Podcast by Rare Candy
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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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We’re bringing you a slice of our lives through humor, tears, drama, games & pop culture, where trying to stay on topic is only half the fun! Join us!
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Karena menulis dan merekamnya dengan suara adalah cara mengabadikan sebuah kenangan yang telah usai. Support this podcast: https://podcasters.spotify.com/pod/show/heirare/support
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Rare Disease Advisor's Rare Care Podcast features exclusive interviews with experts and stakeholders from the rare disease community.
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Welcome to the Dream Rare Podcast! An audio experience aiming to lift you up, make you laugh & help you get healthier all while bringing you some of the best news analysis on Earth.
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Matt Condon and Jonathan Mann explore what it means to own things on the blockchain and beyond.
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Welcome to Jacqueline Rare Antique (http://jacquelinestallone.com), the premier destination for antique collectors! Check Images: Jacqueline Rare antique Pin: https://www.pinterest.com/jacquelinerareantique/ FB: https://www.facebook.com/jacquelinerareantique/ TW: https://twitter.com/jacquelinerare Ins: https://www.instagram.com/jacquelinerareantique/
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Welcome to 'My rare disease' podcast. This is a platform where I raise awareness of something that affects 1 in 15 people, rare disease. By chatting to patients, health professionals and advocates, we talk about all aspects of rare disease including relationships, mental health and much more. I cannot wait for you to hear some truly inspiring stories from some absolutely amazing people. From being diagnosed with a rare disease myself at 10 weeks old, it has given me the motivation to give ot ...
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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/podcasts
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A monthly podcast highlighting the most important news developments and its impact on the orphan drug, cell and gene therapy world. Visit www.partners4access.com/podcasts/955180
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The Rare Elements Sports Cards Podcast


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The Rare Elements Sports Cards Podcast
Aaron Hernandez & Jeremy Aragon, Sports Card Hobbiests, Collectors and Podcasters
We discuss the sports card hobby with our own unique takes and authentic reactions to sports card news!
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General talking of jujitsu jokes movies , music health and mind set ,fitness normal chit chat also looking at my record collection and living in my local community chatting to friends and the wife at some point and anyone who drops in at my secret matted training area The Ninja Loft . .
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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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Welcome to A Podcast of Rare Antiquities! Host’s Harry and Geoff discuss and analyze film and television shows. This podcast mainly delves into more obscure and forgotten films but latest releases are sometimes covered. We hope this is the rare antiquity you are looking for.
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@ericseverson (dj 3r0ck) - deep house, 90s hip-hop, rare grooves


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@ericseverson (dj 3r0ck) - deep house, 90s hip-hop, rare grooves
Eric Severson
Continuous mixes of deep house, 90s hip hop and other groovy goodness...
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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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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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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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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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Podcast by rarebirdlit
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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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Patient Empowerment Program: A Rare Disease Podcast

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Patient Empowerment Program: A Rare Disease Podcast
n-Lorem Foundation
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


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I'm Aware That I'm Rare: the phaware® podcast
phaware global association
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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Podcasts to help business owners accelerate growth and sell their companies for maximum value. Episodes hosted by the team at RareBrain Capital, a leading M&A Advisory. Presenters explore all aspects of growing a business, tackling common performance problems, and selling a business for highest value.
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Conversations started by The Whitworth Group
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Facts are facts if you would like to share your story or be apart of the podcast email me at 1allmostrare@gmail.com
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Funny in Spanish Cover art photo provided by Nahil Naseer on Unsplash: https://unsplash.com/@nahilnaseer
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Welcome to the VeryRarePodcast
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New Simplicity Channel. Robert Bonet's Music No Published
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Every beginning carries within it the seed of its own destruction.
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"Rare & Scratchy Rock 'N Roll" is a rockumentary podcast series that tells the greatest rock and roll stories on record. This includes the untold tales of some great hits that time forgot, but maybe you'll still remember. These programs are hosted by Radio Dave, a veteran disc jockey and published authority on rock and pop music history. He draws his "Rare & Scratchy Rock 'N Roll" stories from his "groove yard," an archive that has more music than most record libraries.
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Funny and........ N O T H I N G
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A series of eclectic mixes from my vinyl record collection- check for regular updates and downloadable classics.
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Two girls dropping gems in all areas of life! From your social to your personal life hopefully what we talk about can help you!
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"Medium Rare is a brand-new talk show podcast from the minds behind G33k P0p. Join us every fortnight for discussions of topics that we think are interesting, regardless of if it's what you want to hear"
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Forty Fivan is a San Francisco based DJ & record collector, highly regarded for his creative mixes, and deep collection of rare Brazilian vinyl.
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This is a podcast tutorial
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Stories and Testimonies about 22Q11.2 and all rare and not so rare disorders and causes
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The home of Schwarzenegger Watch Together, the podcast that chronologically critiques the career of actor, bodybuilder, politician and American hero Arnold Schwarzenegger, and other projects
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A platform that discuss current Topics as well as promote Upcoming Underground Artist And the #1 Goal is to Appreciate the “ REAL” because it’s Rare
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Entertainment jokes life real life
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This podcast covers everything from sex, love, lifestyle,career,health, beauty fashion and relationships with other people and more importantly with yourself .
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RF is devoted to experimental, electronic, noise, improv, electro acoustic, avant-pop, and out-there music. Strange sounds, lovingly presented.
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Dream Rare Podcast by An0maly


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BLM 8.5 Million Deficit Despite Millions In Salaries, Conservatives Possibly Win Against Target & How People Do More Than Politicians.
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Main Kemudian
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Hope you enjoy the Friday show! Secret Episode soon on http://Patreon.com/RareTalk My shop with new merch: http://DreamRare.com Telegram chat: https://T.Me/DreamRareChat Free Email List (Sign up!): https://StayInTouchWIthMe.com Links to my music & channels! Https://DreamRareLinks.comOleh An0maly
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My rare disease


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Koolen-de Vries Syndrome - Becky
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Rare Form Radio with Dan Cleary


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#233 - Too Tight, Too Tired
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#233 - Dan is marrying Sydney Sweeney. Heidi Van Hutchence. Great author, bad wife. Meeting Australian RFR fans! Opening wild presents. Adopting local accents & sayings. Perverted hotel worker. Listener voicemails. Conjoined twin love lives. --- Support this podcast: https://podcasters.spotify.com/pod/show/rareformradio/support…
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The Rare Life


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Confessions of a NICU Nurse w/ Sam Keirsey, RN BSN (Rebroadcast)
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NICU nurses do what we just can’t do for our babies—and that in and of itself is magical and special and makes me over-the-moon grateful whenever I think about it. And while I’m grateful for all nurses that care for my son, there are certainly nurses that are better at their jobs than others. Better at loving, better at caring, better at making the…
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The Rare Elements Sports Cards Podcast


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Episode 93: Fanatics Keeps On Eating!
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In this episode we talk about Fanatics acquiring PWCC, the Drew Jones Bowman 1/1 auto gets pulled, the Greeley Card Show recap and so much more! Check out the YouTube channel and come and interact with us in our socials! Instagram: https://www.instagram.com/rare_elements1/ Twitter: https://twitter.com/RareElements1 Facebook: https://www.facebook.co…
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Rare with Flair


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69. cass & case’s cartoon adventures
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hi hello hey, cuddle up and grab your remote (or streaming device), and let’s watch some cartoons! Case + Cass getting cozy with pizza, 2023Oleh Casey Greer & Cassandra Mendez
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Rare Candy


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Jing w/ Rehmannia Dean Thomas
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Taoist herbalist, Rehmannia Dean Thomas returns to the show and discusses with Glen and Psi how his tonic herb formulas have helped their lives. Also are mushrooms estrogenic? Do they help with alcohol cravings and other vices? Link to purchase Rehmannia Dean Thomas' products https://rdeanthomas.com/Listen to our premium feed for more great content…
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I'm Aware That I'm Rare: the phaware® podcast


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Episode 416 - Katharine Clapham, MD
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Katharine Clapham, MD is an Assistant Professor in the Division of Cardiovascular Medicine at University of Utah Health. @UofUHealth In this episode, Dr. Clapham discusses methamphetamine-associated pulmonary arterial hypertension. Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Follow us on social @phaware Enga…
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Hei Rare


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Referensi Mantra Ketika Kamu Lelah
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Manusia dirancang untuk terluka. Setiap hari manusia terluka. Terluka, adalah tanpa bahwa manusia itu Masih hidup di dunia.--- Support this podcast: https://podcasters.spotify.com/pod/show/heirare/support
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Rare Care Podcast


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79: An Interview With DMD Patient Advocate Christopher Curran
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Christopher Curran, who along with his wife, Jessica, founded Kindness Over Muscular Dystrophy to advocate for patients like their 12-year-old son, Conner, who has Duchenne muscular dystrophy.Oleh Rare Care Podcast
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Jacqueline Rare Antique


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15 Rarest And Most Valuable 2 Dollar Bills Worth Money
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In the year 1862, the first 2 dollar bill was printed with the portrait of Alexander Hamilton, statesman and founding father of the United States of America. Many now living in the United States do not know Alexander Hamilton, except if you are a history buff. Strangely, $2 bills are unfamiliar to some too. According to Business Insider $2 dollar b…
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Cristol Barrett O’Loughlin, founder of ANGEL AID CARES, was a caregiver to 3 of her brothers early in her life; now she works to care for caregivers. Cristol is focused on the mental health and wellness services of caregivers within the rare disease community, her lived experience created a passion to help. In this episode Cristol talks about the g…
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Patient Empowerment Program: A Rare Disease Podcast

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One Year Anniversary: It Takes a Rare Community
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May marks a year of podcasting for us, and we’re thankful for all those who have participated and the growing number of people who have listened to the podcasts. We are pleased with the overwhelming support for the podcast and the willingness of our partners and patients to share their stories. We launched our Patient Empowerment Program with the p…
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“Above all, keep fervent in your love for one another, because love covers a multitude of sins.“ 1 Peter 4:8. What does this mean? How do we cover sin? And what does it mean to rejoice with the truth and how do we practically believe the best about others? I hope you will be encouraged as you listen to the third part of Biblical Love.…
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Amazing to have Pete Robson from Parestra Poole Bjj to come over the loft have a chat about himself his gym and the BudabashoOleh The Rare Savage
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What's up everybody and welcome to a very special episode of Rare Frequency as we celebrate our one year anniversary! This episode contains raw footage of a random conversation had within the past year that you DON'T wanna miss! Thank you to all of our listeners and we hope you enjoy this very special episode!…
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Rare Cuts Media Society


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Movie - Anvil: The Story of Anvil
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Part 4 in the Biography Series! In this episode, we explore the cult classic documentary film "Anvil: The Story of Anvil," released in 2008 and directed by Sacha Gervasi. (Rob's Pick for the month) The film follows the Canadian heavy metal band Anvil, who were pioneers in the genre in the 1980s but struggled to achieve mainstream success. Through i…
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RARECast


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How One Foundation Is Laying the Groundwork to Advance Treatments for an Ultra-Rare Disease
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A week before Deborah Ondrasik’s daughter Gabrielle turned 1, she suffered her first seizure. Within a year, Gabrielle was diagnosed with CACNA1A-related disorder, a rare, neurodegenerative condition. At the time she was the eighth known person to be diagnosed with the disorder. We spoke to Ondrasik, who is a pediatrician, along with CACNA1A Founda…
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@ericseverson (dj 3r0ck) - deep house, 90s hip-hop, rare grooves


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(Deep House) - May DEEP 2023 @ericseverson
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Going DEEP in this mix with some old and new tracks and classics for your eardrums. Get deep and enjoy!
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The Rare hour with Christopher Velona


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Rare thoughts on the #Rarewarrior 5 x 5 challenge!
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In this episode, we break down all of the sponsors and the fun day for the second, annual Rare warrior 5 x 5 challenge
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A Podcast of Rare Antiquities


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Episode 37: Can’t Buy Me Love (1987)
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Can you buy love, or at least a quick way up a clique ladder? A socially inept, lawn-mowing teenager puts that theory to the test. Does his experiment pay off? Harry and Geoff dive into the morality and discuss any resulting consequences as they review the 1987 romantic comedy, Can't Buy Me Love. #APodcastofRareAntiquities #CantBuyMeLove #movies #m…
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Digitally Rare


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Is This Good Material? BINGO w/ Kevin Esherick
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We learn about the latest artistic additions to his jeans (the Material) and about Kevin's latest work, Artist Bingo.
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P4A Let's Talk Rare


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Interview with Xortx Therapeutics CEO, Dr Allen Davidoff discussing their journey from early development to potential launch
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P4A are joined by Xortx Therapeutics' CEO, Dr Allen Davidoff, as he discusses the commercial plans for their novel therapy XRX-008 to treat patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD). Allen discusses the company vision for developing novel therapies for rare progressive kidney disorders, and tells us about the launch journey…
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