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Rebeccasode! Dr Kirk and Rebecca answer patron emails. February 27, 2026This episode is sponsored by BetterHelp. Give online therapy a try at betterhelp.com/KIRK to get 10% off your first month.Become a member: https://www.youtube.com/channel/UCOUZWV1DRtHtpP2H48S7iiw/joinBecome a patron: https://www.patreon.com/PsychologyInSeattleEmail: https://www.psychologyinseattle.com/contactWebsite: https://www.psychologyinseattle.comMerch: https://psychologyinseattle-shop.fourthwall.com/Instagram: https://www.instagram.com/psychologyinseattle/Facebook Official Page: https://www.facebook.com/PsychologyInSeattle/TikTok: https://www.tiktok.com/@kirk.hondaThe Psychology In Seattle Podcast ®Trigger Warning: This episode may include topics such as assault, trauma, and discrimination. If necessary, listeners are encouraged to refrain from listening and care for their safety and well-being.Disclaimer: The content provided is for educational, informational, and entertainment purposes only. Nothing here constitutes personal or professional consultation, therapy, diagnosis, or creates a counselor-client relationship. Topics discussed may generate differing points of view. If you participate (by being a guest, submitting a question, or commenting) you must do so with the knowledge that we cannot control reactions or responses from others, which may not agree with you or feel unfair. Your participation on this site is at your own risk, accepting full responsibility for any liability or harm that may result. Anything you write here may be used for discussion or endorsement of the podcast. Opinions and views expressed by the host and guest hosts are personal views. Although, we take precautions and fact check, they should not be considered facts and the opinions may change. Opinions posted by participants (such as comments) are not those of the hosts. Readers should not rely on any information found here and should perform due diligence before taking any action. For a more extensive description of factors for you to consider, please see www.psychologyinseattle.com(By The Daily Telegraph. Copyright holders of the image of Madeleine at three are Kate and Gerry McCann. The age-progressed image was commissioned by Scotland Yard from forensic artist Teri Blythe for release to the public. Both images have been widely disseminated by the copyright holders, and have been the subject of significant commentary., Fair use, https://en.wikipedia.org/w/index.php?curid=39861556)
In this meeting of The Late Diagnosis Club, Dr Angela Kingdon welcomes Claire Samuels, a proud Autistic speech-language pathologist whose journey to self-recognition unfolded inside the very system she would later question.Claire began her career as a Registered Behaviour Technician (RBT) in the ABA industry, believing what she was told: that ABA was the gold standard for Autistic children. She loved the kids she worked with and believed she was making a positive impact. But as she read autistic voices, learned about interoception, and began recognising her own sensory and regulatory differences, cracks in the framework began to show.Together, Angela and Claire explore ABA, nuance, Autistic self-recognition, masking, sensory processing, burnout, and what it means to move from compliance-based therapy to connection-based communication.This episode is about shifting lenses, from behaviour to nervous systems, from control to connection, and from moral judgment to regulation.
In part one of this two-part series, Dr. Justin Abbatemarco, Dr. Marjo S. van der Knaap, and Romy J. van Voorst discuss vanishing white matter disease, focusing on the clinical and MRI findings that would prompt the consideration of genetic testing. Show citation: van Voorst RJ, Schoenmakers DH, Bonkowsky JL, et al. Consensus-Based Expert Recommendations for Diagnosis and Clinical Management of Vanishing White Matter. Neurology. 2025;105(11):e214320. doi:10.1212/WNL.0000000000214320 Show transcript: Justin Abbatemarco: Hello and welcome. This is Justin Abbatemarco here with Romy J. van Voorst and Marjo S. van der Knaap. After discussing their article published in Neurology, Consensus-Based Expert Recommendation for Diagnosis and Clinical Management of Vanishing White Matter. They both work for Amsterdam University Medical Center in the Netherlands. And we're going to have a two-part episode dissecting maybe two elements of this paper. Marjo, maybe we could start here and just talking about what vanishing white matter disease is and what in the clinic and MRI findings would make us go towards a genetic testing. Dr. Marjo S. van der Knaap: There are two things about vanishing white matter that matter most to families, and one is the stress sensitivity. So any type of physical stress, like fever, viral infection, anything may cause a rapid decline and you never know when it comes. And that brings me to the second item that's very difficult and painful for families. And that's the unpredictability. You never know when a disease is going to hit and then your child is going to go down. So you really need the support of neurologists who know about this disease and help you go through this situation. Dr. Justin Abbatemarco: Right. And this paper serves as a great resource for folks that if they have a patient in clinic like this, medications to avoid, how to manage those stress responses. And so it's a really helpful publication to have there. And then I think another message we talked a lot about on the podcast was the importance of genetic testing when patients aren't fitting a typical bucket and this specific disease has unique characteristics. I think the cystic appearance of the MRI, which you do a great job highlighting, would really lead us down that road. So I think it's all really helpful and it gives us some ways to start in clinic with patients and our caregivers. So thank you. Come back and join us for the second part of The Neurology Minute episode where we're going to talk about the patient management.
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.
In Episode 60 of The Ultimate Assist, Alix Meyer returns with one warning: the trap isn't coming — it's already here.Is Real ID just an airport upgrade… or the foundation of a digital surveillance state?Are we voluntarily opting into a system that could one day decide where we work, whether we travel, or even how much carbon we're “allowed” to consume?Alix breaks down her concept of “weaponized architecture” — systems that appear helpful on the surface but are built to control beneath it. From biometric databases and facial recognition to what she calls the “Internet of Bodies,” she argues that Americans are being nudged — not forced — into a digital identity framework that may ultimately reshape freedom itself.The conversation turns explosive when she questions:Are measles outbreaks being used to manufacture public consent?Has California effectively “medically seceded” from federal authority?Is a social credit-style system closer than we think?Are digital IDs the next opt-in control mechanism?Whether you agree with her or not, this episode will challenge your assumptions about privacy, health freedom, and the true cost of convenience.Are we protecting ourselves… or building our own cage?Understanding Hypophosphatemia: Recognition, Diagnosis, and TreatmentEndocrine experts distinguish Hypophosphatemia from osteoporosis & osteomalaciaListen on: Apple Podcasts SpotifySupport the show
Depuis quand ça existe les TDAH ? Adhérez à cette chaîne pour obtenir des avantages : https://www.youtube.com/channel/UCN4TCCaX-gqBNkrUqXdgGRA/join ERRATUM à 6:21 lésion cérébrale mineure avec un e bien sûr! OUPS 00:00:00 - Introduction à l'histoire du diagnostic de TDAH 00:01:59 - Les premières tentatives 00:08:10 - Le début de la psychopharmacologie pour le TDAH 00:11:54 - L'impact de l'article du Washington Post 00:15:24 - La définition du TDAH par Russell Barkley 00:17:00 - Le diagnostic du TDAH au Québec Pour soutenir la chaîne, au choix: 1. Cliquez sur le bouton « Adhérer » sous la vidéo. 2. Patreon: https://www.patreon.com/hndl Musique issue du site : epidemicsound.com Images provenant de https://www.storyblocks.com Abonnez-vous à la chaine: https://www.youtube.com/c/LHistoirenousledira Les vidéos sont utilisées à des fins éducatives selon l'article 107 du Copyright Act de 1976 sur le Fair-Use. Sources et pour aller plus loin: Marie-Christine Brault, Emma Degroote et Mieke Van Houtte, « Disparities in the prevalence of ADHD diagnoses, suspicion, and medication use between Flanders and Québec from the lens of the medicalization process », Health, 2023, vol. 27 (6), p. 958-979. Lange, K. W., Reichl, S., Lange, K. M., Tucha, L., & Tucha, O. (2010). The history of attention deficit hyperactivity disorder. Atten Defic Hyperact Disord . 2010 Dec;2(4):241-55. doi: 10.1007/s12402-010-0045-8. Epub 2010 Nov 30. Rothenberger A, Neumärker KJ. Wissenschaftsgeschichte der ADHS. Steinkopff, Darmstadt: Kramer-Pollnow im Spiegel der Zeit; 2005. https://neuronup.com/fr/actualites-de-la-stimulation-cognitive/troubles-neuro-developpementaux/tdah/bref-historique-du-tdah-et-de-son-impact-sur-le-fonctionnement-executif/ Barkley 2006a, Barkley RA (2006a) Attention-deficit hyperactivity disorder. A Hand- book for Diagnosis and Treatment, Guilford, New York, Barkley, R. (2002). Niños hiperactivos: cómo comprender y atender sus necesidades especiales. 3a. Ed. Barcelona: Paidós. Barkley, R. (2011). Executive functioning and self- regulation: Integration, extended phenotype, and clinical implications. The Guilford Press. « Early History of ADHD », Russell Barkley, PhD - Dedicated to ADHD Science+, 19 septembre 2023. https://youtu.be/jwrhLpSlMPY?si=-9vm5G3ho2wMg-M8 « Neurodiversity Video #16 A History of ADHD », Thomas Armstrong, 4 juillet 2025. https://youtu.be/KIFFeEFLti4?si=3fpd-bb7KqvBK0ZZ https://www.verywellmind.com/adhd-history-of-adhd-2633127#citation-12 https://www.neurodiverging.com/the-history-of-attention-deficit-disorder/ The Story of Fidgety Philip.” The Evolution of A Disorder. Edward M. Hallowell, M.D. and John J. Ratey, M.D. https://theconversation.com/ritalin-at-75-what-does-the-future-hold-121591 https://daily.jstor.org/adhd-the-history-of-a-diagnosis/ https://www.washingtonpost.com/archive/lifestyle/wellness/1996/03/05/attention-deficit-disorder/c3c72c65-bd93-472d-aa99-3622ad6f5d36/ Robert R. Erk, « The evolution of attention deficit disorders terminology », Elementary School Guidance & Counseling, Vol. 29, No. 4 (April 1995), pp. 243-248. Lawrence H. Diller, « The Run on Ritalin: Attention Deficit Disorder and Stimulant Treatment in the 1990s », The Hastings Center Report, Vol. 26, No. 2 (Mar. - Apr., 1996), pp. 12-18 Autres références disponibles sur demande. #histoire #documentaire #tdah #tda #adhd
I explain how traits once understood as borderline pathology were gradually laundered into bipolar disorder — through expanding criteria, rapid cycling, and the replacement of personality with biology.This isn't about denying suffering.It's about why diagnosis matters, how boundaries collapsed, and what it costs.Upgrade and join us this Saturday the 28th of Febuary at 3 pm Eastern for the next Live Clinical Case Session on psychiatric medications: When, How and How to Taper Safely.00:00 – How mania is portrayed01:00 – What real mania actually looks like03:40 – Performative emotion vs psychosis05:45 – Why mania isn't happiness07:30 – What real bipolar patients experience09:10 – Diagnosis as moral status10:00 – Rapid cycling and diagnostic collapse12:30 – Borderline traits relabeled as bipolar15:10 – Why psychiatry prefers bipolar This is a public episode. If you'd like to discuss this with other subscribers or get access to bonus episodes, visit hannahspier.substack.com/subscribe
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.
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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.
Shine with Frannie Show |Christian health |Christian fitness|Christian wellness| Christian coaching
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.
I'm recording this while driving to work because I'm a busy mom. Today I want to talk about diagnosis—what it means, why we do it, and what my particular take on it is. As a clinical psychologist, I was trained in the medical model alongside psychiatrists. We learned the DSM, the diagnostic manual that classifies psychiatric conditions into discrete categories like depression, anxiety, schizophrenia, bipolar. It's useful because it creates a common language for clinicians and allows us to study treatments and measure whether symptoms are reducing. But the DSM has pitfalls. It's inherently biased—mostly based on Western, predominantly American research and samples. In South Africa, for example, hearing voices might indicate psychosis according to the DSM, but for some cultural groups it's a sign someone is a sangoma, a traditional healer. We have to use the framework for what's useful and leave the rest. So why diagnose at all? For many people, especially women who've been told they're too sensitive or too emotional their whole lives, hearing "you're depressed" or "you have anxiety" is deeply validating. It's not you being difficult—it's a real condition that deserves treatment. I stay away from binaries like "is this real depression or just normal life stress?" If someone is struggling and their quality of life is reduced, they deserve help whether it's a temporary hormonal thing, lack of support, or a diagnosable disorder. The question is: does the diagnosis resonate with someone's lived experience? Adult ADHD diagnosis in women is a perfect example. Women weren't diagnosed as kids because they internalized symptoms, while boys bounced off walls physically. Now women are getting diagnosed in their 30s and 40s and feeling massive relief—finally someone understands what's happening inside their minds. That's when diagnosis is most useful: when it leads to self-compassion, not pathologizing, when it helps us scaffold support systems and treatment plans, not just slap on a label. Follow Carly on: Website: https://onthecouchwithcarly.com/ YouTube: https://www.youtube.com/channel/UCfBi56xQookfRGL3zvWVzCg Instagram: https://www.instagram.com/onthecouchwithcarly/?hl=en Facebook: https://www.facebook.com/onthecouchwithcarly/ TikTok: https://www.tiktok.com/@onthecouchwithcarly Apple Podcasts: https://podcasts.apple.com/za/podcast/on-the-couch-with-carly/id1497585376 Spotify: https://open.spotify.com/show/3t7A2FMnISQ2fz9D5p0Xuw
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.
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
CoROM cast. Wilderness, Austere, Remote and Resource-limited Medicine.
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.
STRONGER BONES LIFESTYLE: REVERSING THE COURSE OF OSTEOPOROSIS NATURALLY
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
VetFolio - Veterinary Practice Management and Continuing Education Podcasts
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
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
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.
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