Podcasts about diagnosed

In this episode, Brent Sanders speaks with former NSW Police officer Justyn Backhouse, who spent 25 years on the front lines of law enforcement. From high-speed pursuits to complex aerial rescues, Justin’s career spanned some of the most intense and demanding roles in policing. But behind the action was a hidden cost. Diagnosed with PTSD in 2021, Justin turned to writing to process his experiences. The result is Hidden Scars: From Crime Scenes to Crisis – The Price of Service, a powerful memoir that reveals the unseen toll of a life spent in uniform. This episode makes mention of self-harm. If you or anyone you know needs someone to speak to, call LifeLine on 13 11 14.See omnystudio.com/listener for privacy information.

In this powerful episode, Jen Delvaux sits down with Dana Donofree, a breast cancer survivor and the visionary founder of AnaOno—a lingerie brand created specifically for women who've undergone breast surgery. Diagnosed at just 27 years old, Dana turned her pain into purpose by designing bras that fit, support, and celebrate post-surgery bodies. Together, they dive into: Dana's personal breast cancer journey and the challenges of treatment at a young age The emotional toll of finding lingerie that didn't fit her new body—and how that frustration became the spark for AnaOno The powerful message behind Cancer Culture's Fashion Show and how it's changing lives The ongoing need for funding and action—specifically for metastatic breast cancer research Why healing is not linear, and how self-love and empowerment are part of the recovery journey Whether you've been through cancer or love someone who has, this episode is a must-listen reminder that beauty isn't lost after breast cancer—it's redefined.

Kaitlyn Oleinik is a chronic illness advocate and the author of Revival: My Journey with Neuropsychiatric Lyme Disease. She was bitten by a tick at age six and spent much of her life fighting an invisible illness while being dismissed by the medical system. Diagnosed with Lyme disease and co-infections in her teens, Kaitlyn has endured everything from hallucinations and involuntary psych holds to IVIG and stem cell treatments. Her book and voice give a name to the unspoken pain of countless others living with Lyme.

Diagnosed at the height of her career, Ann Marie Colapietro of Travelers is one of the nearly 10 million people worldwide living with Parkinson's disease. Ann Marie and Dr. J. Antonelle de Marcaida joined us to offer both personal and medical perspectives on living vibrantly with Parkinson's and other chronic diseases and illnesses.Watch the original Wednesdays with Woodward® webinar: https://institute.travelers.com/webinar-series/symposia-series/parkinsons-resilience.---Visit the Travelers Institute® website: http://travelersinstitute.org/.Join the Travelers Institute® email list: https://travl.rs/488XJZM.Subscribe to the Travelers Institute® Podcast newsletter on LinkedIn: https://www.linkedin.com/newsletters/travelers-institute-podcast-7328774828839100417.Connect with Travelers Institute® President Joan Woodward on LinkedIn: https://www.linkedin.com/in/joan-kois-woodward/.

In this episode of It Takes Balls, husband, father, and testicular cancer survivor Ryan Rayfield shares his powerful story of early detection, recurrence, and the long road through surgery, chemotherapy, and recovery.Ryan's journey began mid-flight on a work trip when unexpected groin pain led to a self-check that changed everything. Diagnosed with stage 1S non-seminoma, he opted for a robotic RPLND at the University of Pennsylvania in hopes of avoiding chemotherapy. With clean scans and pathology, it seemed the worst was behind him - until a month later, rising HCG tumor markers revealed a microscopic recurrence that imaging couldn't catch.Ryan reflects on the mental toll of starting BEP chemotherapy after having hoped to avoid it entirely. He candidly describes chemo's physical and emotional side effects, his experience balancing treatment with fatherhood and grad school, and the strength it took to accept what he once feared most.The episode also explores how Ryan's connection to another survivor, former podcast guest Alex Volynsky, helped guide his treatment choices, highlighting the power of peer support, social media, and storytelling in cancer care. Now approaching two years in remission, Ryan speaks with clarity about scanxiety, post-treatment anxiety, and how cancer reshaped his health, perspective, and purpose.From fertility concerns and proactive surgery to community, parenting, and the lasting impacts of survivorship, Ryan's story is a reminder that healing isn't linear, and that asking for help is a strength, not a weakness.Join 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.twitter.com/testescancer⁠⁠https://www.instagram.com/testescancerhttps://www.facebook.com/tca.orgFollow Steven Crocker: https://www.twitter.com/stevencrockerhttps://www.instagram.com/stevencrockerhttps://www.facebook.com/steven.crocker2Connect with Ryan:https://www.facebook.com/ryan.rayfield.98https://www.instagram.com/rrayfield_44/Theme song: No Time Like Now - Tom Willner www.tomwillner.com

At the start of her second trimester, Rafaela Dreisin was diagnosed with breast cancer at the age of 36. Listen to the episode to hear Rafaela discuss: how she and her doctors decided on a treatment plan how she coped with experiencing the excitement of being pregnant and the fear of her diagnosis at the same time her advice for other people in the same situation

August is recognized in the U.S. as National Minority Donor Awareness Month, an annual observance dedicated to raising awareness and encouraging organ, eye, and tissue donation within multicultural communities. This morning we tell the story of Joshua Lee, Lung Transplant Recipient – Age 64 . Diagnosed with Rheumatoid Arthritis as a teen, Joshua Lee's condition eventually damaged his lungs, making it difficult to breathe or work. By early 2024, he relied on oxygen machines and had to leave his job. In July, he was hospitalized and received a life-saving lung transplant at Temple University Hospital.   Now, Joshua calls himself a “living testimony” and credits his recovery to his wife's support and the gift of organ donation. Learn more about organ and tissue donation at www.donors1.orgFollow:

In this deeply moving and soul-activating episode, Katie Carey sits down with Dominique Trueman, a guest from the Soulful Poems collaboration, to explore her powerful transformation through creativity, cancer recovery, inner child healing, and the path of living with zero limits. Diagnosed with breast cancer for the second time in 2024, Dominique chose not to see it as a curse, but as a divine invitation to reconnect with her authentic self. In this episode, she courageously shares how peeling back the layers of old belief systems—like unworthiness, people-pleasing, and over-responsibility—has allowed her to reconnect with her creativity, rebuild her relationship with her mother, and awaken to a life of freedom, magic, and true expression. ✨ What we cover in this episode: How Dominique's poetry and creativity were reawakened after years of self-abandonment The impact of childhood trauma, parental mental illness, and taking on too much responsibility too young Why illness can be a wake-up call to slow down, heal, and come back home to yourself Her personal practice of writing to God/source to access divine guidance and write poetry How chronic people-pleasing creates toxicity in the body The sacred healing that happened when she sat beside her mother's hospital bed Why reconnecting to joy, family, creativity, and self-expression matters more than hustle and “success” Practical wisdom on living with presence, purpose, and zero limits

On September 3rd 2025, diabetes and sport will go under the global spotlight that is a House of Commons debate. In today's episode the man who made it happen tells us why - and what this could mean for the millions of people living with diabetes in the UK.Chris Bright is one of the community's crusaders. As part of his role as Community Partnerships and Events Lead at Breakthrough T1D in the UK, he has put diabetes in sport on the agenda at the highest possible level. The goal? To improve the inclusivity of physical activity for people with diabetes. The need is clear - the Equality Act that safeguards around 3.5 million people with diabetes in work and education does not currently extend to sport. In fact, recent research found that of 180 existing governing bodies in sport, only four have policies in place for people with diabetes.Diagnosed at the age of 8, Chris overcame stigma and the challenges of a very inflexible insulin regime as a young athlete to represent Wales at futsal. He later used those negative experiences as momentum to build The Diabetes Football Community, bringing young footballers with diabetes together while rewriting attitudes to type 1 diabetes and football.In this episode we dig into different pockets of Chris's work, including some new recommendations for travel, airports and airport security. We touch on his personal journey, and he reveals his strategy for successfully creating change in the face of inequality - perfect for anyone who feels as galvanised as I was listening to Chris's phenomenal story. CONNECT WITH CHRISFollow Chris on Instagram.Find Chris on X.Follow Chris on TikTok.The Diabetes Football Community website.Breakthrough T1D Community Events Calendar.JOIN THE TYPE 1 ON 1 COMMUNITY Come and say hi @studiotype1on1 on Instagram.Visit the Type 1 on 1 website.Subscribe to the Type 1 on 1 newsletter.DISCLAIMER Nothing you hear on Type 1 on 1 should be taken as medical advice. Please consult your healthcare team before making any changes to your diabetes or health management.SPONSOR MESSAGE This episode of Type 1 on 1 is sponsored by Dexcom. Using Dexcom CGM has given me so much confidence to make informed diabetes treatment decisions in the moment.You can choose to wear it on your arm or your abdomen, and all Dexcom CGMs have the share and follow feature even when connected to an insulin pump, so family and friends can see your glucose levels and get alerts, giving that extra bit of support when needed.Head to Dexcom.com to request a free Dexcom ONE+ sample.Always read the user manual for important product aspects and limitations. Talk to your doctor for diabetes management terms and conditions and terms of use. 

Cynthia Ray shares the deeply moving story of her brother Philip's tumultuous journey. Diagnosed with autism later in life, Philip's association with a con artist led to his incarceration and a subsequent prostate cancer diagnosis that went untreated for a year. Cynthia recounts Philip's early challenges, his strong belief in his inventions, and the dire consequences of misplaced trust. She also discusses her ongoing advocacy for his compassionate release due to his severe health issues. This episode sheds light on the intersection of autism, criminal justice, and family resilience. A Brother's Journey Philip's Early Life and Autism Diagnosis The Invention and the Conman Legal Troubles and Incarceration Health Struggles in Prison Hopes for Compassionate Release INTRO Music; T.Wild Mantor Music BMI

In this moving and hope-filled episode, mother-daughter duo Quinn Wyatt and Kirby Larson share the deeply personal story behind their middle grade novel, Gut Reaction. Diagnosed with Crohn's disease as a teen after years of being dismissed, Quinn opens up about her experience living with a misunderstood chronic illness. Kirby, an acclaimed author, reveals what it took to revisit this painful chapter of their lives and co-write a book that helps kids feel seen. Together, they explore diagnosis delays, self-advocacy, parenting through illness, and how their storytelling became a form of healing and community connection. Resources Mentioned: Gut Reaction by Quinn Wyatt and Kirby Larson  Crohn's & Colitis Foundation – https://www.crohnscolitisfoundation.org/ Learn more: https://gutreactionbook.com For Parents & Caregivers: Bring Child Life Home With You The SupportSpot app puts expert child life tools, coping strategies, and emotional support right in the palm of your hand—anytime you need it.

In this episode, Sally is joined by Drew Harrisberg — exercise physiologist, diabetes educator, and founder of Drew's Daily Dose — for a deep dive into how blood sugar, movement, and mindful nutrition can radically transform your body composition and overall health.Diagnosed with Type 1 Diabetes at 22, Drew has turned his condition into a superpower, using it to refine his approach to training, eating, and living. He shares practical, science-backed tools that anyone can use — whether you're living with diabetes or simply want to optimise your metabolism and energy.You'll learn:How Drew uses insulin as a performance toolWhat a plant-based day on a plate looks like for himHis favorite takeout indulgences (yep, he still has them!)Tips to balance blood sugar without overthinking itHow stress and recovery play into physique and performancePlus: his supplement stack, morning routine, and the key mindset shift that changed everything.

Losing a job is never easy, but what if it led to a more fulfilling path? Daniel Incandela, former CMO, opens up about the painful yet transformative experience of being fired in his 50s. In this episode, he shares the emotional toll it took, how he navigated the challenges, and the powerful lessons he learned along the way. Today, I sit down with my good friend, Daniel Incandela, who, like many of us, faced the harsh reality of burnout and being let go. His story is one of resilience and transformation. Despite the painful blow of being fired, Daniel reflects on how the experience helped him realign his priorities, focusing on family, health, and ultimately, finding his path forward through consulting and creative work.We discuss the importance of reflection and accountability, even in the most challenging moments. Daniel's journey sheds light on how career paths don't always go as planned, and how the pressure to “do it all” can weigh heavily on us. From navigating ageism in a competitive job market to embracing AI as a necessary tool for today's workforce, Daniel discusses how he's finding purpose in his new role and working towards a future that aligns more with his values.If you've ever felt like your career took an unexpected turn, this episode is for you. Daniel's story is a powerful reminder that we can find clarity even in moments of doubt.“I've been on this journey that I think I really needed in life, and it has helped me awaken from things I did not see.” ~ Daniel IncandelaIn This Episode:-Daniel's transition from CMO to consultant-Embracing change and realizing what really matters-Leadership in the time of AI-The reality of getting fired in your 50s-Experiencing the immense benefits of slowing down-Looking ahead: Future of work in the gig economy-Why learning how to use AI is no longer optionalAnd much more!Resources:-Free Guide to LinkedIn Job Hunting for the 40+ Crew - https://www.itgetslateearly.com/job-guide-The Gen X Career Meltdown - https://www.nytimes.com/interactive/2025/03/28/style/gen-x-creative-work.htmlConnect with Daniel Incandela:-LinkedIn: https://www.linkedin.com/in/danielincandela/-Substack:https://substack.com/@danielincandela-Newsletter by Daniel Incandela - https://danielincandela.substack.com/Connect with Maureen Clough:-LinkedIn: maureenwclough - https://www.linkedin.com/in/maureenwclough/-Website: itgetslateearly.com - https://www.itgetslateearly.com/-Instagram: @itgetslateearly - https://www.instagram.com/itgetslateearly/-YouTube:...

What happens when a 16-year-old boy runs away from chemotherapy—and survives?   In this gripping episode of the Nutritional Therapy and Wellness Podcast, Jamie Belz sits down with Billy Best, the teen who became a national sensation in 1994 when he fled conventional cancer treatment in search of something different. Diagnosed with Hodgkin's lymphoma, Billy rejected chemotherapy after watching it ravage his aunt's health and instead placed his trust in faith, intuition, and the wisdom of thousands of everyday people who reached out to introduce him to a whole new world of natural healing.   Billy's story is more than a medical anomaly—it's a powerful testimony of medical freedom, holistic healing, and the suppressed potential of natural medicine. His healing protocol included nutritional therapy, Essiac tea, and 714X lymphatic injections, along with a radical mindset shift, spiritual surrender, and a deep belief in the body's ability to heal. Within months, his cancer was gone.   Billy didn't just survive. He healed. And in the early days of his recovery, he believed—with everything in him—that his story would change the world. That people would wake up. That natural medicine would finally be heard. That the truth would matter.   But it didn't.   Instead, Billy faced the crushing reality of censorship, media manipulation, and corporate control. His miraculous outcome wasn't celebrated—it was buried. Stories were pulled at the last minute. Reporters were silenced. And the very system that claims to be searching for a cure wanted nothing to do with the one he'd found.   In this episode, you'll discover:   The viral true story behind Billy Best's escape from chemotherapy What 714X is, how it works, and why it's banned in the U.S. How bio-individuality, nutrition, and mindset played key roles in his healing The power of belief, faith, and spirituality in the healing process Why Billy believed he'd found the cure for cancer—and what happened when no one wanted it The disturbing link between pharma-funded media, cancer fundraising, and censorship Insight into Codex Alimentarius, glyphosate, GMOs, and the global food agenda Why we must reclaim health freedom and medical sovereignty now more than ever   Billy also speaks candidly about the emotional aftermath—how addiction, trauma, and grief shaped the decades following his recovery—and why he's still fighting, 30 years later, to help others awaken, question, and heal.   This is more than a survival story. It's a raw, unflinching testimony of what happens when someone dares to trust their gut, break the rules, and walk a path no one else will. And it's a heartbreaking reminder that sometimes, even when you've found the truth, the world just isn't ready for it.   Whether you're a practitioner, cancer survivor, or someone seeking health freedom, this conversation is a must-listen.     Resources Mentioned:   The Nutritional Therapy Association: ⁠https://www.nutritionaltherapy.com⁠ The Nutritional Therapy and Wellness Podcast Episode with Scott Tips: ⁠https://open.spotify.com/episode/4EkpRYFCciDdwZ1A1gIhf7?si=1334c0b3b24e4440⁠ Make a donation to The National Health Federation to help support health freedom: ⁠https://thenhf.com/make-a-donation/⁠ Learn more about CODEX: ⁠https://thenhf.com/codex/⁠ Checkout Billy's First Book: ⁠https://www.amazon.com/Billy-Best-Story-Alternative-Medicine/dp/1937920283/ref=asc_df_1937920283?tag=bingshoppinga-20&linkCode=df0&hvadid=80401987005810&hvnetw=o&hvqmt=e&hvbmt=be&hvdev=c&hvlocint=&hvlocphy=87545&hvtargid=pla-4584001450967570&psc=1&msclkid=5682c8a9fc9d13ffd119a038cedf016a⁠ ⁠The Billy Best Story⁠ (aka the Pasadena Speech)   If this episode inspired you, please subscribe, leave a 5-star review, and share it with someone who needs to hear this. Follow us on Spotify and help us keep the conversation going about truth, healing, and health freedom.

This week on The RunPod PowerPlaylist, Jenni welcomes an unstoppable force - Iain Ward, aka The King of Chemo. Diagnosed with terminal brain cancer, Iain isn't just fighting - he's running. Running to raise awareness, to raise funds, and to prove that purpose can outrun even the darkest diagnosis.Iain's playlist is what he calls “Licorice Allsorts” - a mix of upbeat tracks with a strong lean into rock. Think powerful riffs, driving beats, and tunes that light a fire in your legs when you need it most.Tune in, turn it up, and run like The King of Chemo.Listen to Iain's Main Episode of RunPod - out now!

This is the All Local noon update for August 5, 2025.

Neuroscientist Dr. Adrienne Benediktsson opens up about her journey with bipolar disorder - from the terrifying moment of trying to jump out of a plane mid-air to retracing lost memories after a psychotic episode. Dr. Benediktsson shares how harrowing experiences with depression and mania led her to discover new ways of living - and thriving - with bipolar disorder, offering a powerful reminder that hope, healing, and a meaningful life are possible.(00:00) Introduction(02:11) Early Signs & School(06:22) What Triggered My Mania(12:07) Jumping Out of My Plane(22:13) Hospitalization & Diagnosis(28:55) Forgetting My Entire Life(34:01) Bill Clinton Induced Psychosis(38:35) Recovery & Getting My Life Back(44:05) Pregnancies & Relapses(51:49) My Supports Saved Me(54:43) You Must Love Yourself AgainDr. Adrienne Benediktsson is an Associate Professor of Biology at Mount Royal University in Calgary and a dedicated neuroscientist specializing in the study of brain cells called astrocytes. Diagnosed with bipolar I disorder during her graduate studies, Adrienne has spent nearly two decades blending her lived experience with rigorous scientific research. Her work aims to deepen understanding of bipolar disorder's biology while breaking down stigma. Passionate about community support, she actively engages in peer advocacy and is committed to fostering acceptance and hope for others living with bipolar disorder.- - -This episode is hosted by Dr. ⁠⁠⁠⁠⁠⁠Erin Michalak⁠⁠⁠⁠⁠⁠ and produced by Caden Poh. #talkBD Bipolar Disorder PodcasttalkBD gathers researchers, people with lived experience, healthcare providers, and top bipolar disorder experts from around the world to discuss and answer the most important questions about living with bipolar disorder. Learn more about talkBD: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://talkBD.live⁠⁠⁠⁠Follow Us

Today's conversation is for every parent who's ever felt a little “different,” a little chaotic, and maybe a little misunderstood. If you or your kids have ADHD, autism, or any kind of neurodivergence, this episode is going to be packed with insights, laughs, and practical wisdom on how to navigate life, work, and parenting with confidence.We're joined by Dr. Kristen Williamson, a licensed professional counselor with a PhD in Behavioral Health Management and a champion for neurodivergent adults. Diagnosed with autism and ADHD in adulthood, Kristen has embraced her “neurospicy” brain as a superpower—and she's here to help others do the same. She's passionate about mental health, leadership, and creating more inclusive spaces for neurodivergent individuals in parenting, work, and life.For those who want to connect with you and learn more about neurodivergence, mental health, and leadership, where can they find you?

After their 21 month old daughter Lily was experiencing stomach pains in April of 2024, Nicky and Dan Rankin took her to an Emergency Room and she was then admitted to Children's Hospital at the Anschulz campus in Aurora, Colorado. Shortly after that, Lily was diagnosed with High Risk Neuroblastoma. 16 months later as we enter August of 2025, Lily is doing as well as possible . Dan will discuss what Lily has been through and the Half Triathlon that he has been training for to raise money because of the great treatment that Lily has received at Children's Hospital.

I'm joined by Sam; mum and CEO of lingerie and sleepwear brand Samaralovesus to chat about her experience in the early months of motherhood. In this solo episode I delve into:

Never Just Surviving: Sophie Holmes on Running 36 Marathons with Cystic FibrosisDespite a schedule packed with training, advocacy, and breaking world records, Sophie Holmes of the U.K. always makes time to share her story, and we're so grateful she did.Diagnosed with cystic fibrosis at just four months old, Sophie was told she might not live past her teens. But rather than letting that define her, she's spent her life rewriting the narrative. Her latest, jaw-dropping accomplishment? Running 36 marathons in 36 days. That's right—36 consecutive days, 26.2 miles each day, driven by pure determination and an unshakable belief in what's possible.Sophie is not only an elite athlete and personal trainer, she's a powerful advocate for chronic illness awareness. In this episode of the Living with Cystic Fibrosis podcast, she talks about what fueled her through each grueling mile, how she manages the intense physical demands of endurance sports while living with CF.“Mindset is everything.” – Sophie HolmesIt's easy to say that exercise is one of the best things someone with CF can do. But Sophie reminds us: that doesn't mean it's easy. Her story is a powerful example of grit, strength, and living fully—even when the odds are stacked against you.Sophie's Story:Diagnosed with cystic fibrosis at four months oldTold she might not live past her teenage yearsRan 36 marathons in 36 days, demonstrating her extraordinary enduranceSet a Lake Cuomo Ultra Ironman World RecordBelieves mindset is the key to overcoming life's toughest challengesWorks as a personal trainer and chronic illness advocateRedefines resilience—not just surviving, but thrivingInspires runners, athletes, and anyone living with chronic illnessLives with relentless drive and purposeShows us what's possible when you push beyond the limits others set for youYou can find Sophie Holmes on IG: https://www.instagram.com/sophiegraceholmes/ 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

Rebecca is a mental health counsellor in Australia. Diagnosed at 47 — with level-two autism and ADHD combined type — she shares her story of self-recognition, complex emotions around diagnosis, and the challenges of navigating neurodivergence in both personal and professional life.Rebecca reflects on masking, internalized ableism, and how people-pleasing tendencies developed as survival strategies. The conversation also explores her work as a counsellor and how parenting neurodivergent children has shaped her own self-understanding.Topics explored include:The slow unmasking processHow late autism diagnosis reframes childhood memories and identityParenting with empathyAvoiding the pitfalls of compliance cultureThe nuanced relationship between sensitivity, empathy, and strengthDisbelief from healthcare professionals and the impact of diagnostic invalidationWatch this episode on YouTube.Rebecca recommends these resources:Camouflaging Autistic Traits Questionnaire (CAT-Q)Embrace Autism websiteIs This Autism? — A Guide for Clinicians and Everyone Else by Donna Henderson and Sarah Wayland, with Jamell WhiteThe Neurodivergent Woman podcast Theme music: "Everything Feels New" by Evgeny Bardyuzha. All episodes written and produced by Kristen Hovet.Send in your questions or thoughts via audio or video recording for a chance to be featured on the show! Email your audio or video clips to otherautism@gmail.com through WeTransfer. Buy me a coffee!Buy The Other Autism merch. Use code FREESHIP for free shipping on orders over $75 USD! The views, opinions, and experiences shared by guests on this podcast are their own and do not necessarily reflect those of the host or production team. The content is intended for informational purposes only and should not be taken as medical or professional advice. Please consult with a qualified healthcare provider before making any decisions related to your health, fitness, or wellness.

Tila huminto ang mundo ni Tippy Valiente nang mabasa ang sagot ng New Zealand Immigration. Hindi na mare-renew and kanyang student visa due to her health condition. Diagnosed with chronic myeloid leukemia si Tippy at mahal ang mga gamot na iniinom niya. Magiging pabigat siya sa health care system ng New Zealand.All Rights Reserved, CBN Asia Inc.https://www.cbnasia.com/giveSupport the show

In this quickfire bonus episode, we're back with the brilliant Cath — skateboard coach, soulful northern lass, and walking proof that you can take a few knocks and still show up fully you.Diagnosed with epilepsy but never one to sit out the ride, Cath has lived a bold, messy, and empowering life on and off the board. Today's episode is just a little slice of her realness, featuring fun questions, big truths, and that signature no-BS warmth we love her for.Expect:Soul-healing superpowers (and why she'd use them on herself too, thank you very much)A billboard message that might just save your brain cells: put your phone downA love/hate relationship with London and the power of going homeWhat she'd say to her 12-year-old self (grab a tissue, just in case)Her challenge to women everywhere: Stop apologising. Start being fully, fiercely you.No fluff. No Instagram quote therapy. Just raw insight, a bit of cheek, and one woman's mission to get more of us living without filters — literal or emotional. Hosted on Acast. See acast.com/privacy for more information.

Website: drmarciaharris.comFacebook: https://www.facebook.com/DrMarciaaharris Marcia A. Harris MD, LHD Dr. Harris has successfully restored hormonal, sexual, and overall health to women & men in the New York & New Jersey area for over 30 years. We provide hormone replacement, erectile dysfunction, vaginal rejuvenation, and all other wellness treatments to residents of New York City, Bronx, Brooklyn, Long Island, Manhattan, New Rochelle, Queens, White Plains, Yonkers, NY, Jersey City, NJ, and all surrounding towns & cities.Many who want to improve their health and wellness often fall victim to one-size-fits-all solutions, and finding the best treatment options can be overwhelming. Our experts are here to listen, understand, and craft a health blueprint that aligns with your specific needs. At The Wellness Restoration Center, we strive to be a welcoming place where your goals can become realized.  

In this deeply reflective episode of It Takes Balls, testicular cancer survivor David Rimmer shares a powerful story of diagnosis, survivorship, and resilience that spans more than 30 years. Diagnosed in 1992 at age 32, long before awareness campaigns or internet support groups, David navigated cancer with little guidance, learning to advocate for himself and seek out the best possible care.From his initial orchiectomy to his choice to travel to Indiana University for a retroperitoneal lymph node dissection (RPLND) under the legendary Dr. Donohue, David walks listeners through the confusion, trauma, and empowerment that defined his treatment journey. He discusses the impact of possible infertility, the psychological toll of recovery, and the importance of acting as a “medical consumer” to ensure the highest level of care.David's story doesn't end with testicular cancer. In the years that followed, he faced multiple additional diagnoses - chronic lymphocytic leukemia (CLL), basal cell carcinoma, and low-grade prostate cancer. Yet through it all, he has maintained a sense of perspective, purpose, and humor. He opens up about how survivorship reshaped his identity, the long shadow cancer casts over even the cleanest scans, and how he finds comfort in staying proactive with his health.A near-death experience during a midair collision over the Amazon adds a surreal layer to David's story - a reminder that surviving isn't just about beating disease, but about what we do with the time we're given. Now, he gives back through bone marrow and stem cell courier missions.Whether you're newly diagnosed, decades into remission, or supporting someone through cancer, David's voice is a reminder of how survivorship evolves over time, and how sharing your story might be the most powerful form of healing.Join 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.twitter.com/testescancer⁠⁠https://www.instagram.com/testescancerhttps://www.facebook.com/tca.orgFollow Steven Crocker: https://www.twitter.com/stevencrockerhttps://www.instagram.com/stevencrockerhttps://www.facebook.com/steven.crocker2Connect with David:djr1010@yahoo.comTheme song: No Time Like Now - Tom Willner www.tomwillner.com

At 28 years old, Joel was navigating life, career, and relationships in bustling London—unaware that the challenges he'd faced with communication since childhood had a name: Developmental Language Disorder (DLD). In this powerful episode of The Talking DLD Podcast, Joel shares what it was like to be diagnosed as an adult, how it reshaped his understanding of himself, and why he's now passionate about breaking the silence around DLD. With honesty, warmth, and insight, Joel walks us through the years before his diagnosis, the moment everything clicked, and how it feels to finally have answers. You won't want to miss this deeply personal conversation as Joel explains how having the diagnosis has changed his life.   Grow your skills with us & support people with DLD Module 1: Diagnosing DLD with Confidence. Learn more. Module 2: Evidence Based Interventions & Strategies for Children with DLD. Learn more. Module 3: Planning Therapy & Measuring Outcomes for people with DLD. Learn more. Module 4: DLD + Co-Occurring Conditions. Learn more. International DLD Research Conference Keynote Series. Learn more.  What is Language + What is DLD - FREE Course. Learn more.  

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Each week on RunPod Jenni meets someone remarkable, inspiring, and fascinating - and this episode is no exception.Joining us in the studio wearing his signature crown is Iain Liam Ward, better known as The King of Chemo.Diagnosed with brain cancer in 2019, Iain made a bold decision: instead of slowing down, he launched a mission to break the world record for the most money ever raised for charity through running. Since then, he's completed marathon after marathon-often while undergoing treatment-proving that cancer might change your life, but it doesn't have to stop it.Iain's story is one of defiance, purpose, and unbelievable grit. With raw honesty, humour, and a crown firmly on his head, he's rewriting what it means to live with terminal illness - and running every step of the way for a cause bigger than himself.If you're looking for motivation, hope, and a reminder that life begins where comfort ends - this episode will stay with you long after the final mileFollow Iain on YouTube, Instagram and TikTok Now! @thekingofchemo

In today's episode of Channel Your Genius, Mellissa Seaman is joined by the radiant and irreverent Cinder Shine, author, musician, and longtime wellness coach, who lives and teaches what she calls rainbow resilience: a joyful, grounded philosophy for navigating life, death, and everything in between. Diagnosed with terminal cancer and still grinning, Cinder shares her hilarious, heartfelt, and deeply real perspective on living fully in the face of pain. From riding motorcycles with brittle bones to being lifted out of a hot tub by trees (yep, really), this episode is a love letter to radical joy, irreverent wisdom, and the power of choosing life even when it hurts. Her new book Terminally Smiling blends memoir, music, and meaning-making in the face of cancer and transformation. This conversation is a must-listen for anyone facing hard things, and craving a little more light.   Talked about in today's episode: 00:01:10 – From Knee Pain to Rainbow Resilience Cinder's journey from body-positive fitness coach to two-time cancer survivor and joy rebel. 00:05:29 – The “F* You Sundial” and Finding Gratitude Cinder shares her irreverent tool for moving from hopelessness to joy, even on the hardest days. 00:08:45 – How to Live Fully with a Terminal Diagnosis What it really means to walk the line between life and death and choose joy anyway. 00:12:33 – Feel Like a Rainbow in the Eye of the Storm The inspiration behind her new song and how she channels emotion through music. 00:14:38 – Death, Ceremony & the Power of Facing the End Mellissa and Cinder explore death as a teacher, and what it means to live fearlessly. 00:21:16 – Hot Tubs, Trees, and the Magic of Asking for Help A story you won't forget, how nature and spirit literally lifted Cinder when she couldn't lift herself.   Guest Bio: Cinder Shine is an author, musician, and irreverent wellness guide who's been helping people move through pain with humor and grit for over 30 years. A two-time cancer survivor and lifelong joy-seeker, she's the author of Plus Size Knee Pain Solution and her latest book, Terminally Smiling, a poignant, playful memoir on living and healing through life's hardest moments. Cinder brings fierce honesty, goofy wisdom, and unapologetic joy to every stage, page, and platform she graces.   Connect with Cinder Shine: Website: https://www.cindershine.com   Facebook: https://www.facebook.com/cinder.shine.ernst  Instagram: https://www.instagram.com/cinder_shine_ernst    Unlock Your Genius with Mellissa Seaman: Discover Your Soul Gift: Take Mellissa's free Soul Gift Quiz to uncover which of the five soul gifts is driving your life's purpose. Dive Deeper into Growth: Explore the Channel Your Genius Academy at channelyourgenius.com for personal and professional development resources. Stay Inspired: Connect with Mellissa on Instagram @channelyourgenius for ongoing wisdom and insights to help you live your purpose, expand your influence, and thrive in your business and personal life as a WiseWoman.   Keywords: Radical Joy, Cancer Survivor, Terminal Illness, Rainbow Resilience, Feminine Leaders, Wellness Coach, Intuitive Guidance, Healing, Humor, Death Ceremony, Living Fully, Emotional Resilience, Channeling Wisdom, Spiritual Growth, Embodied Joy, Creative Healing, Facing Death, Life After Diagnosis, Nature as Healer, Grief and Laughter

This week on the Tom Roland podcast, I sit down with John Gluck, the author of 'An Exercise in Uncertainty.' We dive deep into discussions about fishing, life, and John's incredible journey battling Multiple Myeloma—a rare blood cancer.  Diagnosed with only 18 months to live, John has now thrived for over 21 years, thanks in part to breakthrough treatments and his passion for fishing. We also explore how fishing became a therapeutic escape for John, the power of mindset in overcoming challenges, and the role of family and career in his ongoing battle.  Tune in to hear this inspiring story and learn from John's experiences. You can also buy Jonathan's book, “An Exercise in Uncertainty” wherever books are sold.  00:00 Introduction and Greetings 00:18 Fishing in Idaho and Jackson 00:47 The Glory Days of Fishing 01:16 Challenges of the Salmon Fly Hatch 02:54 Introducing the Book: An Exercise in Uncertainty 03:17 John's Illness and Diagnosis 03:51 Fishing as a Lifeline 04:47 Writing and Fishing Adventures 08:17 Career and Writing Focus 10:23 The Diagnosis Journey 18:26 Coping with Uncertainty 26:02 Purpose and Priorities 29:10 Fishing Dreams and Realities 33:25 Reflections on Health and Life 35:42 Facing Mortality and Embracing Life 36:45 Dealing with Remission and Relapse 39:22 Finding Solace in Fishing 42:36 The Role of Diet and Exercise 44:56 Advice for Cancer Patients 48:08 Writing the Book: A Journey of Reflection 53:53 The Importance of Mindset 01:05:08 Publishing and Promoting the Book 01:13:12 Final Thoughts and Future Plans

In part one of this two-part conversation, Dr. Erin Faules sits down with storyteller and autoimmune survivor Courtney Runyon to explore what it means to heal in the face of uncertainty. Diagnosed with CIDP, a rare autoimmune disease that left her temporarily paralyzed from the neck down, Courtney shares the realities of navigating the medical system when clear answers are scarce. They discuss the importance of mindset, self-advocacy, and the physiological toll of chronic empathy—while also holding space for humor, joy, and post-traumatic growth. Topics include: How paralysis reshaped Courtney's understanding of health and identity The role of mindset and nervous system regulation in recovery Why self-advocacy is non-negotiable in complex illness The double-edged sword of chronic empathy and its link to inflammation Finding humor and meaning in the most unexpected moments Stay tuned for part two next week.

Send us a textIn this inspiring episode of Adulting with Autism, I sit down with Carol Waldman, a lifelong political advocate and community leader, and her son Andrew Waldman, a 23-year-old recent graduate and neurodiversity advocate.Diagnosed with autism at age four, Andrew's journey from navigating social and academic challenges to graduating from the University of Wisconsin–Madison, interning in Washington D.C., and becoming a two-time Global Neurodiversity Conference panelist is nothing short of remarkable.Alongside him, Carol shares how advocacy became personal, from leading parent support groups to serving as an elected California State Democratic Party Delegate, fighting for inclusive policies, accommodations, and opportunities for neurodivergent individuals.

“Something feels off with my child…” “Is this just a phase… or something more serious?” “Should I get them evaluated?” When your child is struggling socially, emotionally, or behaviorally, the pressure to seek a diagnosis can feel overwhelming — from teachers, doctors, friends, even your own inner panic. But what if we're rushing to label what's actually part of normal — if difficult — child development? In this episode, I share 10 things every parent should try before going down the path of evaluation. Not to deny or delay treatment — but to slow down, reconnect, and make sure we're not pathologizing something that's entirely natural… and potentially solvable at home. ❤️ This is NOT about avoiding hard truths. ✅ It's about checking the basics first. There's a powerful bonus tip at the end that might be the most important of all — one that could completely change how your child sees themselves (and how you support them).

Empowerment and Success Against the Odds: Kelsey Lewis' Journey with DiabetesIn this episode of The Pediatric Lounge podcast, hosts George and his co-host welcome Kelsey Lewis, a registered dietitian and certified diabetes care specialist. Diagnosed with type 1 diabetes at 17, Kelsey turned her personal challenges into a professional mission. She shares her journey from being told she couldn't be a collegiate athlete to proving her doubters wrong. After her clinic was shut down due to financial priorities, Kelsey established a thriving private practice that now serves 23 states through telemedicine. Her resilient story underlines the importance of not letting others define your limits, the transformative power of education, and the need for independent practices to prioritize patient outcomes over profitability.00:00 Introduction to The Pediatric Lounge00:37 Meet Kelsey Lewis: A Journey from Athlete to Diabetes Specialist01:28 Kelsey's Diagnosis and Early Challenges02:52 Overcoming Obstacles: From High School to College Athlete11:17 Transition to Professional Life and Systemic Challenges23:50 Establishing a Private Practice and Expanding Nationwide27:47 Telemedicine Success and Future Prospects28:53 Lessons in Resilience and Overcoming Adversity30:45 Partnering with Medical Practices for Better Outcomes35:26 Challenges and Advocacy in Pediatrics40:30 The Impact of Sugar and Salt on Health49:32 Final Thoughts and Advice for ParentsYou can connect with Kelsie here. Diabetes dialogues podcastDiabetes insights for HCPs. Dexcom's expert-led podcast, Diabetes Dialogues.Listen on: Apple Podcasts SpotifySupport the show

Seán's guest suffered a mental health episode during lockdown while living in Italy. Diagnosed as psychosis, a condition she wasn't familiar with, her journey out of it has been a challenging task.Joining to discuss is Lisa Callaghan, an Ambassador for Shine, the mental health charity…Samaritans 24/7 Freephone Helpline - 116 123

This week on The Brave Table, I sit down with the radiant Eliska Vaea, a feminine leadership mentor, ceremonialist, and spiritual teacher whose work has touched thousands of women around the world. Diagnosed with incontinence at just 16, Eliska turned what could have been a lifelong struggle into her sacred calling—guiding women back into the wisdom of their wombs and bodies. From professional athlete to global healer, her journey has taken her through 70+ countries, deep into ancient rites, shamanic teachings, and her own powerful womb-led awakening.In this powerful conversation, we dive into the magic of the feminine body, how to listen to the whispers of your womb, what true success looks like when it's not forced, and how high-performing women can finally soften and return to themselves. This episode is an invitation into your own rebirth—and trust me, you'll feel it.What you'll get out of this episode… The story behind Eliska's feminine awakening and how it changed her life foreverThe powerful (and often misunderstood) truth behind Kundalini awakeningsWhat womb-led leadership really looks like—and how it can shift your business, relationships, and fertilityWhy high-performing women are craving softness and how to give yourself permission to softenSimple daily rituals to connect with your womb and feminine essenceA redefinition of success that centers fulfillment, embodiment, and cyclical powerThis Episode is Powered by Health NagMeet your new daily glow-up: Health Nag's Bioactive Collagen Jelly—the world's first collagen with Types I, II, III & IV for full-body support (skin, gut, joints & more).Tastes amazing. Absorbs fast. One spoon a day = science-backed resilience from the inside out.

Send me a DM here (it doesn't let me respond), OR email me: imagineabetterworld2020@gmail.comI'm honored to introduce you all to: Satanic ritual abuse, mind control, and organized abuse survivor and overcomer, loving mother and devoted wife, artist, podcaster and host of her own podcast ‘Arise and Shine', founder of SHOUT for Help non-profit, facilitator for Relentless Hope, singer and songwriter, writer and blogger, videographer, advocate for future overcomers, author, speaker, videographer, written and spoken word poet, and advocate for current and future overcomers: Sharri BurggraafSharri's life is a testament to the transformative power of faith, resilience, and purpose. Born on Friday the 13th, 1957, in Dubuque, Iowa, to a Catholic family, Sharri's early years were marred by unimaginable trauma. Subjected to ritual abuse, mind control, child pornography, and sex trafficking, her childhood was stolen by multiple perpetrators, including her parents, a priest, a nun, and an elite network of businessmen. Under the guise of a "talented and gifted program," she was bussed from school to a free medical clinic where she endured torture-based mind control, electric shocks, medical experimentation, and psychological programming - deceptively framed as cancer research conducted by German scientists. Her father, a World War II veteran, was also ensnared in these sinister programs, and Sharri believes he was murdered to silence his attempts to escape, with threats used to keep her enslaved.These experiences were designed to fracture and control, yet within her, a spark of resilience refused to be extinguished. Diagnosed in the early 1990s with Dissociative Identity Disorder she embarked on a courageous journey of recovery. Her path was not linear nor easy, but was a winding road marked by pauses to raise her children and moments of profound dedication to healing.As a founding member of Dissociative Writers, and a facilitator for Relentless Hope, Sharri also runs support groups and writing workshops, including her upcoming Project J.U.S.T.I.C.E. training initiative for survivor-clinicians, law enforcement, and advocates. Her work with Relentless Hope aligns with her heart for survivors, emphasizing their value, collective power, and right to be believed. As a beacon of light for survivors, Sharri challenges the stigma and disbelief surrounding ritual abuse and mind control. She confronts the societal denial that often compounds survivors' pain, advocating for awareness of human trafficking and the interconnectedness of ritual abuse and mind control with multigenerational abuse. Her mission is not to rescue single-handedly but to collaborate with others, amplifying voices and fostering hope for those still trapped in darkness.Sharri stands as living proof that one can emerge from the depths of trauma to shine brightly, guiding others toward their own liberation. Her journey reminds us that even in the face of unimaginable evil, the human spirit can reclaim its power, rewrite its story, and inspire a world in need of hope. To every survivor, Sharri's voice echoes: You are not alone. If I can escape, so can you.CONNECT WITH SHARRI: Website: https://ariseandshineafterabuse.com/Spotify: https://open.spotify.com/artist/36X5N0DuOl4xTabqDhKZIITikTok: https://www.tiktok.com/@sharriburgCONNECT WITH EMMA / THE IMAGINATION: 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/theimaginationAll links: https://direSupport the show

Best Of 2GG: Self Diagnosed PART 1 by Two Girls and a Guy

In this episode of Intermittent Fasting Stories, Gin talks to Alyssa Welling from West Des Moines, IA.Gin has a new YouTube Channel! Visit https://www.youtube.com/channel/UC_frGNiTEoJ88rZOwvuG2CA and subscribe today so you never miss an intermittent fasting tip, a support session, or an interview with a past IF Stories guest or expert.Are you ready to take your intermittent fasting lifestyle to the next level? There's nothing better than community to help with that. In the Delay, Don't Deny community we all embrace the clean fast, and there's just the right support for you as you live your intermittent fasting lifestyle. You can connect directly with Gin in the Ask Gin group, and she will answer all of your questions personally. If you're new to intermittent fasting or recommitting to the IF lifestyle, join the 28-Day FAST Start group. After your fast start, join us for support in The 1st Year group. Need tips for long term maintenance? We have a place for that! There are many more useful spaces beyond these, and you can interact in as many as you like. Visit ginstephens.com/community to join us. An annual membership costs just over a dollar a week when you do the math. If you aren't ready to fully commit for a year, join for a month and you can cancel at any time. If you know you'll want to stay forever, we also have a lifetime membership option available. IF is free. You don't need to join our community to fast. But if you're looking for support from a community of like-minded IFers, we are here for you at ginstephens.com/community. Alyssa is an administrative assistant for the parks and recreation department. Alyssa explains how she initially dismissed IF as “unhealthy” when someone first mentioned it to her, but grew curious after plateauing on Weight Watchers following two close pregnancies. She recounts how, beginning in early 2020, she dove into fasting podcasts and adopted a gentle 16:8 approach, gradually shortening her eating window as her comfort and understanding grew. Alyssa describes how immersing herself in fasting resources helped her unlearn pervasive diet culture messages like the need for constant meals and snacks.The conversation delves into Alyssa's challenges and milestones, from her significant weight fluctuations due to multiple pregnancies and postpartum experiences, to the setbacks she faced after a bout of Covid that caused her to regain some of the weight she had lost. Then, Alyssa became pregnant with her third child, which meant she needed to take a break from IF. After her third baby was weaned, Alyssa went back to IF, but she didn't see the weight loss she was hoping for. Despite that, she never abandoned IF, citing the mental clarity and stress reduction it provided as reasons to stick with the lifestyle regardless of the scale.A pivotal point in Alyssa's journey came when she confronted the reality that her eating habits—particularly mindless binging and snacking during her eating window—were undermining her progress. Diagnosed with ADHD and binge eating disorder, she used calorie tracking for awareness and shifted her focus to intentional, satisfying meals, and avoided grazing and finishing her children's leftovers. Alyssa added regular, enjoyable treadmill walks to her routine and cut out alcohol, which improved her food choices and boosted her well-being. These changes, paired with intermittent fasting, helped her shed over 100 pounds, reaching a weight lower than she dreamt possible, and transforming both her confidence and quality of life.Alyssa wraps up by offering heartfelt advice for those starting out with intermittent fasting: don't expect drastic changes overnight and avoid focusing on a specific finish line. She emphasizes that lasting success comes from treating IF as a sustainable lifestyle, allowing ample time to adapt, maintaining a clean fast, making foods work for your body, and not being afraid to make adjustments if progress slows. Alyssa also encourages listeners to be open about fasting without shame and to remember that growing bodies—like those of children—need to eat differently. Ultimately, she underscores that giving yourself the grace to adjust and the patience to persevere are the keys to enjoying the many benefits IF has to offer.Get Gin's books at: https://www.ginstephens.com/get-the-books.html. Good news! The second edition of Delay, Don't Deny is now available in ebook, paperback, hardback, and audiobook. This is the book that you'll want to start with or share with others, as it is a simple introduction to IF. It's been updated to include the clean fast, an easier to understand and more thorough description of ADF and all of your ADF options, and an all new success stories section. When shopping, make sure to get the second edition, which has a 2024 publication date. The audiobook for the second edition is available now! Join Gin's community! Go to: ginstephens.com/communityDo you enjoy Intermittent Fasting Stories? You'll probably also like Gin's other podcast with cohost Sheri Bullock: Fast. Feast. Repeat. Intermittent Fasting for Life. Find it wherever you listen to podcasts. Share your intermittent fasting stories with Gin: gin@intermittentfastingstories.comVisit Gin's website at: ginstephens.com Check out Gin's Favorite Things at http://www.ginstephens.com/gins-favorite-things.htmlSubscribe to Gin's YouTube Channel! https://www.youtube.com/channel/UC_frGNiTEoJ88rZOwvuG2CASee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Want to fall in love with your ADHD brain and make it work for you? Learn more about my patented program, Your ADHD Brain is A-OK Academy  here: programs.tracyotsuka.com/signup___Aging with ADHD isn't about decline—it's about finally coming into your own. Sandy Reynolds is challenging everything we've been told about getting older, especially as neurodivergent women.Sandy is a coach, facilitator, and fierce advocate for women navigating their third act. With more than 25 years of leadership and adult education experience, she helps women untangle themselves from outdated roles, people-pleasing patterns, and identities that no longer fit. Diagnosed with ADHD in her 50s after a fellow grad student pointed out that she "checked out a lot," Sandy brings lived experience to conscious aging—an approach that's about healing the past and embracing the future so you can flourish now.In this conversation, Sandy and Tracy explore why ADHD women often look and feel 10 years younger, how our relentless curiosity keeps us growing when others stagnate, and why so many of us hit our stride in our 50s instead of winding down. They dive into the intersection of hormones, dopamine, and aging, discuss why Sandy's closest friend and she "carry on like they're 35," and explore how conscious aging reframes getting older as gaining wisdom rather than losing relevance.Sandy also shares her approach to life review and life repair, explains why one-third of people don't have wills (hint: executive function), and reveals her number one ADHD workaround that no guest has mentioned in 350+ episodes. From Cambodia's reverence for elders to our culture's ageism, this episode will make you rethink everything about what it means to age as a neurodivergent woman.Resources:Website: https://www.sandyreynolds.com   Instagram: https://www.instagram.com/sandyareynolds  LinkedIn: https://www.linkedin.com/in/sandyreynolds  Substack: A Crone in the Woods: https://crone.substack.com Send a Message: Your Name | Email | Message Learn more by connecting with Tracy through Instagram, Facebook, LinkedIn, Pinterest, or visit adhdforsmartwomen.com.Are You Ready to Discover Your Brilliance? Order Now: https://tracyotsuka.com/book2Join Your ADHD Brain is A-OK: https://tracyotsuka.com/aok Visit our website: https://tracyotsuka.com Join our community of ADHD For Smart Ass Women: https://www.facebook.com/groups/tracyotsuka Join What Do I Do With My Life Masterclass: spyhappy.me/classUnlock your best days with Blends: https://tracyotsuka.com/blends

This week's Misfit Entrepreneur is Skye Waterson. If you've ever struggled with traditional productivity systems or felt like your brain just doesn't fit the mold, Skye's story and work will be a game-changer. She's the founder of Unconventional Organisation, an ADHD support and coaching service designed to help entrepreneurs and executives build focused, sustainable success—without burnout. Diagnosed with ADHD while completing her PhD, Skye realized that the usual productivity advice wasn't built for minds like hers. So she created her own framework—one that now powers the systems used by over 82,000 professionals who follow her work. Her podcast The ADHD Skills Lab has over 200,000 downloads, and her web articles have reached more than a quarter million readers. ​ Skye's belief is that ADHD isn't a flaw to overcome—it's a different operating system that, when properly supported, can be a massive asset. And through her work with founders, executives, and creatives, she's helping people rewire their approach to focus, consistency, and scale. www.unconventionalorganisation.com/ Show Sponsors: Entrepreneurs, what if there was a way to know you were hiring the best salespeople to drive your business? How much would that help your success? Well, with SalesDrive's DriveTest, you can! Drive is composed of three non-teachable traits shared by all top producers: Need for Achievement, Competitiveness, and Optimism. You can get a FREE DriveTest assessment to help you in your hiring efforts at www.MisfitEntrepreneur.com/SalesDrive 5 Minute Journal: www.MisfitEntrepreneur.com/Journal

Today's episode is one of the most powerful we've ever done on Money Rehab. Nicole sits down with a listener named Erin, who reached out after being diagnosed with stage 4 breast cancer. Her message was simple, yet profound: “I need to get my finances in order to make sure my loved ones are taken care of.” What follows is a raw, courageous conversation about life, money, and legacy. Erin shares her fears, her love for her family, and the steps she's taking to give them financial peace of mind. Nicole brings in attorney Veronica Escobar to walk through the essentials of estate planning—from wills and trusts, to power of attorney and beyond. This is not just a conversation about preparing for death. It's about taking control, even in moments when everything feels uncertain. It's about how we can use money as a tool to protect the people we love. This episode is for anyone who wants to plan ahead, not out of fear, but out of love. It's an emotional listen, but an essential one. Tomorrow's episode will be a follow-up, where Nicole answers Erin's questions about saving for medical care. But today, we focus on what Erin wanted most: peace of mind for her family. Check out the company Nicole connected Erin with for estate planning, Trust and Will, here  Learn more about Veronica Escobar's work and practice here This podcast is for informational purposes only and does not constitute financial, investment, or legal advice. Always do your own research and consult a licensed financial advisor before making any financial decisions or investments. All investing involves the risk of loss, including loss of principal. Brokerage services for US-listed, registered securities, options and bonds in a self-directed account are offered by Public Investing, Inc., member FINRA & SIPC. Public Investing offers a High-Yield Cash Account where funds from this account are automatically deposited into partner banks where they earn interest and are eligible for FDIC insurance; Public Investing is not a bank. Cryptocurrency trading services are offered by Bakkt Crypto Solutions, LLC (NMLS ID 1890144), which is licensed to engage in virtual currency business activity by the NYSDFS. Cryptocurrency is highly speculative, involves a high degree of risk, and has the potential for loss of the entire amount of an investment. Cryptocurrency holdings are not protected by the FDIC or SIPC.  *APY as of 6/30/25, offered by Public Investing, member FINRA/SIPC. Rate subject to change. See terms of IRA Match Program here: public.com/disclosures/ira-match.

In this solo, I'm answering all your questions. Starting with fertility - is adoption on the table for us? Do I have an exact infertility diagnosis? Has the fertility process affected our sex life? What shifted between Timmy and I after having Sonny? My thoughts and feelings about being labeled the breadwinner. If you are thinking of having your first baby, I've got some thoughts for you, along with my honest feelings about having kids with a big age gap. You also asked about beauty and I'm always down to wax on about that - where I get Botox, my favorite all-time hair color and cut, if I use at-home light therapy, and a looooot more. I love being able to answer your specific questions so always keep them coming! This episode may contain paid endorsements and advertisements for products and services. Individuals on the show may have a direct, or indirect financial interest in products, or services referred to in this episodeThis episode is brought to you by The RealReal, K12 Education, Venmo, Function Health, and Astral Tequila. With thousands of new arrivals daily, no one does resale like The RealReal. And now, get $25 off your first purchase when you go to therealreal.com/whitJoin the more than 3 million families who have been served by K12, and empower your student to reach their full potential now. Go to K12.com/WITHWHIT today to find a tuition-freeK12 powered school near you and enroll now.Venmo Everything with the Venmo Debit card. Visit Venmo.me/debit to learn more and sign up today. If you're ready to stop guessing and start knowing, learn more and join Function Health. The first thousand get a $100 credit toward their membership. Visit www.functionhealth.com/WITHWHIT or use gift code WITHWHIT100 at sign-up to own your health.House marg summer is here!! Time to stock up! Go to www.astraltequila.com to find Astral near you - and don't forget the limes! Please enjoy responsibly.Produced by Dear MediaSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Managing type 1 when your job means you burn more than 5-thousand calories and lose 10 pounds of water in one day is.. a little different. I caught up with IndyCar driver Conor Daly who is in the middle of the season right now! Diagnosed at 14, Conor talked to me about continuing to chase his dreams of racing, using inhaled insulin – Afrezza – as part of his T1D management for a long time now, how he deals with diabetes during races, and a lot more. This podcast is not intended as medical advice. If you have those kinds of questions, please contact your health care provider. Join us at an upcoming Moms' Night Out event! Learn more about studies and research at Thrivable here Please visit our Sponsors & Partners - they help make the show possible! Learn more about Gvoke Glucagon Gvoke HypoPen® (glucagon injection): Glucagon Injection For Very Low Blood Sugar (gvokeglucagon.com) Omnipod - Simplify Life Learn about Dexcom  Check out VIVI Cap to protect your insulin from extreme temperatures The best way to keep up with Stacey and the show is by signing up for our weekly newsletter: Sign up for our newsletter here Here's where to find us: Facebook (Group) Facebook (Page) Instagram Check out Stacey's books! Learn more about everything at our home page www.diabetes-connections.com  Reach out with questions or comments: info@diabetes-connections.    

This Is How I Got Diagnosed With Narcissistic Personality Disorder (NPD) using the MMPI-2 and the PDQ4. I have been in psychotherapy for nearly 8 years since getting diagnosed. Contact Me - ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://link.me/mentalhealness⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠I'm Lee & I've been diagnosed with narcissistic personality disorder ( NPD ). I've been in therapy since 2017 & It has definitely changed my life because without it, I would have lost everything. My platform is dedicated to giving you the WHYs behind the things that Narcissists do. I'm not here to diagnose ANYONE or to tell you to leave your relationship. I'm just trying to give you the information to make your own informed decisions1 on 1's and all my links - ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://beacons.page/mentalhealness⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Remember, It's not your fault - ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://a.co/d/2WNtdKJ ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Podcast Guest Form -⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ https://tinyurl.com/Mental-Healness-Podcast-Form⁠⁠⁠

Tim, Phil, Mary, & Carter are joined by Six Seven Kevin to discuss Trump being diagnosed with a chronic vein disease, WSJ reporting Trump sent sexy letters to Jeffrey Epstein, CNN losing it over Trump's approval rating surging, and CBS canceling The Late Show.   Hosts:  Tim @Timcast (everywhere) Phil @PhilThatRemains (X) Mary  ⁨@PopCultureCrisis⁩  (everywhere) Carter @carterbanks (X) Serge @SergeDotCom (everywhere) Guest: Six Seven Kevin | SixSevenStories.com

Gavin Newsom, born in San Francisco, California, is the 40th Governor of California, serving since 2019. A Democrat, he was Lieutenant Governor (2011–2019) and San Francisco's youngest mayor in a century (2004–2011), gaining national attention for issuing same-sex marriage licenses in 2004. Diagnosed with dyslexia at age five, Newsom graduated from Santa Clara University in 1989 with a BS in Political Science.  He founded PlumpJack Group in 1992, growing it into a multimillion-dollar enterprise with wineries, restaurants, and hotels. Newsom survived a 2021 recall election and was reelected in 2022 with 59% of the vote.He authored Citizenville (2013), advocating digital governance, and has hosted the podcast This is Gavin Newsom since 2025. Newsom champions progressive policies. Shawn Ryan Show Sponsors: https://aura.com/srs https://americanfinancing.net/srs https://bubsnaturals.com – USE CODE SHAWN https://shawnlikesgold.com https://helixsleep.com/srs https://hexclad.com/srs https://ketone.com/srs Visit https://ketone.com/srs for 30% OFF your subscription order https://moinkbox.com/srs https://mypatriotsupply.com/srs https://patriotmobile.com/srs https://ROKA.com – USE CODE SRS https://shopify.com/srs https://betterhelp.com/srs This episode is sponsored. Give online therapy a try at betterhelp.com/srs and get on your way to being your best self. Gavin Newsom Links: Website - https://www.gov.ca.gov  X - https://x.com/GavinNewsom  Facebook - https://www.facebook.com/GavinNewsom  YT - https://www.youtube.com/@ThisisGavinNewsom PlumpJack Group - https://www.plumpjack.com Learn more about your ad choices. Visit podcastchoices.com/adchoices