Mostrando resultados por autor "RaRo" en Todas las categorías

Un podcast sobre gente poco común en el que hablamos de Lifestyle y Negocios Online. Reflexiones, puntos de fuga e historias de creadores, de hacedores que se arriesgan en lo cotidiano para transitar su deseo. Gente rara es un espacio para pensarse, dudar, divertirse, proyectar y lo que sea que te provoque.

Il podcast gMG Your Way è una serie di otto puntate realizzato con il patrocinio e contributo dell’associazione pazienti Associazione italiana miastenia (A.I.M). Romina Gibertoni, segretaria di A.I.M, ci accompagnerà in un percorso di scoperta all’interno del mondo della gMG, ossia la miastenia gravis generalizzata. In ogni episodio, Romina sarà affiancata da persone che vivono e affrontano questa malattia ogni giorno, clinici, caregiver e altri membri attivi della comunità gMG, che, attraverso la condivisione delle loro storie, esperienze e professionalità ci aiuteranno a capire ...

Sejam todos bem vindos ao Talento Raro Podcast, um podcast semanal voltado para a cultura e mundo pop. Todas as novidades, lançamentos e assuntos mais comentados da semana você encontra aqui! Para não perder nada, nos siga no Instagram: @talentoraropodcast

The Your way Podcast series features Neuromyelitis optica spectrum disorder (NMOSD) patient ambassador Debbie Leticq, alongside healthcare professionals including neurologist Dr Lesley-Ann Hall, Specialist Nurse and Research Fellow, Dr Therese Burke, and psychologist, Dr Sally Shaw, who all share some deeply personal experiences about this rare, auto-immune condition. Their candid conversations shine a light on the day-to-day reality of living with NMOSD, provide some insights and advice to those who may find themselves either newly diagnosed or learning to live with NMOSD. If you would like ...

ABCs of NMOSD brings together the latest information and research about all things NMOSD, from diagnosis and treatment to quality of life and what it’s like to live with NMOSD. We invite medical experts and researchers, to share the latest up-to-date research and clinical knowledge. We have conversations with individuals who have been diagnosed with NMOSD, their caregivers, and allied health professionals. We give tips on how to advocate at school and at work, where to find help and support, navigate health insurance, and work with a team of medical experts.

The goal of our “Ask the Expert” podcast series is to share the latest research and information on rare neuroimmune disorders and provide an avenue for individuals diagnosed with these disorders and their family members to ask questions to experts who specialize in these disorders. The podcasts are moderated based on questions submitted by our community. We would like to hear from you. If there are topics that you would like us to address in our podcasts, you can share your thoughts by sending an email to info@wearesrna.org and please use SRNA Podcast in the subject.

Hosted by Dan Cleary, RFR is a comedy podcast that aims to be just that; in rare form. Sex, race, religion, conspiracy, controversy... nothing is off limits! The faint of heart need not apply. Follow us on Instagram & Twitter: @RareFormRadio - subscribe wherever you get your podcasts - Give us a rating & review if you'd be so kind.

Hunt and Pie talk about adventures as delivery workers, real stories, total knuckleheads

Hi, Welcome to the Strong and Rare parenting podcast. My name is Victoria, and I am a special needs momma of two fun loving boys. In this podcast, we will speak about all things Autism, ADHD, and Rare Diseases. This podcast will bring awareness, acceptance, and knowledge on all things we want to learn as parents raising children with special and medical needs. When you join me, I hope that you will walk away with hope and be empowered to be a driver of change for our community. Support this podcast: https://podcasters.spotify.com/pod/show/strongandrareparenting/support

Comment poser le bon diagnostic sur ces nouveau-nés et enfants atteints par des pathologies rares, des malformations de la tête, du cou et des dents ? Vers qui diriger les familles ? Comment parler de ces maladies, les comprendre et les affronter ? Les différents spécialistes de la Filière TETECOU apportent des réponses. Dans « Mots de têtes », le podcast proposé par la Filière de Santé Maladies Rares TETECOU, nous découvrons l’existence de tout un réseau spécialisé dans des pathologies rares, des malformations de la tête, du cou et des dents présentes à la naissance ...

The NMOSD Your Way Podcast series features Neuromyelitis Optica Spectrum Disorder (NMOSD) patient ambassador, and host, Lelainia, alongside healthcare professionals, patient advocates, and caregivers. In each episode, participants share some deeply personal experiences about this rare, auto-immune condition. Their candid conversations unpack some of the mystery behind this little known condition and delve into the day-to-day realities of living with NMOSD. Participants also provide insights into living well, offering encouragement and information to others who may find themselves either newly ...

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.

pregações do culto

“Tamdem” (pour Training des académiques sur le développement du médicament) est une série de 5 podcasts qui propose de suivre les étapes de développement d’un médicament, de sa création dans un laboratoire académique à sa mise sur le marché par un industriel. Vous découvrirez notamment le mode de fonctionnement et les contraintes de l’industrie ainsi que les apports ciblés des chercheurs académiques pour une collaboration optimale. Chaque épisode thématique donnera la parole à des experts qui aborderont les grands enjeux et les interactions nécessaires entre ...

Over 50 years ago, I was born to a family that ostracized me due to my father’s occupation as a criminal. Although my parents were married, had it not been for my grandfather, we would have been put in orphanages due to the dysfunctional nature of my family. I still have memories of the neglect and abandonment that I experienced.

Everyone has a dream to become something in their life. We all have some kind of desire that doesn‘t leave us. Rare Conversations is where I speak with different business owners about their journeys.- why they started, how they keep going, what they do when things get tough. I want to help others save time so they can learn from mistakes we have made in our own businesses. I hope to inspire you by giving you an honest look at behind-the-scenes and all the stuff no-one really hears about. Episodes drop every Tuesday and Thursdays, so please join us! You may be my next interview!

Podcast by RARE Kind Podcast

We are the newest way to grade and showcase your most valuable collectibles. Elevating the space by bringing transparency back to the collectors.An inside look and discussion of all things collectible with Rare Edition's Staff + Guests.

South London's explosive new podcast discussing pressing topics that are prevalent to young people. Rare talks main host Adz brings uncomfortable and controversial discussions to the forefront of society's attention with special guest speakers from all walks of life.Support this show http://supporter.acast.com/raretalks. Hosted on Acast. See acast.com/privacy for more information.

Welcome to the Rare Cuts Media Society! A Book Club Style show where we dive into Movies, TV, Books, Music, and more. Each month one of us will choose a new piece of media to dive into and discuss. Make sure you watch, listen, and read along with us each month so you will be ready for our discussion. Warning: There will be Spoilers!