Podcasts about diagnosed

What do you when your life starts again? Michelle and Seth talk with Roush Niaghi and Greg Morris, the directors and all around 2-man film crew behind Ali Eats America, a new documentary about the life of Ali Allouche. Diagnosed with cancer, Ali and his mom Jennifer plan a dream trip for after his treatment centered around visiting restaurants across America. Roush and Greg discuss navigating the medical system, dealing with an ever changing story and how sometimes the most difficult things are the ones that bring us life.  This interview is part of a series we are doing to highlight the creative voices behind the films selected for the 30th Stony Brook Film Festival.  Use code MOVIEFRIENDS to save 25% off your pass at the  Stony Brook Film Festival Ad-free versions of all of our episodes are available on our Patreon When you sign up you also get access to our bonus shows, Discord server, decoder ring, shout out on the show AND you get to vote on monthly episodes and themes. That's a lot for only $5 a month! For more info and to sign up visit us on Patreon You can also give a Movie Friends subscription here: Gift a Movie Friends Subscription! Visit our website Send us an email! Follow us on Twitter and Instagram Fill out our listener survey

Sponsor: Timothy Plan aligns your biblical values with your financial stewardship in a way that honors God. Click here to learn more!In this powerful and emotional episode, Abby sits down with singer-songwriter Ryan Tremblay to share the remarkable story of his sister Erica. Diagnosed with terminal cancer while pregnant, Erica made the courageous choice to carry her baby, Ella, to term—refusing abortion and choosing life, even at the cost of her own. Ryan opens up about the heartbreak, hope, and enduring impact of Erica's faith-filled journey. He reflects on how her legacy continues to shape his life, inspire his music, and unite their family. Listeners will hear about the challenges Erica's children, Cade and Ella, have faced and Ryan's heartfelt desire to bring healing and togetherness to their lives.This episode is a testament to the power of faith, the beauty of sacrifice, and the strength of a mother's love. Stay tuned for details on the upcoming film that will bring Erica's story to the screen—and learn how you can support Ryan's music and mission to keep her legacy alive.FOLLOW ABBY ON SOCIAL MEDIA- Instagram- Facebook- Twitter

In this powerful and inspiring episode of UnabridgedMD, host Dr. Isabelle Amigues welcomes Dr. Ward, a chiropractor and functional medicine practitioner, to share his remarkable story of resilience, healing, and clinical transformation. Diagnosed with systemic lupus as a teenager and told he might not live past 30, Dr. Ward defied the odds and turned his diagnosis into a mission to empower others through integrative, lifestyle-based medicine.Together, they explore the intersections of autoimmunity, cognitive decline, and the role of functional medicine in restoring health and hope. Dr. Ward discusses his work using the Bredesen Protocol for Alzheimer's prevention, the impact of lifestyle on chronic disease, and how empowerment and mindset are key to healing.Whether you're a healthcare professional, patient, or simply curious about holistic approaches to wellness, this episode offers a hopeful and science-based roadmap for taking control of your health.

Show notes:Are there people who inspire you, make you want to be better and do better?I have been fortunate to meet with amazing and inspirational people from all walks of life through my podcast The Elephant in the Room. Individuals who refuse to be defined by their circumstances or the challenges they encounter in life. Akashdeep Bansal, CEO of SaralX, and my guest for the 134th episode of the podcast is one such person. Diagnosed with retinitis pigmentosa at a young age, Akash's path took an unexpected turn when a conversation with his master's supervisor prompted him to consider the challenges faced by visually impaired individuals in pursuing STEM education. This pivotal moment not only reshaped his academic trajectory but also inspired the creation of SaralX, a startup focused on enhancing digital accessibility for people with disabilities.In this episode we spoke about

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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___When you're the eldest daughter of immigrants with ADHD and autism, you learn to mask early and master systems—but at what cost? Meral Alizada knows this story intimately, and she's using it to transform how companies think about neurodivergent talent.Meral is the founder of Results of Kindness (ROK), where she helps organizations build workplaces where neurodivergent minds aren't just accommodated, they're celebrated. With degrees in Law and Psychology and a background in organizational psychology, she knows how to navigate systems. But what sets her apart is how she redesigns them with empathy, creativity, and a deep understanding of what actually works for ADHD and autistic brains.Diagnosed with both ADHD and autism in her late twenties while working one-on-one with a brilliant child who shared her traits, Meral's journey from law to psychology to entrepreneurship is as nonlinear as her thinking. In this conversation, she and Tracy explore the weight of being ultra-organized out of anxiety, the loneliness of outgrowing friendships, and why our relentless drive for self-development might be our greatest superpower.Meral also breaks down her "Genius Retention" program, explaining why kindness isn't just nice to have—it's profitable. When 89% of workers want kindness in the workplace but 77% are disengaged globally, she argues that treating people as human beings strengthens the hands with which they contribute to organizations. Born to Afghan-Uzbek parents and raised across Europe, Meral brings both global perspective and deeply personal insight to the future of work.Resources:Website: https://resultsofkindness.co.uk Instagram: https://www.instagram.com/themeralalizada  LinkedIn: https://www.linkedin.com/in/meralalizada 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

What happens when a late ADHD diagnosis meets the powerful potential of AI? Writer, strategist, and sleep coach Lindsay Scola joins Morra to share how she uses AI as a personal productivity partner to manage ADHD challenges, perfectionism, and executive dysfunction—while preserving creativity and rest. Diagnosed with ADHD at 41, Lindsay discovered that AI could act as an accountability buddy, thought partner, and creativity booster. From using AI to overcome the dread of the blank page to automating follow-up emails, Lindsay shares practical ways she leverages AI without losing her humanity. Buy Lindsay's book here: https://www.amazon.com/AI-ADHD-Practical-Starting-Finishing-ebook/dp/B0F5T9QKMH Listen to our interview about the stimulant shortage, narcolepsy and ADHD: https://podcasts.apple.com/us/podcast/the-ritalin-and-adderall-shortage-and-how-it-impacts-work/id1480904163?i=1000611595946 Key Themes: AI as an ADHD Copilot: Lindsay explains how AI helps her manage executive dysfunction, tackle writing tasks, and avoid the overwhelm of perfectionism while maintaining her unique voice. Reducing Shame and Preserving Brain Space: Using AI for small but stressful tasks frees up cognitive space, letting her focus on big ideas and creative work without getting stuck in spirals of self-criticism. Permission to Play: Lindsay urges people with ADHD to experiment with AI and other tools to find what actually works for their brains instead of following rigid systems that suppress creativity. Scheduling for Neurodivergent Brains: From building “dopamine deadlines” to respecting personal circadian rhythms, Lindsay shares how she structures her week to maximize focus while honoring energy dips. AI for Burnout and Loneliness: We discuss how AI can help solo workers feel less isolated and provide accountability without judgment, acting like a team member who says, “let's keep going.” Timestamps: 03:28 ADHD, Midlife, and AI Solutions 08:13 Balancing Perfection and Completion 11:07 Childhood Injustice and Self-Awareness 18:30 Optimize Productivity by Time Awareness 19:37 Embrace Napping for Productivity 25:40 AI-Assisted Writing for Quick Posts 29:06 Podcasting Inspiration for Writing Newsletter 32:32 Flexible Time Management Strategy 35:50 Improvised Charging Solution

“When you heal yourself, it is a spiritual experience.” What if healing isn't something outside of you, but a remembering of what's already within? In today's episode of Soul Talk, I sit down with Donna Eden, world-renowned teacher, energy medicine pioneer, and living example of what's possible when we trust the body's wisdom. At 16, Donna was diagnosed with multiple sclerosis. By her twenties, doctors told her to “get her affairs in order.” But instead of giving up, she turned inward and activated a healing intelligence that transformed her life forever. In this conversation, we explore what true healing means, from chronic illness to emotional trauma, from heartbreak to soul fatigue. Donna shares simple yet powerful energy techniques you can use right now to awaken vitality, move through pain, and reconnect with your joy. We talk about trauma, aging, intuition, seeing energy, and the sacred design of the human body, and why your energy field holds the blueprint for your transformation. Tune in and learn how to regulate your nervous system, release trauma, protect your energy without building walls, and why so many of us feel disconnected. Timestamps: (00:02:30) - Donna's early life: seeing energy as a child (00:04:07) - Diagnosed with multiple sclerosis at 16 (00:05:40) - How Donna healed herself without medical intervention (00:08:09) - Teaching her first energy medicine class (00:12:05) - Why most people can't sense energy and how to reactivate it (00:17:30) - The simple “cross-over” technique to balance energy (00:20:30) - What is the “assemblage point,” and why does it matter (00:26:40) - Can you make someone else happy with energy (00:29:15) - Energy “protection” tips: what works (00:36:30) - Working with trauma and rewiring your stress response (00:43:00) - Heartbreak and how to move energy out of the heart (00:46:55) - Lessons from Donna's journey, forgiveness, and legacy Some Questions I Ask: What sparked your journey into energy healing? Is it possible to heal yourself without medical treatment? Can anyone learn to see or feel energy? Why do most people lose the ability to sense energy? How can we protect our energy in today's chaotic world? What's the first step to activating your energy system? Can everyone heal from trauma, illness, or heartbreak? In This Episode, You Will Learn: How Donna healed herself from multiple sclerosis using energy work. The truth about energy healing, self-healing, and how to awaken your body's innate intelligence. A step-by-step guide to Donna's powerful yet simple “crossover technique” for restoring energetic balance and boosting vitality. How to naturally raise your vibration, strengthen your aura, and become a radiant presence that positively affects others. Why most people lose the ability to feel energy, and how to reactivate your energetic senses. The real secret to protecting your energy in a chaotic or toxic environment, without walls, fear, or withdrawal. How to rewire your nervous system, deactivate stress and trauma responses, and restore emotional regulation through meridian-based techniques.   LINKS DONNA EDEN'S URL:   https://www.edenmethod.com Get in Touch: Email me at kuteblackson@kuteblackson.com Visit my website: www.kuteblackson.com Resources with Kute Blackson: Kute's Life-changing Path to Abundance & Miracles: https://www.8levelsofgratitude.com Free masterclass: Learn the Manifestation secret to Remove Mental Blocks & Invisible Barriers to Attracting the Life of Abundance You Desire. REGISTER NOW:  https://www.manifestationmasterclassonline.com  

“I was pumping in the NICU, feeling completely disconnected—and my husband looked at me and said, ‘Can you invite her in?' That moment changed everything. A nurse handed me a swab, I gave my baby colostrum for the first time, and I thought, ‘I'm a mommy.'” – Tanisha NICU mom and advocate Tanisha shares her deeply moving journey through an unexpected fetal diagnosis, a 157-day NICU stay, and the powerful moments that helped her reconnect with motherhood. Diagnosed at 20 weeks with Lower Urinary Tract Obstruction (LUTO)—a rare, life-threatening condition—Tanisha's son Jaleel faced impossible odds. From transferring care to Cincinnati Children's Hospital, navigating in-utero surgery, to forming a life-saving care team that included her husband and child life specialists, Tanisha's voice is a beacon of strength, love, and resilience.

In this inspiring episode of Living Well with MS, we're joined by Kristen Karasek, a passionate advocate, dance teacher, and vibrant force in the MS community. Diagnosed at 24, Kristen has turned her MS journey into a mission to give back, raise awareness, and uplift others through movement and advocacy. Kristen is also the recipient of the Dorothy Corwin ‘Spirit of Life' Award, a prestigious honour presented by the National MS Society to individuals who exemplify exceptional courage, compassion, and positivity while living with MS. This conversation explores everything from political activism to the healing power of dance, and how to find your voice as an advocate, whether in the doctor's office or the wider world. Topics and timestamps: 01:54 Kristen's MS diagnosis and journey 04:33 How healthy lifestyle habits have supported Kristen 06:02 Why therapy and peer connection matter when you're newly diagnosed 08:07 The personal power of giving back to the MS community 09:10 How to get involved in State Action Days and political advocacy 11:21 The impact of dance and movement on MS symptoms 12:54 Advocating for the right healthcare team 14:32 How to advocate for yourself during appointments 15:33 What winning the Dorothy Corwin Spirit of Life Award meant to her 17:20 Kristen's advice for those newly diagnosed with MS. More info and links: Kristen's dance studio Book: Multiple Sclerosis for Dummies The Pacific Neuroscience Institute where Barbara Giesser, MD practices New to Overcoming MS? Visit our introductory 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 support the ongoing work of Overcoming MS, you can 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.

In this honest and eye-opening episode, Lindsey Maestas dives deep into the impact of ADHD on relationships and friendships. With vulnerability, faith, and research-backed insight, she explores why many people with ADHD subconsciously seek out chaos, conflict, toxic relationships, or emotionally unavailable partners. It isn't out of desire, but as a way of seeking out neurological stimulation. Lindsey discusses how ADHD can intensely heighten feelings of rejection, create a cycle of emotional highs and lows in relationships, often leading to toxic dynamics, chronic arguing, and feelings of inadequacy or isolation. She unpacks the difference between laziness and ADHD Paralysis, explaining the brain science behind task initiation struggles and why shame is often misdirected.  Whether you've been diagnosed with ADHD, have a partner or friend who struggles with it, or simply relate to the patterns of emotional burnout, impulsive decisions, or feeling like you're “too much” in relationships, this episode is a lifeline. Lindsey encourages self-compassion and offers tangible insight to help you understand your brain, regulate your emotions, and build healthier, more stable connections without sacrificing your joy.  Don't forget to give a quick rating and review on Spotify or the Podcasts app (pretty please!) SUBSCRIBE for more conversations like this.  Follow along with me on IG: @livingeasywithlindsey

We're diving into a topic that's generating a lot of buzz in the T1D community: GLP-1s. To break down what these medications actually do, what the research says, and how they might benefit people with type 1 diabetes, we're joined by pediatric endocrinologist Dr. Justin Gregory. We explore what GLP-1s are, how they work in the body, and why they're attracting so much attention in T1D care. Dr. Gregory shares insights on their effects on blood sugar, insulin needs, and insulin sensitivity (and whether those benefits are purely tied to weight loss or something more direct). Whether you've only seen GLP-1s mentioned on social media or you've already started a conversation with your healthcare team, this episode brings clarity to the hype and the hope. Don't miss this conversation - we're answering all the questions the T1D community has been waiting for.Quick Takeaways:Everything you need to know about GLP-1s: What they are, who they are meant for & why they are getting so much hypeThe impact these medications have on T1D: Blood sugar, insulin needs, insulin sensitivity, and more Breaking down the risks: Direct impact on T1D (blood sugars, insulin needs, etc.) and side effects of long-term use How GLP-1s are being prescribed off-label to type 1s and the important conversations people with T1D should have with their provider before starting them Timestamps:[03:13] Dr. Gregory's journey into Endocrinology [03:37] “Diagnosed with T1D and I was told, your Air Force career is over…”[05:21] “My research says, what is the cost of putting too much insulin in the wrong place?”[09:43] One of the most underappreciated aspects of T1D: Insulin sensitivity  [XX:XX] “Insulin sensitivity is 30 to 50% lower in type 1 diabetes compared to mass control.”[12:34] How to determine your insulin sensitivity (and increase it)[21:13] The breakdown of GLP-1s [23:25] Understanding GLP-1s efficacy in T1D [27:09] Who will benefit from these medications vs. who might hurt [30:41] Insulin resistance with a healthy BMI: How is it possible?[34:42] Prescribing these medications to children [38:34] How GLP-1s could be used for the newly diagnosed T1D population[39:00] Dr. Gregory's expectations for the future and evolution of these medications [41:06] Pregnancy + GLP-1s[46:24] “When you come off of it, if you're not staying on it forever, what happens?”What to do now: Follow me @lauren_bongiorno and @riselyhealth on Instagram to stay in the loop when new episodes drop.Apply for coaching and talk to our team so you can reclaim the life you deserve.  Join the PEP (Parents Empowering Parents) Squad, a Facebook group created by the Diabetes Research Institute. This is a place where caregivers of kids with T1D can share stories, ask questions, and learn more about how to get involved with research, advocacy, and fundraising through DRI. 

✦ Can you name a feeling? Dashill Smith and the musicians and vocalists that join him at TenATL certainly think so. City Lights Collective co-host Jon Goode recently went to visit TenATL in East Atlanta to learn more. ✦ In honor of MLB All-Star Week, Truist Park isn’t the only place in Cobb County to see baseball this summer. A new exhibition at the Marietta Cobb Museum of Art features the work of artist Mike Schacht—a prolific painter of baseball legends. ✦ Known to soap opera fans as the hold no prisoners mob by Sonny Corinthos on General Hospital, actor Maurice Bernard has earned several daytime Emmy awards and the attention of millions of fans. However, in recent years, he has stepped into the role of a lifetime: mental health advocate. Diagnosed with bipolar disorder, Bernard has used several platforms, including his podcast, State of Mind, to raise awareness about living with mental illness. He'll share his candid experiences at the Punchline on July 24th with his one-man show, Maurice Bernard: Live on Stage. ✦ Artist, illustrator and educator Faith Ringgold showed us our world through the eyes of young children in every medium you can think of –books, paintings, drawings, sculptures, even quilts. Trained and extensively honored in the fine art and academic circles of New York City, Faith Ringgold nevertheless focused her work on the children who remained her lifelong muse, working as an art teacher in New York City public schools for decades. Now, the High Museum is presenting the most comprehensive exhibition to date of Faith Ringgold’s art from her children’s books, including never-before-seen pieces. ✦ Municipal Support for the Arts ✦ They play on street corners, beneath overpasses, and in MARTA stations — creating the soundtracks of Atlanta’s daily hustle. But who are these street performers, and what drives them? WABE arts reporter Summer Evans explores the city’s vibrant busking scene and learns how it compares to other musical cities.See omnystudio.com/listener for privacy information.

In this SAFE SPACE episode, Jess sits down with Chloe Hayden to explore what it’s really like to live as a Neurodivergent Woman. Chloe is an award-winning actress, author, advocate who's redefining what it means to be neurodivergent in the public eye. Diagnosed with autism at 13 and ADHD at 22, Chloe has spent her life turning difference into power. With her raw honesty and radiant energy, Chloe is the kind of woman young girls need to see in the world. In this conversation, Chloe opens up to Jess about what it's like to grow up autistic in a world that never felt built for her, from the impact of her diagnosis, to masking her way through burnout as an adult. She explains what masking is, why it can lead to physical collapse, and how learning to rest has become the bravest thing she can do while navigating a neurotypical world. This episode is vital listening for anyone who’s ever felt different, or loved someone who is. Is there somebody you'd like to share this episode with? Just tap the 3 dots above ⬆︎ and pass it on LINKS: You can find out more about Kellie’s story in her remarkable book Different, Not Less Chloe is nominated for a Silver Logie for Best Supporting Actress for her brilliant work on Heartbreak High! Vote and show your support here To keep up with all things Chloe, check out her Instagram and website If you or someone you love is seeking support around Autism or Neurodivergence, we recommend reaching out to Autism Spectrum Australia (Aspect). They offer a range of resources, services, and guidance for individuals, families, and carers across the country. Along with Yellow Lady Bugs who are dedicated to the happiness, success and celebration of autistic girls, women and gender diverse individuals. If you love what we do, why not follow the show, and rate and review on Apple or Spotify CREDITS:Host: Jessica RoweGuest: Chloe HaydenExecutive Producer: Nic McClureAudio Producer: Nat MarshallDigital Content Producer: Zoe Panaretos The Jess Rowe Big Talk Show acknowledges the Gadigal people, Traditional Custodians of the land on which we recorded this podcast, and pay our respects to their Elders past, present and extend that respect to all Aboriginal and Torres Strait Islanders peoples here today.See omnystudio.com/listener for privacy information.

In this episode of the BroadEYE Podcast, we welcome inventor, researcher, and MacArthur Fellow Dr. Joshua Miele. Known for his pioneering work in accessible technology for blind users, Dr. Miele shares his journey from early advocacy to his role at Amazon's Lab126, where he continues to develop tools that redefine independence and equity in the built and digital worlds. Explore Dr. Joshua Miele's work, projects, and writings on his personal site, MieleLab, which highlights his innovations in accessible design and disability inclusion. You can visit it here: www.mielelab.com Joining as co-host is Victoria Nolan—a decorated Paralympian, accessibility advocate, and BroadEYE regular. With lived experience navigating vision loss, Victoria brings deep empathy and clarity to the discussion, drawing out the personal and systemic forces that shape accessibility work today. Together, they explore: The real meaning of inclusion, and why accessibility must be baked in—not bolted on. Dr. Miele's development of tactile maps, screen readers, and accessible media interfaces. How institutions can move from compliance to genuine cultural transformation. Dr. Miele also reflects on the resilience required to challenge ableist assumptions and the power of disabled leadership in tech innovation. His message is clear: access is not about charity—it's about justice. About Our Guests Dr. Joshua Miele is a blind scientist, designer, and advocate for accessibility. Currently a Principal Accessibility Researcher at Amazon, he has developed technologies that empower blind and visually impaired people to navigate cities, classrooms, and digital spaces. He is a 2021 MacArthur “Genius Grant” recipient and a prominent voice for disability rights and design justice. Want to learn more? Pick up Dr. Miele's powerful memoir, “Connecting the Dots: From the Blind Side”, now available on Amazon. Victoria Nolan is a Canadian Paralympic rower, author, and passionate advocate for inclusion. Diagnosed with retinitis pigmentosa in her youth, she went on to compete internationally in rowing, including two Paralympic Games. Today, she is an influential public speaker and ambassador for breaking down barriers for people with vision loss.  

In this powerful episode of The O-Studio Podcast, we sit down with Di Foster, a remarkable woman who has faced the unimaginable and emerged with profound wisdom. Diagnosed with terminal secondary breast cancer, Di was given just a year to live, yet well over a decade later, she's here to talk with us about radical responsibility, the power of mindset and living with intention. Di opens up about how she navigated her diagnosis, the mindset that has sustained her, and the importance of listening to your inner voice. This episode is a testament to the power of living fully in the present moment while also preparing for the future. Di shows us how important it is to embrace life's challenges with grace and determination. Di's story will leave you reflecting on your own life choices and inspire you to live each day with purpose.Find Di on...LinkedIn, Instagram, TikTok, Website or email at di@difoster.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

Gisela Chavez's then 4 year old daughter Arianny was experiencing flu like symptoms during the 2024 Christmas season and finally after her fever spiked to the 104-105 range Gisela took Arianny to Advovcate Children's Hospital not too far from Chicago, where she was diagnosed with Acute Lymphoblastic Leukemia. Arianny's diagnosis was given just after her 5th birthday in January of this year, and she has completed 6 months out of a treatment protocol that still has 2 years to go. 

Mike Sullivan and Nancy Jalowiecki had both lost their spouses when they met in 2019 at a grief camp in Pennsylvania. AND One Alabama couple, Kevin and Wendy Wilson, were both diagnosed with stage 4 cancer in the same week. To see videos and photos referenced in this episode, visit GodUpdates! https://www.godtube.com/blog/life-after-loss-and-a-new-beginning.html https://www.godtube.com/blog/both-parents-stage-4-cancer.html Discover more Christian podcasts at lifeaudio.com and inquire about advertising opportunities at lifeaudio.com/contact-us.

In this "Community Spotlight Edition" of "Ask the Expert," Landy Thomas of SRNA talked with Marie Abrego and Dr. Roopa Ramamoorthi about visual impairment and their collaborative book of poetry, Rare Visions, published through the Ipsen Foundation. Dr. Ramamoorthi shared her inspiration for the collection of work from individuals who have been diagnosed with rare diseases [00:02:35]. Landy read select poems from Rare Visions, and the guests offered personal insights into their adapted lives and the significance of accessible technology [00:08:57]. Finally, they discussed the importance of raising awareness about rare diseases and accessibility issues through poetry [00:31:05]. Roopa Ramamoorthi, PhD is a scientist in the field of global health and published poet as well as director for the Catalyst program and Invent fund at UC San Francisco. Her poetry essays and short stories have appeared in over 80 publication including various anthologies and "Perspectives" on NPR. Most recently, she conducted poetry workshops with people living with rare diseases. She feels honored to have now worked with those with rare eye diseases and to help send their voices out into the world. The poetry collections Rare Sounds and Rare Visions were published by the Ipsen Foundation:https://www.fondation-ipsen.org/?s=Roopa+RamamoorthiMarie Abrego is proud to be the Welcome Manager for The Sumaira Foundation. Diagnosed with NMO in 2007 when she was only 14 years old, she shared the story of her diagnosis a few years ago, but as she learned, life doesn't stop with NMO. In 2019, she joined The Sumaira Foundation as one of the first patient TSF Ambassadors representing the state of New Mexico.00:00 Introduction01:18 Meet Marie Abrego and Dr. Roopa Ramamoorthi01:58 The Power of Poetry in Rare Disease Awareness04:37 Challenges of Living with Vision Impairment09:12 Adapting to Vision Loss: Tools and Techniques14:14 Expressing Through Poetry: Marie Abrego's Work21:21 Makeup and Femininity22:33 The Emotional Impact of Blindness25:20 Reading and Discussing Poems by Landy Thomas33:29 Leah Campbell's Powerful Poems38:21 Final Thoughts

This episode of Kiwi Birth Tales is proudly brought to you by In this episode of Kiwi Birth Tales, I speak to Emily. Some of the topics we cover:Diagnosed with PCOS after coming off the pill Worked with a Women's Health Naturopth to reverse PCOS and symptoms Smooth preganancy COVID pos at 26 weeks, issues with Thyroid post that Changed midwives around 28 weeks Your Birth Project course Felt positive as had been surrounded by lots of "natural births" in her life Found out sex in first pregnancyPulled groin muscle while swimming at 38 weeks Almost 41 weeks went into spontaneous labourMidwife had to pull cervix forward Birth in hospital with Epidural Baby born with hand up by her face2nd degree tear Felt rushed to get up and shower post birth, felt alonePostpartum depression 2nd pregnancy wanted a homebirth Searched for positive homebirth stories where their first birth may have been challenging Found comfort and learning in these stories Changed midwives in pregnancy again Spontaneous waters breaking at home Bloom BirthpoolHeatpacks were helpful for pain management Walking up and down stairs and sitting on toilet to help progress at the end of labour Involuntary pushing Birth in the birthpool at home 1st degree tear not requiring stitches Calming, supportive midwife made a huge difference in birth and recovery Prolapse post birth Completely different mental health experience this time, very positive Your Birth Project Online Hypnobirthing Coursehttps://www.fertilityassociates.co.nz/book-a-free-nurse-consultPlease seek support for any mental health concerns, some helpful links are below:Mental Health in PregnancyPerinatal Depression and Anxiety Aotearoa Plunket - Dads Mental HealthLittle Shadow - Private Counselling NZFind me @kiwibirthtales and @yourbirthproject Hosted on Acast. See acast.com/privacy for more information.

Diagnosed with Type 1 diabetes at 11 and later with end-stage renal disease, Suzanne drew on her personal experience to write an MSc thesis exploring the lived challenges of adhering to a highly restrictive dialysis diet. Following her kidney transplant, she was struck by the lack of clear nutrition guidance for transplant recipients, making the transition to managing her new kidney particularly difficult. Determined to fill this gap, she conducted research to develop evidence-based dietary guidelines, which she published in Transplant International and presented at the European Keto Live Conference in Switzerland. X: https://x.com/suzeschneider Instagram: https://www.instagram.com/zanne_schneider/ Timestamps: 00:00 Trailer 00:47 Introduction 05:50 Balancing diet after transplant 07:55 Exploring post-transplant protein needs 14:23 Protein benefits for diabetics 18:35 Optimizing immunosuppressants with diet 21:22 White blood cells and inflammation 26:43 "Life transformation after organ transplant" 30:12 Transplant eGFR limitations 34:04 Challenges of cooking vs. convenience 35:46 Practicing outside NHS 39:37 Managing type 1 with sports 43:53 Double transplant 45:45 Pancreatic transplantation challenges 49:57 Where to find Suzanne Join Revero now to regain your health: https://revero.com/YT Revero.com is an online medical clinic for treating chronic diseases with this root-cause approach of nutrition therapy. You can get access to medical providers, personalized nutrition therapy, biomarker tracking, lab testing, ongoing clinical care, and daily coaching. You will also learn everything you need with educational videos, hundreds of recipes, and articles to make this easy for you. Join the Revero team (medical providers, etc): https://revero.com/jobs ‪#Revero #ReveroHealth #shawnbaker  #Carnivorediet #MeatHeals #AnimalBased #ZeroCarb #DietCoach  #FatAdapted #Carnivore #sugarfree Disclaimer: The content on this channel is not medical advice. Please consult your healthcare provider.

This week's special episode—produced in partnership with Institute for Neuroscience, Neurotechnology, and Society at Georgia Tech – features two powerful stories from individuals whose lives have been shaped by brain-computer interfaces.Part 1: As his Parkinson's symptoms worsen and medications take a toll, Brandan Mehaffie faces a life-altering decision: continue down a difficult path or undergo brain surgery to implant an electrode to stimulate deep areas of his brain.Part 2: After an accident leaves Ian Burkhart with complete tetraplegia, he grapples with losing his independence — until he's offered a chance to participate in a groundbreaking clinical trial using muscle stimulation controlled by a brain implant to help restore movement.Brandan Mehaffie: Graduate University of Pittsburgh School of Pharmacy. Retired Director of Pharmacy Asset Protection Rite Aid Pharmacy. Married 25 years to wife Kelly and have two adult daughters Mae and Riley. Diagnosed with Parkinson's Disease in 2016 and recipient of deep brain stimulation surgery in 2022. I am a huge sports buff and gym rat. I enjoy spending time with and cooking for family and friends.Ian is a C5 complete tetraplegic from a diving accident in 2010. He is the founder and president of the BCI Pioneers Coalition and the North American Spinal Cord Injury Consortium President. After participating in a few clinical trials, he understood the need for engagement of individuals with lived experience from the start. Ian was the first person in the world to restore movement to a paralyzed limb using a BCI neuroprosthetic. He is also the Executive Director of the Ian Burkhart Foundation, which raises funds for medical equipment for other individuals living with paralysis. His research focuses on amplifying the lived experience of people with disabilities. See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Olivia Munn's mother was diagnosed with stage one breast cancer after Olivia battled with it prior. NBA star Klay Thompson was in the back of Megan The Stallion's Instagram photo! And after breakup rumors about Cardi B & Stefon Diggs they confirmed they are still together!See omnystudio.com/listener for privacy information.

After losing 3 lbs out of his less than 30 pound frame and not eating well in late 2021, Shelby Nadeau took her son Stryder to doctors, neither of whom thought that there was anything wrong with him physically. Just a couple of weeks later however, Stryder was diagnosed with Stage 4 High Risk Neuroblastoma after proper tests were ordered at Sacramento Children's Hospital which showed that there were plenty of tumors to be found. 

Type of loss: Infant loss after life-limiting diagnosis (HLHS, heterotaxy syndrome)More about Jenelle's story: In this episode of Confessions of a Grieving Mother, Tracy and Julie talk with Jenelle Romo about the life and loss of her son, Mateo. Diagnosed in utero with Hypoplastic Left Heart Syndrome and heterotaxy syndrome with polysplenia, Mateo was born on July 20, 2023, and spent his entire life in the Cardiovascular ICU.Jenelle shares the complexities of Mateo's medical journey, including multiple surgeries, serious infections, and the moment they were told there was nothing more doctors could do. Mateo passed away at 44 days old, surrounded by love. Jenelle reflects on the heartbreak of watching her son fight so hard and the deep love that carried them through each day. She also shares how her grief led her to start Mateo's Mark, a nonprofit supporting other perinatal loss families through care packages and financial assistance.More about Emma's Footprints:⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠www.EmmasFootprints.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Facebook: @EmmasFootprintsInstagram: @EmmasFootprints

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___People with ADHD are built for the future of work. While everyone else worries about AI taking over jobs, we're the ones who'll figure out what to do with it next.Muxin Li studied at UVA and Rice, but her real education came from following a winding path through anthropology, teaching, journalism, and now AI. Today, she's building tools designed to reduce cognitive overload and help people focus on what actually matters. Diagnosed with ADHD in business school after struggling through chaotic team meetings, Muxin brings a neurodivergent lens to the future of tech—one that sees ADHD not as a barrier, but as a design blueprint.In this episode, Muxin and Tracy explore why the traits we're told to tone down—intuition, creativity, nonlinear thinking—are exactly what the world needs more of. They dive into how ADHD brains connect dots in ways others can't, why we're naturally drawn to entrepreneurship (hello, 50-60% of founders), and how our bottom-up processing gives us superpowers in an AI-driven world.Muxin also shares a profound synchronicity experience that shifted her understanding of intuition, love, and possibility. From Carl Jung's scarab beetle to her own moment of cosmic clarity, she explores how tuning into that deeper intelligence might be the key to creating the future we actually want to live in. Plus, she breaks down the AI tools that are actually helping her manage the chaos of modern life—and previews Maestro, the project management tool she's building for brains like ours.Resources:Website: https://www.muxinli.com  X: https://x.com/muxin_li   LinkedIn: https://www.linkedin.com/in/muxinli 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

On this episode of Integrative Cancer Solutions Dr. Karlfeldt is joined by Rick Hill and we hear Rick's remarkable cancer survival story that spans over four decades and represents a powerful testament to alternative cancer treatments. Diagnosed with cancer and initially treated at the prestigious Mayo Clinic, Rick underwent grueling surgeries that left him questioning the conventional medical approach. A pivotal moment came when he received a letter from John Valentine that convinced him to leave the Mayo Clinic and seek alternative treatments in Tijuana, Mexico. Despite initial skepticism about the dramatic lifestyle changes required, Rick committed to this new path that would ultimately save his life. Central to Rick's recovery was his connection to Dr. John Richardson and the Richardson Protocol, which successfully treated approximately 4,000 patients, many in stage four cancer. Rick criticizes the medical establishment for revoking Dr. Richardson's medical license and imprisoning him despite his remarkable success rate. The treatment protocol centered around vitamin B17 (Laetrile) and other natural extracts, combined with comprehensive lifestyle changes including colonics, fasting, juicing, and strict organic diets. Rick emphasizes how these treatments worked synergistically to support his immune system rather than simply targeting the cancer with toxic drugs. The journey required tremendous personal commitment and lifestyle transformation. Rick describes the challenges of adapting to a completely new diet and treatment regimen, acknowledging the initial difficulty and boredom that came with such drastic changes. He had to navigate skepticism from family members and the medical establishment while maintaining his commitment to alternative treatments. Rick also mentions his involvement in what he calls "low-key smuggling" to obtain necessary treatments across borders, highlighting the regulatory obstacles faced by those seeking alternative cancer therapies. Throughout his interview, Rick strongly criticizes the pharmaceutical industry's financial motivations for suppressing alternative treatments and the medical establishment's focus on drugs rather than immune system support. He expresses optimism about current political developments, particularly mentioning Bobby Kennedy's efforts toward "chemical freedom" and crossing party lines to address these issues. Rick emphasizes that his long-term survival demonstrates the effectiveness of alternative approaches when patients have the persistence and commitment to maintain healthy lifestyle changes. Rick's story extends beyond personal survival to advocacy and education. He authored a book titled "Too Young to Die" to raise awareness about alternative cancer treatments and continues to support other patients seeking similar paths. He expresses interest in collaborating with healthcare providers to help patients access alternative treatments and emphasizes the critical importance of community support, freedom of choice in cancer treatment, and the need for persistence in maintaining the lifestyle changes that support long-term cancer survival. His four-decade journey serves as both inspiration and practical guidance for others facing similar diagnoses.Rick Hill left the Mayo Clinic after receiving a letter from John Valentine and sought alternative cancer treatments in Tijuana, Mexico, leading to over 40 years of cancer-free survival.Dr. John Richardson successfully treated approximately 4,000 cancer patients (many stage four) with the Richardson Protocol using vitamin B17 (Laetrile) and natural extracts, but had his medical license revoked and was imprisoned by the medical establishment.Rick's recovery required dramatic lifestyle changes including strict organic diets, colonics, fasting, juicing, and complete commitment to natural treatments that support the immune system rather than toxic drugs.He criticizes the pharmaceutical industry's financial motivations for suppressing alternative treatments and expresses optimism about current political efforts, particularly Bobby Kennedy's work toward "chemical freedom."Rick authored the book "Too Young to Die" to raise awareness about alternative cancer treatments and continues advocating for patient freedom of choice and community support in cancer treatment decisions.----Grab my book A Better Way to Treat Cancer: A Comprehensive Guide to Understanding, Preventing and Most Effectively Treating Our Biggest Health Threat - https://www.amazon.com/dp/B0CM1KKD9X?ref_=pe_3052080_397514860 Unleashing 10X Power: A Revolutionary Approach to Conquering Cancerhttps://store.thekarlfeldtcenter.com/products/unleashing-10x-power-Price: $24.99-100% Off Discount Code: CANCERPODCAST1Healing Within: Unraveling the Emotional Roots of Cancerhttps://store.thekarlfeldtcenter.com/products/healing-within-Price: $24.99-100% 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

At just 12 years old, Nelson Taylor is turning heads in UK junior racing - fast, instinctive, and fearless on the track. But his path to the podium has been anything but straightforward.Diagnosed as Autistic, Nelson once found it difficult to leave the house, held back by anxiety, sensory overload, and social struggles. Today, he's thriving in the high-pressure world of motorsport and chasing a future in Formula 1.In this chat with Ben, Nelson and his parents, Sophie and Shane, share the story of his remarkable transformation - from shutdowns to starting grids - and reflect on the power of autistic focus, family support, and what it took to move through the darkest days._________________On "The Hidden 20%," host Ben Branson chats with neurodivergent [ADHD, Autism, Dyscalculia, Dyslexia, Dyspraxia, Tourette's etc.] creatives, entrepreneurs, and experts to see how great minds.. think differently.Host: Ben BransonHead of Production: Bella NealeAssistant Producer: Phoebe De LeiburnéVideo Editor: James ScrivenSocial Media Manager: Charlie YoungMusic: Jackson GreenbergBrought to you by charity The Hidden 20% #1203348__________________Follow & subscribe…Website: www.hidden20.orgInstagram / TikTok / Youtube / X: @Hidden20podcastBen Branson @seedlip_benNelson Taylor @nelson_taylor_racing91If you'd like to support The Hidden 20%, you can buy a "green dot" badge at https://www.hidden20.org/thegreendot/p/badge. All proceeds go to the charity. Hosted on Acast. See acast.com/privacy for more information.

Joe DeCamara takes a moment on the 94 WIP Morning Show to acknowledge heartbreaking news: former Eagles special teams standout Bryan Braman has been diagnosed with a rare form of cancer. As the story broke over the weekend, Eagles Nation rallies behind him with thoughts, prayers, and support. A powerful moment of reflection and perspective on life beyond the game.

In this episode of Curing with Sound, we hear the remarkable story of Monica Russell, who has lived with severe obsessive-compulsive disorder (OCD) for nearly 30 years. Diagnosed at age nine, Monica pursued a wide range of conventional and alternative treatments before participating in a focused ultrasound clinical trial at Sunnybrook Hospital in Toronto. Following two noninvasive treatments, she experienced immediate relief from depression and a sustained 35–40% reduction in OCD symptoms over the following year and a half. Monica shares a candid account of her struggles with debilitating OCD, including the painful compulsions and time-consuming rituals that affected her personal and professional life. Her experience offers valuable insight into the challenges of living with treatment-resistant OCD and the life-changing potential of focused ultrasound as a breakthrough therapy for psychiatric conditions.  Discussion highlights: Focused Ultrasound as a Treatment Option: The episode outlines how focused ultrasound helped reduce Monica's depression and OCD symptoms when other therapies had limited effect. Advancing Research Through Clinical Trials: Monica's story underscores the critical role of clinical trials in evaluating new treatment options for patients with treatment-resistant OCD. Her participation highlights the need for continued funding and enrollment in focused ultrasound research to expand access and improve outcomes for others facing similar challenges. EPISODE TRANSCRIPT ---------------------------- QUESTIONS? Email podcast@fusfoundation.org if you have a question or comment about the show, or if you would you like to connect about future guest appearances.  Email info@fusfoundation.org if you have questions about focused ultrasound or the Foundation.  FUSF SOCIAL MEDIA LinkedIn X Facebook Instagram TikTok YouTube FUSF WEBSITE https://www.fusfoundation.org SIGN UP FOR OUR FREE NEWSLETTER https://www.fusfoundation.org/newsletter-signup/ READ THE LATEST NEWSLETTER https://www.fusfoundation.org/the-foundation/news-media/newsletter/ DOWNLOAD "THE TUMOR" BY JOHN GRISHAM (FREE E-BOOK) https://www.fusfoundation.org/read-the-tumor-by-john-grisham/  

Laura Delano, was diagnosed as having bipolar disorder when she was a teenager and would go on to spent 13 years receiving psychiatric care, both as inpatient and outpatient. In the process,  she accumulated more and diagnoses, and was given more and more drugs. But - as she explains in her new book: Unshrunk – How the mental health industry took over my life and my fight to get it back, published by Monoray - there was a problem, Laura wasn't getting better. Despite being a high achieving student for whom it had once appeared a glittering future awaited, her life had fallen apart. She had dropped out of university, was unable to hold down a job and had tried to kill herself. But then one day Laura had a life-changing epiphany - was it possible that rather than the care and medications she was receiving helping her,  might they actually be causing her problems? Gradually over several years, she weaned herself off all her medication – no easy process given the withdrawal effect of many psychiatric drugs . But the impact was transformative and today Laura has completely turned her life around.  So what went wrong with Laura's care?  And why was the medical system unable to recognise how the treatment was making her worse not better? The host of the podcast, Liz Tucker is an award winning medical journalist and former BBC producer and director.  You can follow Liz on Twitter at https://twitter.com/lizctucker and read her Substack newsletter about the podcast at https://liztucker.substack.com If you would like to support this podcast you can do so via Patreon at https://www.patreon.com/WhatYourGPDoesntTellYou or via PayPal at https://www.whatyourgpdoesnttellyou.com/support/ What Your GP Doesn't Tell You has been selected by Feedspot as one of the top 15 UK Medical Podcasts https://blog.feedspot.com/uk_medical_podcasts/

In today's unscripted solo episode, I'm pulling back the curtain and sharing what's really been going on lately... from vacation chaos and a surprise PCOS diagnosis to peeling back the layers of people-pleasing and overthinking everything I create.I talk about:Why I've been MIA from the podcastThe emotional rollercoaster of navigating infertility and finally getting some answersWhat my PCOS diagnosis taught me about my body (and my past)The mindset shift that's helping me stop trying to “fix” everyoneHow therapy is helping me discover who I am without the masksWhy I'm stepping away from overtraining — and how CrossFit is both a stress-reliever and a stressorReal talk on mindful eating, food tracking, and the all-or-nothing mindsetThis episode is messy, real, and full of reflection. No structure, no script, just me talking through life, healing, and learning how to be unapologetically myself again.

Today's guest is Dr. Rachel Orgel, a passionate educator with a lifelong commitment to student success. Diagnosed with a rare form of pancreatic cancer at age 13, Rachel would endure two recurrences and several surgeries in her teens and early 20s before an experimental procedure changed the game.We talk about childhood cancer, spending weeks or months in the hospital at a time, PTSD that still affects her today, the importance of humor, what led her to write her children's book, and so much more. Resources:Rachel's LinkedIn: https://www.linkedin.com/in/rachel-orgel-66a6b914/Rachel's Book on Amazon: But Is It The Bad Kind?Rachel's email: rachelorgelauthor@gmail.comFollow:Follow me: https://www.instagram.com/melissagrosboll/My website: https://melissagrosboll.comEmail me: drmelissagrosboll@gmail.com

Barbara Davis shares how Real Bread - made from freshly-milled flour - played a critical role in her health journey. Diagnosed with Sick Sinus Syndrome—a rare heart condition—Barbara opens up about the challenges she's faced, the lessons she's learned, and how she's choosing to live with purpose and faith. Refusing to let her diagnosis define her, and after years of seeking answers and support, her journey finally led her to the life-changing nutritional benefits of freshly-milled flour, and she shares how this has played a key role in healing her heart, restoring her health, and strengthening her faith. Topic mentioned in this episode: Sick Sinus Syndrome, Carnivore Diet, Wheat Belly LISTEN NOW and SUBSCRIBE to this podcast here or from any podcasting platform such as, Apple Podcasts, YouTube, Spotify, Alexa, Siri, or anywhere podcasts are played. For more information on the Scientific and Biblical benefits of REAL bread - made from freshly-milled grain, visit our website, breadbeckers.com. Also, watch our video, Only Real Bread - Staff of Life, https://youtu.be/43s0MWGrlT8. Learn more about baking with freshly-milled flour with The Essential Home-Ground Flour Book, by Sue Becker, https://bit.ly/essentialhomegroundflourbook. If you have an It's the Bread Story that you'd like to share, email us at podcast@breadbeckers.com. We'd love to hear from you! Visit our website at https://www.breadbeckers.com/ Follow us on Facebook @thebreadbeckers and Instagram @breadbeckers. *DISCLAIMER: Nothing in this podcast or on our website should be construed as medical advice. Consult your health care provider for your individual nutritional and medical needs. The information presented is based on our research and is strictly that of the author and not necessarily those of any professional group or other individuals. #sicksinussyndrome #hearthealth #heartdisease 

Journey Through Music: Fatima Gerendas's Path with Bipolar Paris converses with Fatima Gerendas, a Guatemalan singer and songwriter based in Vienna. Fatima shares her inspiring journey blending pop with alternative vibes to address overlooked societal topics through her music, rooted in personal stories of struggle and growth. Diagnosed with bipolar disorder at 24, Fatima discusses the impact of her diagnosis on her life and relationships, and how music has been a therapeutic outlet for her. She talks about her album 'Two 4 Truce,' which chronicles her experiences with bipolar disorder. Fatima emphasizes the significance of music in helping her process emotions, understand triggers, and find peace. Throughout the discussion, she highlights the support from her family and the importance of self-acceptance and resilience. Listeners are invited to connect with Fatima here and explore her music that not only narrates her story but also resonates deeply with a broader audience.Make sure to check out Love Well Bipolar here if you love someone (partner, son, daughter, etc.) living with bipolar and you want to support them better.00:00 Welcome and Introduction00:20 Meet Fatima Horez: A Journey with Music01:42 First Encounters with Bipolar Disorder03:51 Coping Mechanisms and Support Systems08:43 The Healing Power of Music21:52 Impact and Connection through Music26:42 Future Projects and Final Thoughts

Heather Lino's then 3 year old son James was given a double whammy in 2020 when he was first diagnosed with T Cell Acute Lymphoblastic Lymphoma in July, and then roughly one month into his treatment he was diagnosed with a Chromosomal disorder known as Ring 14 Syndrome. This disorder affects 200-250 people around the world. This affliction causes seizures and intellectual disabilities and can have other problems associated with it as well. James is now 8 years old and is living his best life possible. 

Do you have multiple sclerosis in your family history? Have you been recently diagnosed—or just want to lower your risk of this neurodegenerative autoimmune condition? Then this episode is for you. Dr. Terry Wahls returns to the show to help us connect the dots between MS, menopause, and midlife health. A former athlete turned wheelchair-bound physician, Dr. Wahls reversed her own secondary progressive MS using a radical diet and lifestyle protocol—and now she's teaching others to do the same. We cover: A refresher on what MS is (and why it matters more in midlife) The lifestyle non-negotiables Dr. Wahls uses to keep her MS in remission The overlap between menopause and MS symptoms—and how to tell the difference Why MS affects women 2–3 times more than men How the menopause transition can accelerate MS progression Brain health hacks and supplements to protect cognition in perimenopause and beyond What most doctors still get wrong about Hashimoto's, MS, and other autoimmune conditions in women Why strength, resilience, and radical healing are possible—even in your 60s and beyond Dr. Wahls is an Institute for Functional Medicine Certified Practitioner, author, and clinical researcher specializing in multiple sclerosis. She was awarded the IFM's Linus Pauling Award for her groundbreaking work in patient care and advocacy. Diagnosed with secondary progressive MS and once confined to a tilt-recline wheelchair, Dr. Wahls used diet and lifestyle changes to transform her health. Her Wahls Protocol is now used by thousands of patients worldwide to treat chronic autoimmune and neurological conditions. Books by Dr. Wahls: The Wahls Protocol The Wahls Protocol: A Radical New Way to Treat All Chronic Autoimmune Conditions The Wahls Protocol Cooking for Life Past Episode: https://youtu.be/47M0_GlUkD0?si=6PKl391i9_CUKpNY Learn more about her trials at terrywahls.com/trials Contact Dr. Terry Wahls Website: https://terrywahls.com/ Twitter: https://twitter.com/terrywahls  Facebook: https://www.facebook.com/TerryWahls/  Instagram: https://www.instagram.com/drterrywahls/  YouTube: https://youtube.com/c/terrywahlsmd Give thanks to our sponsors: Qualia senolytics and brain supplements. 15% off with code ZORA here. Try Vitali skincare. 20% off with code ZORA here https://vitaliskincare.com Get Primeadine spermidine by Oxford Healthspan. 15% discount with code ZORA ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠here⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠. Get Mitopure Urolithin A by Timeline. 20% discount with code ZORA at https://timeline.com/zora Try Suji to improve muscle 10% off with code ZORA at TrySuji.com https://trysuji.com Get Magnesium Breakthrough by Bioptimizers. 10% discount with code HACKMYAGE at https://bioptimizers.com/hackmyage Try OneSkin skincare with code ZORA for 15% off https://oneskin.pxf.io/c/3974954/2885171/31050 Join ⁠⁠⁠Biohacking Menopause⁠⁠⁠ before August 1, 2025 to win a free set of SUJI targeted compression bands! 10% off with code ZORA at trysuji.com https://www.trysuji.com/?ref=ZORA   Join the Hack My Age community on: Facebook Page: ⁠⁠⁠⁠⁠@⁠Hack My Age⁠     Facebook Group: ⁠⁠⁠⁠⁠⁠@⁠Biohacking Menopause⁠⁠⁠⁠⁠⁠ ⁠  Private Women's Only Support Group: https://hackmyage.com/biohacking-menopause-membership/ Instagram: ⁠⁠⁠⁠⁠@⁠HackMyAge⁠    Website: ⁠⁠⁠⁠⁠⁠HackMyAge.com⁠   

Send us a textWhat happens when autism representation meets reality? Kaelynn Partlow pulls back the curtain on life before, during, and after Netflix's "Love on the Spectrum" in this candid conversation about authenticity and advocacy in the public eye.Diagnosed with autism at age 10 after years of medical professionals dismissing her mother's concerns ("In the nineties, girls couldn't catch autism," she jokes), Kaylin's journey from struggling student to lead therapist at Project Hope showcases the power of proper identification and support. Now working with autistic clients while managing her growing social media presence, she navigates the complexities of being both clinician and community member with remarkable insight.The conversation reveals surprising truths about overnight fame - the eight-hour filming days, the unexpected social media explosion, and the loneliness of an experience "only you have, by yourself." Most poignantly, Kaelynn articulates the challenge of forming genuine connections when followers seek advice rather than friendship: "There's a power imbalance. When we meet up, you will want something from me." This reality led her to write "Life on the Bridge: Linking my World to Yours as an Autistic Therapist," offering practical guidance to the many families who reach out for support.Between discussions of sensory accommodations (fidget toys, headphones, earplugs) and behind-the-scenes television realities (being excluded from award ceremonies despite the show's success), emerges a portrait of someone determined to create meaningful change through authentic representation. As Kaelynn transitions from direct service to more conceptual advocacy work, her perspective remains invaluable for anyone seeking to understand autism beyond stereotypes and simplifications.Connect with Kaelynn on Instagram, Facebook, TikTok, and YouTube to follow her continuing journey advocating for authentic autism representation and understanding.Support the show

Luke Grenfell-Shaw is a remarkable endurance athlete, and cancer advocate whose story reads like a masterclass in resilience. Diagnosed with stage 4 sarcoma at just 24, he refused to let the label “incurable” define him. Instead, he coined the term “CanLiver”.He's cycled 30,000 km from Bristol to Beijing on a tandem bike, inviting hundreds of others, including fellow CanLivers, to join him along the way. He's since become a professional trail runner for Brooks, and he casually ran an 80-minute half marathon during chemotherapy.https://www.alifeintandemfilm.com/https://www.instagram.com/lukegshaw/ XMILES UK - Listeners now receive 10% of their order value back as store credit via the link below.https://xmiles.avln.me/c/RiwxnARvfHeRRunderwear - Use code TEATRAILS15 for 15% off your orderhttps://runderwear.avln.me/c/GPVNMgMfYfLPSHOKZ - Use code TEA102025 to receive £10 off.https://uk.shokz.com?sca_ref=7394994.MfsDQZBAeLQihiPrecision Fuel & Hydration https://visit.pfandh.com/3GKxHjUPrecision Fuel & Hydration Planner https://visit.pfandh.com/3RuP25zHarrier - Use code TEA10 for 10% off. https://harrierrunfree.co.uk/Fenixlight Limited - Use code T&T5 for 5% off your order.https://www.fenixlight.co.uk/Protein Rebel - Use code Tea15 for 15% off your first order. https://proteinrebel.com/Centurion Running - Use code TEAANDTRAILS10 to receive 10% off *Excluding Sale Items.https://centurionrunning.com/GOODR - Use code GOTEAANDTRAILS to reveive 10% off your order.https://goodr.avln.me/c/VLEmsAIZCDtmLIFE JACKET SKIN PROTECTION - Use code GOTYOURBACK for 10% off your first order.https://lifejacketskin.com/PRIMUS UK - Use code TT-PRIMUS-20 for 20& off.https://primusuk.avln.me/c/kBWmOJaEiByDContent may contain affiliate links which can help support and grow this channel at no extra cost to you. Thanks for your continued support!Brew with the Coaches - CLICK HEREKeeping Dry & Staying Warm - https://amzn.to/42JCexqFix Your Feet - https://amzn.to/3FE4nf0Running Challenges by Keri Wallace - https://amzn.to/3KGdU7eROAR - https://amzn.to/3WU7xB2NEXT LEVEL - https://amzn.to/3Hu15LrUltra Trails - https://www.ultratrails.co.uk/Greener Miles - https://greenermilesrunning.co.uk/Hannah Walsh - https://www.hannahwalsh.co.uk/Punk Panther - https://www.punkpanther.co.uk/Pen Llyn Ultra - https://penllyn.niftyentries.com

Story at-a-glance Most ovarian cysts are harmless and disappear naturally, but some cause severe complications like rupture or twisting the ovary, requiring emergency surgery Vegetable oils like canola and sunflower act as fake estrogens, damaging ovarian tissue and fueling cyst formation due to linoleic acid content PCOS drives recurring cysts through hormonal chaos, particularly insulin resistance and elevated estrogen that disrupts normal ovarian function and cycles Natural pain relief includes heat therapy, massage and gentle movement, while chamomile and ginger teas help reduce inflammation and balance hormones Prevention focuses on eliminating vegetable oils, addressing insulin resistance and considering natural progesterone to restore hormonal balance and stop cyst recurrence

Interview with Rebecca RenckAs an advocate for holistic healing and self-empowerment in the face of chronic illness Rebecca Renck has lived by the motto that “you decide how sick you want to be”. Diagnosed with acute Crohn's disease and then breast cancer, she was determined not to let her illnesses define her life. Instead, for the past 35 years, she has embraced a grounded lifestyle approach centered on self-care, listening to her body and reducing toxins to manage her health. As an author and coach, she shares her journey and insights to inspire others to harness their body's innate ability to heal itself. She is the author of, “Healing Habits: How to Help Your Body Heal itself from Chronic Illness.”https://rebeccarenck.com/https://www.amazon.com/Healing-Habits-Itself-Chronic-Illness/dp/B0F4DV8BK3

⭐️ 24 Hour Content Machine: Want to plan 90 days of content in one afternoon? Here's how

Zibby interviews renowned orthopedic surgeon, Dr. Erin Nance, about her thought-provoking and revealing debut essay collection, LITTLE MISS DIAGNOSED: A Surgeon's Guide to Breaking Bones and Bending Rules, which offers a raw, unfiltered look into the exhilarating but complicated world of healthcare. Dr. Erin Nance shares her journey in medicine, from her first day on the job treating her brother after a life-altering accident to exposing the power imbalances, burnout, and ethical dilemmas doctors face behind closed doors. She also discusses patient advocacy, the gendered challenges of medical training, and the unexpected power of TikTok storytelling!Purchase on Bookshop: https://bit.ly/3I0SrrHShare, rate, & review the podcast, and follow Zibby on Instagram @zibbyowens! Hosted on Acast. See acast.com/privacy for more information.

⭐️ 24 Hour Content Machine: Want to plan 90 days of content in one afternoon? Here's how

⭐️ 24 Hour Content Machine: Want to plan 90 days of content in one afternoon? Here's how

⭐️ 24 Hour Content Machine: Want to plan 90 days of content in one afternoon? Here's how

Skye Waterson is an ADHD strategist, coach, and the founder of Unconventional Organization. Diagnosed with ADHD during her PhD, Skye developed science-based systems to help entrepreneurs and executives stay focused, follow through, and scale without burning out. Her passion is helping business owners with unconventional brains unlock their superpower of focus in a world full of distractions. On this episode we talk about: Skye's first dollar—classic paper run entrepreneurship and her early lessons in hiring (and overpaying her sister) Her journey from academic “nerd” to entrepreneur, and how her family's focus on education shaped her path Being diagnosed with ADHD as an adult and why so many high performers struggle with focus The difference between traditional solutions (like medication) and building custom systems for your brain Why focus is the ultimate entrepreneurial superpower in today's distraction-heavy world Practical strategies for identifying what's truly urgent versus what just feels urgent How to break through “boring,” “confusing,” or emotionally challenging tasks using neuroscience-backed techniques Managing shiny object syndrome and building routines that support working memory and productivity The importance of balancing content consumption and creation as a modern entrepreneur How to build business systems that free up your time and energy for what matters most Top 3 Takeaways Focus is a Superpower: In a world overloaded with distractions, the ability to focus on high-impact tasks is what separates successful entrepreneurs from the rest. Systems Over Willpower: Custom strategies and systems—tailored to your brain—are more effective than relying on medication or brute force alone. Urgent vs. Important: Learning to distinguish between what's truly urgent and what just feels urgent is key to consistent revenue and long-term growth. Notable Quotes “You can get the best strategies and systems, but at the end of the day, it's that consistent focus and time that you need.” “Some of the most successful people I know are either formally diagnosed or self-diagnosed with ADHD—it's their superpower.” “If you can focus on something until that task is completed, that will allow you to have a leg up on all the competition around you.” Connect with Skye Waterson: Connect with Skye Waterson: Instagram: @unconventionalorganisation (DM “makes money” for her Two Minute Focus Formula) Website: http://unconventionalorganisation.com/