Podcasts about diagnosed

Love this clip? Check out the full episode: Episode #346: Voicemails from the ADHD Trenches: Marriage, Faith, Regret, and Rage (Yep, We're Going There)Listen to the full conversation in the original episode HERE.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

In this special episode, host Dr. Cassandre Dunbar takes listeners inside the Johnson & Johnson Healthy eVoices Conference in Princeton, New Jersey — a gathering of hundreds of health advocates from across the country, all living with chronic illness.Cassandre sat down with eight extraordinary women and asked them all the same question: How did you become an advocate?None of them planned it. Most of them were chosen - by a diagnosis, by a moment of crisis, by the simple fact that no one who looked like them existed in the spaces they needed most.From a 7-year-old giving her first speech at a gala, to a woman fired from her job because of epilepsy, to a cancer diagnosis in the middle of a divorce — these stories will move you, challenge you, and remind you why showing up matters.*Disclosure: Johnson & Johnson covered travel and accommodations for the Healthy Voices Conference. They had no involvement in the conversations, participants selected, questions asked, or how this story is told.*Featuring:Alexis - Pulmonary Arterial HypertensionAlexis is a Black disabled advocate and healthcare professional committed to amplifying the patient voice and advancing disability representation. She began her advocacy at age seven with the American Heart Association and was later crowned Miss Amazing National Senior Miss Amazing 2021. Through her work and storytelling—including her love of Disney and fashion—she creates space for honest conversations about disability, identity, and what it means to live well and fully.Asha - Breast Cancer & VitiligoAsha Miller is a nationally recognized breast cancer veteran, speaker, and storyteller who uses her lived experience as a Black woman navigating cancer, divorce, motherhood, and healing to advocate for equity in healthcare. Diagnosed with stage 3 breast cancer in her early 30s, Asha speaks candidly about identity, body image, racial disparities, and reclaiming power after diagnosis. She is the founder of Asha Miller Creative and is known for building transformative spaces where storytelling becomes a catalyst for healing and change.Ayesha - Psoriatic ArthritisFounder of The PsoriaSis Collective and Sistas With Psoriasis Online Support Group, Ayesha Patrick is a long-time psoriasis and psoriatic arthritis patient advocate dedicated to empowering Black women through education, connection, and support. She volunteers with the National Psoriasis Foundation, has written for WebMD and PlaquePsoriasis.com, and serves as a patient research partner advancing psoriatic disease studies. She is a proud Mom of two and resides in NewJersey. Derra - EpilepsysDerra Howard is a content strategist, filmmaker, and the Founder and President of Saving Grace Epilepsy Foundation. She leads initiatives focused on epilepsy awareness, education, and direct community support, working to break stigma and improve access to care for individuals and families affected by seizure disorders.Jenice - Crohn's DiseaseRacquel - LupusLupus In Color founder Racquel H. Dozier is a passionate lupus advocate, educator, speaker, and community builder dedicated to educating, inspiring, encouraging, and empowering lupus warriors around the world. Navigating her own lupus journey, she transformed her experience into purpose, creating a platform that amplifies diverse voices, addresses health disparities, and centers the lived experiences of those often underrepresented in chronic illness spaces.Stephanie - IBD (Crohn's/Ulcerative Colitis)Stephanie A. Wynn is a Certified Patient Leader, Founder and President of The Stephanie A. Wynn Foundation, and Program Director of the IBD Patient Navigator® Program. She leads initiatives that connect patients diagnosed with Crohn's Disease and Ulcerative Colitis two forms of Inflammatory Bowel Disease (IBD)with trained IBD Patient Navigators who provide individualized support to help patients manage their disease and navigate healthcare with confidence. Through advocacy, education, and community-based navigation, she works to reduce healthcare disparities and improve outcomes in underserved communities.Yolanda - Multiple MyelomaYolanda Brunson-Sarrabo, former Fashion Pro, now vocal advocate. She shares her story of being diagnosed and managing multiple myeloma. She's a certified Patient Leader and the founder and CEO of Chronic Fitness. Yolanda is a Content Creator for No Better Time Than The Present, an IG /YouTube Podcast, where she speaks with various Patient Advocates on their trials and Journeys.Connect with Be Well, Sis:Instagram – @bewellsis_podcastSubstack – bewellsis.substack.comFollow, rate, and share this episode!We're supporting St. Jude Children's Research Hospital. Head over to www.stjude.org/bewellsis right now and sign up to be a monthly donor. Together, we can make a real impact.Want to get in touch? Maybe you want to hear from a certain guest or have a recommendation for On My Radar? Get in touch at hello@editaud.io with Be Well Sis in the subject line! Have your own Not Well, Sis rant to contribute? Click here to send it into the show!Be Well, Sis is hosted by Dr Cassandre Dunbar. The show is edited, mixed and produced by Megan Hayward. Our Production Manager is Kathleen Speckert. Be Well, Sis is an editaudio collaboration. Be Well, Sis is hosted by Dr Cassandre Dunbar. This episode was edited by Victoria Marin. Our Production Manager is Kathleen Speckert. Be Well, Sis is an editaudio collaboration. See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

What does it really mean to parent with multiple sclerosis, and how do you talk to your children about something so unpredictable? In this episode of Living Well with MS, we're joined by Julie Stamm – MS advocate, author and mother – for an honest and uplifting conversation about raising a child while living with MS. Diagnosed in 2007, Julie turned her experience into advocacy, determined to be open with her son about her condition in ways that are truthful but age-appropriate. She shares how parenting reshaped her perspective on resilience, how listening to children can ease the guilt many parents carry, and why adapting as a family is a sign of strength, not failure. We explore storytelling as a tool for empowerment, the importance of peer support and community, and why the outlook for people newly diagnosed today is more hopeful than ever. Julie also reflects on her children's book Some Days and her work to promote inclusion and diverse abilities through advocacy and education. This episode will resonate with anyone parenting with MS, considering starting a family, supporting a loved one with MS, or looking to turn lived experience into meaningful advocacy. Keep reading for the key episode takeaways and Julie's bio. 00:00 Introduction and Julie's diagnosis journey 01:23 Why honesty with children matters 02:26 Sharing your story and the power of lived experience 03:37 Parenting guilt, resilience and writing Some Days 04:42 How MS affects the whole family 06:40 Adjusting to change and adapting over time 08:39 Becoming an MS advocate and finding your niche 10:02 Gratitude, grief and staying hopeful 11:23 The importance of peer support and community 13:52 Research advances and hope for the future 14:58 Advice for newly diagnosed parents   Learn more at Julie's website www.iamstamm.com Follow Julie on Instagram at @iamstamm New to Overcoming MS? Learn why lifestyle matters in MS - begin your journey at our 'Get started' page Connect with others following Overcoming MS on the Live Well Hub Visit the Overcoming MS website Follow us on social media: Facebook Instagram YouTube Pinterest Don't miss out: Subscribe to this podcast and never miss an episode. Listen to our archive of Living Well with MS here. Make sure you sign up to our newsletter to hear our latest tips and news about living a full and happy life with MS. Support us: If you enjoy this podcast and want to help us continue creating future podcasts, please leave a donation here. Feel free to share your comments and suggestions for future guests and episode topics by emailing podcast@overcomingms.org. If you like Living Well with MS, please leave a 5-star review.

Subscribers can dive into exclusive, extended conversations from this podcast! To join the adventure, head to BumpInTheRoad.Substack.com. Follow Bump on YouTube @BumpInTheRoadPodcast! Cindy Wageman was diagnosed with multiple sclerosis at just 24 years old, facing a potentially daunting reality that many would find difficult to bear. However, instead of succumbing to despair, she embarked on a personal journey that would ultimately lead her to reclaim her health and happiness. Cindy's path was not an easy one. Faced with the limitations imposed by her diagnosis, she found herself at a crossroads. The medical advice she received left her feeling hopeless, and she realized that she needed to take matters into her own hands. "I decided that I needed to do my own research because the doctors just couldn't help me," she recalls. This pivotal moment marked the beginning of her transformative journey. Through extensive research and a commitment to understanding her condition, Cindy discovered the "eight laws of health" that would guide her towards recovery. These principles—nutrition, exercise, water, sunshine, balance, rest, and trust in divine power—became the foundation of her new lifestyle. She embraced a plant-based diet, incorporated daily exercise, and prioritized her mental well-being. Cindy's journey was also about emotional healing. She learned the importance of forgiveness, not just for others but for herself. "Forgiveness gives you freedom in life when you forgive the other person," she explains. This realization allowed her to let go of past grievances and focus on the present moment. Cindy shares her insights and experiences, encouraging listeners to explore their own paths to health and happiness. Whether you're struggling with a health issue or simply seeking motivation, her story is a powerful reminder that we all have the capacity to overcome life's challenges and emerge stronger on the other side. It's an Award Winning, Amazon best selling book! What they're saying: "This is a beautiful book about life, its imperfections, its challenges, and its joys. It is a book of hope and wisdom for all of us facing a bump in the road." –Pragito Dove "Pat has woven together beautiful stories of life setbacks that have been transformed into spiritual growth. This book is a gift and a must-read for souls experiencing pain and yearning for growth." –Gary Hensel Learn more at BumpInTheRoad.us Follow Bump on: ➡️ Twitter ➡️ Facebook ➡️ Substack ➡️ Instagram ➡️ YouTube

Dr. Kirsten Viola Harrison, trauma psychologist, author, and founder of Soul Wise Solutions, brings over 35 years of experience helping individuals navigate profound psychological and spiritual transitions. In this powerful podcast conversation, she shares her work with clients living with complex PTSD, dissociative identity disorder (DID), schizophrenia, trauma recovery, and near-death experiences, offering deep insights into healing, resilience, and spiritual integration in psychotherapy. Dr. Harrison is the co-author of I, Sean/a: The Story of a Homeless Intersex Woman Who Inspired a Community, the remarkable true story of Sean/a Smith — a homeless intersex woman living with schizophrenia whose life challenges stigma and inspires a movement toward dignity, inclusion, trauma healing, and community transformation. Her story powerfully addresses mental health stigma, homelessness, schizophrenia awareness, and intersex advocacy.

Kendel Davy is a Founding Member of the Riley Rocks Memorial Foundation and Meghan Fessenden is the Director of Social Media and Marketing for the Foundation and is Riley's sister. Together they will talk about Riley who was diagnosed with Esthesioneuroblastoma which is a Pediatric Cancer of the Nasal Cavity when she 6 years old in 2013, and battled for 3 years before her passing on July 20th of 2016 when she was 9 years old. They will also talk about their Foundation which was started by Riley's parents Kamie and Todd.

MEDICARE ADVANTAGE MINUTE:                                                                     CMS (THE GOVERNMENT) TAKES AIM AT MEDICARE ADVANTAGE FRAUD Correspondence: Client Mike writes to ask me to find his wife a Plan G Medicare supplement with a better price. Her current Aetna plan has scheduled a $60+ monthly rate increase so Mike asked me to look for a better deal.  Once again I explained the advantages of High Deductible Plan G (HDG) but Mrs. Mike is very risk averse and wants to stay with regular (expensive) Plan G. A few weeks after, Mike contacted me again to announce that he plans to switch to HDG when his state mandated Birthday Rule period came around. Contact me at: DBJ@MLMMailbag.com (Most severe critic: A+)                   Visit us on: BabyBoomer.ORG Inspired by: "MEDICARE FOR THE LAZY MAN 2026; SIMPLEST & EASIEST GUIDE EVER!" "MEDICARE ENROLLMENT GUIDE!" (Free download from site below) "MEDICARE DRUG PLANS: A SIMPLE D-I-Y GUIDE" For sale on Amazon.com. After enjoying the books, please consider returning to leave a short customer review to  help future readers. Official website: https://www.MedicareForTheLazyMan.com.

"Ever moment, every day is worth celebrating." Somer LoveSomer Love has spent her life choosing hope, dreaming big, and showing up fully for each day. Diagnosed with cystic fibrosis at just 11 months old, Somer has grown into a powerful and compassionate advocate for the CF community.Guided by her belief that “Every moment, every day is worth celebrating,” Somer brings joy and purpose into everything she does. She often reminds others that “laughter is key,” a mindset that has helped carry her, and those around her, through the challenges of life with cystic fibrosis.Through her work, Somer is dedicated to raising awareness, educating others, and offering hope, especially to families navigating a new CF diagnosis. In 2001, she founded Love to Breathe®, a platform created to educate, spread awareness about cystic fibrosis, and share love and connection around the world.Big on birthdays, Somer's parents made celebration part of her story in an unforgettable way. Every year, they placed Somer's photo on a billboard. What began as a birthday tradition became something much bigger, raising awareness about cystic fibrosis in a way that stops people in their tracks. What that billboard did for awareness will give you chills. It's something you will never forget. You'll have to listen to the podcast to hear the story!Somer knows that fighting CF isn't something anyone can do alone. Her journey is deeply rooted in the strength of her support system and the community that stands beside her. She continues to advocate not only for her own future, but for a cure, for everyone living with cystic fibrosis.Somer sums up the reason to advocate. This quote is on her website: "The goal isn't to live forever, but to create something that will"-Chuck Palahniuk 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/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

If your child has just been diagnosed with autism, you might be thinking… now what? In this video I'm sharing what actually happens after the diagnosis, from the emotional rollercoaster of the meeting itself to the practical next steps with school, EHCP or IDP conversations, paperwork, financial support and protecting your own mental health. I've been through this four times with my own children, and I know how overwhelming that day can feel. An autism diagnosis does not change your child. It gives you data. And data helps you support them better. If you're in this space right now, you're not alone. ➡️ Join the conversation in the YouTube comments here - https://youtu.be/0kamuXuGM00 Resources ➡️ Free Autism Signs Guide - https://mummyoffour.com/100asd ➡️ Join my free Neuro-Sparkly community - https://mummyoffour.com/join ➡️ Join the Organised Life Club - https://mummyoffour.com/joinOLC ⸻ UK Financial Support - I can't advise on individual financial circumstances, but you can check eligibility here: GOV.UK benefits calculators https://www.gov.uk/benefits-calculators Turn2us https://www.turn2us.org.uk Citizens Advice https://www.citizensadvice.org.uk/benefits/ ✨ Join My FREE Neuro-Sparkly Community & Resource Hub - https://www.rhiannanmorgan.com/join

Send us a message about the podcast. For questions about MS please contact our helpline 0800 032 38 39Getting an MS diagnosis can be straightforward for some people, but for many it's a long, confusing journey filled with uncertainty. In this episode, we explore one of the questions the MS Trust is asked most often: How is MS actually diagnosed?We look at why diagnosis can take time, what tests are involved, why symptoms aren't always obvious, and what happens when tests give unclear results.We're joined by Professor Alasdair Coles, neurologist and MS specialist, who guides us through the current diagnosis process from first symptoms to MRIs, lumbar punctures, evoked potentials, OCT scans, and what will happen after the point of diagnosis.Episode notesHow MS is diagnosed - info from the MS TrustLumbar puncture  - info from the MS TrustEvoked potentials - info from the MS TrustMcDonald criteria - info from the MS TrustDisease modifying drugs (DMDs) - info from the MS TrustLimbo land - what you can do while you wait for an MS diagnosis - MS Trust podcastWellbeing and MS - information hub to help you support your emotional wellbeingVideo resources from MS TrustWhat happens in a Neurological examination?What is a Lumbar Puncture?What is an Optical Coherence Tomography (OCT) test?

Love the episode? Send us a text!In this powerful episode of Breast Cancer Conversations, Laura Carfang speaks with Kathy Giusti, a two-time cancer survivor who has lived with multiple myeloma for 30 years and later faced a breast cancer diagnosis as well.Diagnosed at 37 after what she thought was a routine visit, Kathy was told she had a fatal blood cancer and would live “three years at best.” Instead of accepting that prognosis, she helped change the trajectory of cancer research by founding the Multiple Myeloma Research Foundation (MMRF)—a model that brought scientists, clinicians, biotech, and the FDA together to accelerate treatments.This conversation explores survivorship, advocacy, and what patients and caregivers can do when the science is moving fast—but the system isn't.In This Episode, We DiscussGetting a shocking diagnosis after a “routine” appointmentWhy multiple myeloma was once considered a “silent killer”How Kathy helped build a research engine that accelerated drug developmentThe difference between fast-moving science and slow-moving systemsHow Kathy's identical twin impacted her breast cancer risk and screeningDCIS decisions and why “there's no right or wrong—only what's best for you”Why “looking healthy” can cause people to underestimate what you're carryingHow to set boundaries when you're in treatment or survivorshipWhy you shouldn't rely on only one or two caregivers—and how to “invite people in”Kathy's book: Fatal to Fearless: 12 Steps to Beating Cancer in a Broken Medical SystemResources & LinksFollow Kathy: @kathy.giustiBook: Fatal to Fearless: 12 Steps to Beating Cancer in a Broken Medical SystemSurvivingBreastCancer.org: Free programs, support groups, and communityDownload the SBC App: Search SurvivingBreastCancer.org in the App Store or Google Play 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.

Carrie Scollon sits down with Diane Heaton to explore her chapter from The Embers We Carry, Lighthouse Book Series Volume 3. Diagnosed with ADHD later in life, Diane shares how this realization reframed decades of self-doubt, masking, and misunderstanding. She speaks candidly about confidence, self-compassion, and why ADHD in women is so often overlooked—and misunderstood. Conversation highlights: - Masking, self-blame, and exhaustion - ADHA in women and missed diagnosis- Self-compassion and reframing identity - Naming truth as a path to healing

Diagnosed just months after childbirth, Kat Robertson reflects on treatment, motherhood, and moving forward with gratitude.

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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

A five-year study has found children are more likely to become sick with the flu or COVID-19 if they have sleep apnea.See omnystudio.com/listener for privacy information.

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

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

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

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!

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.

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. 

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.

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!