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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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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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Celebration Church Rarotonga

Celebration Church Rarotonga

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Heti
 
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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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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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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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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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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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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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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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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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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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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🎙 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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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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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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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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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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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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TE BUSCO es la primera serie de Las Raras, un podcast policial en el que la periodista chilena Catalina May busca al hombre que la atropelló hace 20 años. Una coproducción con Podium Podcast. Las Raras somos un podcast documental independiente con un diseño de sonido único. Contamos Historias de Libertad. Usamos paisajes sonoros y música original. Hablamos de feminismos, medioambiente, derechos humanos, movimientos sociales y más. Encuentra nuestras primeras cinco temporadas en todas las pla ...
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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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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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When we walk in the natural realm, we don't have the strength and fortitude to face our giants. We need to live in the realm of faith so we can rise and confront our obstacles and conquer our trials. Enjoy this message by Pastor Jonathan, as he shares on how we can rise to overcome our battles. • • • • • Our heart at Celebration Church Rarotonga is…
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In this episode of the podcast we sit down with Kari Rosbeck, the president and CEO of the TSC Alliance. That’s a nonprofit dedicated to supporting people living with tuberous sclerosis complex and also driving research into promising treatment, among many other things. The TSC Alliance is also celebrating its 50th anniversary this year! Connect wi…
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Na última quarta-feira, 12 de junho, estreou o programa Pois é, Poesia: Arte no Plural, no youtube.com/@PoisePoesia .Entre muitas das atrações, a primeira edição abre com Reynaldo Bessa entrevistando o curador do Prêmio Jabuti 2024, Hubert Alquéres.Aqui, você confere um dos quadros do programa, o Fazendo Arte, que, na estreia, traz uma matéria sobr…
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#300 - We accidentally celebrate episode 300!!! Whoa. Lisa Rieffel & Zach Tinker help ring in a milestone! Thanks to everyone who has ever watched a single episode. We discuss wimpy workouts, asthma attacks, new podcast announcement, Milf Manor season 2, Naked Attraction, meeting “the one”, evil TikTok, what makes us cry, how to propose, existentia…
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If you’re thinking about traveling with your disabled ormedically complex child this summer but you don’t know what you’ll need or how to plan, we’ve got your back! In this episode, we’re sharing the top ten things youneed to make traveling just a little easier and lighter. This quick episode will make your planning process so much easier. And for …
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Superhero Summer Part 2: Sky High (2005) Rare Cuts Epic Superhero Summer Strikes back with Disney’s Sky High (2005). Eric pick the movie about a Superhero High School where Will Stronghold, son of the most famous super hero Duo, The Commander and Jetstream, is about to start his freshman year. The Movie’s all star cast features Kurt Russell, Kelly …
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Zevra Therapeutics, formerly KemPharm, rebranded itself in early 2023 following the acquisition of the experimental therapy arimoclomol for the rare lysosomal storage disorder Niemann-Pick type C. Zevra is Greek for “zebra,” a symbol of rare disease. The company subsequently built out its rare disease pipeline through the acquisition of Acer Therap…
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En este episodio de Hablemos de Varas Raras Podcast, desentrañamos el misterio de las tentaciones. Aprende sobre sus orígenes, cómo afectan nuestras vidas y estrategias efectivas para superarlas. ¡No te pierdas esta fascinante exploración sobre el poder de las tentaciones!
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We’re recapping the 2023 Nano-rare Patient Colloquium in this special “Best of” episode. For the Colloquium, we gathered the nano-rare community under one single roof for a full day of presentations and panels with experts, partners, supporters, and patients. So, we are bringing some of the top moments directly to your speakers. Discover the origin…
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En este episodio conversamos con Eduardo Pérez, un científico chileno quien se define como "empeñado en desentrañar los misterios genéticos de la epilepsia y los trastornos del neurodesarrollo". En esta entrevista llena de información valiosa, Eduardo nos cuenta cómo su trabajo de investigación en el área de la genética lo llevó de Chile a Alemania…
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Today on the Rarified Heir Podcast, we are talking to Hugo Morley, grandson of actor Robert Morley. Depending on what age you are and what country you grew up in, you might know Robert Morley for different things. If you are an American, you know him from his stint as the spokesman for British Airways or possibly the film Who Is Killing The Great C…
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Author Anna Krivolapova (https://x.com/AnaKrivolapova) joins Glen to talk about her short story collection Incurable Graphomania, Play It As It Lays, Joan Didion, paranoia, ancestry DNA testing, the decline in quality of psyops, and much more Buy Incurable Graphomania NOW https://www.amazon.com/Incurable-Graphomania-Anna-Krivolapova/dp/B0CCW2HGMXFo…
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In this episode, Dr. Dunbar Ivy, a pediatric cardiologist at the University of Colorado, discusses the upcoming World Symposium on Pulmonary Hypertension, where experts from around the world will gather to discuss the progress made and future directions. Dr. Ivy highlights the work of the pediatric pulmonary hypertension task force, which aims to d…
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One of our most influential Founding Father's died a hated man. Sometimes this Founding Father used the pen name "Amicus". When he died, only six people attended his funeral. Watch this episode to learn more and thank you for being a part of Revolutionary War Rarities. Make sure and subscribe to our YouTube Channel, subscribe on your favorite podca…
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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 Luis Posada, director de festivales literarios de La Fábrica, organizadores de la 2º Edición de Festival Fronter…
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"Hey Audrey - I’m wondering if your older grandchildren have phones and if so, if you would mind sharing what they have or use as far as restrictions?" I have been getting a lot of questions about this lately...so I grabbed some time with Maureen and she talks about how she and Jordan have made, and are making these decisions with their children. T…
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We were so blessed as a church to have Murray and Nancy Watkinson share about the power of unity and oneness. • • • • • Our heart at Celebration Church Rarotonga is that this message will greatly bless your walk with Jesus and help bring you closer to Him. We pray that you would be stirred to live a life that is passionate about loving Jesus! We wo…
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Nuevo audio dedicado a la actualidad del cine español, con análisis de 7 estrenos sin spoilers. Incluye reseñas de "Segundo premio", "La mesita del comedor", "Disco Ibiza Locomía", "Tratamos demasiado bien a las mujeres", "Un sol radiant", "El rei Peret" y "El favor". Sin spoilers. Locución de Xavier Vidal y montaje de Mayra Meza. ¡Gracias por escu…
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Send us a Text Message. Join me as I talk to Sky , mother of 3 children. about her daughter Presley's diagnosis with Malan Syndrome. Malan Syndrome is an overgrowth disorder that is considered as ultra rare. Their are only 300 cases of this condition world wide. Join me as I ask about her 8 year journey to diagnosis, Symptoms, Her role in Co-foundi…
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If you’re thinking about traveling with your disabled ormedically complex child this summer but you don’t know what you’ll need or how to plan, we’ve got your back! In this episode, we’re sharing the top ten things youneed to make traveling just a little easier and lighter. This quick episode will make your planning process so much easier. And for …
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Max Blumenthal (https://thegrayzone.com/)returns to the show to talk about Israel vs. Palestine, Stormy Daniels, Trump, Student Protests, and much more For Premium Rare Candy episodes and written content, head to our substack. Free and Paid options https://rarecandy.substack.comRare Candy Merch https://rare-candy-industries.myshopify.com/Rare Candy…
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A compelling and emotional episode that touches on the many challenges young women affected by Cancer go through. Joined by the founder of the not for profit Cancer Chicks, Michele Molnar. We have a candid conversation about relationships, emotional wellbeing, parenting, and grieving our body parts. Although Cancer can take a lot from you, Cancer C…
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For certain rare diseases, therapies derived from human plasma, the largest component of blood, represent critical lifesaving and life-sustaining medicines. In many cases, it may represent the only therapeutic option. Takeda pharmaceutical’s Plasma-Derived Therapies Business Unit works across immunodeficiencies, neuroimmunology, hematology, pulmono…
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In Episode 115 of the Sarc Fighter Podcast, Andrea Maione fights to keep things going as she deals with the aftermath of the pandemic while dealing with the increasing onset of Sarcoidosis symptoms. Show Notes Participate in the aTyr Clinical Trial: https://bit.ly/3EUOxNq More on the Efzofitimod study: https://sarcoidosisnews.com/news/benefits-seen…
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In this episode, John shares his journey of scaling up high-touch support for a small yet demanding customer in Dubai. He delves into the challenges of continuous training due to high staff turnover and how a proactive approach, involving rotating support staff, significantly reduced support requests. Key Takeaways: Proactive Problem-Solving: John …
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Today on another encore episode of the Rarified Heir Podcast, we are talking to the son of actor Albert Eisenmann. While that name might be unfamiliar to some, if you grew up in Houston in the 1960s, you KNEW Albert Eisenmann. This episode is about local television stars and as we hear from guest Ike Eisenmann, the show Cadet Don was a massively po…
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Nola Martin shares her experience with pulmonary arterial hypertension (PAH). Nola describes the physical and mental challenges she faced, including fatigue, weight gain, and the need to ask for help. Nola emphasizes the importance of self-advocacy and fighting for one's own health. She recounts a situation where she had to push her doctor to liste…
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Chema López reseña "FLEISHMAN ESTÁ EN APUROS (FLEISHMAN IS IN TROUBLE)", miniserie disponible en Disney+. Nominada a 5 premios Emmy. ¡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 colaboradores! ¡Contacta c…
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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 Miguel Munárriz, autor de “Empeñados en ser felices” (Ed. Aguilar), Daniel Sardá, director de la editorial DosMa…
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Two of my granddaughters, Claire and Grace, spent a week with us. After my recording a new podcast with their mother, Maureen, which will drop next week, I thought it would be fun to have the girls on the podcast! This week's episode is my conversation with Claire and Grace. We talked about growing up Broggi among other topics. Also, you will hear …
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Descubre los proyectos más sorprendentes y secretos de los nazis durante la Segunda Guerra Mundial. Explora las armas milagrosas que estaban destinadas a cambiar el curso del conflicto y la tecnología avanzada que desarrollaron. ¡No te pierdas este fascinante episodio de Hablemos de Varas Raras Podcast!…
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In this episode of the podcast we sit down with Ronda Thorington, the mother of child living with mixed connective tissue disease. Ronda is also a licensed professional counselor who specializes in empowering parents of children who are living with a rare or chronic diagnosis. Connect with Ronda: Website - Facebook - Instagram Editor's Note: Chroni…
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On this episode we talk to Michelle Fruhschien a mom of two, Noah and Hailey(Jordan Syndrome). The moment she was born, Michelle says she knew it in her bones that something was different about her daughter even though she didn’t start seeing symptoms for another two months. Over the next few months, Michelle spent a lot of her time googling, askin…
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