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RARECast

RARECast

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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.
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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
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Rare Jongens, de podcast

Universiteit van Nederland

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Wie denkt dat klimaatproblemen, feminisme of superrijken typisch dingen van nu zijn, heeft het mis. De Romeinen hadden er ook mee te maken. In de podcast Rare Jongens vertelt historicus Olivier Hekster (Radboud Universiteit) hoe de Romeinen omgingen met dingen waar we ook nu mee te maken hebben. Samen met Merijn Doggen (hoofdredacteur Universiteit van Nederland) bekijkt hij wekelijks onze tijd door de bril van de Romeinen. Met dank aan de Letteren Faculteit van de Radboud Universiteit
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Celebration Church Rarotonga

Celebration Church Rarotonga

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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!
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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.
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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.
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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/
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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.
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Rare with Flair

Casey Greer and Cassandra Mendez

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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
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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!
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Rare But Real

Audrey Broggi

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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.
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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!
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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
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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 ...
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The Rare Life

Madeline Cheney

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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 ...
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El Club de los Negocios Raros

Radio Intereconomía

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Magazine semanal dedicado al apasionante mundo de los libros. Actualidad nacional e internacional sobre novedades editoriales, premios, entrevistas a autores, poesía, libro viejo y ediciones raras o limitadas. Todo esto y más se dan cita en este espacio cultural de Radio Intereconomia, dirigido por Andrés Sánchez-Magro.
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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 ...
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Rare Book Chat

Jeremy O'Connor and Michael DiRuggiero

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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 twice-weekly 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 th ...
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The Rare Disorder Podcast is a podcast created by Shivani Vyas, a high school senior, young changemaker, and rare disease advocate, dedicated to spreading awareness for rare diseases. This podcast is divided into 2 main series. In the "Meet a Fighter," Shivani interviews patients and those affected by rare diseases allowing them to share their inspirational stories. In "Meet An Expert/Partner," Shivani interviews public health experts, rare disease organization leaders, rare advocacy leaders ...
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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 ...
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Patient Empowerment Program: A Rare Disease Podcast

n-Lorem Foundation (Dr. Stan Crooke, Amy Williford, Kim Butler, Andrew Serrano, Jon Magnuson, and Kira Dineen)

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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 ...
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Are you ready to transform your real estate business? The RARE Agent Show is your ultimate guide to closing more deals, building wealth, and thriving as a real estate professional. Hosted by Dylan Tanaka, a multi-award-winning Realtor and coach, this podcast is where top-performing agents share their secrets and strategies to help you achieve consistent closings without the stress. Each episode delivers actionable insights through two dynamic formats: •Exclusive Agent Interviews: Dive deep w ...
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RARBG Proxy List

RARBG Proxy List

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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!
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Rara-Twimee

ratih susilawati

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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
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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 ...
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This show is the learning project of students from Rāroa Normal Intermediate. Each week we choose a recommendation; something for you to watch, read or experience, and then we tell you why you should check it out! Everything about the show is student-run; from the content creating, to the recording and producing.
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Nurse Practitioner, Janette Reyes, from the Pulmonary Hypertension Program at the Hospital for Sick Children shares her extensive experience caring for pediatric patients with pulmonary hypertension. Reyes discusses the unique challenges and developmental considerations involved in treating children from infancy through their teenage years, as they…
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Terry Jo Bichell, PhD, founder and director of CombinedBrain, which advocates for patients with 110 neurogenetic diseases. Dr. Bichell is part of a panel that's studying how the US Food and Drug Administration can do a better job of speeding up clinical trials and becoming more…
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🎙️ What if you could turn market chaos into million-dollar opportunities? In this episode of The RARE Agent Show , Dylan Tanaka sits down with Mike Turner, a real estate powerhouse who has mastered the art of thriving in any market. From navigating the foreclosure crisis to creating lasting passive income streams, Mike shares insider tips that ever…
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In this episode of the Rare Kidney Disease Show, a panel of nephrology experts explore the latest data on sparsentan, as presented at ASN Kidney Week 2024. Dr. Hiddo Heerspink presents a post hoc analysis of the PROTECT trial comprised of patients who achieved complete proteinuria remission. Dr. Chee Kay Cheung shares interim data from the SPARTAN …
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Part 4 of the Holiday Theme Time - January New YearIn today's episode, Mike picks The Phantom Carriage, a silent film to ring in the new year! Hosts Andrew, Rob, Eric, and Mike embark on a captivating journey back to the early days of cinema as they explore the 1921 Swedish silent film, "The Phantom Carriage." Join them as they unravel the film's p…
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Healx, which developed an AI platform to repurpose drugs for rare diseases, is among the first generation of companies built on an AI drug discovery engine. The company’s lead experimental therapy, which the U.S. Food and Drug Administration granted Fast Track designation to in October 2024, is in mid-stage development for neurofibromatosis type 1,…
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Yeerk P returns to talk about the silence about certain atrocities in the UK as well as Playtime (1967) by Jaques Tati. Follow Yeerk P on X https://x.com/PYeerkListen to Bistro Californium https://www.patreon.com/BistroCaliforniumFor Premium RC episodes and written content, subscribe to our substack https://rarecandy.substack.com/Follow Rare Candy …
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Meghan Weaver interviews Bradley Fisher, a dedicated teacher, father, and lifelong Chicagoan, about his experiences in adaptive cycling with his special needs daughter, Lillia. The discussion spans Bradley's journey from early biking adaptations for Lillia, who has GAND, to participating in inclusive bike camping adventures. They explore the proces…
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After3 years in the making, the Joint Clinical Assessment for the EU is in effect. From 12th January 2025 new cancer medicines and advanced therapy medicinal products (ATMPs) will require a JCA across all 27 member states. Join Owen and Georgie, along with guests Darren Callanan and Sam Morrison to discuss the main talking points of the JCA, and wh…
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It's early January and I'm starting a new job -- reflecting on both my early days and the days and years ahead -- while pondering what it all means with sarcoidosis lurking in the background. Show notes: Kerry Wong on The new Netflix show No Good Deed: https://sarcoidosisnews.com/columns/sarcoidosis-storyline-netflixs-no-good-deed-true-patients/ Ke…
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Building connections can feel impossible when life is alreadyoverwhelming. That’s where The Rare Life discussion groups come in. In this episode, I’m pulling back the curtain on our discussiongroups—virtual gatherings that feel more like a book club than anything else. You’ll hear from three amazing facilitators about the friendships, resources, an…
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Walt Whitman’s 1855 poem, I Sing the Body Electric, is a celebration of the human body and its intrinsic connection to the universe. During that era, scientists were just beginning to understand that humans are, indeed, electrical beings. Whitman’s deliberate use of the word "electric" in his tribute to the human body was quite remarkable, as the t…
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