Podcasts about diagnosed

Two-time Emmy and Three-time NAACP Image Award-winning, television Executive Producer Rushion McDonald interviewed Senita M. Hill. Purpose of the Interview To spotlight Peace on Patuxent Incorporated, a nonprofit founded by Sunita M. Hill. To discuss the challenges women face when diagnosed with cancer and how the organization provides sanctuaries for peace, clarity, and empowerment. To inspire entrepreneurs and individuals to prioritize wellness and community support. Key Takeaways About Peace on Patuxent Located in Prince George’s County, Maryland. Offers two-day retreats for women diagnosed with life-leveling cancers. Provides limousine pickup, red carpet welcome, prepared meals, and activities focused on stillness. Launching virtual sessions nationwide in January to reach women who cannot attend in person. Life-Leveling Cancer Defined as any cancer diagnosis that disrupts life and forces major changes. Emphasizes the emotional and psychological impact beyond physical illness. Senita’s Personal Journey Inspired by her mother’s battle with lung cancer to create a space for women to pause and regain control. Empowerment Through Pause Women often feel they have choices, but treatment paths are usually predetermined. Peace on Patuxent offers a moment of stillness to reflect and make informed decisions. Community and Cultural Impact Addresses stigma in African American and ethnic communities around illness. Encourages open conversations and sharing of resources. Access and Application Apply via peaceonpatuxent.org. Requirements: Over 18, healthy enough to be independent, ideally within two years post-diagnosis. Notable Quotes “Every woman should allow herself the opportunity to come to peace.” “She matters—not just as a patient, but as a mother, daughter, coworker, and friend.” “When you hear the word cancer, it changes your life. It’s life-leveling.” “We’re not here to tell you how to run your journey. We’re here to allow you to pause your mind.” “The only way you’ll know your options is if you come out and have the conversation.” #SHMS #STRAW #BESTSupport the show: https://www.steveharveyfm.com/See omnystudio.com/listener for privacy information.

Two-time Emmy and Three-time NAACP Image Award-winning, television Executive Producer Rushion McDonald interviewed Senita M. Hill. Purpose of the Interview To spotlight Peace on Patuxent Incorporated, a nonprofit founded by Sunita M. Hill. To discuss the challenges women face when diagnosed with cancer and how the organization provides sanctuaries for peace, clarity, and empowerment. To inspire entrepreneurs and individuals to prioritize wellness and community support. Key Takeaways About Peace on Patuxent Located in Prince George’s County, Maryland. Offers two-day retreats for women diagnosed with life-leveling cancers. Provides limousine pickup, red carpet welcome, prepared meals, and activities focused on stillness. Launching virtual sessions nationwide in January to reach women who cannot attend in person. Life-Leveling Cancer Defined as any cancer diagnosis that disrupts life and forces major changes. Emphasizes the emotional and psychological impact beyond physical illness. Senita’s Personal Journey Inspired by her mother’s battle with lung cancer to create a space for women to pause and regain control. Empowerment Through Pause Women often feel they have choices, but treatment paths are usually predetermined. Peace on Patuxent offers a moment of stillness to reflect and make informed decisions. Community and Cultural Impact Addresses stigma in African American and ethnic communities around illness. Encourages open conversations and sharing of resources. Access and Application Apply via peaceonpatuxent.org. Requirements: Over 18, healthy enough to be independent, ideally within two years post-diagnosis. Notable Quotes “Every woman should allow herself the opportunity to come to peace.” “She matters—not just as a patient, but as a mother, daughter, coworker, and friend.” “When you hear the word cancer, it changes your life. It’s life-leveling.” “We’re not here to tell you how to run your journey. We’re here to allow you to pause your mind.” “The only way you’ll know your options is if you come out and have the conversation.” #SHMS #STRAW #BESTSee omnystudio.com/listener for privacy information.

Two-time Emmy and Three-time NAACP Image Award-winning, television Executive Producer Rushion McDonald interviewed Senita M. Hill. Purpose of the Interview To spotlight Peace on Patuxent Incorporated, a nonprofit founded by Sunita M. Hill. To discuss the challenges women face when diagnosed with cancer and how the organization provides sanctuaries for peace, clarity, and empowerment. To inspire entrepreneurs and individuals to prioritize wellness and community support. Key Takeaways About Peace on Patuxent Located in Prince George’s County, Maryland. Offers two-day retreats for women diagnosed with life-leveling cancers. Provides limousine pickup, red carpet welcome, prepared meals, and activities focused on stillness. Launching virtual sessions nationwide in January to reach women who cannot attend in person. Life-Leveling Cancer Defined as any cancer diagnosis that disrupts life and forces major changes. Emphasizes the emotional and psychological impact beyond physical illness. Senita’s Personal Journey Inspired by her mother’s battle with lung cancer to create a space for women to pause and regain control. Empowerment Through Pause Women often feel they have choices, but treatment paths are usually predetermined. Peace on Patuxent offers a moment of stillness to reflect and make informed decisions. Community and Cultural Impact Addresses stigma in African American and ethnic communities around illness. Encourages open conversations and sharing of resources. Access and Application Apply via peaceonpatuxent.org. Requirements: Over 18, healthy enough to be independent, ideally within two years post-diagnosis. Notable Quotes “Every woman should allow herself the opportunity to come to peace.” “She matters—not just as a patient, but as a mother, daughter, coworker, and friend.” “When you hear the word cancer, it changes your life. It’s life-leveling.” “We’re not here to tell you how to run your journey. We’re here to allow you to pause your mind.” “The only way you’ll know your options is if you come out and have the conversation.” #SHMS #STRAW #BESTSteve Harvey Morning Show Online: http://www.steveharveyfm.com/See omnystudio.com/listener for privacy information.

In episode 45 of “World of Wishes”, we chat with wish alum Courtney Priede, whose journey from chronic illness to a life-changing adventure will leave you inspired. Diagnosed with ulcerative colitis at just 12 years old, Courtney endured years of hospital stays, surgeries, and emotional challenges during some of the most formative years of her life. But through it all, she held onto hope—and when her doctor referred her to Make-A-Wish, Courtney dared to dream big. Courtney shares how she wished for an unforgettable family trip to Australia, where she swam in the Great Barrier Reef, explored the Outback, and rediscovered joy with her loved ones. Now more than a decade later, she reflects on the lasting impact of that experience, the strength it gave her, and why she continues to give back as a passionate ambassador for Make-A-Wish. This is a story of resilience and the impact of a wish fulfilled. With touching stories, raw emotion, and a genuine heart for service, Alex reveals why she calls Make-A-Wish “her baby”—and how each wish leaves a lasting mark not just on the lives of the children, but on hers as well. Learn more about how can get involved at https://wish.org/sfla!Be sure to follow us @makeawishsfla on Instagram, Facebook, YouTube, Twitter, TikTok, and LinkedIn!Subscribe, Rate, & Review this podcast to support future episodes that will feature wish kids and parents' past and present, volunteers, donors, referral sources and everyone who contributes to this World of Wishes!

Episode 143 - Diagnosed with Alzheimer's 18 years ago, Jim Mann has dedicated his life to reducing the stigma and discrimination associated with Dementia. Disclaimer: Please note that all information and content on the UK Health Radio Network, all its radio broadcasts and podcasts are provided by the authors, producers, presenters and companies themselves and is only intended as additional information to your general knowledge. As a service to our listeners/readers our programs/content are for general information and entertainment only.  The UK Health Radio Network does not recommend, endorse, or object to the views, products or topics expressed or discussed by show hosts or their guests, authors and interviewees.  We suggest you always consult with your own professional – personal, medical, financial or legal advisor. So please do not delay or disregard any professional – personal, medical, financial or legal advice received due to something you have heard or read on the UK Health Radio Network.

Males run this space but females can also be affected. Esme Murphy from WCCO TV joined Vineeta for a look at that topic on The WCCO Morning News on Friday.

Males run this space but females can also be affected. Esme Murphy from WCCO TV joined Vineeta for a look at that topic on The WCCO Morning News on Friday.

What if the key to surviving an “incurable” diagnosis wasn't found in a lab, but in your kitchen? In this extraordinary episode, we follow the true story of Pablo Kelly, who defied every medical prediction after walking away from radiation and chemotherapy for a terminal brain tumor—and used nutrition alone to reclaim his life.Diagnosed with glioblastoma multiforme, the most aggressive form of brain cancer, Pablo was given less than a year to live. But instead of accepting that fate, he began a radical nutritional experiment—one that would change the course of his health, and challenge everything medicine thought it knew about cancer metabolism.Through a strict ketogenic diet, Pablo starved his tumor's primary fuel source—glucose—forcing his body into a state of ketosis that favored healing over growth. Over time, his scans stabilized, his energy returned, and what doctors once called “impossible” became his reality: full remission.By the end of this episode, you'll discover:The remarkable true story of Pablo Kelly's recovery from glioblastoma multiforme—and what his decade of survival reveals about the body's ability to heal.The emerging science of metabolic therapies—and how food can influence cancer metabolism, inflammation, and repair.The shared nutritional patterns seen across documented cases of remission, no matter the diagnosis.Why “one-size-fits-all” diets fail—and how aligning food choices with intuition, feedback, and physiology can become a personal blueprint for healing.You'll also hear how Pablo's journey connects to other stories of remission—from plant-based to ketogenic to carnivore—and what they share at the cellular level: a return to whole, unprocessed, life-giving foods that allow the body to remember how to heal.Listen now to learn how one man's refusal to accept the inevitable—and his willingness to trust his body's intelligence—redefined what healing from cancer can mean. Because sometimes, the most radical act of hope begins with what's on your plate.DisclaimerThis podcast is for educational purposes only and does not offer medical advice. Consult your licensed healthcare provider before making any changes to your treatment or health regimen. Reliance on any information provided is solely at your own risk.This podcast explores stories and science around ALS, dementia, MS, cancer, mind body recovery, healing, functional medicine, heart disease, regression, remission, integrative medicine, autoimmune conditions, chronic illness, terminal disease, terminal illness, holistic health, quality of life, alternative medicine, natural healing, lifestyle medicine, and remission from cancer, offering hope and insights for those seeking resilience and renewal.

When we protect the pace of childhood, everyone in the family heals. In this illuminating conversation, Dr. Natasha Beck—also known as Dr. Organic Mommy—shares how slowing down, simplifying, and removing hidden toxins from our homes can transform not just our kids' health, but our own. Diagnosed as a child with ADHD and dyslexia, Dr. Beck eventually uncovered how diet, environment, and overstimulation were shaping her well-being. Now a pediatric neuropsychologist, she helps families create calmer, more connected lives through practical changes—like her two-week “fragrance-free” challenge that has surprised even the most skeptical parents. (Follow her work on Instagram, Substack, and her podcast When Millennials Become Moms.) From food choices and slow tech habits to the Waldorf philosophy and her “Three S's” framework—sleep, sugar, and screens—Dr. Beck and Ginny Yurich explore how a developmentally appropriate childhood actually restores balance for parents too. This episode is both practical and freeing, showing that you don't need to overhaul your life overnight. One slow evening, one home-cooked meal, one outdoor day at a time—those small shifts might be the self-care your whole family has been missing. Learn more about your ad choices. Visit megaphone.fm/adchoices

"My baby went from fussy to lifeless in hours—by the time we reached the PICU, they said he might have had six hours to live." In this episode, TikTok Influencer and Medical Mom Marlee Brandon, a pediatric speech-language pathologist turned full-time mom, shares the whirlwind diagnosis of her 12-month-old son Bain with Type 1 diabetes and severe DKA, the traumatic hospital stay, and the everyday advocacy that followed. Raw, practical, and deeply hopeful. Why this episode matters Emotional clarity: what a Type 1 diagnosis really feels like in infancy Practical advocacy: scripts, choices, and language that help toddlers cope System gaps: when even major hospitals say "we've never seen this in a baby" Hope forward: raising a confident kid who knows why care matters What You'll Learn Early signs & ER visit: how "ear infection" symptoms masked T1D in a baby DKA in plain language: what "acidic blood" means and how PICU treats it The learning cliff: carb ratios, breastfeeding while dosing insulin, and why it's OK not to "get it" on day one Toddler coping: give choices, narrate care, build independence Rebuilding trust after mistakes: when training/tools aren't perfect Finding your people: groups, podcasts, and creators who answer "what now?" Timestamps 00:00 Meet Marlee (pediatric SLP → motherhood) 01:40 Why speech therapy & pediatrics 03:55 Bain turns one → sudden "ear infection" → nonstop vomiting 06:30 Small-town ER: "He has diabetes" (dismantling stereotypes) 08:35 Life-flight & PICU: severe DKA, hourly sticks, no food for 48 hrs 10:20 Turning the corner: energy returns; the six-hour window 11:22 "I don't understand this"—carb ratios, nursing, overwhelm 13:05 "We've never seen this in a baby" at a major children's hospital 15:23 Tears → handing tasks to partner → first solo shot 17:20 The Chick-fil-A moment: necessity builds confidence 18:44 Finding community: Facebook groups, YouTube, TikTok 19:55 Narrating care for toddlers—SLP tools that build trust & language 21:19 Offering choices: stickers, shot sites, pushing the button 22:53 Caregiver reality: self-care with very young T1D 24:32 Why daycare felt unsafe: syringe mix-ups & trust 25:54 Joy check: rocks, crafts, and a kid excited by everything 27:56 Best resources for newly diagnosed families 29:52 "Diabetes doesn't define your life." Marlee Shares that... "Type 1 isn't about weight or diet—my baby was still nursing." "They told my husband he probably had six hours to live." "I thought I needed nursing school to understand our endo." "I won't chase him with a shot. I explain why—insulin keeps you safe." "You can be anything and do anything…and have diabetes." Resources & Links Support communities Diapers & Diabetes (Facebook group for infants/toddlers with T1D) Juicebox Podcast Related Child Life On Call resources Explaining shots, blood draws and vaccines to kids   SupportSpot App (by Child Life On Call) Procedure guides, coping plans, journals, and parent resources to feel prepared and advocate with confidence 

Transcript: rmad.ac/AIAe081This week's podcast guest is Annie Heathcote. Annie is a multi-business owner, social media influencer, author, Christian and lifelong disability advocate whose life and work embody the belief that disability does not mean inability. Diagnosed with spinal muscular atrophy at just 13 months old, Annie has spent her life breaking barriers, championing accessibility, and inspiring others with her message of resilience and faith. She was crowned Miss Wheelchair Wisconsin in 2023. Using her platform, Caring is Caregiving to reach more than 100,000 people through schools, conferences, organizations, and media appearances across the state.Her advocacy took her to the Miss Wheelchair America national competition where she placed in the top five, earning second runner up and the best speech award. She has since been recognized as a woman of the year for Dane County for her leadership and community impact beyond advocacy. Annie is the founder of Annie Designs and Annie Speaks LLC, where she works as a freelance web and graphic designer and transformational speaker. She also brings creativity and joy into her everyday life through travel, art, music, and her past achievements as an elite athlete in the adaptive sport of power soccer. Annie's mission is simple but powerful. Love, serve God and others, work hard and never give up. Connect with Annie: Annie Speaks | Disability. Dignity. Destiny.Annie's Portfolio – Intentional. Impactful. Invigorating.Annie Speaks | FacebookAnnie Heathcote I Disability Advocate & Speaker (@annieheathcote) • Instagram photos and videosConnect with the Rocky Mountain ADA Center at RockyMountainADA.org or find us on social media. Don't forget to subscribe, rate and review us on Apple Podcasts, Stitcher, Spotify, or anywhere else you get your podcasts!

Subscribe to the video podcast: https://www.youtube.com/@DrTazMD/podcastsWhat Is PCOS in Women, How It's Diagnosed? PCOS is not just a gynecology label, it is a whole-body syndrome that is widely missed in the exam room. In this episode, Dr. Taz explains why nearly seventy percent of women go undiagnosed, how PCOS often begins in the prenatal environment, and why it behaves like a metabolic and autoimmune condition. You will learn the signs most people overlook, the labs that actually matter, and a step-by-step plan that starts with the gut, supports the liver, balances blood sugar, and calms cortisol so real healing can begin.Dr. Taz shares: • Why the old Rotterdam criteria miss metabolic, inflammatory, and immune drivers • How prenatal hormones, medications, and toxins can program PCOS risk • The role of hyperandrogenism in insulin resistance, inflammation, acne, and hair loss • Why PCOS looks different by life stage and race, and what that means for care • The exact labs to request: DHT, AMH, free and total testosterone, DHEAS, 17-OHP, fasting insulin, lipids, CRP and more • A holistic protocol that begins with gut repair and liver support, then adds androgen and metabolic tools • How daily stress and the cortisol hum keep PCOS active, and practical ways to turn it downWhether you feel off but cannot explain why, are chasing a diagnosis, or want a long term plan for energy, fertility, and hormone balance, this episode gives you a clear roadmap to understand PCOS and take action.Connect further to Hol+ at https://holplus.co/- Don't forget to like, subscribe, and hit the notification bell to stay updated on future episodes of hol+.Get your copy of The Hormone Shift: Balance Your Body and Thrive Through Midlife and MenopauseStay ConnectedSubscribe to the audio podcast: https://holplus.transistor.fm/subscribeSubscribe to the video podcast: https://www.youtube.com/@DrTazMD/podcastsFollow Dr. Taz on Instagram:https://www.instagram.com/drtazmd/https://www.instagram.com/liveholplus/Join the conversation on X: https://x.com/@drtazmdTikTok: https://www.tiktok.com/@drtazmdFacebook: https://www.facebook.com/drtazmd/Don't forget to like, subscribe, and hit the notification bell to stay updated on future episodes of hol+Chapters 00:00 The PCOS epidemic and misdiagnosis 00:27 Dr. Taz's PCOS story 03:06 Why old criteria fall short 05:09 PCOS as metabolic and autoimmune 08:20 Why PCOS rates are rising 09:14 Prenatal and medication influences 11:05 Childhood and teen clues 15:44 Symptom checklist you can spot 18:42 Eastern medicine patterns to notice 20:32 What to test for PCOS 23:56 How presentation varies by race 30:03 Building a holistic plan 33:37 Gut and liver first 35:16 Androgen, metabolic, and inflammation tools 37:30 Managing cortisol and stress 39:13 Long term roadmap and next steps

When Atira Roberson was in first grade, she was evaluated and diagnosed with ADHD, dyscalculia, and a specific learning disability. But she didn't find out about those diagnoses until college — when she went through all of her old paperwork herself. Growing up, Atira knew she was different and was bullied because of it. Her mother was her biggest advocate, but her parents chose not to tell her about her diagnoses at the time. In this episode, Atira — now an English language arts teacher — shares how learning the truth changed the way she saw herself, and how it shaped her passion for teaching and education policy today.For more on this topic: Why Black girls with learning disabilities need more visibility, from the Opportunity Gap podcastTo be Black in America with a learning disability, by Atira RobersonWhat are learning disabilities?For a transcript and more resources, visit ADHD Aha! on Understood.org. You can also email us at adhdaha@understood.org. Understood.org is a nonprofit organization dedicated to empowering people with learning and thinking differences, like ADHD and dyslexia. If you want to help us continue this work, donate at understood.org/give Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Because he was Developmentally Delayed at birth, Aliyah Vida was not that surprised when her son Joshua, who was affectionately known as Goose,  slipped while walking to the bathroom and hit is eyebrow, causing a small bump.  Unfortunately this bump continued to grow, as did his feeling lethargic, and then not eating or drinking. Goose was then diagnosed with Stage 4 Neuroblastoma in April of 2022, and this form of Pediatric Cancer led to his passing in April of 2024, before he was to turn 4 years of age. 

Try our FREE burnout quiz.Grab your burnout workbook HERE. To sign up for our difficult conversations and workplace culture workshop go here.Cancer has a devastating effect both on those it afflicts and those around them.For Melanie Staudt her cancer journey was full of challenges that often felt insurmountable.Melanie is 51 years old, lives in the US in Ohio and is married with two girls age 22 and 18.She was diagnosed with breast cancer in February 2021. It was three years of intensive healing and has had no evidence of disease for a year and a half. She continues to work on physical, mental and spiritual health and looks forward to life's next chapter. In this episode she shares:- Why she identifies most with a monarch butterfly- What happened for her in the early days leading up to breast cancer discovery- Getting her biopsy and preparing for bad news- How the initial bad news led to positivity in her life- The moment she got more bad news and her experience of detaching from her body- How she discussed her reservations about chemo with her husband- What her treatment options were and what she decided- When she saw a naturopathic doctor and her experience with craniosacral massage- When she got imaging done and got the all clearKey Quotes“I couldn't process anything, it was like I was out of my body.”“I probably spent between 20 and 40 hours a week researching breast cancer.”More about MelanieYou can contact Melanie via Facebook or Instagram.The pre surgery meditation link she mentioned is here. On facebook in our community: https://www.facebook.com/groups/challengesthatchangeusOr on Instagram: @challengesthatchangeusIf you want to contact the podcast, email us here: support@challengesthatchangeus.comOr check out our website: www.Challengesthatchangeus.com If you want to find out more about what Ali does, check out her business via the website:http://www.trialtitudeperformance.com.au Hosted on Acast. See acast.com/privacy for more information.

In this week's episode of Home Gadget Geeks, I'm joined by Kevin Schoonover for a packed discussion that jumps from health and fitness to EV trucks, from Windows 10's sunset to ARM's rise, and all the way down to the small stuff — batteries, smart home gear, and the realities of modern tech maintenance. Thanks for listening! Episode Summary We open the show by talking about the weather rolling into Omaha and catching up on the World Series, before Kevin dives into something a little different — his personal health journey. Diagnosed with type 2 diabetes a few years ago,

In this week's episode of Home Gadget Geeks, I'm joined by Kevin Schoonover for a packed discussion that jumps from health and fitness to EV trucks, from Windows 10's sunset to ARM's rise, and all the way down to the small stuff — batteries, smart home gear, and the realities of modern tech maintenance. Thanks for listening! Episode Summary We open the show by talking about the weather rolling into Omaha and catching up on the World Series, before Kevin dives into something a little different — his personal health journey. Diagnosed with type 2 diabetes a few years ago,

In this week's episode of Home Gadget Geeks, I'm joined by Kevin Schoonover for a packed discussion that jumps from health and fitness to EV trucks, from Windows 10's sunset to ARM's rise, and all the way down to the small stuff — batteries, smart home gear, and the realities of modern tech maintenance. Thanks for listening! Episode Summary We open the show by talking about the weather rolling into Omaha and catching up on the World Series, before Kevin dives into something a little different — his personal health journey. Diagnosed with type 2 diabetes a few years ago,

11-07-25 - Vincent Emails In The He Was Just Diagnosed w/Early Onset Alzheimers - Someone Thought John Was Doug Hopkins' Son At The RaRa Room - Guys Odd Guest At Suns Game - Antonio Brown Arrested In Dubai For Attempted MurderSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Jordyn Zimmerman is a passionate educator, disability advocate, and accessibility innovator. Diagnosed as autistic and denied access to augmentative and alternative communication (AAC) until age 18, Jordyn's work centers on ensuring every learner has the tools and supports they need to thrive. Their advocacy is rooted in personal experience with segregation and inclusion, making their voice essential for building more inclusive schools.In this episode, Jordyn Zimmerman shares their journey from segregation to meaningful inclusion in schools. The conversation covers the importance of presuming competence, the need for accessible communication, and how policy and practice must evolve to create truly inclusive communities. Jordyn also discusses their work with the Nora Project and Center for Enriched Living, and what it means to measure success beyond just placement numbers.Complete show notes and transcript: https://mcie.org/think-inclusive/designing-schools-for-belonging-jordyn-zimmerman-on-inclusion-and-aac-tools-1310/

11-07-25 - Vincent Emails In The He Was Just Diagnosed w/Early Onset Alzheimers - Someone Thought John Was Doug Hopkins' Son At The RaRa Room - Guys Odd Guest At Suns Game - Antonio Brown Arrested In Dubai For Attempted MurderSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Welcome to Perimenopause WTF!, brought to you by ⁠Perry⁠—the #1 perimenopause app and safe space for connection, support, and new friendships during the menopause transition. You're not crazy, and you're not alone!  Download the free Perry App on ⁠Apple⁠ or ⁠Android⁠ and join our live expert talks, receive evidence-based education, connect with other women, and simplify your perimenopause journey.Today's episode is titled “Full Menopause before 40: Long-term Health Effects and Practical Solutions” with Dr. Jackie Piasta & Teyonna Bowman isn't just a discussion—it's a roadmap. If you or someone you know is facing early or medically induced menopause, this episode is mandatory listening. Physician Dr. Jackie Piasta lays out the crucial medical facts on long-term health effects, while Teyonna Bowman offers a raw, honest look at the emotional turbulence and practical steps for coping. It's a powerful 360-degree view, combining clinical knowledge with lived experience, to help you move from feeling overwhelmed to informed.

Dr. Venkatkiran Kanchustambham, or Dr. K, joins It Takes Two for an in depth conversation about pneumonia and why it Is misdiagnosed, missed and so worrisome to hospitals during the winter months. See omnystudio.com/listener for privacy information.

How do you turn a life-altering diagnosis into a life-affirming mission? In this deeply inspiring episode, Kenny Perkins speaks with Elissa, the powerhouse behind WeGotThis.org, who's redefining what it means to live and thrive with stage 4 breast cancer. Diagnosed just after her daughter's first birthday, Elissa shares how she found meaning in the chaos, leaned into community, and built a nonprofit to help others ask for and receive the help they need during cancer. Whether you're a caregiver, patient, or someone navigating your own hard season, this is a must-listen. Key topics discussed: Navigating diagnosis during early motherhood and the pandemic Creating WeGotThis.org: A registry for cancer patients to ask for real help Redefining creativity, career, and identity in the face of cancer Mental health, chemo fatigue, and choosing treatment that prioritizes quality of life Supporting young children through a parent's diagnosis Marriage, caregiving, and keeping connection alive in hard times Date nights, Air Force 1s, and Lego bouquets—her feel-good rituals Why prioritizing living is just as important as surviving 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

Just a few days after complaining of a headache and vomiting on his way to school the next day in August of 2017, Gunner Smith, who was a 4th grade student was having emergency brain surgery at the Vanderbilt University Medical Center, after being diagnosed with a High Grade Multi Form Glioma. This operation was so serious that there was a question as to whether Gunner would even be able to wake up from this surgery. Gunner's parents Brittany and Brandon will talk about their son who showed so much bravery while he fought his disease and uttered these words after his diagnosis. "We Got This." Gunner passed away from this Pediatric Brain Cancer on May 28th of 2021.

A mum from Margate has died just three months after being diagnosed with cancer.53-year-old Michelle Bailey was told in July she had an incurable form of the disease after initially suffering what doctors thought was a stroke.Also in today's podcast, the leader of Kent County Council has hit back at the Chancellor, after she criticised the local authority during a speech at Downing Street.Rachel Reeves was speaking ahead of her Budget later this month. Hear what she had to say and the response from Reform UK's Linden Kemkaran. The boss of a Kent charity's admitted they got too big, too quickly.Gillingham Street Angels, which runs a number of shops and a food bank, announced at the start of the week it was going to close after supporting hundreds of homeless and vulnerable people since 2018.People living on Prince Andrew Road in Broadstairs have told the podcast the name is now embarrassing, and they want it changed.It's after Andrew Mountbatten Windsor was stripped of his Royal title over his links to disgraced financier Jeffery Epstein. Andrew has always denied any wrong doing.A campaign is underway to organise a Christmas dinner for young care leavers in north Kent.Many of those who grow up in foster homes are left with nowhere to go on the big day after they turn 18.An event is already held every year in Folkestone, and now volunteers want to put on a meal in the north of the county.And in sport, Gillingham manager Gareth Ainsworth has returned to oversee training this week following heart surgery.He's been absent from the club for a month after having an operation in early October. Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Diagnosed with cancer at 16, Emily hadn't dared hope she would graduate from high school or college, let alone fall in love and get engaged.  

Endometriosis is a painful disease that occurs when endometrium-like tissue grows outside of the uterus. It's extremely common—if you have a uterus, you have a 1 in 10 chance of getting it. Yet, it takes seven years on average to receive a formal diagnosis. What does the latest science tell us about the biology of the condition and how to treat it? And why do so many people have such a difficult time getting diagnosed? Host Flora Lichtman is joined by endometriosis researcher and patient Linda Griffith to answer those questions and more. Guest: Dr. Linda Griffith is a biological engineer and Scientific Director of The MIT Center for Gynepathology Research.Transcripts for each episode are available within 1-3 days at sciencefriday.com. Subscribe to this podcast. Plus, to stay updated on all things science, sign up for Science Friday's newsletters.

Being put in a garbage can by a fellow classmate while in Junior High School, and having a teacher laugh at her as she was being forced to clean up the spill of a lunchroom tray which she did not cause, are just a few of the things that Mariah Forster Olson talks about in her recently published book HOPE OVER DESPAIR which details her life of the physical and mental after effects of her Neuroblastoma battle that she has lived with since her diagnosis of this form of Pediatric Cancer when she was a year old in June of 1980. Now at the age of 46, Mariah has proven without a doubt that it is possible to live a meaningful and successful life, despite being forced to endure the many unfortunate details that she describes so eloquently in her book.

Fresh off her stunning appearance on America's Got Talent, 9-year-old Izabela De Vera Giron joins us on this week's episode of the #UnidentifiedPodcast. Diagnosed with alopecia at a young age, Izabela has turned what many see as a challenge into a symbol of strength.Alopecia may take the hair, but it can never touch the courage, confidence, or voice within. With every performance, she shows the world that beauty, bravery, and talent come in many forms—and that confidence shines brightest when it comes from within.Her voice—powerful, pure, and full of heart—has moved audiences across the nation and inspired countless others to embrace their uniqueness. In this episode, we explore Izabela's journey: from her early love of music to the AGT spotlight, and now to the podcast with us. Hear how this young Filipina powerhouse is rising above expectations and using her gift to uplift the community.

He could barely move at 15 and now he's redefining strength. When doctors told Zac Spinosa he might never train again, he refused to accept it. Diagnosed with Systemic Juvenile Idiopathic Arthritis and Macrophage Activation Syndrome, he refused to let that be the end of his story. Instead, he built Forge Fitness, a community where disability doesn't mean limitation and pain becomes power. In this episode of Take a Pain Check, Zac opens up about hitting rock bottom and choosing to fight back, building a gym that truly includes people with chronic illness, the mindset shift that changed everything, and what strength really means when your body is working against you. If you've ever been told you can't, this episode will make you believe you can. Watch now, get inspired, and rethink what strength looks like.Donate to Take a Pain Check Today: ⁠https://www.gofundme.com/f/takeapainc...Don't forget to like, comment, and subscribe for more episodes.Our socials:https://www.takeapaincheck.com/https://www.instagram.com/takeapaincheck_/ https://www.tiktok.com/@takeapaincheckhttps://ca.linkedin.com/company/take-a-pain-checkhttps://www.youtube.com/@takeapaincheckhttps://www.facebook.com/TakeaPainCheckhttps://www.x.com/takeapaincheckZac's socials:  @ZacTheArthritisCoach 

In this powerful episode, Dr. Robert Kiltz sits down with Izzy Watson—athlete, holistic nutritionist, and carnivore advocate—to explore her remarkable transformation from chronic illness to peak performance. Diagnosed with colitis after years of misdiagnoses, Izzy shares how she took her health into her own hands, embraced the carnivore lifestyle, and went on to break a Guinness World Record and complete a 50-mile ultramarathon.

Rapper, producer, and entrepreneur Robert “B-Cide” Cardillo joins Rich to share the raw story behind his memoir, Myelin My Shoes—from underground tours and handing out mixtapes to launching a streetwear brand from a wheelchair after an MS diagnosis at 28. He breaks down how creativity became therapy, what the music business really teaches you, and why he refuses to let chronic illness define the art—or the hustle. If you need proof that purpose outlasts pain, this one's for you. Sponsored by Daniel McGhee and the Victory Team Guest Bio:  Robert “B-Cide” Cardillo is a New York–based rapper, producer, and entrepreneur known for his gritty underground catalog, collaborations with cult-favorite acts tied to the Insane Clown Posse scene, and his 55 Strong streetwear brand. Diagnosed with multiple sclerosis at 28, he chronicles the journey in his memoir Myelin My Shoes and continues creating—releasing new music, narrating his audiobook, and building businesses that turn resilience into a platform. Main Topics: ·         Early underground days: mixtapes, DIY touring, and creative freedom·         MS at 28: symptoms, diagnosis, and navigating good vs. poor care·         Music as therapy: writing through anger, grief, and isolation·         From stage heat to new rules: adapting performance and goals with MS·         Branding & entrepreneurship: 55 Strong origin and product design·         Bookmaking with AI help: editing workflow and audiobook narration·         Industry realities: politics in music, why authenticity matters·         New ventures with his father: helping businesses avoid political pitfalls·         Advice for dreamers facing fear or chronic illness: “Do it—don't wait.” Resources mentioned: ·         Robert's site & merch: b-cide.com·         Book: Myelin My Shoes (audiobook narrated by Robert)·         Music: B-Cide on Send us a texthttps://harfordcountyhealth.comThe Victory TeamLOOKING TO BUY OR SELL A HOME Go with the Agent that was voted Harford's Best & won the Harford CouDisclaimer: This post contains affiliate links. If you make a purchase, I may receive a commission at no extra cost to you.Support the showRate & Review on Apple Podcasts Follow the Conversations with Rich Bennett podcast on Social Media:Facebook – Conversations with Rich Bennett Facebook Group (Join the conversation) – Conversations with Rich Bennett podcast group | FacebookTwitter – Conversations with Rich Bennett Instagram – @conversationswithrichbennettTikTok – CWRB (@conversationsrichbennett) | TikTok Sponsors, Affiliates, and ways we pay the bills:Hosted on BuzzsproutSquadCast Subscribe by Email

Grandma Hobbies to Try This Winter:CrochetingCompleting a coloring bookKnittingPuzzlingBakingScrapbookingPlaying a board gameJewelry makingNeedlepointingEmbroideringMost Americans Spend a Third of Their Paycheck within 12 hours: Feel like your paycheck is gone as soon as you get it? Researchers find that's pretty much true for a lot of us. According to new research, the average American spends more than a third of their paycheck within the first 12 hours of receiving it.  What's Trending: Bay Area restaurants are coming together to support families affected by the SNAP benefit suspension, offering free or discounted meals to help ensure no one goes hungry, starting November 1st.  San Francisco:The Rusty LadleAl Pastor PapiOakland:Monster PhoUnderstoryPuerto Rican Street CuisineSan Jose:Toni and Alba's PizzaShrimp'n Ain't Easy(Food Truck)Santa Clara:Gamers HeavenConcord/Antioch:OG TacosSecond Date Update: Josh thought his tapas date with Tamara was a hit—great food, flirty banter, and zero awkward silences. They agreed: team books, not screens. He left confident. She left… and never texted back  The Most Successful Marriage Proposals Happen at Home: What were the other somewhat successful places?Outdoors (18.4%)Beach (12.4%)Restaurant (5.6%)Mountains (3.9%)Good News: Meet Poppy, 10, from Holborough Lakes. Diagnosed with dyslexia, she calls it her ‘superpower'—and with an IQ of 136, she just joined Mensa! Poppy hopes her story will show that thinking differently is a gift, not a limitation.

Kerri Steele's husband Will ran 13 miles each day, went home to help get his young children ready for the day afterwards, and then put in a full day of work. Needless to say, it was a total shock to Kerri and Will when he was diagnosed with a rare form of  cancer that was determined to be terminal upon his diagnosis in February of 2010, and which led to his passing on Christmas Eve of 2012. Kerri will talk about Will, and about the difficult years ahead for her and their children who were 2,4, and 6 when their father got sick. 

Nikola Topić Diagnosed with Testicular Cancer. Todd Fuhrman Week 10 Picks! Thunder/Wizards Tonight! High School Round Up! OU/Tennessee! MUCH MORE!!!See omnystudio.com/listener for privacy information.

Today's guest Richard Dixon has been living with type 1 diabetes for nearly 40 years.Diagnosed with the condition at the age of 2, Richard has spent a lot of his life in fear of his next injection due to a debilitating fear of needles.Every mealtime would cause huge amounts of worry, and the multiple daily injections he had no choice but to take steadily impacted every aspect of his life. Like so many people, Richard believed that insulin pumps were huge, bulky and incompatible with his lifestyle.He's been amazed to discover that this is not the case, and while deciding to change your diabetes management or try diabetes technology is an individual choice, the changes he's personally experienced in the last couple of years have transformed life for not only himself, but his young family too. DISCLAIMER Nothing you hear on Type 1 on 1 should be taken as medical advice. Please consult your healthcare team before making any changes to your diabetes or health management.JOIN THE TYPE 1 ON 1 COMMUNITY:Come and say hi @studiotype1on1 on Instagram.Visit the Type 1 on 1 website.Subscribe to the Type 1 on 1 newsletter.SPONSOR MESSAGEThis episode of Type 1 on 1 is sponsored by Dexcom. Using Dexcom CGM has given me so much confidence to make informed diabetes treatment decisions in the moment.You can choose to wear it on your arm or your abdomen, and all Dexcom CGMs have the share and follow feature even when connected to an insulin pump, so family and friends can see your glucose levels and get alerts, giving that extra bit of support when needed.Head to Dexcom.com to request a free Dexcom ONE+ sample.Always read the user manual for important product aspects and limitations. Talk to your doctor for diabetes management terms and conditions and terms of use. 

For years, I thought I was just busy. Running a podcast, a charity, doing my doctorate, working full-time, raising a child - that's just life, right? But when I was diagnosed with combined ADHD (moderate to severe) in my 40s, everything finally made sense. In this deeply personal episode, I'm stepping away from our usual dyslexia focus to share my own ADHD diagnosis journey - the signs I missed for decades, the internal chaos I thought was normal, and why getting help changed everything. What I cover: - Why I never thought I could have ADHD (despite working with it for years) - The signs I dismissed: constant internal dialogue, unfinished tasks, extreme fatigue, childhood anxiety - How medication helped me in ways I never expected - Why the "everyone's a bit ADHD" narrative is harmful - Addressing the over-diagnosis myth - and why women in their 40s+ are finally getting diagnosed - Why men are likely underdiagnosed (and what we can do about it) - The link between ADHD and dyslexia (they highly correlate) Key takeaway: If these traits are impacting your quality of life consistently - not just occasionally - that's when it might be ADHD. Everyone forgets things sometimes, but if it's life-altering where you can't function, that's different. Resources mentioned: ADHD Australia: https://adhdaustralia.org.au/ (trusted partner with excellent resources and conference content) Contact Rethink Dyslexia for support with ADHD diagnosis: rethinkdyslexia.com.au Shae's book: Dyslexia: Insights into the hidden disability in and out of the workplace https://rethinkdyslexia.com.au/dyslexia-insights-into-the-hidden-disability-in-and-out-of-the-workplace/ About Dr. Shae: Shae is a Doctor of Public Health, Certified Practicing Speech Pathologist, founder of Rethink Dyslexia, and host of the Dear Dyslexic Podcast. She was diagnosed with combined ADHD (inattentive and hyperactive, moderate to severe) in her 40s. Timestamps: 00:00 "I never thought I could have ADHD" 01:09 Why I'm sharing this now 03:25 When the narrative around ADHD became harmful 04:12 My journey: from focus on dyslexia to recognizing ADHD 06:00 The signs I dismissed for years 08:00 The "unfinished tasks" pattern 10:00 Childhood anxiety and sleep struggles 11:00 Getting assessed: the diagnosis process 11:10 How medication changed everything 13:00 "Everyone's a bit ADHD" - why this narrative is wrong 14:00 What medication actually did for me 17:17 The over-diagnosis myth (and the UK data) 19:00 Why women seek help more than men 21:03 Encouraging everyone to seek support 23:04 What diagnosis gave me: understanding, language, calm If you're struggling with constant mental fatigue, internal chaos, or feeling like life is harder for you than everyone else - you're not alone. Reach out. Get assessed. There is support.

Tired of ADHD strategies that don't work? Here's what actually does. FREE training here: https://programs.tracyotsuka.com/signup_____You walk into a room and forget why you're there. You miss deadlines even though you care deeply about the work. You can remember a random conversation from 15 years ago but not what someone just told you five minutes ago.Welcome to life with an ADHD brain and a memory system that works differently.Dr. Daniella Karidi knows this firsthand. Diagnosed with ADHD in her fifties after a therapist friend sent her a book she initially dismissed as "for kids," Daniella finally understood why she'd always felt "off" despite being highly successful. A researcher who earned her doctorate from Northwestern University studying memory and ADHD, Daniella is now the founder of ADHDtime, where she works as a professional ADHD and executive coach. She's spent years translating complex memory research into practical strategies that actually work for ADHD brains and in this conversation, she breaks down exactly why our memory fails us and what we can do about it.Daniella and Tracy dive deep into prospective memory (remembering to remember in the future), why time-based cues are terrible for ADHD brains, and the five steps where memory can break down. Daniella explains why we forget we took our medication, why she needed multiple cues instead of just one, and why she believes people who master their own memory patterns can finally stop feeling like they're failing at life. She also shares the grief and relief of late diagnosis, and why she'll never stop advocating for better understanding of how ADHD women's brains actually work.Resources:Website: https://www.adhdtime.comInstagram: https://www.instagram.com/ADHDtime Facebook: https://www.facebook.com/ADHDtimeSend a Message: Your Name | Email | Message If this podcast helps you understand your ADHD brain, Shift helps you train it. Practice mindset work in just 10 minutes a day. Learn more at tracyotsuka.com/shift Instead of Struggling to figure out what to do next? ADHD isn't a productivity problem. It's an identity problem. That's why most strategies don't stick—they weren't designed for how your brain actually works. Your ADHD Brain is A-OK Academy is different. It's a patented, science-backed coaching program that helps you stop fighting your brain and start building a life that fits.

In this week's episode, I'm joined by Cindy Shufflebarger, who shares the story of her daughter, Ashlynn Faith, and how God's immeasurable love met her family in the midst of unimaginable loss. Diagnosed with Trisomy 18, Ashlynn lived for three precious days — days filled with both deep sorrow and sacred joy. Cindy reflects on those moments, the way her faith was reshaped through lament, and how journaling became a lifeline that led to her book Dancing in the Rain: Finding Joy in the Midst of the Storm.We also talk about the Shufflebarger's beautiful ministry, P23 Retreat, which provides grieving parents with a private, prayer-covered space to rest and heal. Through this ministry, couples and singles are able to pause, reflect, and experience the peace of Psalm 23 in their own grief journeys.Here are some of the resources we mention in this episode:P23 Retreat Website: p23retreat.org — Learn more about how to request a retreat, donate a stay, or access the free downloadable resources available there.Free Downloadable Checklist for Grieving Parents — A simple tool to help you communicate your needs and boundaries to family and friends during grief. (Find it under “Resources” on the P23 website.)P23 Retreat on Social Media: Facebook    | Instagram    | LinkedInMy Messy Grief Podcast — Listen on Spotify or watch video episodes on YouTubeCindy's Book: Dancing in the Rain: Finding Joy in the Midst of the Storm — A look at how God brings joy and growth even through the hardest seasons.My Messy Grief Journal — Available on Amazon; a creative, colorful guide filled with prompts and activities to help you process grief in practical, sensory ways.Cindy's story is a powerful reminder that God's love truly has no limits — even in our deepest pain.If this episode encouraged you, please share it withI would love to hear your thoughts on the show. Click here to send me a message! (Though I read every message, I am unable to respond through this format.) ** IMPORTANT** - All views expressed by guests on this podcast are theirs alone, and may not represent the Statement of Faith and Statement of Beliefs of the While We're Waiting ministry. We'd love for you to connect with us here at While We're Waiting! Click HERE to visit our website and learn about our free While We're Waiting Weekends for bereaved parentsClick HERE to learn more about our network of While We're Waiting support groups all across the country. Click HERE to subscribe to our YouTube channelClick HERE to follow our public Facebook pageClick HERE to follow us on Instagram Click HERE to follow us on Twitter Click HERE to make a tax-deductible donation to the While We're Waiting ministryContact Jill by email at: jill@whilewerewaiting.org

In this compelling episode of Healthy Mind, Healthy Life, we sit down with Shant Cimenian—author, film producer, and entrepreneur—to explore his extraordinary journey from battling Familial Mediterranean Fever to inspiring thousands globally. Diagnosed at 23 with a rare and excruciating genetic condition, Shant turned his pain into purpose, chronicling his experiences in the memoir My Life, My Victory, now read in over 25 countries and soon to be a feature film. We dive deep into the mental strength it takes to live victoriously despite chronic illness, the role of faith in finding meaning through adversity, and the power of turning personal struggles into global missions of hope. This conversation is a raw and uplifting reminder that resilience isn't about avoiding hardship—it's about rising through it. About the Guest:Shant Cimenian is an internationally recognized author, producer, and entrepreneur. His memoir My Life, My Victory captures his personal battle with a rare genetic illness and has sparked worldwide conversations about perseverance, faith, and the human spirit. Shant's work is expanding into film, and his mission is to inspire others to see their own strength, no matter their struggle. Key Takeaways: How writing became a tool for healing and advocacy. Shant's raw account of living with chronic illness and transforming suffering into empowerment. The mental shift from feeling defeated to reclaiming purpose. Why victory often looks different than we expect—and why it matters. Practical wisdom on staying grounded and finding meaning in adversity. Connect with Shant:Website: www.shantcimenian.comInstagram: @shantcimenian  Get Shant's BookFacebook: My Life, My Victory Page (for updates on the book and upcoming film) 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 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-healthylife•⁠ Instagram – https://www.instagram.com/healthyminds.pod•⁠ Threads – https://www.threads.net/@healthyminds.pod•⁠ Facebook – https://www.facebook.com/podcast.healthymind•⁠ LinkedIn – https://www.linkedin.com/in/reemachatterjee/ | https://www.linkedin.com/in/avikchakrabortypodcaster #podmatch #healthymind #healthymindbyavik #wellness

Leland Vittert didn't speak until age three. Diagnosed with what we now know as autism, he spent middle school crying himself to sleep while his father repeated one message: "The qualities that make you bullied now will make you successful later." In this raw conversation, Leland opens up about his memoir Born Lucky, a father-son story about choosing resilience over accommodation and truth over popularity. We talk about the decision his parents made not to shelter him from adversity, but to hold his hand through it. About learning to turn isolation into independence, and pain into purpose. This isn't a polished highlight reel. It's an honest look at neurodivergence, parenting choices, bullying, and what it costs to stand your ground when the truth matters most. Key moments: Growing up neurodivergent before we had the language for it The parenting decision that changed everything Why middle school bullying prepared him for Washington newsrooms Finding your voice when you literally couldn't speak The father-son relationship that became his foundation Whether you're a parent of a struggling kid, someone who's faced isolation, or anyone trying to find strength in their story, this conversation offers hope, honesty, and the reminder that your hardest seasons might be preparing you for something greater. Guest: Leland Vittert is a journalist and author of Born Lucky, chronicling his journey from a nonverbal child with severe learning disabilities to a voice millions trust. Get the book Born Lucky: https://bornlucky.com/ Chapters: (00:00) Trailer (01:09) Intro (01:44) Introducing Leland Vittert (02:41) Overcoming Childhood Challenges (08:16) The Power of a Nickname: 'Lucky' (11:37) Navigating Autism and Social Challenges (20:41) Journalism and Personal Growth (27:30) Facing Adversity in the Newsroom (40:06) Covering the George Floyd Protests (43:37) The Challenges of Neutral Journalism (47:54) The Role of Media in Political Polarization (50:02) Interviewing Extremists (58:02) Personal Sacrifices for Integrity (01:05:08) Autism and Personal Growth (01:11:24) Faith and Family (01:19:56) A Father Tribute (01:20:58) Rapid Fire Questions SPONSORS: ElevenLabs: Thanks to ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ElevenLabs⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ for supporting this episode and powering Tim's voice. SOCIAL: Website: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠nlupod.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ Twitter: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠@nlutimgreen⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ Facebook: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠facebook.com/NLUpod⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ Instagram: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠@nlupod⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ AUDIO ONLY: Spotify: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Listen on Spotify⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ Apple Podcasts: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Listen on Apple Podcasts⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ PERSONAL: Tackle ALS: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠tackleals.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ Tim Green Books: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠authortimgreen.com⁠⁠⁠⁠ ROCKET ARM: ⁠⁠⁠⁠ https://www.amazon.com/dp/0062796895/ Learn more about your ad choices. Visit megaphone.fm/adchoices

Coming up this week on Pets Who Thrive Radio. Angela Ardolino, a certified cannabis and fungi clinician, and founder of CBD Dog Health and Myco Dog, joins Tammy to discuss her journey into holistic pet wellness. Diagnosed with rheumatoid arthritis, she found relief through cannabis oil and extended her expertise to pets. It's all this week on Pets Who Thrive Radio with Tammy King!

Katie and Dina dish about how ADHD coaching can help people harness their strengths to achieve their full potential, misinformation in science and health literacy, and the power of body-doubling.Katherine Karayianis, B.S, M.A, CALC is the founder of KDHD Coaching & Academic Consulting, where she empowers students with ADHD and learning differences to embrace their strengths and thrive academically. Diagnosed with ADHD and dysgraphia as a child, Katherine understands the frustrations of navigating school systems that aren't built for neurodivergent learners. Her lived experience inspired a lifelong passion for understanding how sleep, stress, and environment affect learning and performance.Katherine holds a B.S. in Psychology and Neuroscience from the University of Maryland and an M.A. in Social Ecology from UC Irvine, where her research focused on cognitive development and educational equity. Today, she offers coaching, tutoring, and advocacy services—including IEP support—to help families feel confident and informed.Learn more about Katie at:https://www.kdhdcoach.com/https://www.instagram.com/kdhdcoach/Mentioned in this episode:Body doubling/ND Hive: https://neurodivergentoutloud.com/nd-hive----Check out our podcast in video format on DishWithDinaTV:https://www.youtube.com/user/DishWithDina?sub_confirmation=1Join our mailing list to stay connected, stay informed, receive exclusive offers, and be a part of the DishWithDina community:https://forms.gle/MzV7gVAPEsqEyEFH6If you enjoyed this podcast, please subscribe, leave a review, and share it with others!You can also submit listener feedback or request to be a guest on a future episode by completing this form:https://forms.gle/EFYX7Gshbjx9cCKfA----DISCLAIMER: The purpose of this podcast is to entertain, educate, and inform, but it is not to be taken as medical advice. Please seek prompt, qualified medical care for any specific health issues and consult your physician or health practitioner before starting a new fitness regimen, herbal therapy, or other self-directed treatment.

Jannell and Keith Royer's daughter McKenna was experiencing headaches before her Diffuse Midline Glioma diagnosis in August of 2023. This Pediatric Brain Cancer behaves in a similar manner to DIPG, leaving little room for a lifespan which is normally expected to be 9-12 months.  McKenna did not even make it that far, passing away on February 26th of 2024, 6 months after being diagnosed. Jannell and Keith will talk about how McKenna felt surprisingly well during almost all of her battle, until 8 days before her passing when she suddenly went downhill health wise. Jannell and Keith will also about their Brave Like McKenna Foundation and their advocacy work for the cause of Pediatric Cancer.

Send us a textGetting diagnosed with type 2 diabetes can feel overwhelming. Fear, denial, guilt, sadness — it's an emotional rollercoaster that many people don't talk about enough. In this episode of The Beating Diabetes Lifestyle Podcast, Oscar gets real about what happens after that diagnosis and how to move forward with hope and purpose.November is National Diabetes Awareness Month, and if you've recently been diagnosed — or you've been living with diabetes for less than a year — this message is especially for you. Oscar shares his own story of being 268 pounds, newly diagnosed, and determined to turn things around through small, consistent steps.You'll learn:How to process the emotional side of a diabetes diagnosisWhy mindset and self-compassion are key to lasting changeSimple, practical ways to start reclaiming your health todayHow physical and mental wellness work hand-in-handOscar also challenges listeners to take action this month — whether that means signing up for a 5K walk or run, reading one book on nutrition, or simply learning more about how your body works. Progress starts with one small step.If you've been wondering where to start, this episode will help you see that your story isn't over — it's just getting started.Download your FREE Weight Loss Planner to help you stay focused and consistent at BeatingDiabetesLifestyle.com_____________________Connect With MeTo submit a question or join my mailing list, use the information below to connect with me. Join My Facebook Group - https://www.facebook.com/groups/beatingdiabeteslifestyle Web - www.beatingdiabeteslifestyle.com Email - hello@beatingdiabeteslifestyle.com Instagram - @beatingdiabeteslifestyle _____________________ ©2025 Oscar Camejo - The Beating Diabetes Lifestyle

Just got the prediabetes news and not sure what to do next? Jess walks you through the very first steps—without shame, overwhelm, or extreme diets. You'll learn how to start tracking patterns, what simple food and lifestyle shifts to make, and why small changes (like breakfast and a 10-minute walk) can actually move the needle. Real results, real encouragement.If you're living with diabetes or prediabetes and want personalized support from a Registered Dietitian Nutritionist covered by insurance, visit diabetesdigital.co to connect with our culturally aware and weight-inclusive team. And if you love the show, don't forget to rate and review us on iTunes or Spotify—it makes a huge difference! For additional resources and show notes, head to diabetesdigital.co/podcast.

In this episode, Myrna Young and guest Kate Moryoussef dive deep into **adult ADHD** and its significant impacts on **women's mental health**. Diagnosed at 40, Kate reveals her journey of navigating life with undiagnosed ADHD, shedding light on the unique, often unseen symptoms women face, particularly those influenced by hormonal changes. This enlightening discussion highlights the intersections between ADHD and everyday life challenges, including maintaining healthy relationships, managing work stress, and developing emotional regulation strategies. Tune in to discover practical tools and holistic approaches to women empowerment amidst the complexities of ADHD. Join us in embracing authentic selfhood and harnessing the potential within!Key Takeaways:Broadened Understanding of ADHD: ADHD encompasses much more than the inability to focus and can significantly impact emotional regulation, hormonal sensitivity, and relationships.Symptoms in Midlife: Hormonal cycles, anxiety, depression, and coping mechanisms are all connected to undiagnosed ADHD, highlighting the importance of awareness and diagnosis.Impact on Relationships: ADHD's influence on communication, emotional regulation, and addictive behaviors can strain relationships significantly.Toolkit for Well-Being: Kate promotes a comprehensive approach, combining medication, lifestyle modifications, holistic practices, and deeper self-awareness to manage ADHD effectively.Authentic Living: The call to embrace one's authenticity and thrive by aligning life choices with personal passions and innate strengths.Sponsors of this podcastShopifySign up for your one-dollar-per-month trial period at SHOPIFY.com/transformResources Kate Moryoussef's Book: ADHD Women's Wellbeing ToolkitPodcast: ADHD Women's Wellbeing PodcastWebsite: ADHD Women's WellbeingInstagram: @adhd_womens_wellbeing_podTo advertise on our podcast, visit https://advertising.libsyn.com/TransformyourMindor email kriti@youngandprofiting.com See this video on The Transform Your Mind YouTube Channel https://www.youtube.com/@MyhelpsUs/videosTo see a transcripts of this audio as well as links to all the advertisers on the show page https://myhelps.us/Follow Transform Your Mind on Instagram https://www.instagram.com/myrnamyoung/Follow Transform Your mind on Facebookhttps://www.facebook.com/profile.php?id=100063738390977Please leave a rating and review on iTunes https://podcasts.apple.com/us/podcast/transform-your-mind/id1144973094 https://podcast.feedspot.com/personal_development_podcasts/

Paris speaks with Daniela Skinner, an artist, corporate professional and mother who shares her journey navigating bipolar to raise her now 9 year old son. Diagnosed at 27, Daniela recounts her challenging experiences with postpartum mania, hospitalizations and navigating life as a new mother under immense stress. She details her struggles, the pivotal role of finding the right medication and how she managed to rebuild her life through creative practices and strong family ties. Daniela opens up about her fears, coping strategies and how she found balance, ultimately showing that it's possible to lead a full, meaningful life with bipolar. This episode is a compelling testament to resilience, offering hope and insightful advice to others on a similar path.Stay connected with Daniela here! Learn to support someone you love with bipolar here!00:00 Introduction and Guest Introduction01:27 Daniela's Bipolar Diagnosis and Early Episodes03:34 Postpartum Challenges and Manic Episode07:42 Hospitalization and Personal Struggles10:16 Custody Battle and Road to Recovery14:03 Finding Stability and Creative Reconnection18:46 Living Well with Bipolar24:53 Motherhood and Family Conversations33:32 Final Thoughts and Closing Remarks

I want to hear your thoughts about the show and this episode. Text us here...What happens when life changes overnight? When the world literally goes dark?In this powerful episode, Julie DeLucca-Collins sits down with Laura Bratton, motivational speaker, coach, and author of Harnessing Courage. Diagnosed with a rare retinal disease at nine years old, Laura faced the reality of losing her sight. Over the next decade, she navigated denial, grief, and transformation to rebuild her identity and discover her purpose.Laura shares how she became the first blind student to graduate from Princeton Theological Seminary, what “grit and gratitude” really mean, and how she helps others embrace change through her company, Ubi Global.In this episode, you'll learn: • How grief and gratitude can coexist in healing • What real grit looks like in daily practice — one tiny goal at a time • Why permission to feel is key to growth • How to move forward when you can't see the path ahead • The importance of faith, mindset, and self-advocacy in creating a meaningful lifeLaura reminds us that courage isn't the absence of fear — it's choosing to move anyway.Connect with Laura Bratton: