Podcasts about diagnosed

Ava N. Simmons, also known as Ava The S.T.E.M. Princess®, is a 12-year-old S.T.E.M. Ambassador, Entrepreneur, Toy Designer, Author, and the creator of educational toy brand Team Genius Squad. Diagnosed with dyslexia and dysgraphia in 2021, Ava used S.T.E.M. (Science, Technology, Engineering and Mathematics) and S.T.E.A.M. (Science, Technology, Engineering, Art, and Mathematics) and entrepreneurial activities to help overcome her academic challenges and build her confidence.  To share her learning journey and encourage others, Ava creates engaging S.T.E.M.-based educational videos, authors S.T.E.M. books, conducts peer-to-peer S.T.E.M. activities in the community, and develops S.T.E.M. toys for children ages 5-13, including children who are neurodivergent or in underserved areas. She has conducted thousands of peer-to-peer S.T.E.M. experiments with children in the community, over 700,000 households have viewed her educational videos, she has authored 3 books, and developed 15 branded S.T.E.M. Educational Toys.  Additionally, she is the Host of the PBS Kids Channel Show from PBS North Carolina called Mini Fab Science Lab, and her STEM-STEAM kits are featured in the Scholastic Catalog. During this episode, you will hear Ava talk about: ●    Her experience in school as a student with dyslexia and dysgraphia ●    How she got interested in S.T.E.M. at a young age ●    How Team Genius Squad helps make S.T.E.M./S.T.E.A.M. more accessible to kids everywhere ●    Where she gets ideas for her experiment kits ●    The origin of her PBS Kids Channel show, Mini Fab Science Lab Learn more about Ava: Team Genius Squad store Mini Fab Science Lab (PBS Kids show) Team Genius Squad on Facebook, Instagram, LinkedIn, TikTok and YouTube Team Genius Squad in the Scholastic Dollars 2025-2026 Catalog on page 33: (M) STEM Genius Lemon Light Experiment Kit with Interactive Experience Item No: 794043 Kits and Virtual Session with Ava Item No: 793745 4-Pack of Kits Only Watch the video of this interview on YouTube. Read the episode transcript. Follow the Beyond 6 Seconds podcast in your favorite podcast player. Subscribe to the FREE Beyond 6 Seconds newsletter for early access to new episodes. Support or sponsor this podcast at BuyMeACoffee.com/Beyond6Seconds! *Disclaimer: The views, guidance, opinions, and thoughts expressed in Beyond 6 Seconds episodes are solely mine and/or those of my guests, and do not necessarily represent those of my employer or other organizations. These episodes are for informational purposes only and do not substitute for professional medical advice. Consult a medical professional or healthcare provider if you are seeking medical advice, diagnoses, or treatment.*

When oncology nurse and mum of three, Lauren Rayner, found a lump on her neck, she never imagined it would flip her world upside down. Diagnosed with a rare and aggressive stage 4 neuroendocrine carcinoma, she was given 14 months to live - but Lauren wasn’t having it. In this raw and powerful chat, she shares what it’s like being both the nurse and the patient, why she calls Australia’s health system “the Hunger Games of cancer,” and how she ended up in Germany fighting for her life with treatments that aren’t even available here. Today, her scans show no evidence of disease. This one’s about hope, advocacy, and the fight to stay alive in a bullsh*t system that doesn’t make it easy. Donate to Lauren here https://give.rarecancers.org.au/.../helping-lauren-rayner Follow Lauren @l_k_rayner SPONSORED BY TESTART FAMILY LAWYERS Website: testartfamilylawyers.com.au TIFFANEE COOK Linktree: linktr.ee/rollwiththepunches/ Website: tiffcook.comSee omnystudio.com/listener for privacy information.

The More Sibyl Podcast Presents: 새로운 나 | The One With Mr. Roland Odeleye, Esq. – Redefining Survival: On Prostate Cancer, Purpose, and the Power of Openness |Episode 30 (2025)At five or six years old, Mr. Roland Odeleye walked miles through the chaos of Nigeria's 1966 military coup, guided by an inner compass that brought him home safely. That moment became a defining spark in his journey, from Bodija's fruit-filled streets to a life of purpose, advocacy, and resilience in the face of prostate cancer.In this deeply moving episode of The More Sibyl Podcast, I sit down with Mr. Roland Odeleye, a Nigerian-born patent attorney, nonprofit leader, and prostate cancer advocate, whose story redefines what it means to live with purpose after illness.From his joyful childhood in Bodija, Ibadan, surrounded by fruit trees and family warmth, to decades of service providing free prostate screenings in Nigeria, Mr. Odeleye's life reflects resilience rooted in community, faith, and knowledge. But when the advocate became the patient, his mission took on a new meaning.Diagnosed with prostate cancer in 2017, he chose active surveillance (regular checkups) instead of immediate surgery, leaning on his family and faith through the journey. Years later, when surgery became necessary, he faced the realities of recovery: physical limitations, emotional healing, and redefined manhood.In this candid conversation, he opens up about:Growing up in Ibadan and the lessons of love, diversity, and resourcefulness.Building a foundation that offered free prostate and cataract screenings across Oyo State.His prostate cancer journey, from diagnosis to surgery, and what “healing” really means.Honest reflections on manhood, quality of life, and faith after prostate surgery.Why he rejects the label “survivor” and calls himself “a man who lived through cancer and carries its legacy.”His ongoing mission to track and support men from his foundation's past medical outreaches.Mr. Odeleye's story is not one of mere survival, but a call to redefine strength through vulnerability, to talk openly about men's health, and to find purpose even in pain.Whether you're on a health journey, supporting a loved one, or seeking inspiration, listen in to be inspired by a story that blends courage, humor, faith, and service, and reminds us all that healing is not a destination, but a daily act of purpose. Because, as the Yoruba saying goes, ”T'aba Mọ Ọna A kò baje”: if we know the way, we won't get lost.

Welcome to my podcast, The Wellness Project with Des, where I speak about all things mental health and wellness to bring you actionable tips you can implement in your own life to help improve your mental health and overall well-being.On today's episode, I speak with Licensed Professional Counselor, Meghan Ashley, about receiving a diagnosis of Autism in adulthood. For detailed show notes and where to find Meghan: accordingtodes.com/206Want to work together? Schedule your free 30-minute consultation call:https://calendly.com/thewellnessprojectwithdes/coaching-consultationShow your love and support for the podcast by buying me a cup of coffee: buymeacoffee.com/thewellnessprojectwithdesShop wellness and positivity products from my Redbubble store:https://www.redbubble.com/people/AccordingtoDes/shop?asc=uCheck out books and products written or recommended by my amazing podcast guests:https://www.amazon.com/shop/influencer-3be311d1?ref_=cm_sw_r_cp_ud_aipsfshop_aipsfinfluencer-3be311d1_GRVS2AR62H5TFFHR13RQBecome a part of my Facebook community: facebook.com/groups/accordingtodesFollow me on Instagram: instagram.com/thewellnessprojectwithdesFollow me on TikTok: tiktok.com/@therapywithdes.lcswI would greatly appreciate it if you would take a moment to leave a review for my podcast on iTunes and/or Spotify. Thank you! https://podcasts.apple.com/us/podcast/the-wellness-project-with-des/id1477570126

Come and join this episode of "Heal Yourself" with myself and Adrienne Scharli, a lady who has successfully reversed her MS symptoms naturally. Diagnosed with Multiple Sclerosis in 2015, Adrienne shares her inspiring journey from a devastating prognosis to a mission of hope.We discuss the pivotal role of the Dr. Terry Wahls protocol, her anti-inflammatory diet (eliminating sugar, dairy, and gluten) and the power of mindset for physical healing. This conversation also explores the connection between emotional trauma, stress and chronic illness. A must-listen for anyone interested in natural remedies for Multiple Sclerosis.In this powerful episode, you will learn:Adrienne's inspiring story, from a life-altering Multiple Sclerosis diagnosis to her journey of seeking natural healing methods.The critical role of diet, including specific food changes like eliminating sugar, dairy, and gluten, that dramatically reduced her MS symptoms.How to use the power of the mind and visualization for physical healing and recovery.The often-overlooked but crucial connection between emotional trauma, stress, and chronic illness.Why a holistic approach to health can be more effective than the traditional medical model for MS.Timestamps:01:28 Adrienne's Shocking Multiple Sclerosis Diagnosis04:18 17 Years of Symptom Reprieve: How it Happened09:40 Why Insurance Didn't Cover Her MS Drugs (The Turning Point)13:51 Seeing Symptoms Improve in Just 6-8 Weeks (The Wahls Protocol)16:13 The Crucial Role of Addressing Past Trauma in the Healing Process18:12 The Power of the Mind: Using Visualization for Physical Healing20:38 Why Stress Management is Critical for Healing Multiple Sclerosis23:33 Adrienne's #1 Tip for Someone with a New MS DiagnosisAdrienne's Bio Adrienne was diagnosed with multiple sclerosis in 2015. This was a very dark and confusing time until about three weeks later when she discovered that a change in her diet could turn her life around. After about six weeks, with a dietary change, she noticed that her brain fog, fatigue, and the numbness in her hands and legs started to fade. She felt great after about 12 weeks and she even healed the blind spot in her eye 4 months later. She was amazed she had this ability to heal. Adrienne later found out that lifestyle with mental and emotional also play a big part in healing. Later, she realized that we are NOT taught about how we can heal naturally. It's her life's mission to spread the word that MS can be healed with education, desire, and action—no matter what stage someone may be in.Connect with Adrienne www.nourishyourway.comFacebook: https://www.facebook.com/groups/1349152931901644You Tube: https://www.youtube.com/@UCzWBzFImqDrVzK9Q9McyL5AWho am I?Sarah is a Holistic Health and Healing Coach, International Speaker and the Author of HEAL YOURSELF.She's also a Multi-Award-Winning Entrepreneur and Award Winning Host of the popular health-focused podcast, Heal Yourself with Sarah Dawkins. As a former Registered Nurse with over twenty years of medical experience, Sarah brings a unique, integrative perspective to her work. Sarah's expertise spans from self-healing multiple chronic health issues to supporting clients in uncovering and addressing the root causes of their symptoms, empowering them to achieve vibrant, lasting health and transformative wellness.www.sarahdawkins.com#multiplesclerosis #naturalhealing #healingms

Tired of ADHD strategies that don't work? Here's what actually does. FREE training here: https://programs.tracyotsuka.com/signup_____What happens when doing everything "right" still leaves you miserable? You start asking better questions.Shell Mendelson was a successful CEO of KidzArt, an international children's art franchise she founded, when everything fell apart. Despite looking accomplished on paper, she was disconnected, dysregulated, and drowning in work that no longer fit. At her lowest point, she found an ADHD book a therapist friend had sent years earlier, opened it, and finally understood why she'd always felt like an outcast. Diagnosed in her fifties, Shell realized the masking, hypervigilance, and constant feeling of being "off" had been ADHD all along.Now, after 35+ years as a career coach, Shell helps ADHD and neurodivergent adults stop job-hopping and start building careers that actually fit. She's the author of Unlock Your Career Path and creator of the Career Galaxy framework—a process that helps people define their must-haves in writing so they never forget what they need to thrive. In this conversation, Shell and Tracy explore why career assessments fail neurodivergent people, how DEI rollbacks are pushing ADHD professionals into hiding, the rise of workplace surveillance, and why people who need accommodations are often just in the wrong job.Shell also shares her recent move to Puerto Vallarta, Mexico, where she's building a life by the beach with her two dogs—a story about reinvention, clarity, and refusing to stay somewhere that doesn't serve you, even when it looks successful from the outside.Resources: Website: www.careercoachingwithshell.com Facebook: https://www.facebook.com/CareerCoachingwithShellLinkedIn: https://www.linkedin.com/in/yourpassiontocareerWebsite: https://unlockyourcareerpath.comSend a Message: Your Name | Email | Message Instead of Struggling to figure out what to do next? ADHD isn't a productivity problem. It's an identity problem. That's why most strategies don't stick—they weren't designed for how your brain actually works. Your ADHD Brain is A-OK Academy is different. It's a patented, science-backed coaching program that helps you stop fighting your brain and start building a life that fits.

Hey friends, Welcome to a very special podcast series called Faith & Justice. In this series, we're diving into what it looks like to follow Jesus in a world that is deeply in need of hope, healing, and justice. Over the next four episodes, we're honored to be partnering with International Justice Mission, or IJM - an incredible organization working to end violence, exploitation, and modern-day slavery in some of the darkest corners of the world.  Today, I sit down with singer/songwriter Ellie Holcomb who has supported IJM in lots of different ways. We talk about why justice and compassion matter so deeply to her, and some practical ways you and I can make a difference too. Ellie also shares how she was diagnosed with ADHD at the age of 42 and how it has deepened  her relationships. She also opens up about how she navigates the challenges of parenting while pursuing her passion for music (oh, and she's got a brand-new album coming out too!).  This conversation is honest, encouraging, and full of hope. I can't wait for you to hear it. Learn more about becoming a Freedom Partner: ijm.org  Check out Ellie's new album Far Country Thanks to our amazing partners on this episode: International Justice Mission & Vern Eide International Justice Mission is a global nonprofit working to end slavery and violence around the world, taking special care of survivors from the moment they're rescued all the way through their healing and restoration. To learn more and support their mission, visit ijm.org  Vern Eide Motorcars is a growing employee-owned company that offers sales, service, and financing of automotive, motorcycle, and power sports lines, including Acura, Ford, Chevy, GMC, Honda, Hyundai and Mitsubishi brands. Whether you live locally or across the country, visit verneide.com Subscribe to The Conversation on YouTube and watch the full interview with Ellie: youtube.com/@adamaweber  Sign up for The Crew: adamweber.com/thecrew    

In this episode, Ben sits down with Rory the Vet - veterinary surgeon, TV presenter, author, and ambassador for the British Dyslexia Association.Diagnosed with dyslexia late during his veterinary studies, Rory is now a passionate advocate for early identification, school support, and embracing ND brains.They explore the realities of dyslexia in high-pressure work environments, the mental health crisis among vets, and the therapeutic (and often overlooked) role of animals in wellbeing.Rory also shares practical tips for revision and ND brains, insights from his charity work, and gives a playful way to find out how you might discover if your dog thinks differently…!CW: This episode contains references to mental health and suicide.Join us at hidden20.org/donate._________Host: Ben BransonProduction Manager: Phoebe De LeiburnéVideo Editor: James ScrivenSocial Media Manager: Charlie YoungMusic: Jackson GreenbergHead of Marketing: Kristen FullerThe Hidden 20% is a charity founded by ADHD & autistic entrepreneur Ben Branson.Our mission is simple: To change how the world sees neurodivergence.No more stigma. No more shame. No more silence.1 in 5 people are neurodivergent. That's 1.6 billion of us - yet too many are still excluded, misunderstood, or left without support.To break the cycle, we amplify voices, challenge myths, and keep showing up. Spotlighting stories, stats and hard truths. Smashing stereotypes through honest voices, creative campaigns and research that can't be ignored.Every month, over 50,000 people turn to The Hidden 20% to feel safe, seen and to learn about brilliant brains.With your support, we can reach further, grow louder, and keep fighting for the 1 in 5 who deserve more.Join us at hidden20.org/donate.Become a monthly donor.Be part of our community where great minds think differently.Brought to you by charity The Hidden 20% #1203348______________Follow & subscribe…Website: www.hidden20.orgInstagram / TikTok / Youtube / X: @Hidden20charityBen Branson @seedlip_benRory The Vet @rorythevetIf 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.

When Australian doctor Steve Coates suddenly developed severe abdominal pain during a hospital shift, he never imagined he'd become the patient himself. Diagnosed with testicular cancer that had already spread to his retroperitoneal lymph nodes, Steve's experience as both physician and patient offers a rare, deeply human perspective on the realities of testicular cancer diagnosis, chemotherapy, and recovery.In this episode of It Takes Balls, Steve shares how his unique vantage point reshaped the way he practices medicine, from understanding the emotional toll of cancer treatment to recognizing the long-term anxiety that follows remission. He also discusses the challenges of balancing fatherhood, mental health, and vulnerability while going through orchiectomy, BEP chemotherapy, and the ups and downs of follow-up scans and tumor markers.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.x.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 Steve:https://www.instagram.com/bris_steveTheme song: No Time Like Now - Tom Willner www.tomwillner.com

“Dad will tell you he believed fixing me was only possible because of my ‘intelligence,' but I would counter and say it couldn't have happened without his love.” So writes Leland Vittert, anchor at NewsNation and former foreign correspondent for Fox News. Diagnosed with what we now understand as autism, Vittert was labeled as “retarded” […]

This week on The ToosDay Crue, we dive deep with Darlene Marshall—a holistic wellness expert and master of transformation who helps people create meaningful lifestyle change through movement, mindfulness, and mindset work. Diagnosed with a chronic illness at 23, Darlene defied the odds and became a wellness pioneer. With thousands of hours in real-world coaching and a Master's in Applied Positive Psychology, she shares her formula for personal transformation.

In this episode, I sit down with Kuyunda to talk about her courageous journey through breast cancer. Diagnosed with ER/PR+ invasive ductal carcinoma (IDC), she opens up about what it was like to face treatment, the day she lost her hair, and how those moments tested both her strength and her identity.Kuyunda shares not just the challenges, but also the beauty she found in community, the friends, family, and support systems that carried her when she couldn't carry herself. Her story is one of resilience, vulnerability, and the reminder that no one has to go through cancer alone.This conversation is more than just about illness, it's about transformation, healing, and the power of being surrounded by love.

As we enter Breast Cancer Awareness Month, Dominique is joined by Kristina Keller, author of Touch Your Tatas, to share her powerful journey of resilience, faith, and hope.Diagnosed on Valentine's Day 2024, Kristina's story is both deeply personal and universally inspiring. Whether you're facing breast cancer yourself, supporting someone who is, or simply seeking encouragement, her words will remind you of the strength of faith, love, and hope in the hardest of times.In this conversation, Dominique and Kristina discuss:Kristina's stage 4 breast cancer diagnosis on Valentine's Day.The rare “lace-like” cancer that mammograms missed and the importance of self-exams.Balancing traditional treatments with alternative approaches that provided hope.Her journey through a double mastectomy and learning self-acceptance.How faith, motherhood, and living fully guide her daily life.Kristina's advice for women on early detection and self-advocacy.For more on Kristina, follow her on:Facebook: http://facebook.com/TouchYourTaTasFacebook: https://www.facebook.com/kristinamkeller Blog: https://isaiah3816.blogspot.com/Book: https://a.co/d/famPD7Z This episode is brought to you by:Nature's Sunshine: Get 20% off your first order and free shipping by using checkout code FLOURISHING at ⁠⁠⁠⁠⁠⁠⁠https://naturessunshine.com Gruns: Visit ⁠⁠⁠⁠⁠⁠⁠https://gruns.co and use code FLOURISHING at checkout for up to 52% off your first order. Clean Simple Eats: Visit ⁠⁠⁠⁠⁠⁠⁠https://CleanSimpleEats.com and use code FLOURISHING20 at checkout for 20% off your first order.The Real Real: Go to ⁠⁠⁠⁠⁠⁠⁠https://TheRealReal.com/over50 to get an extra $100 site credit when you sell for the first timeLeesa: Go to ⁠⁠⁠⁠⁠⁠⁠https://Leesa.com and use promo code OVER50 for 25% off PLUS get an extra $50 off with promo code OVER50Keep in Touch:Website: ⁠⁠⁠⁠⁠⁠⁠https://dominiquesachse.tv/⁠⁠⁠⁠⁠⁠⁠Book: ⁠⁠⁠⁠⁠⁠⁠https://dominiquesachse.tv/book/Insta: ⁠⁠⁠⁠⁠⁠⁠https://www.instagram.com/dominiquesachse/Facebook: ⁠⁠⁠⁠⁠⁠⁠https://www.facebook.com/DominiqueSachse/TikTok: ⁠⁠⁠⁠⁠⁠⁠https://www.tiktok.com/@dominiquesachse?lang=enYouTube: ⁠⁠⁠⁠⁠⁠⁠https://www.youtube.com/@dominiquesachsetvHave a question for Dominique? Submit it here for a chance to have it answered on the show! https://forms.gle/MpTeWN1oKN8t18pm6 Interested in being featured as a guest? Please email ⁠⁠⁠⁠⁠⁠⁠courtney@dominiquesachse.tv⁠⁠⁠⁠⁠⁠⁠ We want to make the podcast even better. Help us learn how we can: ⁠⁠⁠⁠⁠⁠⁠https://bit.ly/2EcYbu4⁠⁠⁠⁠⁠⁠⁠Please note that 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 episode.Produced by Dear Media.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

He's the youngest man in the US to be diagnosed with breast cancer. And now it's back.  Bret Miller shares his recent cancer battle. We'll also hear from the experts about the latest treatments.

Emily joins us this week to talk about her experience in early-diagnosis and what her friends/family suggest for navigating this time period! Send us a text message to be anonymously read and responded to! Support the showYou can find Sara on Instagram @borderlinefromhell. You can also find the podcast on IG @boldbeautifulborderline Corey Evans is the artist for the music featured. He can be found HERE Talon Abbott created the cover art. He. can be found HERE Leave us a voicemail about your thoughts or questions on the show at boldbeautifulborderline.comIf you like the show we would love if you could rate, subscribe and support us on Patreon. Patreon info here: https://www.patreon.com/boldbeautifulborderline?fan_landing=true Purchase Sara's Exploring Your Borderline Strengths Journal at https://www.amazon.com/Exploring-Your-Borderline-Strengths-Amundson/dp/B0C522Y7QT/ref=sr_1_1?crid=IGQBWJRE3CFX&keywords=exploring+your+borderline+strengths&qid=1685383771&sprefix=exploring+your+bor%2Caps%2C164&sr=8-1 For mental health supports: National Suicide Pr...

In this special Fashion Friday episode of Skin Anarchy, Dr. Ekta Yadav sits down with actress-turned-entrepreneur Lois Robbins, founder of WATSKIN, the sun-protective lifestyle brand that proves fashion and function can coexist beautifully.Lois's journey began with a personal health scare that forced her to rethink her relationship with the sun. Diagnosed with squamous cell carcinoma and genetically predisposed to melanoma, she was determined to protect her skin without giving up her love for chic, sophisticated style. When she couldn't find options that matched her needs, she designed her own—and strangers quickly began asking where they could buy them. That moment sparked the birth of WATSKIN.Unlike traditional swimwear or activewear, WATSKIN bridges the gap with UPF 50+ designs that feel like a second skin while offering body-inclusive fits and effortless sophistication. From the pool to dinner, each piece is made to transition seamlessly, creating a new category in fashion: stylish sun-protective lifestyle wear.In this episode, Lois opens up about what it takes to build a brand with purpose, the cultural shift toward prioritizing sun safety, and how WATSKIN is reshaping the way we think about skin health and everyday style. She also shares candid lessons from her own entrepreneurial journey—why resilience, curiosity, and the courage to ask the right questions matter most.

Teepa and Greg address the tough but vital topic of planning when a dementia diagnosis is received. What happens when dementia takes away the ability to make decisions—and why can waiting too long to make plans cause significant issues? They share practical ways to start conversations about medical care, finances, and end-of-life wishes—while voices and opinions can still be clearly shared. ✨ Want more guidance on planning and readiness? Explore The Journey of Dementia (Streaming)—over three hours of insight on what to expect, how to prepare, and how to plan for the future.

Emily Kircher-Morris welcomes Dr. Jennifer Dall, a grief-informed neurodivergence specialist and the founder of ADHD Holistically. Jennifer was diagnosed with ADHD in her 50s, and is now an educator, administrator, coach, and grief specialist. They talk about grieving over what might have been, a struggle that often accompanies late-diagnosis. They discuss Jennifer's lived experience with late diagnosis, as well as some common misconceptions about ADHD, especially those faced by women. They also talk about the challenges of identifying ADHD in school settings, particularly for girls and students who may not present with typical disruptive behaviors, and how dependence on a behavioral lens can lead to greater consequences, rather than providing necessary support. TAKEAWAYS There's a lack of training about the diverse presentations of ADHD among educators and professionals. It's a persistent myth that people "grow out of" ADHD. There can be profound grief and trauma after a late diagnosis, stemming from lost time, opportunities, and years of internalizing negative narratives. ADHD often compounds the symptoms of grief. Dr. Jennifer Dall is a Grief-Informed Neurodivergence Specialist and the founder of ADHD Holistically, where she helps individuals—particularly women—navigate ADHD with practical, personalized strategies that prioritize self-awareness and sustainable growth. With over 25 years of experience as an educator and a background in ADHD coaching, yoga instruction, and grief education, her holistic approach is rooted in both professional expertise and lived experience. Diagnosed with ADHD in her 50s, Dr. Jennifer brings deep insight into the challenges of late diagnosis, masking, and misinformation—especially for women. Through her courses, workshops, and speaking engagements, she supports neurodivergent individuals and the professionals who serve them, including therapists, coaches, and HR leaders. Her work centers on reframing ADHD as a source of strength, helping others unlock their potential with strategies that work in real life. BACKGROUND READING Website, Instagram, Facebook, LinkedIn The Neurodiversity Podcast is on Facebook, Instagram, BlueSky, and you're invited to join our Facebook Group.

The First Lady of Nutrition welcomes Lauren Vaknine, and for anyone living with rheumatoid arthritis, this is a story you won't want to miss. Diagnosed with juvenile RA just before her second birthday, Lauren was wheelchair-bound by 18 with every joint in her body locked. Most people would have lost hope—but not Lauren, and not her mother. Lauren's mom had already defied convention years earlier, saying no to steroids and choosing homeopathy instead. That decision opened the door to a lifetime of natural healing. At 21, Lauren had her own turning point: realizing her recovery was in her hands, she committed to rebuilding her health one choice at a time. Now, more than 11 years in remission, Lauren shares with Ann Louise the practices that made the difference—whole, organic foods instead of processed ones, key supplements like magnesium, cod liver oil, and black seed oil, and daily rituals with turmeric and frankincense that continue to keep her strong. From a child defined by illness to a global voice in holistic health, Lauren's message is both simple and powerful: the body knows how to heal when we give it what it needs. Learn more at laurenvaknine.co.uk The post From Rheumatoid Arthritis to Complete Remission: The Lauren Vaknine Story first appeared on Ann Louise Gittleman, PhD, CNS.

As a 1:1 gluten free coach there are some things a new celiac patient absolutely needs to know. Today I talk about those! If you feel like you still need specific help because your case in unique or extra difficult, please schedule a 1:1 call here: https://forms.gle/gxLLq8kp4RCHZ9jP8SHOW NOTES:Favorite bite:  Buttermilk Biscuits https://www.instagram.com/goodlovefoods/Favorite IG account: Rustic Scoop https://www.instagram.com/rusticscoop/Favorite brand: Love Me Gluten Free Subscription Box  https://www.lovemeglutenfree.com/products/subscription-boxFollow me on IG: https://www.instagram.com/goodglutenfreegrub/

Diagnosed with juvenile idiopathic arthritis as a child, author and 2020 Bush Fellow Jenna Udenberg turned lifelong challenges into a mission: make accessibility the norm, not the exception. She shares how “Within My Spokes” captures resilience, why “committed over compliant” changes everything, and how her nonprofit Above & Beyond With U helps businesses and communities design with disabled people from the start. Expect practical truths on housing, travel, education, and what true inclusion really requires. Sponsored by Real Life Prosthetics Guest Bio:  Jenna Udenberg is an accessibility advocate, author of Within My Spokes: A Tapestry of Pain, Growth and Freedom, founder of the nonprofit Above & Beyond With U, and a 2020 Bush Fellow. A wheelchair user and bugler for veteran funerals, she consults with communities and organizations to go “above and beyond code,” centering lived experience to create spaces where everyone belongs. Main Topics: ·         Juvenile rheumatoid → idiopathic arthritis: what changed and why it matters. ·         Growing up disabled pre-ADA: school, IEP/504 gaps, and systemic ignorance. ·         “Committed vs. compliant” accessibility; housing and new-build failures. ·         Travel barriers (airlines breaking wheelchairs) and policy change needs. ·         Bush Fellowship: investing in leadership, learning from disability history hubs. ·         Adaptive movement, diabetes management, and aquatic training. ·         Above & Beyond With U: funding, rural access, and promoting accessible events. ·         The book Within My Spokes: writing trauma with care; audiobook in progress.  Resources mentioned: ·         Above & Beyond With U (nonprofit): aboveandbeyondwithu.org (said verbally as “dot org”) — donations and book sales support the org. ·         Book: Within My Spokes: A Tapestry of Pain, Growth and Freedom — by Jenna Udenberg. ·         Bush Foundation & Bush Fellowship (MN/ND/SD & tribal nations). ·         DiSend us a textDonate HereReal Life ProstheticsCutting-Edge Solutions. Restoring Ability Since 2001.Disclaimer: This post contains affiliate links. If you make a purchase, I may receive a commission at no extra cost to you.Support the showRate & Review on Apple Podcasts Follow the Conversations with Rich Bennett podcast on Social Media:Facebook – Conversations with Rich Bennett Facebook Group (Join the conversation) – Conversations with Rich Bennett podcast group | FacebookTwitter – Conversations with Rich Bennett Instagram – @conversationswithrichbennettTikTok – CWRB (@conversationsrichbennett) | TikTok Sponsors, Affiliates, and ways we pay the bills:Hosted on BuzzsproutSquadCast Subscribe by Email

What happens when a music executive's precision meets a life-changing diagnosis? In this candid episode of All Talk Oncology, Kenny Perkins sits down with Mathew Knowles—music executive, author of The DNA of Achievers, and male breast cancer survivor. A tiny sign on a white T-shirt (nipple discharge) led Mathew to insist on a mammogram, a Stage 1A diagnosis, surgery, and the discovery of a BRCA2 variant. Drawing on his 20-year background in medical imaging, he breaks down early detection, building a winning care team, and why he now lives by quarterly labs, therapy, movement, and joy. From COVID-era anxiety to laughter-filled nights with his wife, Mathew shares the mindset shifts and habits that helped him rebuild a life he loves—one mindful walk and measured plate at a time. Key Topics Discussed Men get breast cancer: the overlooked red flags (nipple discharge) and why Mathew demanded a mammogram BRCA2 explained: risk implications for men (melanoma, pancreatic, prostate, male breast cancer) and for women (breast, gynecologic) Diagnosed at Stage 1A: survival odds, surgery, and five years on Tamoxifen From isolation to a care team: oncologist, therapist, spiritual support—and why isolation increases risk COVID anxiety & mental health: therapy to confront fear of dying and regain balance Diet, weight loss (~40 lbs), and daily 2-mile brisk walks—“cancer loves obesity” Portion control and practical nutrition: measuring plates, lighter foods, consistent habits Quarterly labs for peace of mind (not just annual checkups); self-advocacy with your clinicians “Look out the window”: stillness, nature, laughter, and marriage strengthened through survivorship Family history & genetics: why genetic testing + knowing your lineage should start early Men's health advocacy: PSA tests, breaking cultural conditioning, and getting over outdated fears   Immortalize your voice by being an ALL TALK ONCOLOGY GUEST! Just fill-out this FORM.   SOCIAL MEDIA LINKS: All Talk Oncology: Instagram & Facebook JOIN OUR FREE COMMUNITY: Facebook Community WEBSITE: https://www.alltalkoncology.com

This week, I'm talking with Ashley Orr, the powerhouse baker behind Sweet Nothings Bakery and Cafe—a 100% gluten-free bakery operating out of a shared kitchen space. Yes, you read that right. Shared kitchen. Not a dedicated gluten-free facility. Sound familiar? For any planner who's been told by a convention center or hotel that “we can't do gluten-free,” Ashley's story is proof that it can be done—with the right knowledge, systems, and commitment. Diagnosed with a gluten allergy in 2019, Ashley didn't just change how she ate—she reimagined how to bake, launching her business to fill the flavor gap in gluten-free baked goods. Now baking alongside other (non-GF) businesses at Little Blue Bakehouse, she takes meticulous care to protect her products and her customers from cross-contact, and the results speak for themselves. In our conversation, we'll explore: • How Ashley safely operates in a non-dedicated kitchen • The protocols that protect her gluten-free guests • What venues and planners can learn from her model • Why SOPs—not just suppliers—are key to safe dining Whether you're serving 10 people or 10,000, this is a must-watch for anyone who's been told “we just can't do that.” Ashley is doing it—and doing it well. Let's talk about how.

Delve into this episode as host Dr. Matt Davis and MBU graduate Jonathan Gilliam chat about a range of topics from cross-country running to marriage, from Jonathan's current camp staff responsibilities to God's calling. Tapping into his recent graduation, they address his college expectations and what aspects prepared him for life. Jonathan appreciates his extension involvement in a small church and highlights his internship, which challenged him to devote time daily in silent reflection. When Dr. Davis asks, “What would you tell your younger self as a student, if you had the chance,” Jonathan thoughtful responds, “How to interact with suffering.” Diagnosed with Chron's disease as a teen and having had potentially fatal complications from it, he judiciously comments that he would not mourn those difficulties or seek immediate release because, he concludes, trials are often the means of growth and sanctification.

Dr. David Fajgenbaum, MD, MBA, MSc, is a pioneering physician-scientist, tenured professor at the Perelman School of Medicine at the University of Pennsylvania, and national bestselling author who transformed his personal battle with the rare, deadly Castleman disease into a global mission to accelerate cures for humanity's 12,000 known diseases. Diagnosed after losing his mother to cancer, Fajgenbaum endured five near-death experiences before using his medical training to identify sirolimus—a repurposed drug—as a life-saving treatment, achieving remission marking over a decade cancer-free as of 2025. A Georgetown University graduate with advanced degrees from Oxford and Wharton, he co-founded the Castleman Disease Collaborative Network (CDCN) and Every Cure, leveraging AI and drug repurposing to unlock hidden treatments, earning spots on TIME's 2025 TIME100 Health list and major media recognition for his "cure thyself" story. Through his book Chasing My Cure and speaking engagements, Fajgenbaum inspires hope, advocates for patient-driven research, and pushes for policy changes to speed up cures for rare diseases affecting millions worldwide. Shawn Ryan Show Sponsors: https://americanfinancing.net/srs NMLS 182334, nmlsconsumeraccess.org. APR for rates in the 5s start at 6.327% for well qualified borrowers. Call 866-781-8900, for details about credit costs and terms. https://bunkr.life – USE CODE SRS Go to https://bunkr.life/SRS and use code “SRS” to get 25% off your family plan. https://shawnlikesgold.com https://ROKA.com – USE CODE SRS https://simplisafe.com/srs https://USCCA.com/srs https://ziprecruiter.com/srs https://gemini.com/srs Sign up for the Gemini Credit Card: https://Gemini.com/SRS #GeminiCreditCard #CryptoRewards #Advertisement This video is sponsored by Gemini. All opinions expressed by the content creator are their own and not influenced or endorsed by Gemini. The Bitcoin Credit Card™ is a trademark of Gemini used in connection with the Gemini Credit Card®, which is issued by WebBank. For more information regarding fees, interest, and other cost information, see Rates & Fees: gemini.com/legal/cardholder-agreement. Some exclusions apply to instant rewards; these are deposited when the transaction posts. 4% back is available on up to $300 in spend per month for a year (then 1% on all other Gas, EV charging, and transit purchases that month). Spend cycle will refresh on the 1st of each calendar month. See Rewards Program Terms for details: gemini.com/legal/credit-card-rewards-agreement. Checking if you're eligible will not impact your credit score. If you're eligible and choose to proceed, a hard credit inquiry will be conducted that can impact your credit score. Eligibility does not guarantee approval. The appreciation of cardholder rewards reflects a subset of Gemini Cardholders from 10/08/2021 to 04/06/2025 who held Bitcoin rewards for at least one year. Individual results will vary based on spending, selected crypto, and market performance. Cryptocurrency is highly volatile and may result in gains or losses. This information is for general informational purposes only and does not constitute investment advice. Past performance is not indicative of future results. Consult with your tax or financial professional before investing. Dr. David Fajgenbaum Links: Website - https://davidfajgenbaum.com X - https://x.com/DavidFajgenbaum IG - https://www.instagram.com/dfajgenbaum LI - https://www.linkedin.com/in/davidfajgenbaum Every Cure - https://everycure.org Castleman Disease Collaborative Network - https://cdcn.org TED talk - go.ted.com/davidfajgenbaum TED YT - https://youtu.be/sb34MfJjurc Chasing My Cure (Amazon) - https://www.amazon.com/Chasing-My-Cure-Doctors-Action/dp/1524799637 Learn more about your ad choices. Visit podcastchoices.com/adchoices

The longtime owner of a marquee NFL team in New York is battling cancer. Correspondent Gethin Coolbaugh reports.

Longtime partners, parents of three, and now both cancer survivors, Matt and Chrissy Stewart's journey is one of resilience, faith, and the power of choosing hope in the face of adversity. Diagnosed within months of each other—Chrissy with angiosarcoma and Matt with colorectal cancer—they turned their trials into testimony, leaning on family, community, and kindness to carry them through. Their story reflects how even in life's hardest seasons, love and purpose can shine brighter than fear, inspiring others to live fully in each moment.  Key Takeaways:  Hope is a powerful choice that can carry us through life's hardest seasons.  Resilience is built by leaning into faith, family, and community support.  Kindness—both given and received—becomes a lifeline during adversity.  Sharing your story can inspire healing and courage in others.  Even in challenges, living with intention brings deeper purpose and meaning.  Join us for the Kindness Campaign and help create a ripple of compassion in your community! Sign up today at SmallChangesBigShifts.com/Kindness to receive daily acts of kindness and inspiration.   We're also inviting sponsorship partners to help us expand this movement and touch even more lives. If your organization would like to be part of spreading kindness across communities, explore the opportunities here: https://smallchangesbigshifts.com/download/9926/?tmstv=1757105005    About Matt and Chrissy Stewart:  Chrissy and Matt have been married for 23 years and have three kids. Jackson is 20, Alex is 18, and Madeline is 15. They lived in Lenexa for 23 years. Chrissy was diagnosed with angiosarcoma four years ago. It's a very rare and aggressive cancer of the blood vessels. Hers stemmed from a cyst her ovary. Matt was diagnosed with colorectal cancer one year ago. It spread to his lungs and his brain, but chemo is helping both of them stay alive. Theye are in the process of writing a memoir about our cancer experiences. Matt published author of six books while Chrissy is in the process of writing her first children's book.    Connect with Matt and Chrissy Stewart at:  https://www.instagram.com/allthethingsmemoir/   https://mattstewartbooks.com/   https://www.facebook.com/matt.stewart.4/     Connect with Dr. Michelle and Bayleigh at:  https://smallchangesbigshifts.com  hello@smallchangesbigshifts.com  https://www.linkedin.com/company/smallchangesbigshifts  https://www.facebook.com/SmallChangesBigShifts  https://www.instagram.com/smallchangesbigshiftsco    Thanks for listening! Thanks so much for listening to our podcast! If you enjoyed this episode and think that others could benefit from listening, please share it using the social media buttons on this page.  Do you have some feedback or questions about this episode? Leave a comment in the section below!  Subscribe to the podcast If you would like to get automatic updates of new podcast episodes, you can subscribe to the podcast on Apple Podcasts or Stitcher. You can also subscribe in your favorite podcast app.  Leave us an Apple Podcasts review Ratings and reviews from our listeners are extremely valuable to us and greatly appreciated. They help our podcast rank higher on Apple Podcasts, which exposes our show to more awesome listeners like you. If you have a minute, please leave an honest review on Apple Podcasts. 

In this episode, Avik Chakraborty talks to Sue Day—ADHD coach, author of ADHD Brilliance, and founder of Pathways Forward Coaching. Diagnosed in 1988, Sue shares her raw, real, and insightful journey from burnout in nonprofit finance to thriving as a coach, writer, and entrepreneur. Together, they explore the chaotic brilliance of ADHD, the challenges of navigating a neurotypical world, and how embracing your mind's uniqueness can lead to powerful transformation. Sue debunks toxic positivity while reframing ADHD as a potential strength—when understood and managed with self-awareness. She also offers practical encouragement for creatives and entrepreneurs who feel stuck, urging them not to go it alone. About the Guest:Sue Day is the founder of Pathways Forward Coaching and author of ADHD Brilliance. Diagnosed with ADHD in 1988, she has spent decades turning chaos into creativity. Her work empowers adults with ADHD to move from overwhelm to ownership. Sue is known for her compassionate, no-fluff approach to neurodivergent coaching and advocacy. Key Takeaways: ADHD isn't something to fix—it's something to understand. Burnout often comes from trying to fit into neurotypical systems. Chaos can become productive when you stop working against your brain. Mindset shift: Accept where you are and take one small step forward. Real support and community are critical for ADHD entrepreneurs. Connect with Sue Day:Visit Pathways Forward CoachingCheck out her book ADHD BrillianceFollow her work and updates through her website or social media     Want to be a guest on Healthy Mind, Healthy Life? DM on PodMatch DM Me Here: https://www.podmatch.com/hostdetailpreview/avik Tune to all our 15 podcasts: https://www.podbean.com/podcast-network/healthymindbyavik Subscribe To Newsletter: https://healthymindbyavik.substack.com/ Join Community: https://nas.io/healthymind Stay Tuned And Follow Us!YouTube – https://www.youtube.com/@healthymind-healthylifeInstagram – https://www.instagram.com/healthyminds.podThreads – https://www.threads.net/@healthyminds.podFacebook – https://www.facebook.com/podcast.healthymindLinkedIn – https://www.linkedin.com/in/reemachatterjee/ | https://www.linkedin.com/in/avikchakrabortypodcaster #podmatch #healthymind #healthymindbyavik #wellness

(0:00) Joe opens Friday night's show discussing the Patriots-Panthers game this weekend and why he believes the Patriots should get a win this weekend. (11:40) Joe discusses the unfortunate news coming out earlier today that Patriots defensive coordinator Terrell Williams has been diagnosed with prostate cancer. Joe also gets upset with Apple TV and their broadcast of the Red Sox game tonight. (22:30) Joe discusses the Red Sox playoff push and the team only needing 1 win to advance to the postseason as their series against the Tigers starts tonight. (34:10) The first hour wraps with Joe discussing Bill Chisholm's press conference yesterday and his biggest takeaways from the Celtics new owner. See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

(00:00) Zolak & Bertrand are joined by RJ Bell of Pregame.com to discuss the best bets for Week 4 of the NFL season.(11:00) Patriots HC Mike Vrabel announces that DC Terrell Williams has been diagnosed with prostate cancer.(23:00)The crew finishes up the day by hitting on a bunch of different Patriots thoughts. (34:23) We close out the show with the takeaways from today.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Today we're joined by Mark Mulholland—a local news legend, steak enthusiast, and founder of Kelly's Angels, a nonprofit created in honor of his late wife. His organization helps bring smiles to kids and families who have lost a parent or sibling to cancer or other illness, and they're hosting their 15th Annual "Calling All Angels" gala on October 11 in Saratoga.Episode Notes:A shocking fact about Mark (2:15)Pitching Mark an idea (8:30)Counterfeit Labubus (11:45)Mark's Facebook page (15:35)What's on Mark's phone? (21:15)The start of Jack & Taylor's creative careers (25:05)Team Kimmel or Team Fallon? (27:20)Talking steak (35:00)The start of Mark's creative career (43:20)Whitehall's most famous resident (45:50)Mark's marriage advice for Jack (50:28)Remembering Mark's late wife, Kelly (57:50)Diagnosed at 32 (1:00:30)Spreading smiles through Kelly's Angels (1:04:25) To learn more about Kelly's Angels, or to join us at their gala in Saratoga on October 11, visit www.kellysangelsinc.org This episode is brought to you by Wellnow Urgent Care, open 7 days a week – no appointment needed. Visit WellNow.com to find the location closest to you.  The Buttonista Show is presented by the Superior Light Beer – Michelob Ultra

Program notes:0:40 Private equity takeover of hospitals1:40 Reduced salaries or staffing2:40 Patients likely to cost system3:30 Use of anti thymocyte globulin to slow down T1D in youth4:30 Diagnosed within 9 weeks prior5:30 Serum sickness in 82% of highest dose group6:30 Incidence increasing by 2% per year over 20 years7:00 Aspirin in CRC8:00 1100 patients with mutation9:00 Can this mutation be acquired?9:15 Alcohol and dementia10:15 Confounding factors relative to alcohol use11:15 Is there a safe level of consumption?12:40 End

Hey Diabuddy thank you for listening to show, send me some positive vibes with your favorite part of this episode.In this episode, I sits down with Renee Puleo, who shares her powerful story of living with type 1 diabetes. Diagnosed at a young age, Renee has faced the highs, lows, and daily challenges of T1D while also carving her own path toward resilience and strength.Renee opens up about the importance of mindset, how her approach to health and life has evolved, and what she's learned about balancing diabetes with personal growth, relationships, and self-belief. Her story is a reminder that diabetes doesn't define you—it shapes you into someone stronger, more compassionate, and more capable.This episode is filled with honesty, encouragement, and practical lessons for anyone navigating life with a chronic condition.

In this episode of Healthy Mind, Healthy Life, host Avik Chakraborty sits down with Dr. Bryan Quoc Le—food scientist, consultant, entrepreneur, and documentary creator—to explore the intersection of adult ADHD, resilience, and the evolving future of food consulting. Bryan shares his journey from being diagnosed with ADHD in his 30s to reframing it as a strength that fuels creativity, adaptability, and entrepreneurial success. From building Mendocino Food Consulting to honoring his mother's legacy through rituals, Bryan's story reveals how systems of growth are deeply tied to both science and humanity. This conversation dives into mental health, resilience, the highs and lows of entrepreneurship, and the evolving science of food innovation. Listeners will walk away with practical insights on reframing challenges, trusting intuition, and designing life systems that support both success and well-being. About the Guest  : Dr. Bryan Quoc Le is a food scientist, consultant, and founder of Mendocino Food Consulting, a firm that supports startups and global food and beverage brands. He holds multiple patents, has walked across America, and is producing a documentary on flavor. Diagnosed with adult ADHD, Bryan has built unique systems of productivity and resilience, transforming challenges into pathways of growth. His work lives at the intersection of science, entrepreneurship, and creativity. Key Takeaways  : ADHD can become a source of strength when reframed as a system for creativity and adaptability. Productivity improves when energy flows are honored instead of forcing strict schedules. Entrepreneurship with ADHD requires strong boundaries, intuition, and the willingness to cut loose from unaligned projects or clients. Rock-bottom moments can spark resilience by removing the fear of failure and creating space for outrageous but achievable goals. Grief and loss can become guiding forces, shaping purpose and fueling momentum to honor loved ones' legacies. Rituals, such as creating shrines or daily reflections, provide grounding and carry forward wisdom into both life and business. The future of food consulting blends science, creativity, and intuition—revealing new possibilities in innovation and flavor. Connect with the Guest   Website: www.mendocinofoodconsulting.comSocials: Search “Bryan Quoc Le” Want to be a guest on Healthy Mind, Healthy Life? DM on PM - Send me a message on PodMatch DM Me Here: https://www.podmatch.com/hostdetailpreview/avik Disclaimer: This video is for educational and informational purposes only. The views expressed are the personal opinions of the guest and do not reflect the views of the host or Healthy Mind By Avik™️. We do not intend to harm, defame, or discredit any person, organization, brand, product, country, or profession mentioned. All third-party media used remain the property of their respective owners and are used under fair use for informational purposes. By watching, you acknowledge and accept this disclaimer. Healthy Mind By Avik™️ is a global platform redefining mental health as a necessity, not a luxury. Born during the pandemic, it has become a sanctuary for healing, growth, and mindful living. Hosted by Avik Chakraborty—storyteller, survivor, and wellness advocate—this channel brings powerful conversations on: • Mental Health & Emotional Well-being• Mindfulness & Spiritual Growth• Holistic Healing & Conscious Living• Trauma Recovery & Self-Empowerment With over 4,400+ episodes and 168.4K+ global listeners, join us to unite voices, break stigma, and build a world where every story matters.

Send us a textIn today's episode, Dawn sits down with Kristen Silverberg—a nurse practitioner turned high-level healthcare administrator turned organic gardener—to explore how the principles of nature offer a surprising path to finding a better balance with autoimmune conditions like rheumatoid arthritis.Diagnosed with two autoimmune diseases before age 40, Kristen felt dismissed by the very system she once worked in. But the game changed when she began focusing on whole foods which led to growing her own food. Within two years, she was off all medications—and today she teaches others how to create garden ecosystems that nourish the soil and ultimately the body.Together, Dawn and Kristen unpack the surprising connections between soil health and gut health, how gardening can help calm inflammation, and why slowing down to work with nature—not against it—can radically shift your health journey.Whether you're managing RA or just feeling disconnected from your body, this conversation will leave you inspired to reconnect with the rhythms of the earth—and reclaim your health from the ground up.Happy Listening!Connect and Grow with Kristin Silverberg:www.diggingintohealth.com@diggingintohealthResources Mentioned in this Episode:Ready to bust through the MYTHS that may be stealing your energy? Grab your free resource below.RA Doesn't Win:  10 Myths Stealing Your Energy, Stamina, & Spark.Rate, Review, and Subscribe!Don't miss a single episode! Make sure you go HERE to hit the subscribe button so you know when the next episode drops.If you found this episode helpful in any way, please leave me a Rating + Review. When you do, it helps me reach and support other people, just like you, so that they can move toward living a healthier and happier life with RA. Click HERE, scroll down to the bottom, tap to rate with 5 stars, then scroll down and tap 'Write a Review'. Then share what resonated with you in the episode! What did you love the most?Learn More From Dawn Online:

In episode 153, host Kevin Schaefer talks with Annie Heathcote from Mazomanie, Wisconsin. Annie is a multi-business owner, social media influencer, author, and lifelong disability advocate whose life and work embody the belief that disability doesn't mean inability. Diagnosed with Spinal Muscular Atrophy (SMA) at just 13 months and in a wheelchair by age 2, she has dedicated her life to breaking barriers, championing accessibility, and inspiring others with her message of resilience and faith. Visit our website at www.smanewstoday.com Follow us: IG: instagram.com/smanewstoday Facebook: facebook.com/SMAnewstoday X: x.com/smanewstoday To take part in our ongoing discussions regarding SMA, please visit www.smanewstoday.com/forums

Staci Kirk, a six-time cancer survivor, shares her remarkable journey of resilience and advocacy in this episode of Integrative Cancer Solutions with Dr. Michael Karlfeldt. Diagnosed with follicular lymphoma at just 14, and later facing Hodgkin's lymphoma twice and breast cancer twice by the age of 31, Staci's story is one of perseverance through repeated adversity. She recounts the emotional and physical challenges of each diagnosis, emphasizing the importance of self-advocacy, clear communication with medical teams, and the value of having a strong support system throughout treatment and recovery. Throughout the conversation, Staci highlights the lessons she learned from navigating multiple cancer diagnoses. She stresses the need for patients to educate themselves about their conditions, ask questions, and bring someone to appointments for support and to help remember important information. Staci also discusses the evolution of chemotherapy and radiation treatments, sharing her experiences with side effects such as nausea, hair loss, neuropathy, and bone pain, and underscores the importance of self-care and managing expectations during treatment. A significant portion of the episode is dedicated to the power of community and support. Staci describes her efforts to connect with other patients and provide encouragement through her organization, Warrior Boxes, and her involvement with Black Girls Fighting Cancer. She advocates for mentorship programs, networking, and education, particularly for women and young girls of color who may face additional health disparities. Her authenticity and transparency in sharing her journey have inspired many, as reflected in her memoir, "Hold On, Sis." Staci also opens up about navigating personal trauma, including childhood molestation, sexual abuse, and dealing with addiction in her marriage. She explains how these experiences have shaped her advocacy work and highlights the importance of addressing mental health and trauma in cancer patients. Staci encourages the use of tools like meditation, deep breathing, and journaling to manage stress, find clarity, and maintain a sense of purpose and joy even in the face of significant challenges. In conclusion, Staci provides information about her organizations, including the Letter Foundation and Black Girls Fighting Cancer, and offers resources for support and information through her website, social media, and coaching services. She urges listeners to reach out for help, build community, and embrace authenticity on their own journeys. Staci's story is a testament to the power of resilience, the importance of advocacy, and the transformative impact of community support for those facing cancer and other life challenges.Staci Kirk recounts her journey as a six-time cancer survivor, emphasizing the importance of self-advocacy and communication with medical teams.She discusses the physical and emotional impacts of chemotherapy and radiation, including long-term effects like neuropathy and bone pain.Staci highlights the value of community, mentorship, and support networks, especially for women and young girls of color facing health disparities.She openly addresses personal trauma and mental health, advocating for tools like meditation and journaling to manage stress and find purpose.Through her organizations and memoir, Staci provides resources and encouragement, inspiring others to seek support and embrace authenticity on their healing journeys.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

Maria Montoya shares her personal experience as a two-time breast cancer survivor. Diagnosed first at 30 and later at 37, she discusses dealing with Li Fraumeni Syndrome—a rare genetic predisposition to various cancers. Maria also talks about the systemic gaps she encountered in the healthcare system, such as limited genetic testing and inadequate fertility counseling, and what can be done to fix this. She also shares how getting treatment during the isolating early months of the COVID-19 pandemic fueled her passion for cancer care advocacy and systemic change. Now pursuing a Master's in Social Work, Maria aims to address systemic healthcare challenges, focusing on improving psychosocial support and survivorship care.Maria's bio and LinkedIn profileTell us your thoughts on this episode!Support the showBecome a member of The Cancer Pod Community! Gain access to live Q&As, exclusive content, and so much more! Join us today! Check out our website! Looking for more information? We have blogs, merch, and all of our episodes listed by season and category. Shop our favorite reads! We've joined with Bookshop.org to offer some of our fave books! Have a comment or suggestion? Email us at thecancerpod@gmail.com Follow us wherever you browse. We're always @TheCancerPod: Instagram Bluesky Facebook LinkedIn YouTube THANK YOU!!

Episode 109 of Trail Society features an inspiring conversation with Daisy Martinez, the rabbit x Trail Society 100K scholarship winner whose story embodies resilience and representation. A Mexican American ultrarunner from Los Angeles, Daisy started trail running in 2016 and has since transformed personal challenges into fuel for her running journey. As a teen parent and now single mother, she credits the endurance and grit she built while raising her son with helping her push through the mental and physical demands of ultrarunning. Diagnosed with Multiple Sclerosis in 2023, Daisy has been learning how to continue pursuing the sport she loves while managing the realities of an autoimmune disease. Beyond her personal racing goals, Daisy is driven by a deep commitment to community. She co-founded Chingonas on the Run to empower women, especially women of color, to take up space in trail running and the outdoors. From racing her first ultramarathons, to training for Javelina 100K, Daisy embraces each challenge as a way to learn, grow, and inspire others. Through her scholarship, she hopes to show what's possible when passion meets support, and to blaze a trail for more underrepresented runners at start lines everywhere.  We are so excited to see what she can do at Javalina! Follow Daisy on instagram here: @elementsofdaisy   HUGE thanks to our sponsor rabbit for helping us with this scholarship. Shop their fall looks with 10% off using CODE → TRAILHOP10  at https://www.runinrabbit.com/ Articles: 2025 Canadian guideline for physical activity, sedentary behaviour and sleep throughout the first year post partum: https://bjsm.bmj.com/content/bjsports/59/8/515.full.pdf  

Episode 205 of The Hitstreak, a podcast where we talk about anything and everything!  This week we are joined by the Founder & CEO of Unblurred Media & Founder of POTSies, Kristen Kukta!Let us know in the comments what YOU want to hear about next!Episode in a Glance:In this episode of the Hitstreak, I get to welcome back Kristen Kukta, founder of Unblurred Media and POTSies. We discuss the importance of authenticity in marketing, the challenges of living with POTS syndrome, and the evolving landscape of public relations in the digital age. Kristen shares her personal journey with POTS, the significance of community support, and the realities of the supplement industry. The episode emphasizes the need for education and awareness around invisible illnesses, as well as a call to action for listeners to support those with invisible illnesses and to seek out reliable information and community resources.Key Points:- Authenticity is crucial in marketing and branding.- POTS syndrome is often misunderstood and misdiagnosed.- The supplement industry is filled with challenges and regulations.- Community support is vital for those with invisible illnesses.- Education on POTS is essential for both patients and healthcare providers.- Holistic approaches can complement traditional medical treatments.- The media landscape has changed, affecting how PR works today.About our guest: Kristen Kukta is the founder and CEO of Unblurred Media, a Nashville-based PR and marketing agency, and the creator of POTSies, a supplement brand supporting those with Postural Orthostatic Tachycardia Syndrome (POTS). Diagnosed with POTS in 2016, Kristen turned her personal health journey into a mission, developing POTSies alongside medical experts to provide real solutions for patients. Through Unblurred Media, she's helped businesses nationwide cut through the noise with bold PR campaigns, e-commerce growth, and high-impact storytelling. Beyond business, Kristen supports community initiatives like Change the Stars, an annual event benefiting children in Haiti. Her work bridges health, entrepreneurship, and empowerment—giving both people and brands the tools to be seen, heard, and supported.Follow and contact:Instagram: @kkukta | @unblurredmedia | @potsies.counblurredmedia.com | potsies.coCheck it out! For a limited time, use the keyword “Hitstreak” for 20% off your order at potsies.co!Subscribe to Nick's top-rated podcast The Hitstreak on Youtube: ⁠https://www.youtube.com/NickHite⁠rFollow and Rate us on Spotify: ⁠https://spotify.com/NickHiter⁠Follow and Rate us on Apple Podcast: ⁠https://podcasts.apple.com/NickHiter⁠Follow and Rate us on iHeartRadio: ⁠https://www.iheart.com/NickHiter

Awakening The Warrior with J.R. Hutter | The Hopeaholics PodcastIn this episode, J.R. Hutter shares his raw and transformative life story, opening up about his upbringing, his father's struggles with alcoholism, and how his own battles with PTSD, bipolar disorder, and addiction spiraled after serving in Iraq. He recounts years of heavy drinking, cocaine use, and the chaos of life as a DJ in South Florida, describing the cycle of self-destruction that left him suicidal, ashamed, and on the verge of losing everything. A breaking point came after cheating on his girlfriend and realizing he had become someone he despised, which pushed him to reach out for help and attend his first AA meeting. From there, J.R. reflects on the long, difficult path of sobriety—learning that quitting alcohol wasn't enough, and that true change required rebuilding his character, embracing spirituality, committing to fitness, and creating healthier routines. He explains how his journey led him to share his story publicly, transition into coaching, and inspire others in recovery, even as he lost thousands of social media followers when he shifted from photographing models and wrestlers to talking about sobriety. Through honesty and vulnerability, J.R. paints a picture of redemption, showing how discipline, purpose, and service to others transformed his life and gave him a new mission.#thehopeaholics #redemption #recovery #AlcoholAddiction #AddictionRecovery #wedorecover #SobrietyJourney #MyStory #Hope #wedorecover #treatmentcenter #natalieevamarieJoin our patreon to get access to an EXTRA EPISODE every week of ‘Off the Record', exclusive content, a thriving recovery community, and opportunities to be featured on the podcast. https://patreon.com/TheHopeaholics Go to www.Wolfpak.com today and support our sponsors. Don't forget to use code: HOPEAHOLICSPODCAST for 10% off!Follow the Hopeaholics on our Socials:https://www.instagram.com/thehopeaholics https://linktr.ee/thehopeaholicsBuy Merch: https://thehopeaholics.myshopify.comVisit our Treatment Centers: https://www.hopebythesea.comIf you or a loved one needs help, please call or text 949-615-8588. We have the resources to treat mental health and addiction. Sponsored by the Infiniti Group LLC:https://www.infinitigroupllc.com Timestamps:00:07:11 – Family Curse00:09:16 – Diagnosed & Declining00:11:59 – Trapped in the Cycle00:13:01 – Suicidal Spiral00:14:10 – The Breaking Point00:16:04 – Losing It All00:17:14 – Rebuilding00:24:02 – Sobriety Date00:25:00 – Best Friend Bond00:26:24 – The Transformation00:29:15 – Fighting Through Fitness00:34:00 – Behind the Lens00:36:52 – Losing Followers

After experiencing stomach pains and fevers in the spring of 2023, Jordan Vanstee's then 2 year old son Kian was diagnosed with B Cell Acute Lymphoblastic Leukemia. Kian went through very difficult treatment at McMaster's Children's Hospital in Canada , but with the help of his Disney Hero Mickey Mouse and the Make a Wish Foundation, Kian is now in remission and is living his best life possible. 

Family, this week on Queer News Anna DeShawn continues to bring you the stories that matter most to our community. In top news, The Okra Project Expands Nationwide with BetterHelp to Deliver Free Mental Health Care for Black Trans Communities. In politics, In a 6-3 vote the Supreme Court declined to immediately overrule a lower court's block on South Carolina's bathroom ban law, Texas A&M president steps down after upheaval over classroom video. In culture & entertainment, Jason Collins, the man who made history as the first openly gay player in the NBA, has been diagnosed with a brain tumor and Se7en Bites owner Trina Gregory turned 49 parking spots outside her restaurant into a dazzling rainbow in direct protest to Florida crackdown on rainbow crosswalks. Let's get into it.  Want to support this podcast?

An elite swim coach known for training Olympic hopefuls suddenly finds themself on the other side of perseverance. Diagnosed with acute myeloid leukemia (AML), they face their toughest challenge yet- a fight for their life. After grueling rounds of chemotherapy and a bone marrow transplant, The University of Kansas Cancer Center helped them emerge with a renewed purpose and perspective.

Discover how prayer brings breakthrough in mental health battles. Dayne Kamela shares his powerful testimony of deliverance from bipolar disorder and how God brought complete freedom through prayer   Purchase Kathy's book Healed at Last – Overcome Sickness to Receive your Physical Healing on Amazon https://a.co/d/6a6mt8w or at: https://www.kathydegrawministries.org/healed-at-last/   Purchase Anointing Oil with a prayer cloth that Kathy has personally mixed and prayed over on Kathy's Website or Amazon. Order anointing oil by Kathy on Amazon look for her brand here https://amzn.to/3PC6l3R or Kathy DeGraw Ministries https://www.kathydegrawministries.org/product-category/oils/    Training, Mentorship and Deliverance! Personal coaching, deliverance, e-courses, training for ministry, and mentorships! https://www.kathydegrawministries.org/training/# In this episode of Prophetic Spiritual Warfare, Kathy DeGraw sits down with Dayne Kamela, author of Choose Prayer Not Despair, to share a powerful story of healing and freedom from mental illness. Diagnosed with severe bipolar disorder, Dayne experienced deliverance through prayer, the Word of God, and the power of agreement. His testimony reveals how renewing the mind, declaring scripture, and choosing prayer daily can break fear, depression, and anxiety. This conversation dives deep into spiritual warfare, healing, and deliverance, while offering practical tools for your own mental freedom. Kathy and Dayne discuss how biblical heroes overcame despair, how to partner with the Holy Spirit for breakthrough, and how consistent prayer creates victory in the mind. You'll also hear about Dayne's Prayer Project app and his daily prayer reels designed to strengthen your walk with God. If you or a loved one are battling mental illness, neurological conditions, or emotional torment, this message will inspire hope. Freedom belongs to you through Jesus Christ, and prayer is the key to unlock it. #deliverance #mentalhealthhealing #spiritualwarfare #mindbattles #healingtestimony **Connect with Dayne** YouTube: https://www.youtube.com/@litwithprayer  Purchase Choose Prayer not Despair at https://a.co/d/jgcp3cu Get the app at https://www.prayerprojectapp.com/   **Connect with Us** - Website: https://www.kathydegrawministries.org/  - Facebook: https://www.facebook.com/kathydegraw/  - Instagram: https://www.instagram.com/kathydegraw/    Podcast - Subscribe to our YouTube channel and listen to Kathy's Podcast called Prophetic Spiritual Warfare, or on Spotify at https://open.spotify.com/show/3mYPPkP28xqcTzdeoucJZu  or Apple podcasts at https://podcasts.apple.com/us/podcast/prophetic-spiritual-warfare/id1474710499    **Recommended Resources:** - Receive a free prayer pdf on Warfare Prayer Declarations at https://kathydegrawministries.org/declarations-download  - Kathy's training, mentoring and e-courses on Spiritual Warfare, Deliverance and the Prophetic: https://training.kathydegrawministries.org/  - Healed At Last ~ Overcome Sickness and Receive your Physical Healing: https://www.kathydegrawministries.org/healed-at-last/  - Mind Battles – Root Out Mental Triggers to Release Peace!: https://www.kathydegrawministries.org/product/mind-battles-pre-order-available-january-2023/  -Kathy has several books available on Amazon or kathydegrawministries.org   **Support Kathy DeGraw Ministries:** - Give a one-time love offering or consider partnering with us for $15, $35, $75 or any amount! Every dollar helps us help others!  - Website: https://www.kathydegrawministries.org/donate/   - CashApp $KDMGLORY - Venmo @KD-Ministries - Paypal.me/KDeGrawMinistries or donate to email admin@degrawministries.org - Mail a check to: Kathy DeGraw Ministries ~ PO Box 65 ~ Grandville MI 49468  

Today we tackle the common issue of how parents should handle planned emancipation when their teenager carries one or more diagnoses like ADHD or Oppositional Defiant Disorder or Autism Spectrum Disorder or Dyslexia or Depression or Anxiety or Trauma etc. etc. etc. This question comes up a lot! Dr. Ken's take is clear and freeing—the diagnosis shapes how you coach but not whether you give freedoms. Parents can adjust their approach, offer tools, and expect some natural consequences, but lowering the bar only delays the growth they'll need when the world stops making accommodations. If you have a minute, please leave us a review. We love hearing listeners encouraging other listeners. You can order Dr. Ken's book "Feeding The Mouth That Bites You" here.Got questions or feedback? We want to hear from you! podcast@feedingthemouth.com Music provided by the great John David Kent 

Sophie Sargent walked into the studio already owning the mic. A pandemic-era media rebel raised in New Hampshire, trained in Homeland Security (yep), and shaped by rejection, she's built a career out of DM'ing her way into rooms and then owning them. At 25, she's juggling chronic illness, chronic overachievement, and a generation that gets dismissed before it even speaks.We talk Lyme disease, Lyme denial, and the healthcare gaslighting that comes when you “look fine” but your body says otherwise. We dive into rejection as a career accelerant, mental health as content porn, and what it means to chase purpose without sacrificing identity. Sophie's a former morning radio host, country music interviewer, and Boston-based creator with a real voice—and she uses it.No fake podcast voice. No daddy-daughter moment. Just two loudmouths from different planets figuring out what it means to be seen, believed, and taken seriously in a system designed to do the opposite.Spoiler: She's smarter than I was at 25. And she'll probably be your boss someday.RELATED LINKSSophie on InstagramSophie on YouTubeSophie on LinkedInMedium article: “Redefining Rejection”See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Special Guest Willie Blake   https://coachwillieblake.com/freegift   In this episode of Profits Unleashed, I dive into a conversation that hits close to home for so many of us: the belief that we're “behind.” My guest, Coach Willie Blake—a dyslexic career and high-performance coach—shares his journey of transforming self-doubt into confidence and clarity, and why it's never too late to start. His story is proof that progress doesn't come from comparing yourself to others—it comes from taking small, consistent steps toward your goals. Key Takeaways I want you to hear today: You're not behind—you simply haven't started yet. Labels don't define you. You're not “lazy” or “a procrastinator”; you just have habits you can shift. Small daily action compounds. Willie's “2% Rule” shows how steady progress leads to extraordinary change. Clarity is essential. His GPS Method (Get clarity, Plan it, Start now) is a simple framework to break down any big goal. Flexibility in the journey matters more than rigid control—hold onto the vision, but stay open to how you get there. Willie's personal story is inspiring. Diagnosed with dyslexia in first grade, he spent years feeling “behind” his peers. Instead of giving up, he reframed his challenges into fuel for growth. By leaning into tools like audiobooks and coaching, he went from struggling to read a single book to consistently absorbing 60 books a year. That shift didn't just expand his knowledge—it helped him step into his calling as a coach who empowers neurodivergent entrepreneurs and professionals to see their unique edge as an advantage. What stood out to me most is Willie's perspective on labels. When we say “I am this,” we box ourselves in. But when we shift to “I have this,” we reclaim power. That subtle language shift opens the door for growth, self-compassion, and change. If you've ever felt stuck, compared yourself to others, or believed you were too far behind to start—this conversation is for you. You can connect with Willie at coachwillieblake.com, where he shares resources, coaching opportunities, and his podcast. And stay tuned—after the break, I'll be debunking the myth that it's too late to start your own podcast. Spoiler: it's not. YouTube – Dyslexic Achievers Hub https://www.youtube.com/@DyslexicAchieversHub   LinkedIn https://www.linkedin.com/in/willieblake-light/   Community (Skool) https://coachwillieblake.com/community   Instagram https://www.instagram.com/willieblake_light/   Facebook (Personal Profile) https://www.facebook.com/WillieBlake.Light/   YouTube – Coach Willie Blake https://www.youtube.com/@WillieBlake_Light So many people believe the myth that it's too late to start a podcast. After listening to my conversation with Coach Willie Blake, I couldn't help but notice how often we fall into the trap of thinking we're behind just because we compare ourselves to those further along. And the truth? You're not behind—you simply haven't started yet. Key Takeaways from this episode: It's not too late to start a podcast—there's more room than you think. Over 80% of podcasts are inactive, meaning consistency is your greatest advantage. Most podcasters quit too soon; those who keep going quickly stand out. Listeners crave authenticity and niche voices, not just celebrity shows. Your story matters—the people who need it are still waiting to hear it. Here's the reality: there are around 5 million podcasts worldwide, but fewer than 20% are actively producing new episodes. That means the space isn't oversaturated—it's full of abandoned shows. Consistency, not timing, is what separates the ones that thrive from the ones that disappear. I've said this before and I'll say it again: 90% of podcasts don't make it past three episodes, and of the ones that do, most never get past 20. That's not discouraging—it's an opportunity. If you commit to showing up, you're already ahead of the majority. Podcasting is still growing, audiences are expanding, and new listeners are tuning in every day. They're not just searching for big names; they're searching for voices that resonate with their unique struggles, interests, and goals. That could be you. Just like Willie's story reminded us, your challenges don't disqualify you—they can become your strength. Whether you're navigating dyslexia, ADHD, or simply the doubts that whisper “you're too late,” the moment you start and stay consistent, you've already set yourself apart. I'm grateful every day that I kept going, that I didn't stop when it felt tough, and that I get to share this platform with you. Your story deserves to be heard, and the world is waiting for it. If you're ready to finally start, head over to podcastprofitsunleashed.com and book a call. Let's get your voice out there.

In this intimate and profoundly moving episode of Choosing Joy, host Deborah Joy Winans Williams sits down with her mother, Deborah Kerr Winans, to share a deeply personal story of love, legacy, and faith in the face of Alzheimer’s. What began as a conversation meant for family became something much more—a testament to the power of memory, God’s grace, and choosing joy in the midst of unimaginable challenges. Diagnosed with Alzheimer’s in 2020, Deborah Kerr Winans may not remember everything, but she never forgets her children, her faith, or the goodness of God. From growing up in Detroit and becoming the first in her family to earn a college degree to raising four children with fierce love and intention, this conversation honors a mother’s journey, strength, and unwavering belief. It’s a story about what remains even when memory fades—love, faith, and joy. ✨ Whether you’re a caregiver, a daughter, or someone facing hard truths about health and aging, this episode will wrap you in warmth and remind you: You’re not alone. And joy is still possible. Chapters 00:00 – Why This Conversation Matters01:00 – Living With Alzheimer's: A Daughter's Reflection03:00 – How the Diagnosis Changed Everything05:00 – Sitting in Gratitude, Not Just Grief07:00 – What My Mom Remembers Most09:00 – Holding Faith in the Middle of Memory Loss11:00 – Raising Us with Intention & Love13:00 – Faith, Detroit, and Family Values15:00 – A Mother's Unshakable Joy17:00 – The Gift of Her Legacy19:00 – Final Reflections, Birthday Song & A Blessing #DeborahJoyWinansWilliams #ChoosingJoyPodcast #DeborahKerrWinans #AlzheimersAwareness #FaithAndFamily #LegacyOfLove #BlackWomenCaregivers #ChoosingJoyInGrief #MotherDaughterLove #SpiritualHealingSee omnystudio.com/listener for privacy information.