Podcasts about Charcot

Listener Appreciation Week Day 4 Renowned French explorer Jean-Baptiste Charcot explored the polar regions for many years aboard his ship, the Pourquoi Pas. When fellow explorer Roald Amundsen's plane went missing in 1928, Charcot joined the search for the Norwegian. Amundsen himself was searching for the crashed Italian airship, Italia, and its captain Umberto Nobile. As a thank you to all Shipwreck and Sea Dogs listeners, I am bringing you a bonus mini-episode each day this week. As another bonus, all merchandise is 25% OFF during Listener Appreciation Week! Go to ⁠⁠⁠shop.shipwrecksandseadogs.com⁠⁠⁠ and use code LISTENER2025 at check out. Please share this episode with a friend, family member, or coworker, and help Shipwrecks and Sea Dogs reach a larger audience. ⁠⁠https://www.shipwrecksandseadogs.com/⁠⁠ Written, edited, and produced by Rich Napolitano. Original theme music for Shipwrecks and Sea Dogs by ⁠⁠⁠⁠⁠Sean Sigfried⁠⁠⁠⁠⁠. Go AD-FREE by becoming a Patreon Officer's Club Member! Join at ⁠⁠⁠⁠⁠https://www.patreon.com/shipwreckspod⁠⁠ Join the Into History Network for ad-free access to this and many other fantastic history podcasts! ⁠⁠⁠⁠⁠https://www.intohistory.com/shipwreckspod⁠⁠⁠⁠⁠ You can support the podcast with a donation of any amount at: ⁠⁠⁠⁠⁠https://www.buymeacoffee.com/shipwreckspod⁠⁠⁠⁠⁠ Follow Shipwrecks and Sea Dogs ⁠⁠⁠⁠⁠Subscribe on YouTube⁠⁠⁠⁠⁠ ⁠⁠⁠⁠⁠Follow on BlueSky⁠⁠⁠⁠⁠ ⁠⁠⁠⁠⁠Follow on Threads⁠⁠⁠⁠⁠ ⁠⁠⁠⁠⁠Follow on Instagram⁠⁠⁠⁠⁠ ⁠F⁠⁠⁠⁠ollow on Facebook⁠⁠⁠⁠ Learn more about your ad choices. Visit megaphone.fm/adchoices

In the conclusion of this series on Charcot, guest host Eitan Ingall discusses treatment strategies with Drs. Carroll Jones, Kaitlin Neary, and Matt Conti. For additional educational resources, visit AOFAS.org

Ecoutez Ecran Total avec Isabelle Morini-Bosc du 13 juin 2025.Distribué par Audiomeans. Visitez audiomeans.fr/politique-de-confidentialite pour plus d'informations.

[GRAINE DE METAMORPHOSE] Xavier Pitois reçoit Lorène Vivier, 37 ans, atteinte de Sclérose Latérale Amyotrophique (SLA) ou maladie de Charcot. Comment continue-t-on à avancer quand le corps lâche ? Que fait-on du temps, quand l'avenir se rétrécit ? Et comment transforme-t-on un diagnostic bouleversant en énergie d'action, pour soi, mais aussi pour les autres ? Lorène Vivier a choisi de faire de son quotidien un engagement : sensibiliser, témoigner, mobiliser. Une réflexion profonde sur le sens de la vie. Épisode #127Quelques citations du podcast avec Lorène Vivier :"On est en 2925, on va sur Mars, on ne peut toujours pas aller investiguer le système neurologique du corps humain.""Je n'ai plus envie de ramener du chiffre d'affaires, j'ai envie de ramener de l'argent pour la recherche, pour moi c'est ça le plus important.""C'est important de vivre pleinement les choses aujourd'hui."Thèmes abordés lors du podcast avec Lorène Vivier :00:00 Introduction03:22 Les origines du livre de Lorène Vivier06:47 L'importance de parler de la SLA07:16 Qu'est-ce que la maladie de Charcot ou SLA ?09:02 L'annonce de la maladie14:20 Les phrases qui apaisent16:38 La phase de lutte19:38 Le sens de l'engagement associatif22:04 Recherche et moyens financiers23:16 L'importance d'impliquer les entreprises25:10 Le goût du voyage26:27 La spiritualité : un vrai soutien30:05 Maladie progressive et sens de la vie32:14 Les aménagements au quotidien33:44 Comment aider ?34:51 Le regard des autres36:39 Le rapport au corps38:52 Les deux experts indispensables39:20 La place des aidants et de la famille41:28 Mettre en lumière la maladieAvant-propos et précautions à l'écoute du podcast Découvrez Objectif Métamorphose, notre programme en 12 étapes pour partir à la rencontre de soi-même.Recevez chaque semaine l'inspirante newsletter Métamorphose par Anne GhesquièreFaites le TEST gratuit de La Roue Métamorphose avec 9 piliers de votre vie !Suivez nos RS : Insta, Facebook & TikTokAbonnez-vous sur Apple Podcast / Spotify / Deezer / CastBox/ YoutubeSoutenez Métamorphose en rejoignant la Tribu MétamorphosePhoto © Christophe Martin Hébergé par Acast. Visitez acast.com/privacy pour plus d'informations.

[GRAINE DE METAMORPHOSE] Xavier Pitois reçoit Lorène Vivier, 37 ans, atteinte de Sclérose Latérale Amyotrophique (SLA) ou maladie de Charcot. Comment continue-t-on à avancer quand le corps lâche ? Que fait-on du temps, quand l'avenir se rétrécit ? Et comment transforme-t-on un diagnostic bouleversant en énergie d'action, pour soi, mais aussi pour les autres ? Lorène Vivier a choisi de faire de son quotidien un engagement : sensibiliser, témoigner, mobiliser. Une réflexion profonde sur le sens de la vie. Épisode #127Quelques citations du podcast avec Lorène Vivier :"On est en 2925, on va sur Mars, on ne peut toujours pas aller investiguer le système neurologique du corps humain.""Je n'ai plus envie de ramener du chiffre d'affaires, j'ai envie de ramener de l'argent pour la recherche, pour moi c'est ça le plus important.""C'est important de vivre pleinement les choses aujourd'hui."Thèmes abordés lors du podcast avec Lorène Vivier :00:00 Introduction03:22 Les origines du livre de Lorène Vivier06:47 L'importance de parler de la SLA07:16 Qu'est-ce que la maladie de Charcot ou SLA ?09:02 L'annonce de la maladie14:20 Les phrases qui apaisent16:38 La phase de lutte19:38 Le sens de l'engagement associatif22:04 Recherche et moyens financiers23:16 L'importance d'impliquer les entreprises25:10 Le goût du voyage26:27 La spiritualité : un vrai soutien30:05 Maladie progressive et sens de la vie32:14 Les aménagements au quotidien33:44 Comment aider ?34:51 Le regard des autres36:39 Le rapport au corps38:52 Les deux experts indispensables39:20 La place des aidants et de la famille41:28 Mettre en lumière la maladieAvant-propos et précautions à l'écoute du podcast Découvrez Objectif Métamorphose, notre programme en 12 étapes pour partir à la rencontre de soi-même.Recevez chaque semaine l'inspirante newsletter Métamorphose par Anne GhesquièreFaites le TEST gratuit de La Roue Métamorphose avec 9 piliers de votre vie !Suivez nos RS : Insta, Facebook & TikTokAbonnez-vous sur Apple Podcast / Spotify / Deezer / CastBox/ YoutubeSoutenez Métamorphose en rejoignant la Tribu MétamorphosePhoto © Christophe Martin Hébergé par Acast. Visitez acast.com/privacy pour plus d'informations.

Join guest host Eitan Ingall as he discusses the challenges and strategies of treating Charcot with Drs. Carroll Jones, Kaitlin Neary, and Matt Conti in part 1 of this 2 part series. For additional educational resources, visit AOFAS.org

L'année dernière, il relançait le défi givré. Un seau d'eau glaçé et un don en faveur de la lutte contre la maladie de Charcot. Depuis qu'il se sait atteint de cette maladie incurable, Olivier Goy met à profit chaque seconde de son temps pour faire progresser la recherche. Alors pour la nouvelle campagne de mobilisation de l'institut du cerveau dont il est l'ambassadeur, il a cette fois-ci sauté en parachute. On reçoit Olivier Goy aux côtés de Jacques Séguéla qui l'a aidé à mettre en place cette nouvelle campagne. L'émission « Invincible été » sera diffusée le samedi 14 juin à 21h sur paris première puis disponible après diffusion sur M6+Tous les soirs, du lundi au vendredi à 20h sur France 5, Anne-Elisabeth Lemoine et toute son équipe accueillent les personnalités et artistes qui font l'actualité en direct de Cannes.

« Caroline, c'est quelqu'un qui croit très fort dans ses rêves », quelqu'un qui la connaît bien, a parlé ainsi de Caroline Delage.Née à Paris mais originaire de Nice, Caroline est journaliste - une vocation précoce dans sa vie. Elle a été grand reporter, présentatrice du journal pendant des années, encore récemment sur C8 avant que la chaine ne disparaisse à la suite de la décision de l'ARCOM, chroniqueuse et enseignante en journalisme.Caroline est devenue depuis quelques mois productrice TV. Principalement à la faveur d'une émission qui a rencontré d'emblée un grand succès avant les élections présidentielles de 2017 : « Au Tableau ! » qui voyait, concept génial, des écoliers ou des collégiens interpeller et questionner des adultes, à commencer par des candidats à l'Elysée.Du reste sa boîte de production s'appelle « Au Tableau ». Depuis cette émission qui a été exportée dans de nombreux pays du monde, elle en a produit bien d'autres ainsi que des documentaires. Parmi ceux-là, un documentaire absolument bouleversant, signé Myriam Seurat, sur Lorène Vivier. Cette jeune femme a été diagnostiquée à 35 ans de la maladie de Charcot, qu'on appelle aussi la SLA (Sclérose Latérale Amyotrophique). Elle se bat depuis pour sa santé mais aussi pour que la recherche avance vite et trouve un remède à sa maladie malheureusement à ce jour incurable et mortelle. J'ai eu la chance d'interroger Caroline Delage dans les locaux de sa société de production. Un moment intense que d'apprendre sa perception du bonheur qui passe pour elle par l'action en permanence. Elle dit qu'elle a besoin de faire, d'agir, de construire et se dit très inspirée par le principe du « Tikoun olam », une expression hébraïque qui signifie « réparer le monde ». Caroline veut se sentir utile, apporter quelque chose à la société dans laquelle elle vit et pour l'avenir de ses deux filles. Elle l'est assurément, utile !   Bonne découverte ! #interview #culture #philosophie #bonheur #action #télévision #radio #SLA #AuTableau #documentaires #littérature #enseignement #production #rêves #ésotérisme #politique #démocratie #doute Retrouvez ces interviews sur toutes les plateformes de podcast, sur YouTube, ainsi que sur Instagram (@bla.bla.lebonheurlesautres)et Facebook (https://www.facebook.com/Lebonheurcestlesautres).Hébergé par Ausha. Visitez ausha.co/politique-de-confidentialite pour plus d'informations.

Le combat pour la vie de Lorène Vivier, jeune femme atteinte de la maladie de Charcot est le sujet du documentaire “Du côté de la vie”, réalisé par Myriam Seurat. Elle a suivi d'octobre à décembre dernier Lorène Vivier malgré un quotidien qui est déjà totalement chamboulé par cette maladie mais elle veut témoigner pour alerter sur le manque de moyens dont dispose la recherche. Il y a aussi de la beauté dans sa vie car ce documentaire lui permettra de monter les marches de cannes ce dimanche pour présenter "Du côté de la vie". Le documentaire sera disponible sur LCP à la rentrée prochaine.Pendant la durée du festival de cannes le samedi à 19h sur France 5, Anne-Elisabeth Lemoine et toute son équipe accueillent les personnalités et artistes qui font l'actualité en direct de la croisette.

Nos invités du samedi 17 mai 2025 : Emmanuelle Bercot et William Lebghil, pour le film “Baise-en-ville” avec son réalisateur Martin Jauvat. Lorène Vivier, jeune femme atteinte de la maladie de Charcot à qui le documentaire “Du côté de la vie”, réalisé par Myriam Seurat est consacré. Aliocha Schneider interprète en live “L'océan des amoureux”. Avec également comme chaque soir le 5 sur 5 de Lorrain Sénéchal avec un focus sur l'Eurovision.

Prof. Comi stellt die Arbeit der Europäischen Charcot-Stiftung vor, die dazu beiträgt, das Leben von Menschen mit MS weltweit zu verbessern. Auf meinem Blog kannst Du den Beitrag nachlesen: https://ms-perspektive.de/303-ecf Diese Podcast-Folge ist dem Andenken an Prof. Giancarlo Comi gewidmet – einen herausragenden Neurologen, engagierten Forscher und langjährigen Präsidenten der European Charcot Foundation. Er hat mit seinem Wirken die Versorgung und das Verständnis für Menschen mit Multipler Sklerose entscheidend geprägt und hinterlässt ein beeindruckendes wissenschaftliches und menschliches Vermächtnis. Ich hatte die große Ehre, dieses Interview mit ihm auf Englisch zu führen – nur wenige Monate vor seinem Tod. Ohne die Unterstützung der Gemeinnützigen Hertie-Stiftung wäre dieses Gespräch nicht möglich gewesen. Dafür danke ich von Herzen. Das Gespräch ist ursprünglich auf Englisch erschienen und kann weiterhin in der Originalfassung gehört werden. In dieser überarbeiteten und übersetzten Version möchte ich Dir Prof. Comis Arbeit zugänglich machen und seine Gedanken und Visionen weitertragen. Inhaltsverzeichnis Einführung – Wer ist Prof. Giancarlo Comi? Die European Charcot Foundation Der Charcot Multiple Sclerosis Master Weitere Aktivitäten der European Charcot Foundation Schnellfragerunde Verabschiedung Einführung – Wer ist Prof. Giancarlo Comi? Prof. Giancarlo Comi: Ich bin Professor Giancarlo Comi, Neurologe. Zurzeit bin ich Ehrenprofessor an der Vita-Salute-Universität in Mailand, Präsident der European Charcot Foundation und Vorsitzender des Wissenschaftlichen Komitees der Human Brains Initiative der Prada Foundation. Außerdem leite ich das MS-Zentrum an der Casa di Cura Igea in Mailand. Nele von Horsten: Das klingt nach einem sehr engagierten und erfüllten Berufsalltag! Welche ermutigende Botschaft möchten Sie Menschen mit MS mitgeben? Prof. Giancarlo Comi: Für neu diagnostizierte Patient:innen: Seien Sie zuversichtlich. Dank moderner Therapien ist ein Leben ohne schwerwiegende Einschränkungen heute in vielen Fällen möglich. Für Menschen mit längerer Erkrankungsdauer oder bestehenden Einschränkungen: Es gibt vielversprechende Entwicklungen – auch im Bereich der modernen, interdisziplinären Rehabilitation. Und für alle gilt: Eine engagierte Zusammenarbeit zwischen Patient:innen, Ärzt:innen und Organisationen ist der Schlüssel zum Fortschritt. Nele von Horsten: Prof. Comi, vielen herzlichen Dank für das spannende Gespräch, Ihr Engagement und Ihre Zeit. Herzliche Grüße nach Mailand! Prof. Giancarlo Comi: Es war mir ein Vergnügen. Alles Gute – auf Wiedersehen! --- Bis bald und mach das Beste aus Deinem Leben, Nele Mehr Informationen und positive Gedanken erhältst Du in meinem kostenlosen Newsletter. Hier findest Du eine Übersicht zu allen bisherigen Podcastfolgen.

Dans C Ce Soir, un débat à la fois politique, intime et philosophique : l'aide à mourir. Les députés examinent un projet de loi, réclamé de longue date, mais qui crispe déjà une partie des politiques. Une large majorité de Français le soutiennent, mais qu'est-ce que ce consensus raconte de nous ? Une société individualiste, qui laisse les plus vulnérables de côté ? ou au contraire, un mouvement d'émancipation inexorable vers la liberté pour chacun de choisir jusqu'au bout ? On en débat ce mercredi 16 avril avec nos invités : ▶︎ Antoine MESNIER, Médecin, atteint de la maladie de Charcot, auteur de « Bon anniversaire Antoine ! » aux éditions Bouquins / Mollat (05/10/2023)▶︎ Eugénie BASTIE, Essayiste, journaliste au Figaro, chroniqueuse sur CNews et Europe 1▶︎ Jean-François COLOSIMO, Historien, théologien, documentariste, éditeur▶︎ Claire FOURCADE, Médecin, présidente de la Société française d'accompagnement et de soins palliatifs (SFAP)▶︎ Véronique FOURNIER, Cardiologue, médecin de santé publique, fondatrice du Centre d'éthique clinique de l'AP-HP▶︎ Cédric ENJALBERT, Rédacteur en chef adjoint Philosophie magazine

durée : 00:02:26 - Le billet sciences - Des scientifiques chinois ont identifié une anomalie génétique dans l'ADN des mitochondries des malades. Un espoir pour mieux comprendre et peut-être, dans le futur, mieux prendre en charge cette maladie dégénérative qui touche environ 8 000 personnes en France.

Dean's Chat hosts, Drs. Jensen and Richey, welcome Dr. Narenda Patel to the podcast! Narendra Patel, DPM is a highly skilled podiatric foot and ankle surgeon based in the Northwest Suburbs of Chicago, Illinois. He is a partner surgeon at Barrington Orthopedic Specialists. He is known for his expertise in diagnosing and treating a wide range of foot and ankle conditions, including sports injuries, fractures, peripheral nerve injuries, ankle replacement, and Charcot and Trauma expert. Dr. Patel earned his Doctor of Podiatric Medicine degree from the New York College of Podiatric Medicine in New York City and completed a comprehensive three-year post-doctoral surgery residency. He has been in practice since 1997. Dr. Patel is Faculty Attending Surgeon for the Ascension St. Joseph's Surgical Residency Program and Fellowship Trainer for the Complex Deformity Correction & Microsurgical Limb Reconstruction at Ascension St. Joseph. Dr. Patel has built a reputation for providing compassionate and personalized care to his patients. He is committed to staying up to date with the latest advances in foot and ankle surgery and uses state-of-the-art techniques and equipment to ensure the best possible outcomes for his patients. Dr. Narendra R. Patel, DPM is a skilled and compassionate podiatric foot and ankle surgeon who is dedicated to providing the highest level of care to his patients. With his expertise and commitment to excellence, he has become one of the most trusted foot and ankle surgeons in the Northwest Suburbs of Chicago, Illinois. When he's not seeing patients, Dr. Patel enjoys photography, traveling abroad, and electronic dance music. Dr. Patel enjoys going on humanitarian mission trips. https://bakodx.com/ https://bmef.org/ www.explorepodmed.org https://podiatrist2be.com/  

Cette semaine LeChair reçoit Pauline Messier. Originaire de Chambly dans l'Oise, Pau' comme elle se fait surnommer à vu le jour il y'a 22 ans. Aînée de la famille, c'est une fille pétillante et vive d'esprit. Épicurienne, Pau' est une passionnée de musique et pratique la salsa occasionnellement. Sa vie a changé de manière drastique lorsqu'on lui a annoncé qu'elle était atteinte de la maladie de Charcot... Au fil d'un bel échange, Pauline nous parle avec franchise des conséquences de la maladie sur sa vie, de ses ambitions et n'hésite pas à distiller de précieux conseils.Hébergé par Ausha. Visitez ausha.co/politique-de-confidentialite pour plus d'informations.

Comme en 2024, je fais un pas de côté avec cet épisode dans le cadre du Podcasthon. Le Podcasthon c'est cette opération qui réunit des centaines de podcasteurs en France ainsi qu'à l'étranger et qui permet de mettre en avant des associations.Cette année, je mets à l'honneur l'association Les Invincibles. Créée en juin 2023, ses membres mènent des actions pour aider des malades atteints de SLA. SLA pour Sclérose latérale amyotrophique ou encore maladie de Charcot. En plus du soutien aux personnes atteintes, ils financent directement la recherche pour comprendre la maladie et développer des traitements.Pour mieux comprendre tout ça, j'ai rencontré le président de l'association et sa femme, Ludovic et Clarisse Besombes. Ludovic est lui-même atteint de la maladie (ayant perdu l'usage de la parole, il communique maintenant grâce à un ordinateur) et avec Clarisse ils font un travail de titan que je suis très heureux de partager avec vous aujourd'hui. J'ai également rencontré Sévérine Boillée, chercheuse à l'Institut du Cerveau qui va nous permettre de lever le voile sur cette maladie et d'en saisir les mécanismes.Et comme un Podcasthon ne serait rien sans une aide concrète, je vous invite à cliquer sur le lien suivant pour contribuer à la collecte de dons en faveur des Invincibles :

Nonepileptic events are prevalent and highly disabling, and multiple pathophysiologic mechanisms for these events have been proposed. Multidisciplinary care teams enable the efficient use of individual expertise at different treatment stages to address presentation, risk factors, and comorbidities.   In this episode, Kait Nevel, MD, speaks with Adriana C. Bermeo-Ovalle, MD, an author of the article “A Multidisciplinary Approach to Nonepileptic Events,” in the Continuum® February 2025 Epilepsy issue. Dr. Nevel is a Continuum® Audio interviewer and a neurologist and neuro-oncologist at Indiana University School of Medicine in Indianapolis, Indiana. Dr. Bermeo-Ovalle is a professor and vice-chair for Faculty Affairs in the Department of Neurological Sciences at Rush University Medical Center in Chicago, Illinois. Additional Resources Read the article: A Multidisciplinary Approach to Nonepileptic Events Subscribe to Continuum: shop.lww.com/Continuum Earn CME (available only to AAN members): continpub.com/AudioCME Continuum® Aloud (verbatim audio-book style recordings of articles available only to Continuum® subscribers): continpub.com/Aloud More about the American Academy of Neurology: aan.com Social Media facebook.com/continuumcme @ContinuumAAN Host: @IUneurodocmom Full episode transcript available here Dr. Jones: This is Dr Lyell Jones, Editor-in-Chief of Continuum, the premier topic-based neurology clinical review and CME journal from the American Academy of Neurology. Thank you for joining us on Continuum Audio, which features conversations with Continuum's guest editors and authors who are the leading experts in their fields. Subscribers to the Continuum Journal can read the full article or listen to verbatim recordings of the article and have access to exclusive interviews not featured on the podcast. Please visit the link in the episode notes for more information on the article, subscribing to the journal, and how to get CME. Dr Nevel: Hello, this is Dr Kait Nevel. Today I'm interviewing Dr Adriana Bermeo about her article on a multidisciplinary approach to nonepileptic events, which she wrote with Dr Victor Petron. This article appears in the February 2025 Continuum issue on epilepsy. Welcome to the podcast, and please introduce yourself to our audience. Dr Bermeo-Ovalle: Hello Dr Neville, it's a pleasure to be here. Thank you very much for inviting me. My name is Adriana Bermeo and I'm an adult epileptologist at Rush University Medical Center in Chicago, and I am also the codirector of the NEST clinic, which is a treatment clinic for patients with nonepileptic seizures within our level four epilepsy center. Dr Nevel: Wonderful. Well, thank you so much for being here, and I can't wait to talk to you about your article and learn a little bit about NEST, maybe, during our conversation, and how you approach things. To start us off talking about your article today, could you share with us what you think is the most important takeaway from your article for the practicing neurologist? Dr Bermeo-Ovalle: Wonderful. There's some messages that I would like people to get from working with patients with functional neurologic disorders in general. The first one is that functional neurologic disorders are very common in presentation in the neurologic clinic, almost no matter what your practice of self-specialty care is. The second is that for people who treat patients primarily with seizures or epilepsy, they account for between 5 to 10% of our patients in the clinic, but about 30% of our patients in our epilepsy monitoring unit because the seizures typically do not respond to anti-seizure medication management. Also, that in order to diagnose them, you don't need to have a neuropsychological stress already be available for the patient or the clinician. And the most important thing is that there are available treatments for these patients and that there are options that we can offer them for them to have less seizures and to be more integrated to whatever activities they want to get integrated. Dr Nevel: Wonderful. What do you think a practicing neurologist might find surprising after reading your article? Dr Bermeo-Ovalle: I think still many neurologists feel very hopeless when they see patients with these conditions. They do not have very good answers right away for the patients, which is frustrating for the neurologist. And they don't think there's too much they can do to help them other than send them somewhere else, which is very difficult for the neurologist and is crushing to the patients to see these doctors that they're hoping to find answers to and then just find that there's not much to do. But what I want neurologists to know is that we are making strides in our understanding of the condition and that there are effective treatments available. And I hope that after reading this and engaging with this conversation, they will feel curious, even hopeful when they see the next patient in the clinic. Dr Nevel: Yeah, absolutely. I find the history of nonepileptic seizures really interesting and I enjoyed that part of your article. How has our understanding of nonepileptic seizures evolved over the centuries, and how does our current understanding of nonepileptic seizures inform the terminology that we use? Dr Bermeo-Ovalle: Yeah. The way we name things and the way we offer treatment goes along to how we understand things. So, the functional seizures and epileptic seizures were understood in ancient times as possession from the spirits or the demons or the gods, and then treatments were offered to those kind of influences and that continues to happen with functional seizures. So, we go through the era when this was thought to be a women-only condition that was stemming from their reproductive organs and then treatments accordingly were presented. And later on with Charcot and then Freud, they evolved to even conversion disorders, which is one understanding the most conversion disorders, which is one of the frameworks where this condition has been treated with psychotherapy, psychoanalytic psychotherapy. And in our current understanding, we understand functional neurologic disorders in general as a more like a connection, communication network disorder, between areas of the brain that modulate emotional processing and movement control. And therefore, our approach these days is much more geared towards rehabilitation. You know, I think that's the evolution of thinking in many different areas. And as we learn more, we will be acquiring more tools to help our patients. Dr Nevel: Yeah, great. Thanks so much for that answer. Just reading the historical information that you have in your article, you can imagine a lot of stigma with this diagnosis too over time, and that- I think that that's lessening. But I was wondering if you could talk about that a little bit. How do we approach that with our patients and loved ones, any stigma that they might feel or perceive from being diagnosed with nonepileptic seizures? Dr Bermeo-Ovalle: Thank you for asking that question. Stigma is actually an important problem even for people living with epilepsy. There's still a lot of misunderstanding of what epilepsy is and how it affects people, and that people living with epilepsy can live normal, healthy lives and do everything they want to do with appropriate treatment. And if a stigma is still a problem with epilepsy, it is a huge problem for patients living with functional neurologic symptoms in general, but particularly with functional seizures or nonepileptic seizures. Because the stigma in this population is even perpetuated by the very people who are supposed to help them: physicians, primary care doctors, emergency room doctors. Unfortunately, the new understanding of this condition has not gotten to everybody. And these patients are often even blamed for their symptoms and for the consequences of their symptoms and of their seizures in their family members, in their job environment, in their community. Living with that is really, really crushing, right? Even people talk about, a lot about malingering. They come back about secondary gain. I can tell you the patients I see with functional seizures gain nothing from having this condition. They lose, often, a lot. They lose employment, they lose ability to drive. They lose their agency and their ability to function normally in society. I do think that the fight- the fighting of stigma is one that we should do starting from within, starting from the healthcare community into our understanding of what these patients go through and what is causing their symptoms and what can we do to help them. So there's a lot of good work to be done. Dr Nevel: Absolutely. And it starts, like you said, with educating everybody more about nonepileptic seizures and why this happens. The neurobiology, neurophysiology of it that you outlined so nicely in your article, I'm going to encourage the listeners to look at Figure 1 and 4 for some really nice visualization of these really complex things that we're learning a lot about now. And so, if you don't mind for our listeners, kind of going over some of the neurobiology and neurophysiology of nonepileptic seizures and what we're learning about it. Dr Bermeo-Ovalle: Our understanding of the pathophysiology of functional neurologic seizure disorder is in its infancy at this point. The neurobiological processes that integrate emotional regulation and our responses to it, both to internal stimuli and to external stimuli and how they affect our ability to have control over our movement---it's actually amazing that we as neurologists know so little about these very complex processes that the brain do, right? And for many of us this is the reason why we're in neurology, right, to be at the forefront of this understanding of our brain. So, this is in that realm. It is interesting what we have learned, but it's amazing all that we have to learn. There is the clear relationship between risk factors. So, we know patients with functional neurologic symptom disorder and with functional seizures, particularly in many different places in the world with many different beliefs, relationship to their body, to their expression of their body, have this condition no matter how different they are. And also, we know that they have commonalities. For example, traumatic experiences that are usually either very strong traumatic experiences or very pervasive traumatic experiences or recurrent over time of different quality. So, we are in the process of understanding how these traumatic experiences actually inform brain connectivity and brain development that result in this lack of connections between brain areas and the expression of them, and that result in this kind of disorder. I wish I can tell you more about it or that I would understand more about it, but I am just grateful for the work that has been done so that we can understand more and therefore have more to offer to these patients and their families and their communities that are support. Dr Nevel: Yeah, absolutely. That's always the key, and just really exciting that we're starting to understand this better so that we can hopefully treat it better and inform our patients better---and ourselves. Can you talk to us a little bit about the multidisciplinary team approach and taking care of patients with nonepileptic seizures? Who's involved, what does best practice model look like? You have a clinic there, obviously; if you could share with us how your clinic runs in the multidisciplinary approach for care of these patients? Dr Bermeo-Ovalle: The usual experience of patients dealing with functional seizures, because this is a condition that has neurological symptoms and psychiatric symptoms, is that they go to the neurologist and the neurologist does not feel sufficiently able to manage all the psychiatric comorbidities of the condition. So, the patient is sent to psychiatry. The psychiatry really finds themselves very hopeless into handling seizures, which is definitely not their area of expertise, and these patients then being- “ping-ponging” from one to the other, or they are eventually sent to psychotherapy and the psychotherapist doesn't know what they're dealing with. So, we have found with- and we didn't come up with this. We had wonderful support from other institutions who have done- been doing this for a longer time. That bringing all of this specialty together and kind of situating ourselves around the patient so that we can communicate our questions and our discrepancies and our decision between who takes care of what without putting that burden on the patient is the best treatment not only for the patient, who finally feels welcome and not burden, but actually for the team. So that the psychiatrist and the neurologist support the psychotherapist who does the psychotherapy, rehabilitation, mind the program. And we also have the support and the involvement of neuropsychology. So, we have a psychiatrist, a neurologist, social worker, psychotherapist and neuropsychology colleagues. And together we look at the patient from everywhere and we support each other in the treatment of the patient, keeping the patient in the middle and the interest of the patient in the middle. And we have found that that approach has helped our patients the best, but more importantly, makes our job sustainable so that none of us is overburdened with one aspect of the care of the patient and we feel supported from the instances that is not our most comfortable area. So that is one model to do it. There's other models how to do it, but definitely the interdisciplinary care is the way to go so far for the care of patients with functional neurologic symptom disorders and with functional seizures or nonepileptic seizures in particular. Dr Nevel: Yeah, I can see that, that everybody brings their unique expertise and then doesn't feel like they're practicing outside their, like you said, comfort zone or scope of practice. In these clinics---or maybe this happens before the patient gets to this multidisciplinary team---when you've established a diagnosis of nonepileptic seizures, what's your personal approach or style in terms of how you communicate that with the patient and their loved ones? Dr Bermeo-Ovalle: It is important to bring this diagnosis in a positive term. You know, unfortunately the terminology question is still out and there's a lot of teams very invested into how to better characterize this condition and how to- being told that you don't have something is maybe not that satisfying for patients. So, we are still working on that, but we do deliver the diagnosis in positive terms. Like, this is what you have. It's a common condition. It's shared by this many other people in the world. It's a neuropsychiatric disorder and that's why we need the joint or collaborative care from neurology and psychiatry. We know the risk factors and these are the risk factors. You don't have to have all of them in order to have this condition. These are the reasons why we think this is the condition you have. There is coexisting epilepsy and functional seizures as well. We will explore that possibility and if we get to that conclusion, we will treat these two conditions independently and we- our team is able to treat both of them. And we give them the numbers of our own clinic and other similar clinics. And with that we hope that they will be able to get the seizures under better control and back to whatever is important to them. I tell my trainees and my patients that my goals of care for patients with functional seizures are the same as my patients with epileptic seizures, meaning less seizures, less disability, less medications, less side effects, less burden of the disease. And when we communicate it in that way, patients are very, very open and receptive. Dr Nevel: Right. What do you think is a mistake to avoid? I don't know if “mistake” is necessarily the right word, but what's something that we should avoid when evaluating or managing patients with nonepileptic seizures? What's something that you see sometimes, maybe, that you think, we should do that differently? Dr Bermeo-Ovalle: I think the opportunity of engaging with these patients is probably the hardest one. Because neurologists have the credibility, they have the relationship, they have- even if they don't have a multi-disciplinary team all sitting in one room, they probably have some of the pieces of this puzzle that they can bring together by collaborating. So, I think that missing the opportunity, telling the patient, this is not what I do or this is not something that belongs to me, you need to go to a mental health provider only, I think is the hardest one and the most disheartening for patients because our patients come to us just like all patients, with hopes and with some information to share with us so that we can help them make sense of it and have a better way forward. We as neurologists know very well that we don't have an answer to all our patients, and we don't offer zero seizures to any of our patients, right? We offer our collaborative work to understand what is going on and a commitment to walk in the right direction so that we are better every day. And I do think wholeheartedly that that is something that we can offer to patients with functional seizures almost in any environment. Dr Nevel: Yeah, absolutely. And using that multidisciplinary approach and being there with your patient, moving forward in a longitudinal fashion, I can see how that's so important. What do you find most challenging and what do you find most rewarding about caring for patients with nonepileptic seizures? Dr Bermeo-Ovalle: The thing that I find more challenging are the systemic barriers that the system still places. We discuss with the patients, what is the right time to go to the emergency room or not? Because the emergency room may be a triggering environment for patients with functional seizures and it may be a place where not everybody is necessarily attuned to have this conversation. Having said that, I never tell any of my patients not to go to the emergency room because I don't know what's happening with them. As a matter of fact, we're getting a lot of information on high mortality rates in patients with functional seizures, and it's not because of suicide and is probably not related to the seizure. Maybe this is---you know, this is speculation on my part---that is because they get to more severe conditions in other things that are not the functional seizures because they just experienced the healthcare system as very hostile because we are very in many instances. So, navigating that is a little bit difficult, and I try to tell them to have the doctors call me so that I can frame it in a different way and still be there for them. But I can tell you this clinic is the most rewarding clinic of all my clinical activities. And I love with all my heart being an epileptologist and seeing my patients with epilepsy. But the number of times my patients with functional seizures say, nobody had ever explained this to me, nobody had ever validated my experience in front of my family so that I'm not- like, feel guilty myself for having this episode, I can't tell you how many times. And obviously patients who come to the nonepileptic seizure clinic already know that they come to the nonepileptic seizure clinic, so that- you can say it's a selection of patients that are already educated in this condition to come to the clinic. But I would love everybody to know managing this population can be enormously, enormously satisfying and rewarding. Dr Nevel: Especially for, I imagine, patients who have been in and out of the ER, in and out of the hospital, or seen multiple providers and make their way to you. And you're able to explain it in a way that makes sense and hopefully reduces some of that stigma maybe that they have been feeling. Dr Bermeo-Ovalle: And along with that, iatrogenic interventions, unnecessary intubations, unnecessary ICUs; like, so much. And I think, I have no superpower to do that other than understanding this condition in a different way. And by I, I mean all the providers, because I'm not alone in this. There's many, many people doing excellent work in this state. And we just need to be more. Dr Nevel: Yeah, sure. Absolutely. So, on that note, what's next in research, or what do you think will be the next big thing? What's on the horizon in this area? Dr Bermeo-Ovalle: I think the community in the functional neurologic disorder community is really hopeful that more understanding into the neurobiology of this condition will bring more people over and more neurologists willing to take it on. There was an invitation from the NIH, I think, about four or five years ago to submit proposals for research in this area in particular. So, all of those studies must be ongoing. I'm much more a clinician than a researcher myself, but I am looking forward to what all of that is going to mean for our patients. And for- I think there's other opportunities in that further understanding of the clinical manifestations of many other conditions, and for our understanding of our relationship with our patients. I feel we are more attuned to align with a disease that, when the experience of the patient- and with a disease like this, a condition like this one, we have to engage with the personal experience of the patient. What I mean by that is that we are more likely to say,  I'm an epileptologist, I'm an MS doctor, you know, and we engage with that condition. This condition, like, just makes us engaging with the symptom and with the experience of the person. And I think that's a different frame that is real and rounded into the relationship with our patients. So, I think there's so much that we can learn that can change practice in the future. Dr Nevel: Yeah. And as your article, you know, outlines, and you've outlined today during our discussion, that- how important this is for the future, that we treat these patients and help them as much as we can, that comes with understanding the condition better, because wow, I was really surprised reading your article. The mortality associated with this, the healthcare costs, how many people it affects, was just very shocking to me. So, I mean, this is a really important topic, obviously, and something that we can continue to do better in. Wonderful. Well, thank you so much. It's been really great talking to you today. Dr Bermeo-Ovalle: Thank you, Katie, I appreciate it too. Dr Nevel: So again, today I've been interviewing Dr Adriana Bermeo about her article on a multidisciplinary approach to nonepileptic events, which she wrote with Dr Victor Petron. This article appears in the most recent issue of Continuum on epilepsy. Be sure to check out Continuum audio episodes from this and other issues. And thank you to our listeners for joining today.  Dr Monteith: This is Dr Teshamae Monteith, Associate Editor of Continuum Audio. If you've enjoyed this episode, you'll love the journal, which is full of in-depth and clinically relevant information important for neurology practitioners. Use the link in the episode notes to learn more and subscribe. AAN members, you can get CME for listening to this interview by completing the evaluation at continpub.com/audioCME. Thank you for listening to Continuum Audio.

In this podcast episode, I tackle the theme of functional neurological disorders, and I explore their almost endless types and diverse presentations. I particularly highlight functional seizures, noting their risk factors, their characteristic, even if diverse, presentations, the ways by which they may be distinguished from organic seizures. I also review functional movement disorders with a special emphasis on functional tremors. I also highlight the negative attitudes by which people with FND are treated by medical staff, who are themselves often poorly trained in the condition, and the tendency for FND to be misdiagnosed. I highlight the principles of communicating the diagnosis of FND and the often negative emotions the diagnosis elicits in many patients and their families on account of the stigma associated with it. I also review the challenges that doctors face with making a diagnosis of FND, and the management approach to the disorder. I illustrate functional neurological disorders with the books The Shaking Woman or A History of My Nerves by Siri Hustvedt, FiNDing Hope, by Jocelyn Bystrom, and FND Stories by Greg Rawlings and colleagues. The podcast also discussed the evolving scientific understanding of functional neurological disorders, and for this I cited the book by neurologist Suzanne O'Sullivan titled It's All in Your Head. I also explore the fascinating history of the study of functional neurological disorders with reference to the role played by Jean-Martin Charcot, the acknowledged father of clinical neurology. In this context, I cited the book Medical Muses, written be Asti Hustvedt, which vividly captured the nature of hysteria, and the personalities of the famous hysterics that Charcot studied in Paris. This especially reviewed Blanche Wittman, Charcot's most famous patient, and factors of her life that predisposed her to developing hysteria. I also used this text to highlight the less well-known positive contributions that Charcot made to the subject.

On a réunit deux médecins légistes: une fausse, Julie Depardieu dans la série “Alexandra Ehle" sur France 3. Un vrai, Philippe Boxho, qui a plus de 400 autopsies à son actif mais également des livres à succès sur son métier. Son dernier en date est « La mort en face » disponible aux éditions kennes. Philippe Boxho donnera une conférence à but caritatif le 18 avril au théâtre du gymnase. ça s'appelle "Les morts ont la parole" et les bénéfices seront reversés pour aider la recherche contre la maladie de Charcot.“Alexandra Ehle: Feu Sacré” avec Julie Depardieu sera diffusé mardi 11 mars à 21h05 sur France 3.Tous les soirs, du lundi au vendredi à 20h sur France 5, Anne-Elisabeth Lemoine et toute son équipe accueillent les personnalités et artistes qui font l'actualité.

durée : 00:04:16 - Chroniques littorales - par : Jose Manuel Lamarque - La Généreuse est la première régate caritative de France qui vise à engager les participants de la régate et leur entourage, à soutenir la recherche médicale pour la maladie de Charcot par l'Institut du cerveau. Son fondateur Laurent de Bernède, la présente dans les Chroniques littorales...

La chanteuse américaine Roberta Flack nous a quittés hier à l'âge de 88 ans. On la savait atteinte depuis 2022 de la maladie de Charcot. Le premier à avoir été subjugué par la voix magique de Roberta Flack, c'est Clint Eastwood. En 1971, il signe son premier film de réalisateur, "Un frisson dans la nuit", et pour accompagner les images de la côte californienne, il choisit cette merveilleuse chanson d'amour qu'il a entendue à la radio. Interprétée par Roberta Flack... Ecoutez La star du jour avec Anthony Martin du 25 février 2025.

Regardez notre émission avec Florent, fondateur de EWIGO ➡️ https://youtu.be/03u3Hm1VRfIPour accéder au site d'EWIGO : https://link.influxcrew.com/EWIGO-LEGENDMerci à Christophe d'être passé nous voir chez LEGEND ! Christophe, 37 ans, a été diagnostiqué de la maladie de Charcot le 25 avril 2024, une maladie incurable qui paralyse progressivement les muscles et empêche de respirer sans assistance. Marié et père de deux enfants, il a dû arrêter son métier de surveillant pénitentiaire au fur et à mesure que la maladie progressait. La maladie de Charcot, ou SLA, est décrite par l'organisation mondiale de la santé, comme la maladie la plus cruelle du Monde, laissant au malade une espérance de vie allant de 24 à 36 mois.Suivez le quotidien de Christophe et sa famille sur Instagram ➡️ https://www.instagram.com/famille_rovere_et_la_sla?igsh=N3FoM3hvZ3BoZWR2&utm_source=qrPour les contacter ➡️ Famillerovereetlasla@gmail.comL'association ARSLA (Association pour la recherche sur la SLA) ⬇️Instagram : https://www.instagram.com/arsla_?igsh=MTlucjlmc2tnYzFkOQ==Site : https://www.arsla.org/Merci à notre ami Matthias Baccino de chez Trade Republic pour le cadeau offert à Christophe et sa famille lors de l'émission ! Retrouvez l'interview complète sur YouTube ➡️ https://youtu.be/wtDaxwcYBccPour toutes demandes de partenariats : legend@influxcrew.comRetrouvez-nous sur tous les réseaux LEGEND !Facebook : https://www.facebook.com/legendmediafrInstagram : https://www.instagram.com/legendmedia/TikTok : https://www.tiktok.com/@legendTwitter : https://twitter.com/legendmediafrSnapchat : https://t.snapchat.com/CgEvsbWV Hébergé par Acast. Visitez acast.com/privacy pour plus d'informations.

Stéphane n'avait que 46 ans lorsque le diagnostic est tombé: maladie de Charcot foudroyante. Il a décidé de prendre sa dose de pentobarbital le 25 janvier 2021. Dans quel état d'esprit? Une semaine avant sa mort, famille et amis lui rendent visite, chez lui, à Cudrefin. Reportage de Francesca Argiroffo (première diffusion le 30 mars 2021) Réalisation : Jean-Daniel Mottet Production : Laurence Difélix

All the logical answers to Charcot's escape and disappearances had come up... but why should an escaped convict be logical? Solitary by Robert Silverberg. That's next on The Lost Sci-Fi Podcast.Thanks to Phee808 for another 5 star review on Apple Podcast, “The perfect narration to a treasure trove of incredible talent. They don't make them like this anymore but fortunately we can still hear them. The narration is on point and passionate and matches the mood of the stories perfectly.” Thanks Phee808!If you are a fan of Robert Silverberg, as I am, you will be happy with today's episode which was the cover story in Future Science Fiction number 32 in Spring 1957. Open this 35 cent magazine to page 4, Solitary by Robert Silverberg…Next on The Lost Sci-Fi Podcast, What happens when a secret society demands your fortune—or sacrifices innocent lives instead? An electrifying tale of power, greed, and morality that will keep you in suspense until the very end. The Minions of Midas by Jack London.☕ Buy Me a Coffee https://www.buymeacoffee.com/scottsV===========================

Joel était passé au sujet de son ami atteint de la maladie de Charcot. Depuis, il a réussi à gérer son approche face à son handicap. Il espère l'aider à trouver une logement adapté. Cette saison, Joseph Agostini accueille les auditeurs le dimanche soir de 23h à 1h sur RTL au 09 69 39 10 11

Au cœur de la nuit, les auditeurs se livrent en toute liberté aux oreilles attentives et bienveillantes d'Olivier Delacroix. Pas de jugements ni de tabous, une conversation franche, mais aussi des réponses aux questions que les auditeurs se posent. Un moment d'échange et de partage propice à la confidence pour repartir le cœur plus léger.

Two Short stories from the 1800s. The Tell-Tale Heart and The Masque of the Red Death by Edgar Allan Poe. That's next on The Lost Sci-Fi Podcast.Did you know we take requests? We do, and both of the stories you are about to hear have been requested a number of times. If there is a vintage science fiction story you'd like to hear send us an email, scott@lostscifi.com. He was born Edgar Poe in Boston in 1809, orphaned at the age of 2 and taken in by a wealthy merchant, John Allan and his wife, Francis. And that's how he came to be known as Edgar Allan Poe. John Allan did not adopt Poe and that's why he didn't take Allan as his last name. Let's travel back in time 182 years to January 1843. Our story was first published in The Pioneer, The Tell-Tale Heart by Edgar Allan Poe…Up next, a story published 9 months earlier, in Graham's Magazine in April 1842, The Masque of the Red Death by Edgar Allan Poe...Next on The Lost Sci-Fi Podcast, All the logical answers to Charcot's escape and disappearances had come up... but why should an escaped convict be logical? Solitary by Robert Silverberg.☕ Buy Me a Coffee https://www.buymeacoffee.com/scottsV===========================

En 2010, Léonard, 37 ans, est atteint de la maladie de Charcot (Sclérose Latérale Amyotrophique) qui le prive, peu à peu, de tous ses muscles et le rend prisonnier d'un corps qui ne répond plus. Malgré l'épreuve et la souffrance, Léonard cultive sa joie de vivre jusqu'à sa mort survenue 4 ans plus tard…

Joel s'est lié d'amitié à un homme rencontré lors d'un séminaire. Plus tard, celui-ci lui confie être atteint de la maladie de Charcot. Depuis, Joel s'interroge sur la meilleure attitude à adopter vis-à-vis de son ami. Cette saison, Joseph Agostini accueille les auditeurs le dimanche soir de 23h à 1h sur RTL au 09 69 39 10 11.

Today's guest is Emily Capley, who has an amazing success story reversing very serious health issues and getting back to a normal life, even with type 1 diabetes. See her bio below and enjoy the video! Emily's bio: I am a 43-year-old woman who has type 1 diabetes. After following the ADA guidelines for 29 years i now have numerous long-term complications. Kidney failure, retinopathy, neuropathy that led to Charcot foot disease, frozen shoulder in both arms to name a few. Using a ketogenic diet starting in August 2020 I was able to better control my diabetes with much less insulin. I've been strict carnivore since January 2024 and my complications are now slowly reversing and my last A1C was 5.4. My body is healing eating only meat/animal products.   ✅ Dr Chaffee's website: www.thecarnivorelife.com ✅Join my PATREON for early releases, bonus content, and weekly Zoom meetings! https://www.patreon.com/AnthonyChaffeeMD ✅Sign up for our 30-day carnivore challenge and group here! https://www.howtocarnivore.com/ ✅Stockman Steaks, Australia Discount link for home delivered frozen grass-fed and grass finished pasture raised meat locally sourced here in Australia! Use discount code "CHAFFEE" for free gift with qualifying orders! http://www.stockmansteaks.com.au/chaffee ✅ 60-minute consultation with Dr Chaffee https://calendly.com/anthonychaffeemd/60-minute-consultation   Sponsors and Affiliates: ✅ Brand Ambassador for Stone and Spear tallow and soaps referral link https://www.stoneandspeartallow.com/?ref=gx0gql8b Discount Code "CHAFFEE" for 10% off ✅ Carnivore t-shirts from the Plant Free MD  www.plantfreetees.com ✅THE CARNIVORE BAR: Discount Code "Anthony" for 10% off all orders!   https://the-carnivore-bar.myshopify.com/?sca_ref=1743809.v3IrTuyDIi ✅Schwank Grill (Natural Gas or Propane) https://glnk.io/503n/anthonychaffeemd $150 OFF with Discount Code: ANTHONYMD ✅X3 bar system with discount code "DRCHAFFEE" https://www.kqzyfj.com/click-100676052-13511487 ✅Cerule Stem cells https://DrChaffee.cerule.com ✅CARNIVORE CRISPS: Discount Code "DRCHAFFEEMD" for 10% off all orders! www.carnivorecrisps.com ✅Shop Amazon https://www.amazon.com/shop/anthonychaffeemd?ref=ac_inf_hm_vp   And please like and subscribe to my podcast here and Apple/Google podcasts, as well as my YouTube Channel to get updates on all new content, and please consider giving a 5-star rating as it really helps!   This podcast is for general informational purposes only and does not constitute the practice of medicine, nursing or other professional health care services, including the giving of medical advice, and no doctor/patient relationship is formed. The use of information on this podcast or materials linked from this podcast is at the user's own risk. The content of this podcast is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Users should not disregard or delay in obtaining medical advice for any medical condition they may have and should seek the assistance of their health care professionals for any such conditions. Music Credit: Music by: bensound.com License code: MPTEUCI8DAXJOKPZ Music: bensound.com License code: FJQPPMCJLHEOYGQB Music: Bensound.com/royalty-free-music License code: KQAKMWSXIH3MJ4WX Music I use: https://www.bensound.com License code: 58NN4QOSKWJ7ASX9   

Dr. Burns earned his bachelor's degree from the University of Pittsburgh, graduating with honors in biological sciences. He then graduated summa cum laude from the Dr. William M. Scholl College of Podiatric Medicine in Chicago. He returned to the University of Pittsburgh to complete his surgical residency, and joined the Foot and Ankle Division of the University of Pittsburgh Department of Orthopedic Surgery where he worked for 17 years before recently joining West Virginia University Medicine as part of their foot and ankle reconstructive team.  Join us as we discuss all things podiatric medicine as we talk with Dr. Burns about his experience educating students, residents and fellows. He has written and lectured extensively regarding External fixation and Charcot neuroarthropathy as well as issues related to the diabetic foot. Tune in as we discuss his Fellowship in Kurgan Russia as well as his role as Co-Chair of the International External fixation Symposium.    Dr. Burns also participates in local, state, and national committees and associations and has been named to the “Most Influential” DPM's across the country twice and has been given the “Distinguished Service Award” by the Pennsylvania Podiatric Medical Association for his work in education. He is considered a thought leader within the profession and has served in various leadership positions including medical director for UPMC Mercy Hospital. Listen in, as he describes the importance of relationship building and how trying to be 1% better each day can translate into future opportunities.  Dr. Burns is board certified in foot surgery and reconstructive rearfoot and ankle surgery. He is a member of the American Podiatric Medical Association and a diplomate of the American Board of Foot and Ankle Surgery. Dr. Burns is the Associate Editor of the surgical section of the Journal of the American Podiatric Medical Association, Clinics of Podiatric Medicine and Surgery and the Foot and Ankle Specialist He also has served on the editorial board of several other publications including UpToDate, and functioned as the Editor in chief for Diabetic Foot and Ankle. His interests include complex foot and ankle deformity and preservation techniques. He has extensive experience with complex foot and ankle surgery, revision surgery, trauma and fracture care, Charcot neuroarthropathy and limb preservation.  https://wvumedicine.org/wheeling/education/podiatric-medicine-and-surgery-residency/ https://www.acfas.org/ https://www.abfas.org/residents https://www.aofoundation.org/aona https://www.apma.org/  

durée : 00:09:03 - L'invité de 7h50 - par : Sonia Devillers - Affaibli et sous respirateur, le sénateur LR de la Drôme Gilbert Bouchet lance un appel pour faire évoluer la loi concernant la prise en charge de la maladie de Charcot, lui-même atteint par la pathologie.

durée : 02:58:38 - Le 7/10 - par : Nicolas Demorand, Léa Salamé, Sonia Devillers, Anne-Laure Sugier - Ce jeudi 19 décembre 2024, les invités de France Inter sont le sénateur Gilbert Bouchet atteint de la maladie de Charcot à 7h50, les auteurs du podcast sur l'Affaire Dreyfus à 8h20, la gastronomie française à l'honneur dans le Débat de 9h05, Philippe Descola à 9h20, et des cheerleadeuses à 9h50 !

durée : 00:09:03 - L'invité de 7h50 - par : Sonia Devillers - Affaibli et sous respirateur, le sénateur LR de la Drôme Gilbert Bouchet lance un appel pour faire évoluer la loi concernant la prise en charge de la maladie de Charcot, lui-même atteint par la pathologie.

In this episode, Dr. Jeremy Pettus and Dr. Steve Edelman address the most common musculoskeletal and neuropathic conditions that affect people with diabetes. They explore how complications like frozen shoulder, carpal tunnel syndrome, and trigger are linked to long-term diabetes, and how they can significantly impact daily life. Focusing on real-life scenarios and actionable advice, they offer strategies to help individuals with diabetes recognize early warning signs, navigate treatment options, and take preventive measures to protect their overall health and quality of life.Key Topics:What is frozen shoulder, and why is it more common in people with diabetes?What are the early signs of trigger finger and Dupuytren's contracture in diabetes?How does diabetes increase the risk of carpal tunnel syndrome?What are the dangers of Charcot joint, and how can people with diabetes prevent it?How can managing blood sugar and mobility exercises help prevent diabetes-related complications?What are the long-term impacts of peripheral neuropathy on daily life for people with diabetes?How can early detection of diabetes-related musculoskeletal issues improve outcomes?What role does physical therapy play in managing diabetes-related complications?How does poor glucose control contribute to inflammation and joint stiffness?What lifestyle changes can help people with diabetes prevent hand and foot complications?Useful links to discover:Learn more about Musculoskeletal Complications: https://tcoyd.org/2022/05/diabetes-is-a-pain-in-the-neck-and-the-shoulders-and-the-hips-and-the-knees/Watch our LIVE Broadcast on this topic: https://tcoyd.org/live-oct-2024/ ★ Support this podcast ★

Si vous aimez "Dans les yeux d'Olivier", le podcast qui donne la parole à ceux qui ne l'ont jamais, laissez des étoiles et des commentaires sur votre plateforme d'écoute préférée !Olivier Delacroix part à la rencontre de Rio Mavuba. Ce joueur professionnel de football a surmonté de nombreuses épreuves avant de pouvoir atteindre ses objectifs. Il a accepté de confier son histoire dans cet épisode du podcast “Dans les yeux d'Olivier” produit par Europe 1 Studio. En 1984, Rio Mavuba voit le jour sur un bateau de fortune alors que ses parents fuient la guerre civile en Angola. Arrivée en France, la famille Mavuba s'installe dans un quartier populaire de Mérignac. À deux ans, Rio Mavuba perd sa mère de la maladie de Charcot, puis son père alors qu'il a 13 ans. Orphelin, il est élevé par la belle-mère Suzanne avant d'entrer en équipe de France Espoirs. Mais pour devenir footballeur professionnel, le jeune garçon doit impérativement être naturalisé français… Rio Mavuba a accepté de confier son histoire dans cet épisode du podcast « Dans les yeux d'Olivier », produit par Europe 1 Studio. Crédits : Présentation : Olivier DelacroixProduction et rédaction : Raphaëlle MariatteRéalisation : Christophe Daviaud Promotion et distribution : Marie Corpet Graphisme : Cosa Vostra

Profitez des meilleurs rabais sélectionnés par Noovo Moi à l'approche du Black Friday! https://www.noovomoi.ca/style-et-maison/maison/aubaines-pre-vendredi-fou-amazon.html https://amzn.to/3CovKL6 Guylaine Guay devient critique de cinéma et nous donne son avis sur « Le cyclone de Noël » Tammy Verge se demande : si les Fantas devaient donner une classe de maître, ça serait sur quoi ? Rémi-Pierre Paquin cherche les plus beaux endroits au Québec !   BONNE ÉCOUTE !

durée : 00:05:26 - Déjà debout - Pierre-Yves Caillaud, gestionnaire dans l'immobilier, témoignant de son rôle d'aidant suite à la maladie de Charcot de son épouse, est l'invité "Déjà debout"

durée : 00:05:26 - Déjà debout - Pierre-Yves Caillaud, gestionnaire dans l'immobilier, témoignant de son rôle d'aidant suite à la maladie de Charcot de son épouse, est l'invité "Déjà debout"

Le 9 juin dernier, le projet de loi sur la fin de vie était abandonné avec la dissolution de l'Assemblée nationale. Depuis, le texte laissé en suspens est au centre des préoccupations de nombreux malades qui espèrent la légalisation prochaine d'une « aide à mourir ». Code source fait le point sur cette réforme « mise en pause » à travers l'histoire de Loïc Résibois, un homme atteint de la maladie de Charcot, qui avait témoigné dans Code source, en mai 2024, et qui est mort, à 47 ans, le 24 septembre.Cet épisode de Code source est raconté par Bérangère Lepetit, journaliste au service société du Parisien. Écoutez Code source sur toutes les plates-formes audio : Apple Podcast (iPhone, iPad), Amazon Music, Podcast Addict ou Castbox, Deezer, Spotify.Crédits. Direction de la rédaction : Pierre Chausse - Rédacteur en chef : Jules Lavie - Reporter : Barbara Gouy - Production : Raphaël Pueyo, Clara Garnier-Amouroux, Barbara Gouy, Clémentine Spiler et Thibault Lambert - Réalisation et mixage : Julien Montcouquiol - Musiques : François Clos, Audio Network - Archives : France 2 Hébergé par Acast. Visitez acast.com/privacy pour plus d'informations.

Philippe Caverivière aborde avec humour la maladie de Charcot, à l'occasion de la sortie du livre Invincible.

Condamné par la maladie de Charcot, Olivier Goy se bat avec les armes qui lui restent, sa détermination, son intelligence et son amour de la vie pour lever des fonds en faveur de la recherche et pour mieux faire accepter le handicap. Olivier Goy et la journaliste Anne Fulda publient "Invincible, derrière le sourire le combat d'une vie", aux éditions de L'Observatoire. Ils sont les invités de Amandine Bégot. Ecoutez L'invité d'Amandine Bégot avec Amandine Bégot du 25 septembre 2024.

Philippe Caverivière aborde avec humour la maladie de Charcot, à l'occasion de la sortie du livre Invincible.

Condamné par la maladie de Charcot, Olivier Goy se bat avec les armes qui lui restent, sa détermination, son intelligence et son amour de la vie pour lever des fonds en faveur de la recherche et pour mieux faire accepter le handicap. Olivier Goy et la journaliste Anne Fulda publient "Invincible, derrière le sourire le combat d'une vie", aux éditions de L'Observatoire. Ils sont les invités de Amandine Bégot. Ecoutez L'invité d'Amandine Bégot avec Amandine Bégot du 25 septembre 2024.

Aux Etats-Unis, un homme handicapé parvient à interagir avec sa maison connectée grâce à un implant cérébral via l'assistant Alexa d'Amazon.Ce qui semblait autrefois relever de la science-fiction est désormais une réalité. Aux États-Unis, un homme de 64 ans, atteint de la maladie de Charcot, a réussi un exploit technologique et médical sans précédent. Grâce à une interface cerveau-ordinateur (BCI) de l'entreprise américaine Synchron, il peut contrôler des appareils chez lui, comme allumer les lumières ou lancer de la musique, en utilisant uniquement son cerveau. Et cela sans même prononcer un mot. Il peut, entre autres, passer des appels vidéo, lire des livres sur Kindle ou même faire des achats en ligne, simplement en pensant aux actions correspondantes. L'idée d'utiliser Alexa pour interagir avec l'environnement est une première. Une avancée technologique qui ouvre de nouvelles perspectives pour les personnes handicapées.-----------♥️ Soutien : https://donorbox.org/monde-numerique

It has been assumed that diabetic patients with peripheral neuropathy should not have pain associated with Charcot foot arthropathy.   In conclusion, this small series of patients would suggest that nonunion of the Charcot neuroarthropathy process was responsible for complaints of pain not able to be managed with therapeutic footwear. Successful arthrodesis resolved the pain. CT imaging may help identify a treatable source of pain in this population.     Click here to read the article.

Send us a Text Message.Emily is a 42-year-old woman who lost 90 pounds and reversed her diabetic complications by following a carnivore diet. Initially, she struggled with her health from aged 9. Eventually, Emily discovered the low-carb and ketogenic way of eating and found success. She believes that nothing good is easy but making the change to a carnivore diet made life the easiest it had been. The speaker was diagnosed with diabetes at an early age and had struggled with managing her condition for many years. She was on multiple medications, constantly dealing with high blood sugar, and had various complications such as kidney failure and diabetic retinopathy. She also experienced broken bones, foot ulcers, and anemia. When she discovered the ketogenic diet in 2017, her life took a drastic turn for the better. Emily was on a knee scooter for almost three years. Due to Charcot foot disease and the horrific foot ulcer.Thank you so much for listening to my podcast. I hope you enjoyed it. Your support means the absolute world to me. And if you're enjoying the show, I've got a small favor to ask you. I'd be incredibly grateful if you would consider becoming a supporter and make a small monthly donation. Your contribution will really help to improve the show. It's a small monthly contribution. You can cancel at any time, and the link is in the show notes. Support the Show.All my links in 1 easy list, including booking and personal training workout plans at LINKTREE You can now download the carnivore experience appApple direct link for apple devices Google play store direct link to app for Android Coach Stephen's Instagram Book me for coaching My growing UK carnivore YouTube channel I have set up a community that is all about eating low-carb and specifically carnivore. CLICK HERE Support my podcast from just £3 per monthBECOME A SUPPORTER Success stories Optimal Health 5 Star reviews All my facebook and other reviews are here Thanks to www.audionautix.com for any music included. Ple...

Send us a Text Message.Episode 2 of Season 2 and the boys are already hot on the trail of celebrities.This week Martin and Patrick are overwhelmed to be interviewing one of this Countries (UK) Mega-Star's Mr Jimmy Tarbuck OBE (Tarby).Jimmy's first television show was "It's Tarbuck " on ITV in 1964, though he had been introduced on Sunday Night at the London Palladium in October 1963 by Sir Bruce Forsyth. He then replaced Forsyth as the last original host of the show from 1965 until it was axed in 1967. He has also hosted numerous quiz shows, including Winner takes all, Full Swing and Tarby's Fame game. In the early 1970s he hosted a variety show called Tarbuck's Luck on the BBC.In the 1980s, he hosted similar Sunday night variety shows, Live from Her Majesty's, Live from the Piccadilly and finally Live from the Palladium.He appeared on the fourth series of BBC One's Strictly Come Dancing in but was forced to pull out due to high blood pressure, and needed surgery to fit 3 stents in his heart. In 2008, he returned to a variety format on television screens when he co-hosted, alongside Spice Girl's Emma Bunton an edition of ITV's variety show For One Night Only. He appeared on Piers Morgans Life Stories on 25 May 2012, while on 3 December that year he was invited to celebrate 100 years of the Royal Veriety Performance along with Bruce Forsyth, Ronnie Corbet and Des O'connor. In February 2020, Jimmy revealed that, the day after his 80th birthday, he had been diagnosed with Prostate Cancer.In 2022 Jimmy then 81-years-old was back in hospital having a cancerous mole removed from his back.Listen to Jimmy's fascinating stories over 60 years in show business and how he coped with his Heart issues and Cancer diagnosis and treatments.We have a special "Joke of the week" this time by a British Legend in Comedy, Jimmy takes on Martin for top spot on "Who's Tom & Dick"Next we the boys have another special guest Norman Hume who has Emphysema, Charcot-marie-tooth Disease, Bronchiectasis and Prostate cancer, Norman is battled with illness most his life, Listen to his Inspirational story next week.#Prostate Cancer#Bronchiectasis#CharcotmarietoothDisease#Emphysema#The after life#Ghosts#Spirts#Ouija boards#Mediums#Psychics#Reincarnation#HeartTransplant#EbsteinsAnomaly#RareCondition#HealthJourney#LifeChangingDiagnosis#MentalHealth#Vulnerability#SelfCompassion#PostTraumaticGrowth#MedicalMiracle#BBCSports#Inspiration#Cardiology#Surgery#Podcast#Healthcare#HeartHealth#MedicalBreakthrough#EmotionalJourney#SupportSystem#HealthcareHeroes#PatientStories#CardiologyCare#MedicalJourney#LifeLessons#MentalWellness#HealthAwareness#InspirationalTalk#LivingWithIllness#RareDiseaseAwareness#SharingIsCaring#MedicalSupport#BBCReporter#HeartDisease#PodcastInterview#HealthTalk#Empowerment#Wellbeing#HealthPodcast#ChronicIllness#mywishcharity#comedy#funny#joke#BBCuploads#Cancer#BreastCancer#Lungcancer#Childcancer#Bowlcancer#Canceruk#mywishcharity#MacmillancancersupportCheck out our new website at www.whostomanddick.comCheck out our new website at www.whostomanddick.com

In this episode, we review the high-yield topic of⁠⁠ ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Diabetic Charcot Neuropathy⁠⁠⁠⁠⁠ ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠from the Foot & Ankle section. Follow ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Orthobullets⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ on Social Media: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Facebook⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Instagram⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Twitter⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠LinkedIn⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠YouTube

In this episode, we review the high-yield topic of⁠ ⁠Neuropathic Charcot Arthropathy ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠from the MSK section. Follow ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Medbullets⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ on social media: Facebook: www.facebook.com/medbullets Instagram: www.instagram.com/medbulletsofficial Twitter: www.twitter.com/medbullets