Résultats de "RaRa" dans Toutes les catégories

Historias de un Artista es un emocionante podcast que presenta una serie de entrevistas con algunos de los artistas más innovadores y talentosos de nuestra región. En cada episodio, el anfitrión conversa con un artista diferente, explorando su vida, su proceso creativo y su trayectoria profesional.Desde pintores y escultores hasta músicos y escritores, Historias de un Artista presenta una amplia variedad de artistas de diferentes disciplinas, ofreciendo una visión única de las mentes creativas detrás de algunas de las obras más impresionantes e influyentes de nuestro tiempo.Con una ...

THREE amigos give you the up to date in sports and entertainment.. Also TAP IN ▶️ on @iheartradio, Spotify, and YouTube!! Hosted by: 0V0$kIp, Zee Gawd, Pressure P,!! #podcastBecome a supporter of this podcast: https://www.spreaker.com/podcast/the-rich-rare-podcast--5690445/support.

Very rare old school hip hop Nothing but classic hip hop from the forgotten era......

Ippo kekudha ?? is the voice of 4 Chennai girls. Join them as they navigate adulthood, make tough choices, and grow through life together. Please enjoy!

On January 5, 2026, all episodes of "Ask the Expert, ABCs of MOGAD, ABCs of NMOSD, ADEM Academy, and Community Meets Clinic" - past and present - will now be found in one feed called “SRNA Soundwaves” on all podcast streaming platforms. Make sure to subscribe to "Ask the Expert," which will be renamed “SRNA Soundwaves” on January 5th: https://creators.spotify.com/pod/profile/srna-ask-the-expert/ If you have questions about the upcoming change, please email: podcast@wearesrna.org ADEM Academy is a podcast series designed to create awareness regarding acute disseminated encephalomyelitis...

Podcast by Rare Candy

Advanced spoken Latin podcast by Irene Regini. In each season I interview some "rarae aves", incredibly talented persons who achieved amazing results in the field of the Latin language. You'll learn how they started, how their daily Latin routine looks like and how they grew their projects from scratch. The interviews in full video format are available on my YouTube channel. Your very special journey to becoming a "rara avis" starts here: https://pages.saturalanx.eu/yplc-waitlist/ This is a Satura Lanx production (listen to my other podcasts: Satura Lanx, Litterae Latinae Simplices).

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.

How would you like to be given a new identity to live by and then removed from your sisters and brothers—never to be legally permitted to contact them again—even upon your deathbed? This is just one of many examples of red tape adoptees are forced to contend with. This book reveals the making of the current child welfare system. The pioneers who built and profited from the industry continue to deny adoptees access to documents that could lead them back to their families. This book protects you against adoption profiteers and traffickers who profess God is on their side.

This page features multiple Podcasts for the gem of a text based game, torn.com - The original Torn Underground w/ Ara & TheFelan. Beers With Balashi and Recruit Radio w/ TexasTuberTim. Lastly, Women of Torn w/ Jairyll & Glandem!

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 ...

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 ...

On January 5, 2026, all episodes of "Ask the Expert, ABCs of MOGAD, ABCs of NMOSD, ADEM Academy, and Community Meets Clinic" - past and present - will now be found in one feed called “SRNA Soundwaves” on all podcast streaming platforms. Make sure to subscribe to "Ask the Expert," which will be renamed “SRNA Soundwaves” on January 5th: https://creators.spotify.com/pod/profile/srna-ask-the-expert/ If you have questions about the upcoming change, please email: podcast@wearesrna.org ABCs of NMOSD brings together the latest information and research about all things NMOSD.

SRNA Soundwaves is a podcast network that brings together expert insight, research updates, and experiences from the rare neuroimmune disorder community. Through multiple series, SRNA Soundwaves connects those living with rare neuroimmune disorders, caregivers, clinicians, and researchers with trusted information and meaningful conversations that educate, empower, and inspire. Topics include acute disseminated encephalomyelitis (ADEM), acute flaccid myelitis (AFM), MOG antibody disease (MOGAD), neuromyelitis optica spectrum disorder (NMOSD), optic neuritis (ON), and transverse myelitis (TM).

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.

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.