Podcasts about Diagnosis

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

In this Winter News & Notes episode of The Celiac Project Podcast, Mike and Cam share powerful listener updates and real life celiac journeys. From insurance battles and refractory celiac disease to mental health, OCD, and navigating college gluten free, this episode highlights both the challenges and the progress happening in the community. They also discuss advocacy efforts around FDA labeling and helpful resources for checking whether medications are gluten free.

For years people were told the body can only decline with age, but what if that isn't the full story? I sit down with Toni and Kerri to explore remarkable testimonies that left even their own doctors saying what they experienced should have been impossible, as their strength, mobility, and vitality returned in ways they never expected. When you hear what happened, it may challenge what you believe about how the body was designed and what is still possible for you.   Podcast Episode 2039: Woman Faced With Scary Diagnosis Gets a Breakthrough They Said Couldn't Happen | don't miss this! Listen to more episodes of the Lance Wallnau Show at lancewallnau.com/podcast

Contributor: Travis Barlock, MD Educational Pearls:  Foul-smelling urine and cloudy urine are commonly misinterpreted as indicators of a UTI. However, these findings alone are not diagnostic. Criteria for UTI: Presence of localized urinary symptoms: Suprapubic pain Dysuria Hesitancy Urgency Urinalysis with WBC > 10 Urine culture with > 100,000 CFU/mL Colonization differs from infection - many patients harbor asymptomatic bacteria but do not have a true infection. Consequences of overtreatment One review showed 45% of patients treated with antibiotics for a presumed UTI actually had asymptomatic bacteriuria and were incorrectly treated. Unnecessary antibiotic treatment can have deleterious effects on the gut microbiome, increasing the risk of multidrug-resistant infections. Another problem with overdiagnosing UTI is missing the real diagnosis by explaining symptoms away as "just a UTI." Be mindful of the risk of overtesting versus not testing at all. Clinicians must navigate a balance between moving patients efficiently through the ER and testing appropriately when a UTI is truly suspected. References: Baghdadi JD, Korenstein D, Pineles L, et al. Exploration of primary care clinician attitudes and cognitive characteristics associated with prescribing antibiotics for asymptomatic bacteriuria. JAMA Netw Open. 2022;5(5):e2214268. doi:10.1001/jamanetworkopen.2022.14268 Colgan R, Williams M. Acute uncomplicated urinary tract infections in adults. Am Fam Physician. 2024;109(2):167-174. Accessed February 21, 2026. https://www.aafp.org/pubs/afp/issues/2024/0200/acute-uncomplicated-utis-adults.html#afp20240200p167-ta1 Summarized by Ashley Lyons OMS3 | Edited by Ashley Lyons & Jorge Chalit OMS4 Donate: https://emergencymedicalminute.org/donate/ Join our mailing list: http://eepurl.com/c9ouHf

Congenital Muscular Dystrophy (CMD) is an ultra-rare diagnosis that often requires a long, complex journey toward answers.In this episode, Brigitte Cutshall sits down with Kelly Berger and Avery Roberts, hosts of the Wheel Talk with Kelly & Avery Podcast, to explore their lives with the same rare subtype of CMD. From meeting on a Zoom call to becoming close friends and collaborators , they share how they navigated the transition to mobility devices for independence and safety , the frustrations of a world not built for them , and their mission to amplify disabled voices through female empowerment.3 Key Takeaways(1) Diagnosis is a Spectrum: Avery was diagnosed at age seven after extensive testing , while Kelly lived with a misdiagnosis until her late 20s ; their experiences highlight that CMD is a spectrum disorder where every individual's journey is unique(2) The Difference Between Compliance and Access: The ADA provides only a "bare minimum" for public spaces , but many private or older venues, such as New York theaters, remain inaccessible , forcing those with disabilities to perform exhausting "pre-planning" just to run basic errands.(3) The Power of Allyship and Unlearning: Being a supportive ally starts with a willingness to "unlearn" misconceptions and assumptions about the disability community , understanding that there is power in collective action to enact meaningful, lasting change.Action items: - Support and listen to people with disabilities- Advocate for accessible environments- Stay informed about genetic testing and healthCheck out Kelly and Avery's stories on the Wheel Talk with Kelly & Avery Podcast—available on Apple, Spotify, and YouTube—and follow their mission to uplift and empower rare voices.

Helping you diagnose a common cause of hypertension!Hypertension is a growing disease globally, affecting millions of individuals and increasing the risk of heart disease and stroke. Along with the expert help of Dr. Vaidya (Brigham and Women's Hospital), we help reimagine the approach of clinicians in terms of hypertension and help them navigate common diagnostic dilemmas! @AnandVaidya17 (Bluesky) @AnandVaidya17 (X)Claim CME for this episode at curbsiders.vcuhealth.org!Patreon | Episodes | Subscribe | Spotify | YouTube | Newsletter | Contact | Swag! | CMEShow Segments Introduction and Personal Interests Advice and Wisdom in Medicine  Case 1 Defining Primary Aldosteronism Screening for Primary Aldosteronism How common is Primary Aldosteronism Challenges in Diagnosis and Testing Medication Management and Testing Protocols Managing indeterminate cases Aldosterone Suppression Testing and its role Discussing treatment options with patients Case 2 Considering genetic causes of Primary Aldosteronism The need for AVS for lateralization Upcoming imaging modalities for Primary Aldosteronism Case 3 Medical Management of Primary Aldosteronism Future Directions in Treatment Credits Producer, Writer, Show Notes:Mobeen Ahmad MBBS  Infographic:Kate Grant MBChB MRCGP Cover Art:Kate Grant MBChB MRCGP Hosts: Matthew Watto MD, FACP; Paul Williams MD, FACP    Reviewer: Emi Okamoto MD Showrunners: Matthew Watto MD, FACP; Paul Williams MD, FACP Technical Production: PodPaste Guest:  Anand Vaidya MD, MMSc DisclosuresDr. Vaidya has disclosed the following: Financial Relationships: Astra Zeneca-Consulting Fee and Corcept-Consulting Fee, relationships have not ended. The Curbsiders report no relevant financial disclosures. Sponsor: The Sanford GuideCurbsiders listeners can get 20% off the already very moderately priced yearly subscriptions directly at sanfordguide.com. Go to sanfordguide.com and use the code, CURB at checkout.Sponsor: MedStudy PodcastCurbsiders listeners get 15% off with code CURB15 atmedstudy.comSponsor: Panacea Legal Visit Panacea.Legal and use code CURB20 for 20% off contract review services.Sponsor: DeleteMeGet 20% off your DeleteMe plan when you go to joindeleteme.com/CURB and use promo code CURB at checkout.

Dr. Justin Abbatemarco talks with Dr. Marjo S. van der Knaap and Romy J. van Voorst about expert consensus recommendations for the diagnosis and management of vanishing white matter and the importance of standardizing care worldwide. Read the related article in Neurology®.  Disclosures can be found at Neurology.org. 

Dominion is in your DNA. Y O U have the power to move mountains.Jesus never told us to beg mountains to move — He told us to speak to them. He gave us clear instruction for facing trials, obstacles, and adversity with Kingdom authority.In today's episode, I'm sharing my three-part Mountain Moving Protocol — the exact framework I use to identify the obstacle, activate spiritual authority, and take aligned action that sets miracles in motion.We all face adversity. Debt. Diagnosis. Delays. Relationship strain. The question isn't if you'll face a mountain — it's whether you'll stand before it as a victim… or a daughter with dominion.If you're ready to stop circling the mountain and start commanding it to move, this episode is for you.Press play. Activate your authority. And try the protocol for yourself.Want to learn more about Kingdom coaching? Contact me here on Instagram or email me at shinewithfrannie@gmail.comAnd if this episode blessed you, I have a huge ask--please share comment and leave a rating! And of course, sharing is caring! Please share this with a fellow sister who might be facing a mountain of her own! Love you to life!:) Frannie

A coworker diagnosed with ALS: how to pray?

Shawn Jorgenson, MD facilitates a debate between Dave Preston, MD and Richard Lewis, MD: Should Neuromuscular Ultrasound be Routinely Used in the Diagnosis of CIDP?

WD tells what was so special about the USA beating Canada for the gold in hockey, reacts to Duke's defense against Michigan, attached letter grades to the ACC basketball weekend in "WD's Diagnosis", breaks down the best things he saw over the weekend including Wemby saying he would do the slam dunk contest, and Hayes Permar, of Sports Channel 8, joins the show to reveal the inside story of Chad Ochocinco pulling up to The Rialto in Raleigh.

In this powerful and heartfelt conversation, Kathy Carvalho shares her journey through challenge, uncertainty, and ultimately transformation. What happens when your body forces you to confront everything you thought you knew about strength, control, and identity?Kathy opens up about the emotional realities behind a life-changing diagnosis, the fear and frustration that followed, and the pivotal mindset shifts that helped her reclaim her power. This episode dives deep into resilience, self-trust, nervous system regulation, and the often-overlooked connection between belief and healing.If you've ever felt defined by your symptoms, stuck in fear, or unsure how to move forward, this conversation will remind you that your identity is not your diagnosis and that healing begins the moment you decide to see yourself differently.This is more than a story. It's a roadmap back to possibility.

Welcome to the Heal and Restore Podcast with Randy and Cathy Boyd—where we engage in honest conversations that help you heal, grow, and strengthen your relationships.In today's deeply personal and timely episode, “When the Diagnosis Changes Everything: Navigating the Emotional Shock of Unexpected Medical News,” we explore the moment life suddenly shifts—when a diagnosis arrives that you never saw coming, and the emotional ground beneath you begins to move.A medical diagnosis doesn't just affect the body—it impacts the heart, the mind, and every relationship connected to it. In an instant, certainty can turn into fear, strength into vulnerability, and plans into questions. Many people experience shock, denial, anxiety, grief, and even anger—all while trying to remain strong for those around them.We'll unpack the emotional impact of unexpected medical news and how it affects not only the person diagnosed, but also their spouse, family, and support system. We'll talk about the internal battles no one sees—the fear of the unknown, the loss of control, and the quiet questions about the future. Without awareness and support, these emotions can lead to isolation, emotional shutdown, or overwhelming anxiety.In this episode, you'll learn how to recognize and honor the emotional shock that follows a diagnosis, how to stay emotionally connected to yourself and your loved ones, and how to navigate uncertainty without losing hope. We'll share practical, grace-filled steps to help you slow down, process what you're feeling, and begin finding emotional steadiness—even when the future feels unclear.Because the truth is, a diagnosis may change your circumstances—but it does not define your identity, your value, or your capacity to live with purpose and hope.Healing is not only physical. It is emotional, relational, and spiritual.If this episode speaks to your heart, be sure to follow, rate, and share the Heal and Restore Podcast. When we face life's hardest moments with honesty, courage, and support, we don't just survive them—we grow through them.

In this episode, Annika Kroger is joined by Corina Bruckmann and Ian Needleman to explore how clinicians can support patients at every stage of the periodontal journey, from communicating risk and setting expectations at diagnosis, to maintaining motivation and managing recurrence during long-term supportive care. They also discuss the importance of incorporating patient perspectives, the challenges faced in everyday practice, and how integrating the entire dental team can strengthen engagement, improve adherence, and support better long-term outcomes.

Sixteen months ago my primary care doctor told me I had developed Mild Cognitive Impairment(MCI). In lay terms that means I am losing my mind. It could happen slowly over the next few years or it could happen more quickly. That seems like a life changer.

In Part 2, Marta and Denise explore what happens after survival — when the crisis passes, but life is permanently changed.This is a conversation about faith, surrender, letting go of control, and learning to trust life even when certainty is impossible. Denise shares how walking through her daughter's illness reshaped her understanding of motherhood, love, and purpose, and how learning to “let go and trust” became not just an idea, but a daily practice.Together, they reflect on what it means to support loved ones without trying to control their path, how hardship can deepen connection and spiritual meaning, and why sometimes the most powerful thing we can offer someone is presence, not protection.A grounded, deeply human reminder that transformation doesn't always come from comfort. Sometimes it comes from learning how to live fully in the unknown.

In this week's message, Pastor Lawrence digs into Romans 1:18-32 to show us that the best news ever actually starts with some bad news. God — the Great Physician — has given us a clear diagnosis: our world is sick, and we are the cause. But understanding what's wrong is the first step to receiving what's right.This episode explores the wrath of God (and why it's actually a sign of His goodness), two forms of truth suppression, what it means when "God gave them up," and why the gospel is truly good news for every kind of sinner — regardless of background, struggle, or story.

There's a long-held idea that autism is more prevalent in boys than girls—the CDC says it's three times as common. But a growing body of research suggests the reality is more complicated. In a new study, researchers tracked autism diagnoses in millions of Swedish people born from 1985 to 2022. They found that the prevalence of autism is actually pretty even across the sexes, but people with “female” stamped on their birth certificate are often diagnosed later in life.  Host Flora Lichtman speaks with epidemiologist Caroline Fyfe about what this study teaches us about the prevalence of autism. Then, psychology researcher Rachel Moseley, an autistic woman herself, shares how late and missed diagnoses can affect autistic people. Guests: Dr. Caroline Fyfe is an epidemiologist at the University of Edinburgh who studied sex differences in autism diagnoses.  Dr. Rachel Moseley is a researcher in psychology at Bournemouth University in the UK, studying the experiences of autistic adults.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.

The Visionary Artisté, formerly known as [blake{Art}]®, embodies the artist from the get-go — driven by curiosity, allergic to hollow fame, and aligned with #ArtsTask, a mantra inspired by Terence McKenna that calls creators to midwife culture rather than chase clout. Moving from pyramid to spiral, from Magical Egypt to the Mandelbrot set, from the golden mean to the "thumbprint of God," this perspective weaves ancient wisdom with modern complexity To gain access to the second half of show and our Plus feed for audio and podcast please clink the link http://www.grimericaoutlawed.ca/support. For second half of video (when applicable and audio) go to our Substack and Subscribe. https://grimericaoutlawed.substack.com/ or to our Locals  https://grimericaoutlawed.locals.com/ or Rokfin www.Rokfin.com/Grimerica Patreon https://www.patreon.com/grimericaoutlawed Support the show directly: https://open.spotify.com/show/2punSyd9Cw76ZtvHxMKenI?si=ImKxfMHgQZ-oshl499O4dQ&nd=1&dlsi=4c25fa9c78674de3 Watch or Listen on Spotify https://grimericacbd.com/ CBD / THC Tinctures and Gummies https://grimerica.ca/support-2/ Our Adultbrain Audiobook Podcast and Website: www.adultbrain.ca Our Audiobook Youtube Channel:  https://www.youtube.com/@adultbrainaudiobookpublishing/videos Check out our next trip/conference/meetup - Contact at the Cabin www.contactatthecabin.com Other affiliated shows: www.grimerica.ca The OG Grimerica Show Join the chat / hangout with a bunch of fellow Grimericans  Https://t.me.grimerica grimerica.ca/chats   Discord Chats Darren's book www.acanadianshame.ca Eh-List Podcast and site: https://eh-list.ca/ Eh-List YouTube: https://www.youtube.com/@TheEh-List www.Rokfin.com/Grimerica Our channel on free speech Rokfin Leave a review on iTunes and/or Stitcher: https://itunes.apple.com/ca/podcast/grimerica-outlawed http://www.stitcher.com/podcast/grimerica-outlawed Sign up for our newsletter http://www.grimerica.ca/news SPAM Graham = and send him your synchronicities, feedback, strange experiences and psychedelic trip reports!! graham@grimerica.com InstaGRAM https://www.instagram.com/the_grimerica_show_podcast/  Purchase swag, with partial proceeds donated to the show www.grimerica.ca/swag Send us a postcard or letter http://www.grimerica.ca/contact/ ART - Napolean Duheme's site http://www.lostbreadcomic.com/  MUSIC Tru Northperception, Felix's Site sirfelix.bandcamp.com    

Join us for an exciting discussion all about the world of **jeep** and **offroad** adventures. We dive deep into various aspects of **automotive** care and **car repair** specific to these rugged vehicles. Learn about the latest in **automotive technology** that keeps your ride performing at its best. Join host Tony Muckleroy from the Jeep Talk Show for an in-depth return interview with Jay Voltovan, General Manager of Steer Smarts – the go-to brand for heavy-duty aftermarket steering and suspension upgrades on Jeeps, Ford Broncos, and trucks. In this episode (a follow-up to our August 2024 chat on fixing death wobble), we dive deep into: - How Steer Smarts eliminates death wobble, numb steering, wandering, and insecure highway feel on JL Wranglers, JT Gladiators, and more – even on stock or mildly lifted rigs. - Real-world explanations: What *actually* causes death wobble (harmonics, deflection in factory components like track bars), vs. "wiggles" or shimmy. - Preventative upgrades: Start with the beefy solid-forged track bar + sector shaft brace for massive improvements (~$600-650 budget combo) – then add drag link, tie rod, and stabilizer. - Why Steer Smarts' Yeti XD series linkages (forged in-house, minimal outsourcing, no jam nuts, clamp-style retention) transform ride quality, reduce fatigue, and handle big tires/lifts. - Tony's personal experience: Full Steer Smarts install on his 2021 Jeep Talk Show Gladiator – night-and-day difference, wife-approved confidence, no more babysitting on the highway. - New RōMR Suspension line (launched at SEMA 2025): Fully integrated chassis systems (Trail, Ascent, Summit kits) for JL/JT – 2.5" or 3.5" lift options, tuned for 90% of enthusiasts (daily driving + moderate trails), reduced body roll, firmer/plant feel, pairs perfectly with Steer Smarts steering. - Summit Chassis System: Comprehensive overhaul (sway bars, shocks, springs, geometry corrections, steering reinforcements) – takes the guesswork out. - Tips: Diagnose first (torque checks, bushings), prevention over cure, install yourself or via dealer network, works on stock Jeeps too – not just lifted monsters. - Bonus: Tony's million-dollar ideas (candy cane tie rods? "I Survived Death Wobble" shirts?), social media handles, and tech support (888-8GO-YETI). If you're tired of white-knuckling your Jeep, chasing wobble, or wanting that confident, planted drive – this is for you!

In this meeting of The Late Diagnosis Club, Dr Angela Kingdon welcomes Julie Farrell, a late-diagnosed Autistic and ADHD writer, activist, and co-founder of The Inklusion Guide, a resource dedicated to making literature events accessible to disabled people.Julie shares her slow, layered journey toward understanding her neurodivergence — from burnout, migraines, and chronic illness labels, to finding herself mirrored in Autistic writers like Katherine May, to sobbing through the documentary Seeing the Unseen and finally knowing in her bones.Together, Angela and Julie explore masking, shutdowns mislabelled as anxiety, CPTSD, creative identity, freelance work as nervous system regulation, and the relief of receiving a diagnosis in a supportive, affirming environment. They also talk about ADHD medication, menstrual cycle titration, EMDR therapy, and what it feels like to “precipitate out of the hot goo” and become solid for the first time.This episode is also about Autistic joy — about stars, navigation, grief, and how Julie's late father taught her to look up at the night sky and find her way.

Nocardioform placentitis is a frustrating and sometimes devastating diagnosis in broodmares. In this episode of StallSide, Theriogenologists, Dr. Maria Schnobrich and Dr. Karen Von Dollen take a closer look at how this condition develops, what makes it different from other forms of placentitis, and why early detection is important. They explain how expanding the definition to focal mucoid placentitis better describes this condition, then explore the clinical presentation, diagnostic tools, treatment strategies, and what current research and field experience suggests about prognosis and outcomes. Whether you're managing mares on the farm or supporting breeding operations, this episode offers practical, experience-driven insight into navigating high-risk late-term pregnancies. @roodandriddle Watch episodes on YouTube @roodandriddle or visit us at www.rrvp.com

This week, Aebhric is joined by Dr Harrison Steins, who is finishing his MSc in Austere Critical Care with CoROM. He also finished medical school and is starting his emergency medicine training. His master's thesis was on the complexities of swimming-induced pulmonary oedema (SIPE), a rare condition affecting athletes, particularly in high-altitude environments. The speaker, Harrison Steins, discusses the pathophysiology, clinical presentation, diagnosis, and management strategies for SIPE, emphasising the importance of context in medical practice. He shares case studies, research findings, and future directions for understanding and treating this condition, highlighting the role of ultrasound in diagnosis and the need for tailored prevention strategies.TakeawaysSwimming-induced pulmonary oedema is a rare condition with a prevalence of less than 1%.Understanding the context of patient presentation is crucial for diagnosis.Acute-onset cough and dyspnoea are key symptoms of SIPE.Diagnosis requires a broad differential, ruling out other conditions first.Management focuses on immediate life threats before addressing SIPE.Hydration strategies can prevent SIPE, especially in athletes.Sildenafil may be effective in preventing SIPE, but it is not widely recommended.Handheld ultrasound is a reliable tool for diagnosing pulmonary oedema in the field.Females may have a higher incidence of SIPE at lower elevations than males do.Knowledge of population-specific pathology is essential for effective treatment.Chapters00:00 Introduction to Swimming-Induced Pulmonary Oedema04:47 Understanding the Pathophysiology of Swimming-Induced Pulmonary Oedema09:18 Case Studies and Clinical Presentation13:48 Diagnosis and Imaging Techniques19:26 Management Strategies and Treatment24:17 Research Findings and Future Directions

Uncle Si discovers his brand-new smile helped reveal a health issue that had been affecting his whole body for years. The boys shift gears as Si, Phillip, and Godwin are joined by Mark Neumann of LifeCampUSA as they support middle school boys and girls who've lost a parent in military, law enforcement, or first responder service. Plus, Martin jokes that after hearing Si's stories of backyard pellet-gun injuries and kitchen-table “field surgery,” he's just hoping his own boys survive childhood without needing the same kind of homegrown medical care. Duck Call Room episode #528 is sponsored by: https://nutrafol.com — Get $10 off your first month's subscription and free shipping when you use promo code DUCK at checkout! httsp://fastgrowingtrees.com — Get 20% their first purchase when using the code DUCK at checkout. https://trybeef.com/duck — Get 10% off your first TriTails box straight from their ranch to your door. https://myphdweightloss.com — Find out how Godwin is losing weight! Schedule your one-on-one consultation today by visiting the website or calling 864-644-1900 and be sure to mention "Godwin" so they know we sent you! - Learn more about your ad choices. Visit megaphone.fm/adchoices

Tara Daniels is now 33 years old , married, working at a job that she enjoys , and living as good of a life as she can. Back in 2009 when Tara was 16 years old this was not the case as she was diagnosed with Acute Lymphoblastic Leukemia . Tara relapsed twice, with the last relapse coming in 2016. Tara then received a Bone Marrow transplant and since that time period, she has been cancer free. Tara will talk about all that she has been through, including survivorship on today's podcast.

In Part 2 of this important two-part conversation, Debi Robinson continues her discussion with Dr. Nick Birch, a former spinal surgeon who began questioning conventional bone density testing after decades of surgical experience.While Part 1 explored the limitations of DEXA scans and the difference between bone density and bone strength, this episode goes deeper into the broader implications: informed consent, the blind spots of specialty medicine, polypharmacy, and why bone health must be viewed through a whole-body lens.Dr. Birch explains how REMS technology evaluates bone fragility and toughness — not just density — and why women deserve access to better information when making decisions about their bone health.This episode is about empowerment through education.What You'll Learn in This EpisodeWhy bone density and bone strength are not the sameHow REMS measures fragility and bone toughnessThe limitations of the traditional “T-score model”What medical “blinkers” are — and how they affect careThe risks of polypharmacy in aging womenHow medications can unintentionally impact bone healthWhy informed consent must include lifestyle optionsWhy bone health reflects overall metabolic, hormonal, and digestive healthAction Steps You Can Take TodayLook beyond your T-score and ask about fracture risk.Ask your provider about all options, including lifestyle interventions.Evaluate medication interactions if you are on multiple prescriptions.Support digestion and gut health to improve nutrient absorption.Address inflammation and stress, which directly impact bone remodeling.Think holistically — bone health is whole-body health.Resources & LinksDebi's website: https://debirobinson.comLearn more about REMS (Radiofrequency Echographic Multi Spectrometry) technology (as discussed in the episode): https://www.osteoscanuk.com/about-usHealthy Gut Healty Bones Program: https://debirobinsonwellness.thrivecart.com/hghb-self-paced-group-program-pp/Join the Community: https://debirobinson.com/the-stronger-bones-lifestyle-community/Yoga Therapy MasterClass: https://debirobinson.com/yoga-therapy-for-bones-health-mc/Instagram: https://www.instagram.com/debirobinsonwellness/Youtube Channel: https://www.youtube.com/@debirobinsonwellness/Debi's TakeawayYou are not your T-score.You are not a prescription.You are not a number on a scan.Bone health is influenced by hormones, digestion, stress, inflammation, movement, and metabolic balance. When we expand the conversation beyond density alone, we give women the information they need to make empowered decisions.Information replaces fear.Understanding builds confidence.And empowered women build stronger bones.

Welcome to OncLive On Air®! I'm your host today, Courtney Flaherty.OncLive On Air is a podcast from OncLive®, which provides oncology professionals with the resources and information they need to provide the best patient care. In both digital and print formats, OncLive covers every angle of oncology practice, from new technology to treatment advances to important regulatory decisions.In today's episode, Philippos Costa, MD, and Hari Deshpande, MD sat down to discuss and answer frequently asked questions about chondrosarcoma in honor of International Chondrosarcoma Awareness Day. This included common pitfalls in the diagnostic process for this rare, heterogenous bone malignancy; the central role of surgery as the primary treatment for localized chondrosarcoma; and the potential application of IDH1-targeted therapy, DR5 agonists, and other emerging targeted therapies in this sarcoma subtype.Dr Deshpande is an associate professor of medicine, clinical research team leader in sarcoma, and the director of Medical Oncology Inpatient Consult Service in the Section of Medical Oncology at Yale School of Medicine. Dr Costa is an oncologist and assistant professor of medicine (Medical Oncology and Hematology) at Yale School of Medicine._____That's all we have for today! Thank you for listening to this episode of OncLive On Air. Check back throughout the week for exclusive interviews with leading experts in the oncology field.For more updates in oncology, be sure to visit www.OncLive.com and sign up for our e-newsletters.OncLive is also on social media. On X and BlueSky, follow us at @OncLive. On Facebook, like us at OncLive, and follow our OncLive page on LinkedIn.If you liked today's episode of OncLive On Air, please consider subscribing to our podcast on Apple Podcasts, Spotify, and many of your other favorite podcast platforms,* so you get a notification every time a new episode is posted. While you are there, please take a moment to rate us!Thanks again for listening to OncLive On Air.*OncLive On Air is available on: Apple Podcasts, Spotify, CastBox, Podcast Addict, Podchaser, RadioPublic, and TuneIn.This content is a production of OncLive. The current episode was filmed in advance of Chondrosarcoma Day, observed on February 6, 2026

Gil Alderete of Catholic Men's Fellowship (CMF) serves as host of Men of Faith; in this episode he continues his conversation with businessman Mark Prather about Gil's embrace of the Catholic faith after experiencing turmoil in life.Listen live to Gil's show Men of Faith at https://www.spiritfilledevents.com/radio-podcast Monday -Friday at and 12:30pm Pacific Time. Podcast is available https://www.spiritfilledevents.com/men-of-faith and other podcast outlets. Support the show

Unlike a simple infection with a clear-cut cure, canine atopic dermatitis (CAD) is an inflammatory, chronic condition with complex causes. Treating it with a one-size-fits-all approach is like trying to put a Yorkshire terrier's sweater on a Great Dane—it will not work. In this episode of the VetFolio Voice podcast, discover the nuances in treating atopic dermatitis and finding the best fit for the individual patient. We explore how to alleviate pruritus while ruling out pruritic diseases that mimic atopy. Join us as we go from syndrome to solution in providing relief for your patients with CAD.

Dizziness, fatigue, brain fog, and a racing heart are often brushed off as anxiety or stress. But sometimes there's a real reason behind these symptoms: Postural Orthostatic Tachycardia Syndrome (POTS). Dr. Wendy talks with pediatric autonomic specialist Dr. Jeff Boris about POTS, an often-missed nervous system condition. We explain what POTS looks like, how it's diagnosed, why it can show up after viral infections like COVID, and treatments that help kids feel better.    Find Jeffrey Boris, MD and learn more about POTS  Download the POTS Exercise program at dysautonomiainternational.org    Send your questions to hello@pediatriciannextdoorpodcast.com or message me online here.  Find products from the show on the shop page.   *As an Amazon Associate, I earn commission from qualifying purchases.    More from The Pediatrician Next Door:    Website: Pediatrician Next Door Podcast  Instagram: @the_pediatrician_next_door  Facebook: facebook.com/wendy.l.hunter.75  TikTok: @drwendyhunter  LinkedIn: linkedin.com/in/drwendyhunter    This is a Redd Rock Music Podcast  IG: @reddrockmusic  www.reddrockmusic.com Learn more about your ad choices. Visit megaphone.fm/adchoices

In this week's podcast episode, Jessica shares the remarkable story of becoming a NICU mom through adoption. She opens up about her and her husband's journey through foster care, infertility, and the unexpected call that would introduce them to their son, Noah. Just weeks before his birth, they learned he had a complex congenital heart defect, along with other medical concerns that left doctors unsure if he would survive.Jessica vulnerably walks us through Noah's early arrival, his emergency transfer to a Level IV NICU, a terrifying code event at one month old, and ultimately his open heart surgery at just four months of age. She shares what it felt like to hand her baby over at the operating room doors, how NICU nurses carried hope for her when she could not carry it herself, and the tension of learning to fully embrace her role as mom while honoring Noah's birth mother. Jessica also reflects on the emotional transition home after 84 days in the hospital and what it looked like to slowly rebuild life and create new memories beyond survival mode.Today, Noah is thriving and living a full, joyful life. His story is one of resilience, courage, and deep trust in the midst of fear!As you listen to Jessica's story, we hope that any heart mama, adoptive mama, or NICU mama in the thick of it feels seen and heard. You are not alone.To get connected with DNM:Website | Private Facebook Group | InstagramSupport the show

In this episode of The Ultimate Assist, John Stockton and Ken Ruettgers sit down with naturopathic physician Dr. John Lieurance for a wide-ranging conversation about the hidden drivers of modern chronic illness — and why he believes the conversation around health is only just beginning.Dr. Lieurance explains how mitochondrial health, inflammation, toxic exposures, and chronic infections may play a larger role in disease than many people realize. He discusses emerging research around cellular energy production, oxidative stress, and the body's ability to adapt to environmental stressors, outlining how lifestyle, detoxification pathways, and microbiome balance can influence long-term resilience.The conversation also explores controversial topics in modern health care, including medical freedom, evolving approaches to chronic disease, and why individualized protocols — rather than one-size-fits-all solutions — may shape the future of wellness. Dr. Lieurance shares clinical insights from his practice, discusses new therapeutic approaches being explored in integrative medicine, and highlights the importance of empowering individuals to take an active role in their own health decisions.Whether you're curious about biohacking, longevity science, or the future of preventive medicine, this episode challenges conventional thinking and asks an important question: Are we focusing on managing disease instead of addressing its root causes?Understanding Hypophosphatemia: Recognition, Diagnosis, and TreatmentEndocrine experts distinguish Hypophosphatemia from osteoporosis & osteomalaciaListen on: Apple Podcasts SpotifySupport the show

Love the show? Have any thoughts? Click here to let us know!On this week's episode, we welcome one of Kenzie's best friends, Lindsay, as we travel to the Show-Me State, Missouri! Kenzie shares the strange and unsettling story of the prominent Swope family, whose household was rocked by a series of sudden deaths in a very short period of time. The family's trusted in-house doctor insisted the deaths were from natural causes, but the nurses caring for the patients began to question his treatment methods and the care being provided. Was the Swope family simply the victim of tragic coincidence? Or was something far more sinister unfolding behind closed doors? Join us as we dig into a century-old case that remains controversial and debated to this day.Follow us on Social Media and find out how to support A Scary State by clicking on our Link Tree: https://instabio.cc/4050223uxWQAl--Have a scary tale or listener story of your own? Send us an email to ascarystatepodcast@gmail.com! We can't wait to read it!--Thinking of starting a podcast? Thinking about using Buzzsprout for that? Well use our link to let Buzzsprout know we sent you and get a $20 Amazon gift card if you sign up for a paid plan!https://www.buzzsprout.com/?referrer_id=1722892--Works cited!https://docs.google.com/document/d/1Dq_0tJvFgEFuU1ZpZQ3E_LcuLc-RrTML8fSt9ILWb6k/edit?usp=sharing --Intro and outro music thanks to Kevin MacLeod. You can visit his site here: http://incompetech.com/. Which is where we found our music!

Dr. Raymond Barnhill on Diagnostic Drift, Uncertainty, and the MPATH-Dx V2.0 Approach to Melanocytic LesionsIn this episode of The Girl Doc Survival Guide, Christine interviews Dr. Raymond Barnhill, a world-recognized dermatopathology expert known for work on diagnostically challenging melanocytic lesions, melanoma pathology references, and contributions to WHO skin tumor classification and AJCC melanoma staging. Dr. Barnhill shares career anecdotes and key communities at Yale and in Boston, collaborations with numerous melanoma leaders, and the founding of the North American Melanoma Pathology Study Group and the International Melanoma Pathology Study Group, as well as participation in the NIH-funded MPATH Study Group. The discussion focuses on overdiagnosis, underdiagnosis, and diagnostic discordance in melanocytic lesions, including evidence of diagnostic drift toward calling more lesions melanoma over time and the overlap between melanoma criteria and atypical/dysplastic nevi. He describes MPATH research, explains the revised MPATH-Dx V2.0 schema, explicitly recognizing uncertainty along a continuum rather than a strict benign/malignant threshold. He emphasizes practical diagnostic approaches including measuring lesion size (noting a 4 mm threshold associated with conventional dysplastic nevi and increasing concern at larger sizes), focusing on key architectural features (junctional nest variation/disarray and lentiginous proliferation), using nuclear size relative to keratinocyte nuclei (including a 1.5× threshold and counting atypical cells per high-power field) while accounting for site-specific pitfalls such as scalp nevi. The conversation also covers “gestalt” versus systematic review, the importance of due diligence using full clinical and morphologic information before ancillary testing, and cautions against overreliance on immunohistochemistry or molecular tests. Dr. Barnhill closes with career advice ends with a message that setbacks can be opportunities for growth.00:00 Welcome + Meet Dr. Raymond Barnhill (Dermatopathology Legend)01:51 Career Origins & Melanoma Pathology Mentors (Yale → Boston)03:59 Building Melanoma Pathology Study Groups (North American & International)05:57 Overdiagnosis, Diagnostic Drift & Why Discordance Happens09:43 Inside the MPATH Study: Measuring Interobserver & Intraobserver Agreement11:39 MPATH-Dx V2.0 Explained: Standardized Classes & Treatment Guidance13:59 Redefining “Low-Risk” Melanoma: Stringent pT1a Criteria + Embracing Uncertainty18:47 Practical Grading Tips: Lesion Size, Architecture & Nuclear Atypia Thresholds22:42 Gestalt vs Due Diligence: Avoiding Traps + Using IHC/Molecular Wisely (PRAME)28:39 Career Advice: Passion, Mentors, Community + Final Reflections

Next week our first Brewers Lectures of 2026 takes place at the fantastic Full Circle Brew Co in Newcastle on the 25th February. We’ve got a brilliant line-up of industry talent taking part including Jack Walker, the head brewer at Azvex. Since being founded by Adam Henderson in 2020, Azvex Brewing Company has gone on to become of the UK's most respected producers of hop-forward pale ales and IPAs, fruited sours, and imperial stouts. And head brewer Jack Walker has played a huge part in that journey. Next week Jack will share his brewing expertise and give us an insight into how he produces the brewery’s beautiful West Coast Pils. While we look forward to that talk, Jack also shared some experiences of a different kind during our Manchester lectures last year. In 2025 Jack has found himself in the final stages of a coeliac diagnosis and in his lecture he outlines the challenges that has presented for a brewing professional while also outlining some of the misinformation and misunderstanding that surrounds the condition. 

Does a mental health diagnosis explain why you are suffering, or does it just give your suffering a name?In this episode, I challenge the traditional way we look at mental health labels. While a diagnosis (like depression, anxiety, or ADHD) can be a helpful shorthand for professionals, it often becomes a trap for the person receiving it—convincing them they are "broken" rather than adapting to their life context.To illustrate this, I share the story of two hypothetical clients: Penny and Milton. Both come to therapy with the exact same heavy symptoms.Penny receives a diagnosis, is told she has a disorder to manage forever, and leaves feeling defective.Milton is met with a nervous system perspective, learns his feelings make sense based on his history, and is given the tools to actually heal.Join me as we explore why your diagnosis is a description, not a life sentence. We'll discuss how to shift from "fighting a disorder" to building safety in your nervous system, so you can stop merely managing symptoms and start getting unstuck.In this episode, you will learn:Why a diagnosis in the DSM describes what is happening but rarely explains why.The critical difference between the "Disorder Model" vs. the "Nervous System Model."How to stop rejecting your feelings and start building safety (the "Milton" approach).Why your symptoms are likely a normal response to an abnormal situation.

Dr. Nancy O'Hara, pediatrician and leading expert in PANS and PANDAS, joins me to unpack why some children experience sudden, dramatic changes in behavior, anxiety, OCD, tics, sleep, or emotional regulation following illness. For many families, these symptoms appear almost overnight and are often misdiagnosed as "just anxiety," behavioral issues, or psychiatric disorders, leaving parents confused, dismissed, and unsure how to help their child.   Together we explore:   - What PANS and PANDAS are, and how infections like strep, viruses, or tick-borne illness can trigger sudden neuropsychiatric symptoms in children. - What to assess to help you determine if your child has a generalized anxiety disorder or if it may be PANS/PANDAS that is the root cause of their symptoms. - Why PANS/PANDAS is often missed or misunderstood in both medical and mental health settings. - The three-pronged approach to treatment: Addressing the trigger, the immune system, and the child's emotional and behavioral symptoms. - How therapy, both for parents and children, can support recovery, even when symptoms have a medical origin. - Understanding that there is real hope for healing and that it's never too late to identify and address PANS or PANDAS.   This episode is designed to help parents and clinicians feel more informed, less alone, and more confident in recognizing when a child's behavior may be signaling something deeper. PANS and PANDAS are real, treatable conditions that deserve compassionate, comprehensive care.     LEARN MORE ABOUT MY GUEST:

In Part 1 of this two-part conversation, Marta is joined by Denise Harris, mother of cancer survivor Holly Harris, for a deeply human exploration of caregiving, faith, resilience, and what it means to love someone through a life-altering diagnosis.Together, they reflect on the moment everything changes, the emotional reality of being “the strong one,” and how faith, community, and small moments of kindness can become lifelines during crisis. Denise shares her experience walking beside her daughter through brain tumor diagnosis, surgery, and treatment while navigating her own fear, grief, and responsibility as a mother and caregiver.This is a spacious conversation about love, village support, self-care, and the unseen emotional work of holding others while learning who holds you. A grounded reminder that strength is not the absence of fear, it's the willingness to stay present in the middle of it.

In this episode of Parallax, Dr Ankur Kalra welcomes Dr Rakesh Shah, a former interventional cardiologist, Oxford MBA graduate, and founder of DRS.LINQ. Dr Shah brings a unique perspective on addressing critical delays in heart attack diagnosis through the intersection of clinical medicine, engineering, and business strategy. The conversation explores a pressing challenge in cardiovascular care: the majority of cardiac damage occurs within the first hour of symptom onset, yet treatment activation often takes several hours. Dr Shah introduces mHeart, a mobile EKG platform designed to create a "virtual cardiology office." Unlike consumer wearables that lack critical chest leads, this technology enables patients to initiate comprehensive cardiac evaluation anywhere—at home, at work, or while traveling—transmitting diagnostic-quality data directly to cardiologists. The episode delves into Dr Shah's diverse career path and offers candid advice for physician-entrepreneurs, emphasizing the importance of collaboration with professional business leaders to achieve scalability. Looking ahead, Dr Shah discusses the integration of AI and machine learning into mobile diagnostic platforms as essential tools for an aging workforce and overstretched healthcare system. Questions and comments can be sent to "podcast@radcliffe-group.com" and may be answered by Ankur in the next episode. Host: @AnkurKalraMD and produced by: @RadcliffeCardio Parallax is Ranked in the Top 100 Health Science Podcasts (#48) by Million Podcasts.

In episode #423 of The Hormone Puzzle Podcast, our guest, Katherine Rohland, talks about Beyond the Diagnosis: Decoding Unexplained Infertility. More about Katherine Rohland: Katherine Rohland, M.S, LAc, is a licensed Chinese medicine practitioner with over eight years of experience helping women naturally enhance their fertility and reproductive health. Alongside her clinical practice, she holds advanced training in Chinese medicine gynecology, classical Chinese medicine, nutrition, and pediatric care. In her practice, she supports women holistically by addressing the body, mind, and lifestyle so they feel deeply guided on their path to pregnancy. Nothing brings her more joy than seeing women achieve their optimum health potential, empowering them to show up in the world as their best selves mentally and physically while pursuing their personal and professional dreams. Thank you for listening! This episode is brought to you in partnership with Puzzle Brew Fertility tea - https://hormonepuzzlesociety.com/fertility-tea Follow Katherine on Instagram: @‌manhattan_medicine_woman Follow Dr. Kela on Instagram: @‌kela_healthcoach Get your FREE Fertility Meal Plan: https://hormonepuzzlesociety.com/ FTC Affiliate Disclaimer: The disclosure that follows is intended to fully comply with the Federal Trade Commission's policy of the United States that requires to be transparent about any and all affiliate relations the Company may have on this show. You should assume that some of the product mentions and discount codes given are "affiliate links", a link with a special tracking code This means that if you use one of these codes and purchase the item, the Company may receive an affiliate commission. This is a legitimate way to monetize and pay for the operation of the Website, podcast, and operations and the Company gladly reveals its affiliate relationships to you. The price of the item is the same whether it is an affiliate link or not. Regardless, the Company only recommends products or services the Company believes will add value to its users. The Hormone Puzzle Society and Dr. Kela will receive up to 30% affiliate commission depending on the product that is sponsored on the show. For sponsorship opportunities, email HPS Media at media@hormonepuzzlesociety.com

In this episode of Our Forever Smiles, Laura sits down with Natalie and Alec, parents to Zaid, who was born with a cleft lip and palate. They share their experience navigating a prenatal diagnosis, an unexpected NICU stay, feeding challenges, and learning how to advocate within a complex medical system. This honest conversation highlights the importance of asking questions, finding community support, and trusting your instincts as a parent. A must-listen for families preparing for birth or feeling overwhelmed in the early weeks of the cleft journey.  

In this episode of Find Your Finish Line, I sat down with two incredible guys, eight-time IRONMAN champion Ben Hoffman and Dr. Tommy Martin, a physician at Boston's Chosin Hospital, who are teaming up to take on one of the toughest mountain bike races on the planet: the Cape Epic in South Africa. This eight-day, 400-mile race through some of the most unforgiving terrain in the world is no joke, and what makes their story even more compelling is that Tommy had never ridden a mountain bike until eight months ago. Together, they're racing with the IRONMAN Foundation to raise money to put kids on bikes in South Africa and fund swim lessons, proving that the best finish lines are the ones we chase for something bigger than ourselves. We got into everything from the raw reality of preparing for a race this demanding, to the power of teamwork, to Tommy's deeply moving perspective as a father of a son with a rare genetic disorder called Lamb-Shaffer syndrome. His message that "a diagnosis doesn't define a child's potential" is one that will stick with you long after this episode ends. This one's packed with heart, grit, and a whole lot of inspiration. Follow the Guests: Dr. Tommy Martin: @DrTommyMartin on all social media platforms Ben Hoffman: @BHoffmanRacing on Instagram and Facebook Donate: IRONMANFoundation.org

In this episode of 'Autism for Badass Moms,' host Rashidah welcomes Kanisha, a 40-year-old registered nurse in Houston and mom to five-year-old Zoë (diagnosed at 2.5, verbal with limited communication), shares her journey from early concerns and self-referral for evaluation to an ADOS-based diagnosis and the therapies that followed. She opens up about balancing full-time work, navigating limited support, starting full-day ABA, and witnessing Zoë's significant progress.At the heart of the conversation is disclosure. Kanisha explains why she told only a small circle at first, choosing privacy over overwhelm and commentary. She reflects on finding community online and encourages moms to move at their own pace, trust their discernment, and protect their peace.In this episode, we talk about:00:00 Welcome to Autism for Badass Moms (Show Intro)00:46 Today's Topic: Who Do You Tell First After an Autism Diagnosis?02:18 Meet Kisha & Zoe: A Diagnosis That Changed Everything04:42 Early Red Flags: 12–18 Months, Speech Concerns & Being Dismissed07:58 Two-Year Turning Point: Sensory Signs & Suspecting Autism11:22 The Daycare Wake-Up Call: Social Struggles & “Final Piece” Moment13:52 Taking Control: ECI, Child Find & Getting Evaluated Without Waiting16:45 Diagnosis & Insurance Hurdles: Fighting for Speech/OT Services20:03 School vs. Daycare Reality: When Half-Day Support Isn't Enough21:44 Choosing ABA: Fear, First Days, and Finally Seeing Progress24:26 Breakthroughs & Reframing the Future: From Level 3 to New Milestones26:16 The Grief After Diagnosis: Mourning Dreams, Milestones, and the Unknown32:27 Who We Told (and Who We Didn't): Processing the Diagnosis35:34 Grief, “What Ifs,” and Preparing for Every Outcome36:53 Protecting Your Child: Privacy, Boundaries, and Unwanted Advice38:56 Finding Your Tribe: Podcasts, Threads, and Support Groups That Get It44:14 Real-Life Logistics: Summer Break, Programs, and Working Full-Time47:36 Advice to New Autism Moms: Tell People at Your Own Pace51:48 What Makes Her Badass + Closing Reflections and How to Connect56:58 Final Takeaway: Discernment, Peace Over Pressure, and Guest Call-OutConnect with Kanisha:Instagram: www.instagram.com/mamanish20Resource shared:YouTube: confessionsofanautismmomIf this episode resonated with you:• Follow the Autism for Badass Moms Podcast on your favorite platform• Leave a review to help other autism moms find this community• Share this episode with a parent who may feel unseen or misunderstoodInstagram: www.instagram.com/theabmpodcastFacebook: www.facebook.com/theabmpodcastYouTube: autismforbadassmoms

If you've suspect IBS but have never been diagnosed with it, this episode is for you! Includes:What information to share with your doctor in your appointmentThe diagnostic criteria for IBSWhat conditions your doctor should rule out when considering IBSBuy my book - Inside Knowledge for people with IBS & SIBO (find it on Amazon)Get free weekly IBS & SIBO emails - https://mailchi.mp/goodnessme-nutrition.com/h6acndd1bsWork with me3 month Gut Reset - https://www.goodnessme-nutrition.com/consultations/Ready for your gut reset?

BrainStorm wants to hear from you! Send us a text.Alzheimer's disease is no longer just a memory problem — it's a biological, cultural, and ethical challenge reshaping how we think about aging, identity, and medicine. In this episode of Brainstorm by UsAgainstAlzheimers, host Meryl Comer sits down with Dr. Jason Karlawish, professor of medicine, medical ethics, health policy, and neurology at the University of Pennsylvania. They explore how Alzheimer's evolved from a rare condition into a full-blown public health crisis. Dr. Karlawish unpacks the science behind biomarker testing and early detection, the promise and complexity of new anti-amyloid treatments, and why so many physicians remain reluctant to diagnose cognitive decline at all. From health equity gaps that leave Latino and African American patients chronically underserved, to the ethical weight of disclosing an Alzheimer's diagnosis to someone still in the middle of their career, Dr. Karlawish brings both scientific precision and moral seriousness to one of medicine's most urgent conversations. It's a candid, wide-ranging discussion about what it truly means to confront a disease that strikes at the heart of who we are. You don't want to miss this episode!Produced by Susan QuirkSupport the show

WD reacts to Adam Silver's shocking thoughts on tanking and how he intends to penalize teams for it, breaks down an awesome Daytona 500, details the best things he saw this weekend including Jon Gruden's day at Daytona, tells whether or not the ABS Challenge system in the MLB is a good thing, and he attaches letter grades to the sports weekend that was in "WD's Diagnosis".

A new high blood pressure diagnosis can feel overwhelming, especially when the only advice you hear is “cut the salt” or “lose weight.” In this episode, Kara Carper and Brandy Buro break down what to change first to start lowering blood pressure naturally.

Dr. Frank Peacock and Dr. Damon R. Kuehl join BioTalk for a focused discussion on one of emergency medicine's most persistent challenges: accurately diagnosing and predicting outcomes in mild traumatic brain injury. As Scientific Advisory Board members for BrainBox Solutions, Inc., they walk through what happens when a patient presents to the emergency department after a fall or sports injury and why current tools, including CT scans, often leave clinicians without clear answers. The conversation explores the gap between a "normal" scan and ongoing symptoms, and what missed or uncertain diagnoses can mean for patients weeks later.   Dr. Peacock outlines the HeadSMART II study and explains why combining blood biomarkers with neurocognitive testing provides a more complete assessment than biology alone. Dr. Kuehl discusses how multi-modal data, integrated through artificial intelligence, can generate an objective score to support real-time clinical decision-making and help identify patients at risk for persistent symptoms. The episode also highlights BrainBox's leadership, including CEO Donna Edmonds, a member of the BioHealth Innovation Board of Directors, and the company's role in advancing objective mTBI testing.   Editing and post-production work for this episode was provided by The Podcast Consultant (https://thepodcastconsultant.com).   Dr. W. Frank Peacock IV is Professor of Emergency Medicine at Baylor College of Medicine. Chief Medical Officer at AseptiScope, and the founder of both a contract research organization called Comprehensive Research Associates, LLC and a medical education company named Emergencies in Medicine, LLC. Dr. Peacock received his medical degree from Wayne State University Medical School and completed his Emergency Medicine training at William Beaumont Hospital. He has >900 peer reviewed publications and is also the co-editor of multiple medical textbooks on heart failure, acute coronary syndromes, and traumatic brain injury.   Dr. Damon R. Kuehl is the Vice Chair of Research and Academic Affairs and Professor in the Department of Emergency Medicine at Virginia Tech, School of Medicine. He completed Medical School at University of Minnesota Medical School and his Emergency Medicine Residency at Stanford University. He has also completed residencies in Preventive Medicine and a Research Fellowship in the Center for Policy and Research in Emergency Medicine, at Oregon Health and Science University. Dr. Kuehl's research primarily focuses on diagnostic and prognostic uncertainty in brain injury. He is a lead investigator for HeadSMART II and for HeadSMART Geriatrics, a NINDS funded 3 year study to develop a diagnostic tool for head trauma in older adults.  He is the founder of the Carilion Brain Injury Center and also an investigator with the Virginia Tech Center for Biomechanics studying the boundary conditions associated with injuries in older adult falls.

Norah St Peter never saw herself as an athlete. She grew up in the performing arts, ran cross country in high school but didn't connect with it, and later spent years very sick before finally being diagnosed with Crohn's disease. Once she reached remission, movement became something to celebrate. Rock climbing led to running, running led to a half marathon, and not long after crossing that finish line she signed up for her first full at the Cowtown Marathon in Fort Worth on her birthday weekend.She trained through a cold Texas winter, only for race day to spike into the 80s. When the half marathoners split off and the course got quiet, the race shifted. The wall hit, the heat took a toll, and she crossed the finish line feeling physically and mentally feeling a bit wrecked. We also talk about taper tantrums, leaning on community, racing in remission, and what it means to do everything right in training and still have a hard day. This episode is a great reminder that even if the finish doesn't come with fireworks, you still ran a marathon. Follow along with Norah on Instagram at @norahtriestorun !Support Norah's local chapter of the Crohn's and Colitis FoundationFollow along with the show: 

Today you meet Carra who got diagnosed in 2016, during a very interesting time in our country. Today she talks about her experience with diagnosis, her childhood, relationship, and arguments about chickens. Spoiler alert, I fight with my husband about our chicken coop as well! Thank you, Carra, for joining us on the podcast! 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...