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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.
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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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RareErth Podcast explores work, creativity and entrepreneurship. Over the years we’ve all found ourselves asking that question, “What am I passionate enough about to take risks for?” RareErth podcast is a collection of insights and conversations with some of those who have heeded their creative spirit or entrepreneurial calling. Learn more at https://www.rareerth.com
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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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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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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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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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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 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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A journal through my 20’s.. for everyone seeking to Live unapologetically. On RaRa, we have weekly laidback and chill conversations about matters affecting the millennial youth, ranging from Faith, Love, Relationships, Sexuality, Career choices and everything in between. Let’s become better versions of ourselves together. Reach out to me via rarathepodcast@gmail.com Instagram @zubbey. Love & Light.
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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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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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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. Support this podcast: https://podcasters.spotify.com/pod/show/rareformradio/support
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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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Join us for a one-hour rare disease community support group. Here we will discuss the topics that affect your daily life in rare diseases as well as special needs. Being a parent is hard but having a child in rare disease takes a special kind of person and the journey is filled with potholes along the way. The pathway may never be clear, but together we can navigate by supporting each other. P.S. we are not a glum lot!
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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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Rarzclothing - Trending Fashion In the USA. Rarzclothing is a global online store, where people come together to buy and collect unique items at low prices cost. Contact Info: Website: https://rarzclothing.com/ P: (SMS text recommended) +1(951) 236-0707 E: support@rarzclothing.com A: 2880 Stevens Creek Blvd, San Jose, CA 95128, United State Hastags: #rarzclothing
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🎙 Welcome to Rarified Air: Stories of Inspired Service, a podcast that takes you on a journey into the DNA of InterSystems. I will be your guide as we explore how our unparalleled commitment to customer service fuels limitless human potential. 🤝 Join us as we dive into the culture of InterSystems and share the stories of the people who make it all possible - our customers, partners, and employees. From helping healthcare providers improve patient outcomes to powering the world’s most importa ...
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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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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.
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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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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 ...
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RareWine Podcast - Viden om vin

RareWine Podcast - Viden om vin

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Lær mere om vin og vinens forunderlige verden mens du er på farten - dét er præmissen for denne, ikke helt traditionelle, podcast udgivet af RareWine Group. Vi har kombineret podcastformatet med det bedste fra lydbøger. Således kan du her finde vores yndlingsartikler og portrætter om de største producenter og de mest populære vinområder serveret i en række korte podcast-episoder, som du kan lytte til mens du er på farten. Bliv klogere på selveste Domaine de la Romanée-Conti, lær om hvorfor C ...
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Teología bíblica, que se desprende de confesiones denominacionales y sistemas teológicos a través de la exposición del contexto original del cual las Escrituras son producto. El contenido presentado se basa en el material del Dr. Michael S. Heiser y forma parte de las iniciativas oficiales para extender su legado.
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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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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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Before she had her son, Serena was already a pediatric SLP, business owner, and disability advocate who spent her time empowering families to understand and become more comfortable with their children’s disabilities. So, she was prepared for anything, or so she thought. But as it turns out, no amount of education or experience can prepare you for t…
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As genetic testing continues to expand, it is bringing into focus a shortage of genetic counselors who can work with patients to explain results and answer questions. Igentify is helping genetic counselors manage more patients by providing an AI-based platform that can take some of the load off of them by helping onboard patients, obtaining consent…
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Join us for the second episode of Rare Matters, where we delve into the crucial yet often overlooked topic of medical gaslighting. In this episode, we uncover what medical gaslighting entails, shed light on its subtle manifestations, and equip you with the tools to identify and combat it. Through insightful discussion and a compelling personal narr…
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Overview: In this episode of the Rare Kidney Disease Show, Professor Jonathan Barratt discusses the need to take a long-term approach when managing IgA nephropathy patients. He presents data from the UK National Registry of Rare Kidney Diseases (RaDaR). During this recording you will hear Professor Barratt discussing the continued risk of progressi…
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Dionar Hidalgo y Xavier Vidal comentan las películas del FESTIVAL DE CANNES 2024. Repasamos la sección oficial, Una cierta mirada, Quincena de realizadores, Semana de la crítica y proyecciones fuera de concurso. Todo sobre el festival francés, en nuestro pódcast. ¡Gracias por darle al play! Redes sociales: @CinoscaRarities Blog: https://cachecine.b…
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Today on another encore edition of the Rarified Heir Podcast we are talking to Charlie Matthau, son of actor Walter Matthau. We spoke to Charlie about his amazing father & their special relationship but also his incredible mother, actor/author Carol Matthau. We quickly learn that she was (wait for it), the basis for Truman Capote’s Holly Golightly …
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Glen and Psi talk about Bob Marley, 420, another self-immolation, The Barefoot Contessa, Flint Dibble vs. Graham Hancock, Snowden/Assange, Women's sports, and more Rare Candy Premium Episodes https://rarecandy.substack.com/Merch Store https://rare-candy-industries.myshopify.com/Rare Candy on Apple, Spotify, Rumble, Youtube, X, Instagram https://bea…
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Voor de recreatieve drugs- en drankgebruiker was de Romeinse tijd een walhalla! Alles was legaal. Geen war-on-drugs, laat staan (lokale) machthebbers die drugs uit de criminaliteit wilden halen. Zolang je je maar gedroeg, mocht alles bij de Romeinen. Olivier gebruikt zelf nauwelijks, maar weet wel waar de Romeinen hun drugs haalden. En oh ja, we he…
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Gina Mundy is an attorney specializing in childbirth cases. For over 20 years, her focus has been investigating and analyzing mistakes that arise during labor and delivery. She has spent countless hours meticulously scrutinizing childbirth cases, conducting interviews with delivery teams, and thoroughly examining medical records to understand every…
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In this episode, Joellen Brown shares her experience with pulmonary hypertension (PH) on the 15th anniversary of her diagnosis. Joellen was born with a hole in her heart and had her first open heart surgery at the age of two and a half. She believes she may have had PH since birth, but was not aware of it due to limited research in the 1950s. Joell…
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Joining me today on the FSr Sarc Fighter Podcast is Sanjay Shukla, CEO of aTyr Pharma. Sanjay returns to the podcast with a promising update on Efzofitimod, the most promising candidate to become the first drug developed specifically to fight sarcoidosis. Sanjay joins the podcast from Brazil, just one of the countries around the world, where the dr…
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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 e ediciones raras o limitadas. En esta ocasión tendremos a Aldo García Arias, gerente de librerías Antonio Machado (Plaza de las Salesas 11 y C/ Marqués de Casa Riera 2, e…
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The only way a couple can truly live "happily ever after" is if they live their lives in obedience to the Lord. The bride has learned her loyalty is to her husband, and she wants everyone to know. She wants the world to know there is no way any other man can get to her, can steal her heart, and steal her affections. She stands with her husband, no …
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Vanad sõbrad Gert Kiiler ja Martin Algus ajavad arukat juttu, et kuidas on parimas loomingulises eas elada ja olla. Kirjasõnas, telepildis ja muus maailmas. Huvid ja hobid ja pudipadi ja päevatöö pealekauba. Vestluse juhatab sisse Eesti Rahvusraamatukogu kultuurinõunik Karl Martin Sinijärv. Gert Kiileri sulest on tulnud nii kriminaalromaan „Eranuhk…
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Xavier Vidal reseña el clásico "HERMANOS DE SANGRE (BAND OF BROTHERS)", serie disponible en HBO Max y Netflix. Ganadora del Globo de oro, Emmy y PGA. ¡Gracias por darle al play! Redes sociales: @CinoscaRarities Blog: https://cachecine.blogspot.com.es/ Correo: cinoscararities@gmail.com Escúchanos en Spotify, Ivoox y Apple Podcast ¡Buscamos colaborad…
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Introducing the inaugural episode of Rare Matters Podcast, where host Mikey Stone courageously delves into his personal odyssey living with an undiagnosed rare disease. In this groundbreaking debut, Mikey offers an intimate glimpse into his profound medical journey, unraveling the complexities of his diagnosis quest like never before. Through candi…
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I saw Patrick Bet David & Jason Whitlock taking jabs at each other and I felt inspired to weigh in because this feels like the fundamental disagreement I have with the current Republican Party media apparatus. All My Links (Music, Support, YouTube, Shop) DreamRareLinks.com저자 An0maly
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Friendship, especially with those who don’t have disabled children, gets more complicated once you’ve had your own child with disabilities. It’s not necessarily fair, but it doesn’t change the fact that we often end up interacting differently with friends we had before our children were born. In this episode of The Rare Life, I’m joined by Jillian …
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Duchenne muscular dystrophy is an inherited disease caused by genetic mutations that no longer allow the dystrophin protein to function properly. It turns out that dystrophin not only plays a role in muscle fiber, but in muscle stem cells as well and is critical for regeneration of muscle tissue. Without dystrophin, people with Duchene suffer progr…
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On this episode of Raising Rare we talk with Stacy Lloyd, a rare disease patient and board certified patient advocate. Stacy has dedicated her life, even much of her free time to healthcare in one way or another. She currently works at the American Medical Association, previously at Saavy Co-op, and is on the board of the VHL Alliance. After being …
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Research physicians and their associated institutions are monumental to the mission of the n-Lorem Foundation and are truly transformational to the lives of the nano-rare patients they treat. Olivia Kim-McManus, M.D., was one of four physician panelists at our first Colloquium who participated in "A Physician's Perspective on n-Lorem and Nano-rare"…
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Guillermo Navarro y Xavier Vidal repasan la historia de los Premios Platino. Además, reseñamos las películas de esta edición y hacemos quiniela de la gala del 20 de abril. ¡Gracias por darle al play! Redes sociales: @CinoscaRarities Blog: https://cachecine.blogspot.com.es/ Correo: cinoscararities@gmail.com Escúchanos en Spotify, Ivoox y Apple Podca…
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Join me for an incredibly real chat with Priyanka Raghuvanshi, an artist who's not afraid to be herself. Priyanka opens up about her wild ride, from studying the mind to trying out different jobs before realizing art is her true calling.She drops some serious truth bombs about how important it is to ask questions, even if it makes you look silly. P…
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hi hello hey, it’s springtime, which also means we get to recap one of our favorite things: the annual Hermansky-Pudlak Syndrome family conference! Back in 2021, we explained this very unique conference before back in episode 16 (!), so we recommend giving it a listen if you haven’t already. We love to recap these special times together like we did…
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Today on part two of the Rarified Heir Podcast, we continue our conversation with Patti Weidenfeld, daughter of stand-up comedian Pat Cooper. If you heard part one of our conversation last week, prepare yourself for part two because the second half of Patti’s story is unlike anything you have ever heard before. An idyllic life as the only child of …
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Goed om te weten: deze aflevering is opgenomen voor de aanval van Iran op Israël. Om maar gelijk met de deur in huis te vallen: de Grieken voerden meer oorlog dan de Romeinen. Hoe dat zit hoor je deze aflevering. Olivier Hekster vertelt verder dat 'vrede' in Rome iets anders is dan dat we nu bedoelen met vrede. En we hebben het over speren gooien i…
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In this episode, Chelsea Price shares her experience living with pulmonary arterial hypertension (PAH). She emphasizes the importance of having a good support system, including her church community and connecting with other friends with PAH. Chelsea is grateful for the good days she has and strives to be an active mom for her children. Discover eve…
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Sharon Hesterlee, PhD, chief research officer at the Muscular Dystrophy Association, about the recent proliferation of gene therapies and other treatments for neuromuscular diseases.저자 Rare Care Podcast
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Music has always played an important role throughout the history of this nation and the Revolutionary War was no different. This week’s episode of Revolutionary War Rarities focuses on one song which was intended as an insult to the Colonial Soldiers, a song that many of us grew up singing. Make sure and watch by clicking on the picture below and t…
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Though weddings are beautiful, they are not nearly as beautiful as a marriage that has stood the test of time and commitment. Real beauty emerges after some heartache. Real beauty is when a couple is still dancing after 25, 35, 45, 65 years together. Real beauty emerges when they are forgiving of each other's sins, and when they don't see ugly, eve…
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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 e ediciones raras o limitadas. En esta ocasión tendremos a Pedro Valverde Ogallar, jefe el área del libro y la lectura de la Subdirección General del Libro de la Comunidad…
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Dubbed the man who died twice and Hod brought back to life, Kevin Hills Story appears in 45 national and international Newspapers and Magazines. Listen along as I talk with Kevin about his medical conditions Calcifylaxis and Multiple Endocrine Neoplasia Type 1(MEN1). You can see the full video on YouTube on my channel Rare Chef also as well as many…
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Coincidiendo con el fallecimiento de O.J. Simpson, rescatamos la reseña de Xavier Vidal de la serie documental "O.J.: MADE IN AMERICA", título disponible en Disney+. ¡Gracias por darle al play! Redes sociales: @CinoscaRarities Blog: https://cachecine.blogspot.com.es/ Correo: cinoscararities@gmail.com Escúchanos en Spotify, Ivoox y Apple Podcast ¡Bu…
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Jeremy Loffredo returns to the show to talk about his latest trip to Israel, Rabbi Shmuley, Candace Owens and Ben Shapiro, Diddy/Jay-Z, Trump, Electoral Politics, and much more.Follow Jeremy Loffredo on X https://twitter.com/loffredojeremyFor Premium Rare Candy Episodes and Written Content https://rarecandy.substack.com/Rare Candy on Apple Podcasts…
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In this episode of the podcast we talk with Drs. Julie Gerberding and Courtney Silverthorn from the Foundation for the National Institutes of Health (FNIH). They're bringing us updates on the Bespoke Gene Therapy Consortium's new regulatory playbook that is designed to help get certain types of genetic therapies for rare diseases approved and avail…
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