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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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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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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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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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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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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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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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Rare Cuts Media Society

Rare Cuts Media Society

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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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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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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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Mas Que Raras

BloodStream Media

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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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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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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 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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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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A podcast for parents and families of people living with rare diseases in Ontario. I Care for Rare is a social advocacy campaign, designed to give individuals, families and caregivers living with rare diseases a collective voice for system healthcare AND community support reform.
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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 ...
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Hello, welcome to A Rare Breed Podcast! My name is Avee (Aw-vee) your host. This show will bring you entertainment and enlightenment. My opinions on topics from politics, social ideology, culture, and more! I try to keep it light, sweet and to the point. I want to give you my juicy take on what is going on in the world and keep the movement of conservative's going strong. The left will not win!
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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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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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Rāroa Radio

Rāroa Radio

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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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In this powerful message, Pastor Jonathan confronts the difference between spiritual hunger and hesitancy. Whether we've been in church for a few months or a few decades, we're not called to be spectators - we're called to be on fire for Jesus! Complacency has no place in the Kingdom of God, so we must stir up our faith and reignite the fire! The c…
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Even Matt Walsh called out the ridiculous hypocrisy today over a pretty wild Senate hearing. We need to talk about the elephant in the room because Trump is going way further than most GOP media/politicians will admit! My YouTube Channel: YouTube.com/An0malyhophop My shop: DreamRare.comAn0maly által
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April is Sarcoidosis Awareness Month, and it's time to let people know that we are all "Facing Sarcoidosis Together," which is the theme for 2025. In this edition of the FSR Sarc Fighter podcast, I talk with Cathi Davis, Director of Communication and Marketing for FSR, along with fellow sarc fighters and volunteers Theresa Govan and Susan D'Agostin…
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Eric Austin, MD, MSCI discusses early detection among people who are at risk of pulmonary arterial hypertension (PAH), particularly those who would have genetic susceptibility, or who may have congenital heart disease, or who may have connective tissue disease or other features that would make them more at risk of developing pulmonary arterial hype…
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Möödunud aasta oktoobris esietendus Tartu Uues Teatris koosloomemeetodil valminud lavastus “Abrakadabra”, mille alusmaterjaliks on väljamõeldud sõnade sõnastik. Prooviprotsessi käigus jäi sõelale 28 keeleuuenduslikku sõna ja definitsiooni, mis ka eesti keelde tõlgitud said. Ähmaste tunnete tõlkimisest nii keelde kui teatriruumi räägib lavastaja Joh…
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Tehisarud on korraga kõikjal. Kontoris ja internetis, külmkapis ja kempsupotis. Suured keelemudelid ja pildirobotid, rääkimata tillukestest arumutukatest kujundavad meie igapäevast käitumist juba praegu, ilma et sellest alati arugi (!) saaksime. Kas kirjanik peaks kartma, et tehisaru temalt ta töö ära võtab? Võibolla, aga kas ka eesti kirjanik kart…
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Ajal, kus raamatupoodide letid on täis aina kirjumaid teoseid, on raske noorel selles virvarris orienteeruda. Valik on küllastunud, kuid tase annab tihti soovida. Tänu nutiseadmetele on aga meie ees valla uus ja huvitavam maailm, kus tarbitakse, sotsialiseerutakse ning tekib kõnekeel. https://www.rara.ee/sundmused…
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Kui tahame eesti keelt hoida, oleks hea mõtiskleda selle kahele peamisele väljendusvormile: kõnekeelele ja kirjakeelele. Tundub, et mõlemat on vaja hoida, aga ka teineteise eest teatud piirini kaitsta. Eriti oluline on kõne- ja kirjakeele vaheliste ühenduste ja pingete küsimus ilukirjanduse taustal, sest ilukirjandus on see koht, mis on võimeline a…
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There were many consequences of the American Revolution, some of which we experience to this day. Join us on this week’s episode of Revolutionary War Rarities as we explore some of those consequences. Make sure and Subscribe to our YouTube Channel and click the bell, follow us on Instagram, join our Facebook Group, and subscribe on your favorite po…
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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 Intereconomía, dirigido por Andrés Sánchez-Magro. En esta ocasión tendremos, e…
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"Eu sempre dizia pro Márcio Borges que eu tocava baixo e cantava, mas não era compositor. Ele não aceitava muito. Um dia nós fomos assistir o filme Jules et Jim no cinema, eu fiquei fascinado pela música e, logo na sequência, já entramos na próxima sessão. Assistimos ao filme várias vezes no mesmo dia, me inspirei naquele amor e amizade e logo depo…
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Dionar Hidalgo y Xavier Vidal comentan las polémicas de los Óscar de los últimos 10 años. Hablamos del Oscarssowhite, el Me Too, el lío de sobre entre Moonlight - La La Land o los escándalos de Will Smith, Andrea Riseborough o Karla Sofía Gascón. ¡Acompáñanos! Redes sociales: @CinoscaRarities Blog: https://cachecine.blogspot.com.es/ Correo: cinosca…
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Title: Intro to FSGS Episode Description: In this episode of the Rare Kidney Disease Show, Howard Trachtman, Adjunct Professor of Pediatrics at the University of Michigan, and Chris Gisler, medical director at Travere Therapeutics, explore the complexities of FSGS, covering its pathophysiology, classifications, and clinical presentation. They discu…
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Cody LaDuke joins the show to talk about the life and career of Roman Polanski. Part one covers Polanski's childhood in Poland, Rosemary's Baby (1968), the murder of wife Sharon Tate, all the way up to Chinatown (1974). Part 2 will come out later this week.Follow Cody LaDuke on X x.com/cladu33Rare Candy Premium Episodes available here (40% off unti…
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When the systems your child depends on are under threat, it doesn’t feel political—it feels personal. In this episode, Madeline and Alyssa unpack the deep unfairness of having to constantly justify your child’s worth while watching essential supports unravel in real time. They also discuss the fury that bubbles up when people call your fear “politi…
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In this week's episode of Rarefied, host Meredith Meeker delves into the fascinating world of the American Eel. Despite its slimy and elusive nature, the American Eel is a remarkable and critical species. Meredith is joined by Chris Bowser, Education Coordinator for the New York State Department of Environmental Conservation, who shares his extensi…
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“No sertão da minha terra Fazenda é o camarada que ao chão se deu Fez a obrigação com força Parece até que tudo aquilo ali é seu Só poder sentar no morro E ver tudo verdinho, lindo a crescer Orgulhoso camarada De viola em vez de enxada" (Morro Velho - Milton Nascimento) No documentário MILTON BITUCA NASCIMENTO, dirigido por Flavia Moraes, há muitas…
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Netherton syndrome is a rare and chronic skin condition. One in ten infants with the disease will die as a result of infections and related complications. Azitra has developed a platform for engineering bacteria that naturally colonize the skin to produce proteins with therapeutic benefits to treat Netherton syndrome and other conditions. We spoke …
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En este episodio de Mas Que Raras contamos con una invitada excepcional: La Dra. Pam Pojomovsky McDonnell, destacada médica en la división de neurología del Hospital de Niños de Filadelfia (CHOP). Nacida en Buenos Aires, Argentina, la Dra. McDonnell nos habla de su increíble trabajo de investigación en epilepsia y neurogenética, y de cómo su experi…
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This week on the podcast, you will hear my conversation with our oldest grandchild, Jack. He is 18 and a freshman at UGA. His mom is Maureen, one of the RBR girls, and his dad is my second son, Jordan. I asked Jack if I could interview him and he graciously agreed! I hope you moms of boys especially enjoy listening and that you are encouraged. His …
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Today on the Rarified Heir Podcast, we are talking to Michael Rivers, son of rock n’ roll icon Johnny “Secret Agent Man” Rivers. Retired and in great health at age 82, Johnny Rivers has lived many lives as one of the groundbreaking musicians in the LA music scene since the early sixties. From session man to Sunset Strip headliner to #1 recording ar…
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In this week’s message, Zachary Cargill shares a powerful word about the glory, majesty and awe of our God. Daniel 7 and Revelation 4 give us a picture of what our Lord truly looks like in His glory. This message challenges us to move beyond casual Christianity and live with pure devotion - is Christ truly our solid Rock, or is He a stepping stone …
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Kristin Highland, MD, from the Cleveland Clinic discusses the importance of shared decision-making and patient preferences when treating patients with pulmonary hypertension. Dr. Highland, emphasizes that the patient is the true expert on their own body and that it is crucial to understand their perspective when making treatment decisions. She high…
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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 Intereconomía, dirigido por Andrés Sánchez-Magro.…
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Mayra Meza y Xavier Vidal comentan las 5 ganadoras del Óscar a la mejor película favoritas de los oyentes: "El retorno del rey", "Million Dollar Baby", "Birdman", "Parásitos" y "Oppenheimer". Repaso a 25 años de premios Óscar. ¡Acompáñanos! Redes sociales: @CinoscaRarities Blog: https://cachecine.blogspot.com.es/ Correo: cinoscararities@gmail.com E…
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Our monthly scheduled horse sesh with the Agitator bros. Covering Giza Pyramid developments, Napoleon, and groundbreaking certified hood classic Snow on Tha Bluff (2012). Pre Order Gods Fare no Better by J David Osborne https://ronintrash.bigcartel.com/product/gods-fare-no-betterListen to Agitator https://www.patreon.com/agitatorGet 40% off of Rare…
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In this episode of 'Rarefied,' host Meredith Meeker revisits the past 14 episodes to reflect on the conservation efforts for some endangered and imperiled species across North America. Starting with the central theme of habitat loss and delving into issues like diseases, pests, recreation, and climate change, the episode intertwines powerful succes…
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There are certain moments that never leave you—the sight of your child turning blue, the smell of hospital-grade hand sanitizer, the feeling of helplessness as doctors take over. Medical trauma doesn’t just happen to our kids. It happens to us too. In this episode, therapist Rosey Schaefermeyer joins us for a deep dive into how medical trauma shape…
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Antonio Carvalho nasceu em 21 de março e faria 79 anos se estivesse vivo. Para homenageá-lo, relembre uma edição do quadro Interferência, produzido por mim em 2015, para o antigo "Você é Curioso?", da Rádio Bandeirantes. Em destaque, o programa Bandeirantes Frequência Balançada, que foi conduzido por Carvalho. Um programa de AM que antecipou muito …
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Part 2 of Rowdy Roddy Piper In this episode of Rare Cuts Media Society, Andrew Picks our Second Rowdy Roddy Piper movie as they delve into the classic 1988 film "They Live." This month, the team is continuing their exploration of Rowdy Roddy Piper's cinematic ventures, following their previous look at "Hell Comes to Frogtown." They discuss the film…
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Emerging cell and gene therapies represent areas of great promise for people with rare, genetic diseases, but the translation gap for these medicines can leave them stalled at the lab. Mass General Brigham in 2022 launched the Gene and Cell Therapy Institute, a research hub dedicated to advancing gene and cell therapies for various diseases to brid…
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Our bodies are like bustling cities of cells, always chatting and working together. They don’t just send long-distance messages to organs—they also gossip locally, getting nearby cells to spring into action. Juxtacrine communication is like a handshake between cells—they have to be up close and personal to pass the message along! Unlike long-distan…
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hi hello hey, ready to rock out at a concert? It’s no secret that we love music, especially seeing the artists we love live. This week, we answer a listener question from Delaney, a loyal fan of Jesse McCartney, about shows we’ve seen, artists we’ve met, and accommodations we’ve either requested or made ourselves to make the most of our show experi…
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Special guest Sarah Funke Butler (funkeliterary.com) joins Jeremy and Michael to discuss a fascinating and newly unearthed trove of letters from Ernest Hemingway to the groundbreaking journalist Lillian Ross. You think you knew everything about Hemingway? Well, think again - this collection of letters has forced us to reconsider our understanding o…
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In January, my daughter asked me to share 1 Timothy 3:11 with a group of women in Raleigh, North Carolina. As I walked through the qualifications for deacons' wives, I shared some principles for ALL wives. Husbands need wives in ways that they might not fully understand. God calls men to lead, provide, and protect. Sometimes they do that as pastors…
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Today on another edition of the Rarified Heir Podcast, we are Jason Everly, son of Phil Everly of the famed Everly Brothers. We connected with Jason after listening to his radio show on Sirius XM satellite radio on the Fifties Gold channel. It sparked a memory that Jason and host Josh Mills had attended the same middle school together at the Oakwoo…
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Pastor Jonathan continues to share on the spirit of abdication and brings out biblical examples to provide keys on how to overcoming this spirit. Abdication leads to us avoiding the real issues, never taking responsibility and sulking when things don’t go our way. We can see this with King Ahab, who abdicates his role and allows Jezebel to take con…
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Send us a text Guest: Khartik Uppalapati, Co-founder of RareGen Youth Network Episode Description: In this episode of Rare Connection, host Joanna welcomes Khartik Uppalapati, a remarkable young leader at the intersection of biomedical research and rare disease advocacy. Khartik shares his personal journey with rare conditions, which ignited his pa…
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Jimmy Ford, MD discusses the 7th World Symposium on Pulmonary Hypertension and his work on the Exploring the Patient Perspective in PH Task Force. Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Follow us on social @phaware Engage for a cure: www.phaware.global/donate #phaware Share your story: info@phaware.com …
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The Foundation for Sarcoidosis Research recently awarded two grants to further our knowledge of cardiac sarcoidosis. One of them went to Dr. Ravi Karra, MD, MHS, Associate Professor of Medicine and Pathology at Duke University. Dr. Karra is investigating what causes cardiac sarcoidosis, and the best way to treat it. He joins me on the Sarc Fighter …
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Send us a text Guest(s): Allison & Elizabeth Episode Summary In this episode of Rare Connection, I’m joined by twin sisters Allison and Elizabeth, who both have familial Cerebral Cavernous Malformation (CCM)—a rare genetic condition that causes clusters of abnormal blood vessels in the brain and spinal cord. They share their personal diagnosis jour…
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