Podcast by Rare Candy

RARECast is a Global Genes podcast hosted by award-winning journalist Daniel Levine. It focuses on the intersection of rare disease with business, science, and policy.

Rare Disease Advisor's Rare Care Podcast features exclusive interviews with experts and stakeholders from the rare disease community.

Revolutionary War Rarities is fast, fun, and rarely known history on the American Revolution. All PodCasts are 8-10 minutes long and are released every two weeks. Revolutionary War Rarities is the PodCast from the ”Sons of the American Revolution”. Please subscribe and let’s make history fun again. Thank you for joining us. #americanrevolution #revolutionarywarrarities #americanhistory #foundingfathers #revolutionarywar #sonsoftheamericanrevolution #rarehistory #americanrevolution

We are a thriving church located in the pacific island of Rarotonga. On this podcast, you will find powerful preaching taken right from our church services. We will also be producing bonus content that is designed to help you live a life of breakthrough and make an impact for Christ! Subscribe and become a part of what God is doing!

This is the real, raw, and all the feels of loving a child with disabilities. Episodes feature parent-guests, professionals, and solo episodes with host Madeline Cheney. Their authentic conversations don’t shy away from the strong and mixed emotions that often accompany medically-complex parenting. Parents listen in to feel seen, validated, and receive much-needed solidarity. Professionals working with disabled people listen in to better understand what is often going on under the surface fo ...

We’re bringing you a slice of our lives through humor, tears, drama, games & pop culture, where trying to stay on topic is only half the fun! Join us!

RaRa Raadio toob sinuni saated, mis haaravad endaga kaasa, ärgitavad mõtlema ja kergitavad suunurki ülespoole. Usume, et leiad siit mõtteid, mis teevad sind rikkamaks inimeseks.

Fighting sarcoidosis as well as other rare diseases.

Host Josh Mills brings together a wide variety of adult children of celebrities for a fun, funny, bizarre, jaw-dropping, strange and wonderful look behind celebrity, by the people that know them best: their very own children.

Bienvenidos al Podcast de Cinoscar & Rarities, espacio del blog de cine Cinoscar & Rarities. Reseñas, estrenos, festivales, noticias, especiales y todas las novedades del séptimo arte. Podcast dirigido por @CinoscaRarities y @CineAmateur http://cachecine.blogspot.com.es/

Welcome to the Dream Rare Podcast! An audio experience aiming to lift you up, make you laugh & help you get healthier all while bringing you some of the best news analysis on Earth.

Young women have been growing up with an indoctrination of what womanhood is and what it should be. They've been taught everything that is in direct opposition to the Word of God. Young women who want to be different from the world are rare but they are real. Audrey Broggi will often be joined by her daughter and her daughters-in-law who desire to be discerning in a day when everything seems to go against God's design.

Welcome to A Podcast of Rare Antiquities! Host’s Harry and Geoff discuss and analyze film and television shows. This podcast mainly delves into more obscure and forgotten films but latest releases are sometimes covered. We hope this is the rare antiquity you are looking for.

Parenting tools and life hacks for raising a child with a rare diagnosis. Let’s get to the meat of it!

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.

Casey + Cassandra are a pair of best friends with the same rare disease. Their goal is simple: sharing their lives to showcase the beauty and normalcy in disability, while having fun together. They’ll also touch on accessibility, friendships, style, and everything in between as they live their best, rare, lives! For show notes, go to rarewithflair.com

Continuous mixes of deep house, 90s hip hop and other groovy goodness...

En esta serie mensual entrevistamos a pacientes, familiares, científicos, investigadores y líderes hispanos en el mundo de las enfermedades raras, para que nos compartan sus historias, alegrías, desafíos y aprendizajes. Acompáñanos a compartir estas historias, desde la odisea del diagnóstico (¡hablando un idioma diferente!) a los conceptos erróneos en nuestra comunidad. Hablaremos de la diversidad cultural en los países de habla hispana e intentaremos comprender mejor los diferentes factores ...

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!

siraman rohani ala rarrizi

Welcome to P4A Let’s Talk Rare, a monthly podcast highlighting the most important developments in the world of rare diseases orphan drug, cell and gene therapy, hosted by Georgie Rack and Owen Bryant of Partners For Access. To find out more about Partners For Access and our commitment to sustainable orphan drug access for patients with high unmet need, visit partners4access.com

Dive deep into the fascinating world of rare books with Rare Book Chat. Hosted by Michael DiRuggiero and Jeremy O'Connor, the co-founders of The Manhattan Rare Book Company, this podcast explores the unique and often valuable items that fill the world of rare books, manuscripts, letters, photographs, archives, and more. From historical documents to literary first editions, we'll discuss the stories behind these one-of-a-kind treasures. Join us as we explore the intricacies of the rare book t ...

Intro,obrolan

This podcast is about rare and wonderful creatures that are at risk of disappearing and the amazing people working hard to save them! Have you ever wanted to know why they call the Loggerhead Shrike the Butcher Bird? Have you wondered where have all the bats gone? Or asked yourself what is being done to protect the creatures that can’t stand up for themselves? Well this is the podcast for you!

Escape The World Thru MusiQ.

Conversations started by The Whitworth Group

Formerly Nutrition Equity, rare connection is an extension of the podcast to include all 10,000 rare conditions and not just those covered by the Medical Nutrition Equity Act. Some of the conditions may be the same, but I am trying to turn this into a learning experience for those in the medical feild, policy leaders, and those who are just interested in hearing about rare conditions and patient stories. Rare conditions are called zebras hence the zebra striped ribbon. More common conditions ...

Wait How Do You Spell That? is a rare disease podcast produced by Patient Worthy. We talk about issues affecting people rare and underdiagnosed conditions and interview advocates from across the community. We‘re definitely not doctors, and we can‘t give you medical advice. We‘re just here to chat and learn about the diseases that even doctors can‘t seem to spell. Check out the latest in rare disease news at PatientWorthy.com.

Somos tu podcast favorito donde hablamos de todo lo curioso, extraño y fascinante que el mundo tiene para ofrecer. Desde misterios sin resolver hasta historias extraordinarias, ¡aquí encontrarás de todo! 🔍 ¿Qué encontrarás en nuestro podcast? Análisis de fenómenos inexplicables. 🎧 ¡No te pierdas ni un episodio! Suscríbete para estar al tanto de las últimas publicaciones y únete a nuestra comunidad de exploradores de lo desconocido. ¡Únete a nosotros en esta aventura y descubre las varas más ...

We are in an Acura in a park we came to do yoga but it wasn’t here, so we started talking about stuff in the parking lot.

Imagine the excitement of becoming a new parent and then within hours finding out your child has a serious developmental disorder. That is exactly where Sanath Kumar Ramesh found himself in the summer of 2018. One year later, on his son’s first birthday, they found out that their son, Raghav, had an extremely rare mutation of the GPX4 gene. At the time, doctors told them that Raghav may be the only one on the planet with this genetic variant who had lived beyond one month of life. The progno ...

Welcome to Joslyn Rardon, where amazing things happen.

Caden Rardon Interviewing Chauncey Rardon about his coaching experience

TIXTO son capsulas de tecnología aplicada a la evangelización, su productor y locutor es Roberto Arias (@bettocr) de RARComputacion.com

I'm Aware That I'm Rare: the phaware® podcast is devoted to raising global pulmonary hypertension awareness with dynamic stories from PH patients, caregivers and medical professionals from around the world. Through this series of impactful, insightful and, most importantly, hopeful stories from members of the global pulmonary hypertension community, we hope to further the global #phaware conversation as well as to capture, engage and enable misdiagnosed and undiagnosed PH patients because ea ...

New Simplicity Channel. Robert Bonet's Music No Published

Facts are facts if you would like to share your story or be apart of the podcast email me at 1allmostrare@gmail.com

Whether you want the latest release or something more classic, there's sure to be something for everyone. And with no registration or fees required, it's easy and affordable to get started. So kick back, relax, and enjoy the show!

Join the nano-rare disease community! Interviews features leading physicians, scientists, biotech experts, and patient advocates. Lessons teach core concepts about drugs. Our host Dr. Crooke has led the creation of antisense technology and his foundation, n-Lorem, is using this powerful technology to discover, develop, and provide personalized experimental antisense oligonucleotide medicines to nano-rare patients for free, for life. n-Lorem is a non-profit organization established to apply t ...

Podcast by rarebirdlit

Hai. Aku Rara. Aku seneng banget baca buku. Hehe aku pengen buat episode hal-hal menarik dari buku-buku yang ku baca. Ohya dan juga bisa jadi episode isi dari suara hatiku. Jadi ga melulu tentang buku yaaaa

Funny in Spanish Cover art photo provided by Nahil Naseer on Unsplash: https://unsplash.com/@nahilnaseer

Welcome to the VeryRarePodcast

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 suppor ...

Every beginning carries within it the seed of its own destruction.

For fans of the Rutgers University Scarlet Knights.

El mejor podcast para discutir cualquier vaina rara; que en Venezuela y el mundo, son muchas.

Conozcamos qué son las Enfermedades Raras y porque difundimos sobre ellas!