Résultats pour "Rara" dans Santé et bien-être

Rare Medium with Deb Snyder Celebrating life’s rarities, the people, places and experiences that just might be a little bit weird. This podcast explores all facets of our energetic connections…to each other and beyond We’ll dive into the depths of mediumship, psychic ability, intuition, near death experiences, afterlife research, healing modalities and more. Our focus is to bring you relevant and moving accounts with guests who share their authentic selves and their treks into Spiritual and energetic realms. We’ll learn how those experiences shifted their perspectives on life itself. ...

Das Peutz-Jeghers-Syndrom ist so selten, dass viele Ärztinnen und Ärzte es nie zu Gesicht bekommen. Für Betroffene bedeutet das oft jahrelange Ungewissheit: Untersuchungen ohne Ergebnis, Beschwerden, die niemand einordnen kann, und das Gefühl, nicht ernst genommen zu werden. In "Rare but Aware" sprechen Betroffene und Angehörige genau davon. Unterstützt von Expertinnen und Experten aus verschiedenen Fachgebieten erzählen von ihren Diagnosewegen und vom Alltag mit einer sehr seltenen Erkrankung – auch über die Themen, die sonst niemand anspricht, vom Abführen vor der Darmspiegelung ...

Un relato audaz y épico sobre cómo la coevolución de la psicología y la cultura creó la peculiar mente occidental que ha moldeado profundamente el mundo moderno. En ‘El pueblo más raro del mundo’, Joseph Henrich se basa en investigaciones de vanguardia en antropología, psicología, economía y biología evolutiva para explorar estas cuestiones y otras más. El autor explica los orígenes y la evolución de las estructuras familiares, el matrimonio y la religión, así como el profundo impacto de estas transformaciones culturales en la psicología humana.

This podcast is dedicated to raising awareness and sharing the voices of people living with rare disorders in New Zealand.Around one in seventeen New Zealanders are affected by a rare condition. For many, finding answers and support can take years.Here, we speak with individuals, families, and experts to help build greater understanding, connection, and support for the rare disorder community.Thank you for listening and for being part of the Rare Aware journey. For more information, visit www.raredisorders.org.nz

The Rare Rebels™ Podcast shares unscripted conversations with patients, caregivers, advocates, and researchers who are changing the future of rare disease. These aren’t polished soundbites — they’re real voices from the front lines, revealing the humanity, heartbreak, and hope woven into the rare disease experience.Because change doesn’t happen through statistics alone — it happens through connection.Hosted by award-winning storyteller and advocate Melody Joy Paine, Rare Rebels™ brings lived experiences to the forefront, bridging gaps between families, researchers, nonprofits, ...

Rare Humans is a podcast about what it really looks like to live — and thrive — with a complex biology in today’s world. Hosted by Kevin and Jack, each episode explores chronic health, blood sugar, energy, mindset, and the daily realities of managing a body that doesn’t follow the “normal” playbook. Through honest conversations, personal stories, and practical insights, Rare Humans is here to help you feel more in control of your health — and remind you that being different might just be your greatest advantage.

Your Podcast for Rare Kidney Conversations Life with a rare kidney disease can be complex, isolating, and often misunderstood. Rare Kidney Source brings together voices from across the community to inform, inspire, and connect people living with rare kidney diseases such as C3 glomerulopathy (C3G) and primary immune-complex membranoproliferative glomerulonephritis (IC-MPGN). Through honest conversations and expert insights, we explore the realities of diagnosis, disease management, and everyday life to empower listeners with knowledge, perspective, and a sense of belonging to navigate their ...

In Rare Stories erzählen Menschen von ihren Erfahrungen mit seltenen Erkrankungen. Sie teilen ihre persönlichen Geschichten, geben wertvolle Alltagstipps und schenken Mut. Auch Angehörige berichten von ihren Erlebnissen, und Expert*innen liefern hilfreiche Einblicke. Jeden Monat eine neue Folge mit inspirierenden Geschichten und spannenden Insights. Hör mal rein und lass dich berühren!

What’s it like living with a rare blood or bone marrow disorder? Or parenting a child who is? This brand new podcast invites people living with these conditions to share their perspectives and advice for those facing similar challenges. How do you carry on feeling positive when someone you know dies as a result of the same condition? How do you explain why your child can’t go to a party? How do you speak up at the hospital when you think doctors need to do something different? Stories of strength and real, practical advice for super rare people and families. -------------------------------...

Louis Jolyon "Jolly" West (October 6, 1924 to January 2, 1999), Director Emeritus, Neuropsychiatric Institute, University of California at Los Angeles, was an American psychiatrist and longtime contractor for the Central Intelligence Agency (CIA) and its Project MKUltra. Margaret Thaler Singer, Ph. D., was an Emeritus Adjunct Professor of Psychology, University of California at Berkeley. The following recording is from a 1998 conference.

🎙️ Dessine-moi un cœur – Podcast Le récit intime et courageux d’une battante face à un cancer rare. À travers ce podcast, je partage mon parcours contre une maladie peu connue : la maladie de Paget extra-mammaire secondaire. Quatre années d’errance médicale, de doutes, de douleurs, d’espoir et de combats. Ici, je mets des mots sur l’invisible. Je parle de la peur, de l’annonce, des traitements, de la vie de maman, de femme, et de l’impact d’un cancer rare sur le quotidien. Ce podcast est un espace de vérité, de vulnérabilité et de force. Un témoignage pour ...

Thriving in the Rare is a podcast dedicated to amplifying the voices of individuals living with rare diseases and complex chronic conditions. Through candid conversations with patients, caregivers, and advocates, this series explores what it truly means to move forward in the face of uncertainty, loss, and change.Each episode highlights personal journeys of adaptation—navigating diagnosis, redefining identity, managing invisible symptoms, and finding new ways to live meaningful, connected lives. Guests share how they have transformed challenge into purpose through advocacy, creativity, ...

Programa Dedicado a hablar sobre las Enfermedades Raras, Platica con Pacientes, Familiares, Médicos, Fundaciones y Mas #EnfermedadesRaras #Rarediseases

A podcast focused on rare disease research, created by Share4Rare, an initiative by the Sant Joan de Déu Research Foundation that promotes collaborative research and connects patients and families affected by rare diseases worldwide, and by the Weber Foundation. In each episode, we delve into various topics related to advances in rare disease research, featuring expert insights, patient stories, and family perspectives. Let’s explore the Rare Horizons! Hosted on Acast. See acast.com/privacy for more information.

Dobro došli na podcast! Ovo je naše: “Zašto Rare & Share?”: Tokom lečenja sina od retke bolesti, a posebno nakon izlečenja imali smo prilike da upoznamo sjajne ljude i čujemo vrlo inspirativne priče. Ceo jedan svet sa svojim temama. Ovde ćemo pričati sa onima koji su pokretali lavine događaja, menjali okvire, pomerali granice do tada poznatog. Želimo da razgovaramo o temama koje su važne onima koji se suočavaju sa retkim izazovima kao što su pravni i zakonski okviri, aspekat psihološke podrške, medicinska dostignuća i nove studije. Planiramo razgovarati sa ekspertima, ...

In rarity we unite, connect and find our way to purpose.

À propos : "RARE à l'écoute" est un podcast dédié à la sensibilisation aux maladies rares et au soutien des personnes touchées par ces affections. Créé par un groupe passionné de professionnels de la santé, le podcast vise à informer les professionnels de santé et fournissant des informations sur les dernières avancées médicales et scientifiques dans le domaine des maladies rares, et inspirer les patients et leurs proches en partageant des histoires de courage et de persévérance.Contenu : 🔍 "RARE à l'écoute" sensibilise les professionnels de santé et le grand public aux...

Welcome to the new Rare Kidney Disease Show part of the RKD Scientific Network sponsored by Travere Therapeutics. The Rare Kidney Disease Show is your primary source for cutting-edge insights, expert perspectives, and pivotal updates in nephrology. Led by our panel of experts, explore the advances in glomerular nephropathies through compelling conversations, challenging case studies, and discussions tackling hot topics. Join us as we strive to provide you with the ultimate resource to support your clinical practice and advance patient care.

Hosted by HCPLive, the monthly series tackles the intricate details of the 6,000-plus known rare diseases, featuring an expert guest, one disease at a time.

Conversations started by The Whitworth Group