver, Heather Jose, the MBC thriver living with triple positive metastatic breast cancer for 27 YEARS! Heather Jose is a long-term metastatic breast cancer thriver, advocate, and the host of the podcast I'm Still Here: Lessons from Life with Metastatic Breast Cancer. Diagnosed at 26 and living with metastatic disease for over 25 years, Heather focuses on honest, grounded conversations about what it means to live fully — not just survive — alongside breast cancer. After her diagnosis, Heather went on to adopt a child, redefining what building a family can look like after metastatic breast cancer and showing that life doesn't stop at a diagnosis, it evolves. She has spent decades navigating treatment, motherhood, advocacy, and survivorship, all while helping others feel less alone.Listen to this episode as it breaks down:Who is Heather Jose? – Meeting the woman behind the diagnosisHer MBC story – Diagnosed in 1998, her subtype, and how she's still here decades laterThen vs. now – What MBC treatment looked like then and how far it's comeStrength without the pressure – The moments that carried her through and why the term "inspirational" comes with a heavy weight to itLiving with grief and joy – Mourning the life imagined while fully living the one she hasMotherhood after MBC – Infertility, adoption, and expanding her family against the odds“I'm Still Here” – Why Heather launched her podcast and who it's forLong-term survivorship – What it really means and what she's still dreaming of for the future Living Our Breast Lives Information:Email: livingourbreastlivespodcast1@gmail.comInstagram: @livingourbreastlivesFounder: Wren MorrobelPersonal Instagram: @wren_morrPodcast Guest Speaker: Heather Jose's Information:Email: mail@heatherjose.comInstagram: @heatherbjoseFacebook: Heather JoseWebsite: www.heatherjose.comYouTube: I'm Still Here

Love the episode? Send us a text!What happens when you're diagnosed with stage 2B breast cancer, start a new job, and are asked to lead a COVID response—all at the same time?In this powerful episode of Breast Cancer Conversations, host Laura Carfang sits down with Samira Daswani, founder and CEO of Manta Cares, to talk about what it really means to navigate cancer when the system isn't built for you.Diagnosed at 30 and undergoing chemotherapy during the earliest days of the COVID-19 pandemic, Samira shares how she worked through treatment, wrestled with impossible decisions about hormone therapy, and struggled with the loss of control that so many cancer patients feel—but rarely name.Out of a sleepless night during chemo, Samira created a simple paper planner just to survive her own care. That tool would eventually become Manta Cares: a personalized, cancer-specific platform designed to give patients and care partners the thing most people never get—a map.In this candid, founder-to-founder conversation, Laura and Samira explore:Being diagnosed with breast cancer during COVIDWorking through chemo and surgery while leading critical healthcare programsDeciding whether to stay on hormone therapy—and living with that choiceWhy cancer care feels like being dropped into a hike without a mapHow patient-built tools can restore agency, clarity, and peace of mindThe emotional cost of fixing a system that failed youWhat's next for Manta Cares, including mobile tools and AI companionsThis episode is for anyone who has ever thought: There has to be a better way.Support the showLatest News: Become a Breast Cancer Conversations+ Member! Sign Up Now. Join our Mailing List - New content drops every Monday! Discover FREE programs, support groups, and resources! Enjoying our content? Please consider supporting our work.

In this meeting of The Late Diagnosis Club, Dr Angela Kingdon welcomes Abbey Thompson — a librarian, classically trained vocalist, prize-winning baker, gamer, social justice bard, and self-described random fact machine.Abbey is a fat, queer, neurodivergent woman living in Los Angeles with two orange cats and a deep commitment to creativity without perfection.Diagnosed with ADHD in her 40s and later recognising she was also Autistic, Abbey describes how finally naming her neurodivergence didn't just bring understanding — it brought permission. Permission to be loud, to be big, to be joyful, to be mediocre, and to exist without apology.Together, Angela and Abbey explore late identification, fatness and bullying, perfectionism, burnout, AuDHD, creativity as regulation, and the radical act of letting go of shame. This episode is an invitation to stop fixing yourself — and start living.

What happens after a working dog's service ends—and the real battle begins? In this powerful episode of The ToosDay Crüe, the hosts welcome Chris Bingham, federal law enforcement K9 handler and lifelong partner to K9 Tambo, a decorated retired working dog who spent years protecting people and property at the highest levels of government. After retirement, Tambo faced a new mission: survival. Diagnosed with aggressive cancer at age 11, Tambo's fight became a story of resilience, faith, and community. With the support of Project K9 Hero, life-saving treatment, and a growing national audience, Tambo continues to defy the odds—earning recognition from The Dogist and an upcoming honor at the Philadelphia Eagles Salute to Service game. This episode dives into the unbreakable bond between handler and K9, the realities of life after service for working dogs, and the lessons in loyalty, sacrifice, and perseverance that inspire thousands.

If you've just been diagnosed with cancer, here are the first five things I believe matter most—faith, support, nourishment, gentle movement, and clarity—shared from someone who's been there. All the links, tools & resources I personally share:https://linktr.ee/cfreecancerfree

Persistent colds and a chronic cough were followed by not being able to walk and being constantly tired for Marie Gulliver's 2 year old son Ezra in 2022. These symptoms were finally diagnosed as High Risk Acute Myeloid Leukemia, which was complicated by a genetic mutation and the always difficult Graft vs, Host Disease after Ezra received a successful Bone Marrow Transplant in September of 2022. Ezra has been cancer free for more than 3 years and has ony a 5 percent chance of a relapse which is great news for him and his family.

Diagnosed at three, Shane discusses growing up with T1D, navigating the college party scene, and his transition to adulthood. He covers alcohol, mental health, dating, and improving his A1C. Free Juicebox Community (non Facebook) Type 1 Diabetes Pro Tips - THE PODCAST Eversense CGM Medtronic Diabetes Tandem Mobi ** Use code JUICEBOX to save 40% at Cozy Earth  CONTOUR NextGen smart meter and CONTOUR DIABETES app Dexcom G7 Go tubeless with Omnipod 5 or Omnipod DASH * Get your supplies from US MED  or call 888-721-1514 Touched By Type 1 Take the T1DExchange survey Apple Podcasts> Subscribe to the podcast today! The podcast is available on Spotify, Google Play, iHeartRadio, Radio Public, Amazon Music and all Android devices The Juicebox Podcast is a free show, but if you'd like to support the podcast directly, you can make a gift here or buy me a coffee. Thank you! *The Pod has an IP28 rating for up to 25 feet for 60 minutes. The Omnipod 5 Controller is not waterproof.  ** t:slim X2 or Tandem Mobi w/ Control-IQ+ technology (7.9 or newer). RX ONLY. Indicated for patients with type 1 diabetes, 2 years and older. BOXED WARNING:Control-IQ+ technology should not be used by people under age 2, or who use less than 5 units of insulin/day, or who weigh less than 20 lbs. Safety info: tandemdiabetes.com/safetyinfo Disclaimer - Nothing you hear on the Juicebox Podcast or read on Arden's Day is intended as medical advice. You should always consult a physician before making changes to your health plan.  If the podcast has helped you to live better with type 1 please tell someone else how to find it!  

(00:00) Terry Pegula and Brandon Beane discuss the future of the Bills organization during a press conference yesterday…. It didn't go well.(17:24.31) RYAN JOHNSTON is the voice of the Boston Bruins on the 98.5 Sports Hub Bruins Radio Network and joins Toucher & Hardy to talk all things hockey!(29:48.83) BREAKING: Fred Diagnosed with sleep apnea, but refuses to do the CPAPPlease note: Timecodes may shift by a few minutes due to inserted ads. Because of copyright restrictions, portions—or entire segments—may not be included in the podcast.CONNECT WITH TOUCHER & HARDY: linktr.ee/ToucherandHardyFor the latest updates, visit the show page on 985thesportshub.com. Follow 98.5 The Sports Hub on Twitter, Facebook and Instagram. Watch the show every morning on YouTube, and subscribe to stay up-to-date with all the best moments from Boston's home for sports!See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

David Smith spent years working as a therapist specializing in neurodiversity-affirming care, but it wasn't until age 56, prompted by his wife and his own clients, that he sought his own autism diagnosis. That confirmation fundamentally shifted his clinical approach from that of a white-coated expert to a fellow traveler, deepening the way he accompanies families through unmapped territory. Today, Emily and David discuss the delicate balance between professional curiosity and humility, and why traditional therapeutic models often fail to support the fragile nervous systems of neurodivergent clients. They talk about the nuances of demand avoidance, specifically the high-masking, internalized presentation that often looks like perfectionism, and why "connection before correction" is a neurological necessity, not just a catchy phrase. TAKEAWAYS Effective therapy for neurodivergent clients often requires shifting away from the traditional expert hierarchy. The neurodivergent brain is a "complicated, custom-made car with no user's manual." For neurodivergent nervous systems, stress isn't just negative trauma; it includes any destabilizing experience, including excitement and joy. While we often associate PDA with external defiance, the internalized profile often manifests as high-achieving perfectionism. Rewards and consequences often backfire with neurodivergent children because they increase anxiety. It's ineffective to offer a correction to a child until you have connected with them. There is a massive overlap between complex trauma and neurodivergence. A late diagnosis doesn't instantly fix struggles; it initiates a complex grieving and reframing process. Join our live CE training, Adapting Cognitive-Behavioral Therapy for Autistic and ADHD Pediatric Clients, Friday morning, January 23, at 10:30 eastern/7:30 pacific, or get the recorded version anytime after. Get signed up or learn more here. David Smith, LCSW is a late-diagnosed autistic therapist and licensed clinical social worker specializing in neurodiversity-affirming care for autistic and otherwise neurodivergent individuals and their families. Practicing since 2017, David opened his private telehealth practice in 2023 and now serves clients across five states from his home in southern Oregon. In addition to therapy, he offers consultation, writing, education, and advocacy to expand access to effective, affirming support for the neurodivergent community. Diagnosed with autism in 2024 at age 56 (thanks in part to gentle nudges from his wife and clients) David continues to explore how his autistic identity shapes both his personal and professional life. His work is deeply rooted in curiosity, humility, and a commitment to learning from his clients and the broader neurodivergent community. He is also a devoted listener of this and other neurodivergence-focused podcasts. David lives with his wife, a fellow therapist originally from Peru, and is the proud father of three sons. BACKGROUND READING David's website, LinkedIn, authored articles The Neurodiversity Podcast is on Facebook, Instagram, BlueSky, and you're invited to join our Facebook Group. For more information go to www.NeurodiversityPodcast.com. If you'd like members of your organization, school district, or company to know more about the subjects discussed on our podcast, Emily Kircher-Morris provides keynote addresses, workshops, and training sessions worldwide, in-person or virtually. You can choose from a list of established presentations, or work with Emily to develop a custom talk to fit your unique situation. To learn more, visit our website.

What if the very challenge you think is holding you back is actually the thing meant to launch you into your purpose?In this deeply inspirational and motivational podcast episode, Reginald D sits down with A'Santianna Austin is a 20-year-old award-winning author, speaker, poet, youth advocate and 2027 Grammy Nominated Spoken Word Artist — for a powerful, life-affirming motivational speech conversation on identity, resilience, faith, and purpose.  Less than one year after graduating college, A'Santianna published her debut book, "Melanated, Not Black," a poetic exploration of identity, culture, and self-definition.  "Melanated, Not Black," is now being used in public, private and alternative schools as well as juvenile detention centers. A'Santianna has also toured nationally and performed at HBCU's and college events.  A'Santianna leads Project 500 to empower 500 youth through literacy, mentorship and identity.Diagnosed with severe epilepsy at just eight years old, A'Santianna turned adversity into impact through storytelling, advocacy, and service. This inspirational motivational episode explores how challenges don't disqualify you—they refine you—and how faith, self-belief, and action can motivate you to rise beyond limitations and live with purpose.Many people—especially young adults—feel limited by their health, background, identity, or circumstances. This inspirational and motivational speech-driven episode speaks directly to listeners who feel unseen, unheard, or underestimated. Through.Press play now to experience this inspirational and motivational speech conversation and walk away empowered to turn your pain into purpose and your story into impact.A'Santianna's  Instagram: https://www.instagram.com/asantiannanijeanPurchase A'Santianna's book on Amazon:Amazon.com: MELANATED NOT BLACK: 9798262452439: AUSTIN, ASANTIANSend us a textSupport the showFor daily motivation and inspiration, subscribe and follow Real Talk With Reginald D on social media:Instagram: realtalkwithreginaldd TikTok: @realtalkregd Youtube: @realtalkwithreginald Facebook: realtalkwithreginaldd Twitter Real Talk With Reginald D (@realtalkRegD) / TwitterWebsite: Real Talk With Reginald D https://www.realtalkwithreginaldd.com Real Talk With Reginald D - Merchandise

It's Wednesday, January 21st, A.D. 2026. This is The Worldview in 5 Minutes heard on 140 radio stations and at www.TheWorldview.com.  I'm Adam McManus. (Adam@TheWorldview.com) By Jonathan Clark and Adam McManus Nigerian Muslims kidnapped 160 people, many of whom are Christians Armed bandits raided three church services in Nigeria on Sunday. The suspected Fulani Muslim militants kidnapped over 160 people in Kaduna State. Morning Star News reports it could be the largest mass kidnapping of Christian farmers in the area. Rev. Joseph John Hayab is the chairman of the Christian Association of Nigeria for the country's north. He told media outlets, “The terrorists invaded the churches while worship services were on. They held the worshippers hostage and marched them out into the bushes.” An eyewitness told TruthNigeria, “It was around 10 a.m. on Sunday. I was in our Evangelical Church Winning All church when we suddenly heard gunshots everywhere.  The gunmen were shouting that everyone should lie  down or be killed.” In addition, he said some of the assailants wore black robes with black head turbans, and others were outfitted with “shabby-looking Nigerian Army camouflage uniforms.” The man and his 10-year-old son escaped through a window while the Muslim assailants were forcing the congregation out. Sadly, local police are acting as if nothing happened.  Psalm 14:4 asks, “Have all the workers of iniquity no knowledge, who eat up My people as they eat bread, and do not call on the LORD?” UK court: Men not allowed in female changing room A court in the United Kingdom ruled against a hospital's transgender policy last week. The landmark ruling said that Darlington Memorial Hospital discriminated against eight female nurses. The nurses simply objected to a man, pretending to be a woman, from using their changing room.  The Christian Legal Centre supported the nurses in the case. Andrea Williams, Chief Executive of the Christian Legal Centre, commented, “The [National Health System] and the government should now give up their sabotage of clear judicial decisions and abide by the law which acknowledges that men are men and women are women.” Britain tracks new Christian songs Britain's Official Charts Company is launching a new official singles chart for Christian music this month. AStepFWD, the organization behind the U.K. Christian Charts, has partnered with the Official Charts Company to introduce the Official Christian & Gospel Singles Chart. Christian Today reports the chart will “formally recognize the growing impact of faith-based music within the wider U.K. music landscape.” 10,000 Christians gather in France's March for Life Around 10,000 people gathered in Paris on Sunday for France's annual March for Life. AUDIO:  (Marchers chanting for life in French.) The event highlighted opposition to legislation that would legalize euthanasia and assisted suicide.  Listen to this testimony from a French marcher through a translator. POST-ABORTIVE WOMAN: “I had an abortion under circumstances where my fiancé forced me to do it so that we could get married, and it literally broke me. But God saved me. God healed me and helped me rebuild my life and turned the worst event of my life into a source of greater strength.” Marie-Lys Pellissier is the spokeswoman for the March for Life in France. The 24-year-old said, “Going out into the street seems essential to us. It is the only moment in the year when we can publicly express our opposition to abortion and euthanasia and propose concrete solutions. The rest of the time, the media never give us the floor.” Trump announces tariffs against goods from Denmark On Saturday, President Donald Trump announced tariffs on all goods from Denmark. President Trump said the tariff will be in force “until such time as a Deal is reached for the Complete and Total purchase of Greenland.” The 10% tariff will also apply to all goods from Norway, Sweden, France, Germany, the United Kingdom, the Netherlands, and Finland. 70% of Americans diagnosed with cancer survive More Americans are surviving cancer, according to new findings from the American Cancer Society. The report found the five-year relative survival rate for all cancers combined reached 70% for people diagnosed during 2015-2021. That's up from about 50% in the 1970s. The survival rates for people diagnosed with more fatal cancers is up significantly as well from the 1990s. Gallup poll: Americans trust nurses, not telemarketers Gallup released their latest Honesty and Ethics Survey of the professions that Americans trust the most.  U.S. adults have the most trust in nurses, military veterans, medical doctors, and pharmacists. They have the least trust in members of Congress and telemarketers.  Only 27% of Americans have high levels of trust in clergy, down from 64% in 2001. Hoosier quarterback gives glory to God And finally, the Indiana Hoosiers won their first college football national championship on Monday. ANNOUNCER: “He's gonna take off and run. Mendoza weaves his way first and diving toward the end zone. Touchdown!  A century of futility is forgotten. The Indiana Hoosiers are the kings of college football. The 2026 college football national champions: Coach Curt Cignetti and the Indiana Hoosiers!” The Hoosiers beat the Miami Hurricanes 27 to 21 to cap off an undefeated season. The team's historic victory represents a turnaround led by head coach Curt Cignetti over the past two years. For decades, the Hoosiers were known as the “losingest team” in college football. Members of the tight-knit team are now known for sharing their faith. Quarterback Fernando Mendoza is an outspoken Christian who also won the Heisman Trophy last year, college football's top individual award.  Listen to his comments after the championship victory. MENDOZA: “This victory is so sweet for everybody, for the entire Hoosier nation, but also it's super sweet for myself. I was a two-star recruit coming out of high school. I got declined to walk on offer to the University of Miami. Full circle moment here. Playing in Miami for all the friends and family. I can't thank Coach [Curt] Cignetti enough, and Coach [Chandler] Whitmer and Coach [Ola] Adams for taking a chance on me. I just give all the glory to God.” 1 Corinthians 10:31 says, "Therefore, whether you eat or drink, or whatever you do, do all to the glory of God." Close And that's The Worldview on this Wednesday, January 21st, in the year of our Lord 2026. Follow us on X or subscribe for free by Spotify, Amazon Music, or by iTunes or email to our unique Christian newscast at www.TheWorldview.com.  I'm Adam McManus (Adam@TheWorldview.com). Seize the day for Jesus Christ.

Diagnosed at 45, Erin shares her journey with Type 1 diabetes, Graves' disease, and heart issues, highlighting the vital importance of self-advocacy in a dismissive medical system. Free Juicebox Community (non Facebook) Type 1 Diabetes Pro Tips - THE PODCAST Eversense CGM Medtronic Diabetes Tandem Mobi ** twiist AID System Use code JUICEBOX to save 40% at Cozy Earth  CONTOUR NextGen smart meter and CONTOUR DIABETES app Dexcom G7 Go tubeless with Omnipod 5 or Omnipod DASH * Get your supplies from US MED  or call 888-721-1514 Touched By Type 1 Take the T1DExchange survey Apple Podcasts> Subscribe to the podcast today! The podcast is available on Spotify, Google Play, iHeartRadio, Radio Public, Amazon Music and all Android devices The Juicebox Podcast is a free show, but if you'd like to support the podcast directly, you can make a gift here or buy me a coffee. Thank you! *The Pod has an IP28 rating for up to 25 feet for 60 minutes. The Omnipod 5 Controller is not waterproof.  ** t:slim X2 or Tandem Mobi w/ Control-IQ+ technology (7.9 or newer). RX ONLY. Indicated for patients with type 1 diabetes, 2 years and older. BOXED WARNING:Control-IQ+ technology should not be used by people under age 2, or who use less than 5 units of insulin/day, or who weigh less than 20 lbs. Safety info: tandemdiabetes.com/safetyinfo Disclaimer - Nothing you hear on the Juicebox Podcast or read on Arden's Day is intended as medical advice. You should always consult a physician before making changes to your health plan.  If the podcast has helped you to live better with type 1 please tell someone else how to find it!