Podcast by Rare Candy
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Wie denkt dat klimaatproblemen, feminisme of superrijken typisch dingen van nu zijn, heeft het mis. De Romeinen hadden er ook mee te maken. In de podcast Rare Jongens vertelt historicus Olivier Hekster (Radboud Universiteit) hoe de Romeinen omgingen met dingen waar we ook nu mee te maken hebben. Samen met Merijn Doggen (hoofdredacteur Universiteit van Nederland) bekijkt hij wekelijks onze tijd door de bril van de Romeinen. Met dank aan de Letteren Faculteit van de Radboud Universiteit
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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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Rare Disease Advisor's Rare Care Podcast features exclusive interviews with experts and stakeholders from the rare disease community.
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Parenting tools and life hacks for raising a child with a rare diagnosis. Let’s get to the meat of it!
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Fighting sarcoidosis as well as other rare diseases.
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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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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 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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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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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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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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The Rare Disorder Podcast is a podcast created by Shivani Vyas, a high school senior, young changemaker, and rare disease advocate, dedicated to spreading awareness for rare diseases. This podcast is divided into 2 main series. In the "Meet a Fighter," Shivani interviews patients and those affected by rare diseases allowing them to share their inspirational stories. In "Meet An Expert/Partner," Shivani interviews public health experts, rare disease organization leaders, rare advocacy leaders ...
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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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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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Escape The World Thru MusiQ.
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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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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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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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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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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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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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Rare Treasures is a podcast all about rare conditions and disabilities. Each episode will focus on a rare disability or condition. We will gather information and statistics as well as interview people affected by the condition.
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Conversations started by The Whitworth Group
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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)
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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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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Podcast by rarebirdlit
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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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Are you ready to transform your real estate business? The RARE Agent Show is your ultimate guide to closing more deals, building wealth, and thriving as a real estate professional. Hosted by Dylan Tanaka, a multi-award-winning Realtor and coach, this podcast is where top-performing agents share their secrets and strategies to help you achieve consistent closings without the stress. Each episode delivers actionable insights through two dynamic formats: •Exclusive Agent Interviews: Dive deep w ...
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Ever wonder what makes people take the leap and follow their dreams? That's what RareErth Podcast is all about. I sit down with folks who've turned their passions into careers, asking them the tough questions we all face. How'd they find the courage to start? What keeps them going? Whether it's artists, business owners, or creative thinkers, I'm chatting with people who've taken risks to do what they love. If you're looking for a little inspiration or just enjoy a good story, tune in. Learn ...
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Since 1972, the Book Arts Press and Rare Book School have offered more than 600 public lectures on a wide variety of bibliographical topics.
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Funny and........ N O T H I N G
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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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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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A blockchain informational podcast. We produce an annual blockchain convention called Rare Evo.
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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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"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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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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In rarity we unite, connect and find our way to purpose.
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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 a podcast tutorial
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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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Stories and Testimonies about 22Q11.2 and all rare and not so rare disorders and causes
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#327 - Assassins are the new superhero. Gone missin’. Florida Man. Heidi has all the diseases. Tammy Hull of Fame. Drones are weird. Listener question. The new must listen podcast. House jeans. --- Support this podcast: https://podcasters.spotify.com/pod/show/rareformradio/support
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149: An Interview With Clinical Psychologist Rosalind Kalb, PhD, of Can Do-MS
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews clinical psychologist Rosalind Kalb, lead senior programs consultant for Can-Do MS, a Colorado-based nonprofit health and wellness organization.Bởi Rare Care Podcast
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Q&A - 2024 Nano-rare Patient Colloquium Recap
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Join Stan Crooke, n-Lorem founder, CEO, and host of the Patient Empowerment Program Podcast, alongside Amy Williford, Sr. Director of Communications and Donor Relations, for a special episode. In this post-colloquium Q&A, Stan recaps the 2024 Nano-rare Patient Colloquium and the progress n-Lorem has made as the organization nears its 5-year anniver…
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Einstein's Frubber Face, Plath's Favorite Cook Book, Kafka's Earliest Scribbling, & the Kelmscott Press
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We begin this episode with Michael bemoaning a missed opportunity to buy the head of Albert Einstein, and then we welcome Darren Sutherland, Senior Specialist in the Fine Books and Manuscripts at Bonhams Auctions, to discuss two upcoming sales. The first is a fascinating single-owner complete collection of books from the Kelmscott Press, assembled …
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What’s going to happen if our godly women today don’t invest in the lives of the next generation of young women? I think about this often. So many young women don’t grow up in families that reflect what a biblical family should be. This generation is consumed by social media and influencers, yet God says the primary influencers should be the godly …
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Mario Cuomo joins Glen and Psi to talk about his new single "Leftovers", William Friedkin's Sorcerer (1977), Tangerine Dream, and more Leftovers (Official Video) on Youtube https://www.youtube.com/watch?v=wf0-FLGsb_8Mario Cuomo on Instagram https://www.instagram.com/mcmariocuomo?igsh=NTc4MTIwNjQ2YQ==For premium RC episodes and written content subsc…
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Tanya Stinson shares her journey of being diagnosed with pulmonary hypertension (PH) after persistent symptoms and misdiagnoses. Her struggle highlights the difficulty of finding the right diagnosis and the emotional toll of living with a rare, chronic disease. Tanya’s experience underlines the fear, mental challenges, and hope intertwined in navig…
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Episode 128 | A year of major accomplishments - and how you can help the Foundation for Sarcoidosis Research
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We are making progress against Sarcoidosis, whether it's new treatments or outreach to patients or even the FDA, the foundation for Sarcoidosis Research is making serious progress. In this episode of the FSR Sarc Fighter Podcast, Cathi Davis and Jennifer Bulandr join me to look back at all the advancements we have made in 2024 and they look ahead t…
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How This Solo Agent Closed $14M in Sales Without a Team | RARE Agent Show
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What does it take to crush the real estate game solo and close $14M in sales without a team? In this powerful episode of The RARE Agent Show, Dylan Tanaka—award-winning real estate coach, mentor, and nationally recognized expert—sits down with top-producing agent Chris Griffin to uncover his incredible journey and the strategies that make him one o…
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#326 - Dan is a new age. Playing with gunz. Space ice cream. Afroman the slugger. The Christmas spirit. Empty gestures. Worst Ex Ever. Hawk Tuah isn’t who we thought. --- Support this podcast: https://podcasters.spotify.com/pod/show/rareformradio/support
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Holiday Mini 2: Gift Giving Grief for Disability Parents w/ Amanda Griffith-Atkins
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Holidays are supposed to be full of joy, right? But for disability parents, gift-giving can bring a whole mix of feelings: grief, frustration, and why did they buy this moments. Instead of magic, we’re juggling unconventional (or maybe not age-appropriate) toys for our kids, therapy equipment wrapped in bows, and family members who just don’t get i…
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Terry Pratchett's The Hogfather (2006)
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Part 3 of the Holiday Theme Time - Christmas In today's episode, Andrew Picks Terry Pratchett’s The Hogfather to celebrate the Hogswatch…er um…I mean the Christmas Season! Join hosts Andrew, Rob, Eric, and Mike as they dive deep into the 2006 British TV Miniseries Terry Pratchett’s the Hogfather. The story follows Death, the Grim Reaper, and his gr…
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hi hello hey, and brace yourselves for some disabiliTEA. Discrimination is a topic we wish we didn’t have so much experience with, but it’s an unavoidable reality we face as disabled women. On this episode, we’re diving into some of the most frustrating and heartbreaking situations we’ve endured. From being denied rideshare services because of a gu…
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23. Verkeer. Files, parkeerproblemen en agressie in Rome
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Als je denkt dat de verkeersproblemen van nu zomaar opgelost worden, nou dat zit je er naast. De dealen er al meer dan 2000 jaar mee. Ook in het oude Rome zonder verkeersborden en duidelijke regels was het chaos, vertelt historicus Olivier Hekster. In de rubriek Helpdesk Rome geven we Romeins advies over huisdieren.…
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Innovate, Iterate, Impact: ft. Co-Founder of AdaptTrack, Samuel Taggard
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Welcome to "Innovate, Iterate, Impact" ft. Co-Founder of AdaptTrack, Samuel Taggard. This is a podcast exploring the transformative journey of entrepreneurship through the lens of academic learning and real-world insights. Join Shivani Vyas, a Duke University student studying Financial Economics and Entrepreneurship, as she reflects on key lessons …
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The Role of AI in Medicine feat. Joe Lennerz, BostonGene
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On this episode of the podcast, we discuss the role of artificial intelligence (AI) in medicine – specifically in the areas of analysis and diagnosis. Our guest, Dr. Joe Lennerz, is the chief scientific officer at BostonGene, an American clinical technology company that studies and produces new diagnostic tools in the areas of oncology and immunolo…
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CNN Says Kash Patel Hacked By Iran, Biden Gives Our Money To Africa, Eric Adams Border Czar Comments!
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Lot's of topics covered in today's show & just kicked it at the end with some live viewers. Was fun! Hope you enjoy. Get a Christmas gift: DreamRare.comBởi An0maly
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012: My Top 10 Must-Have Toys Over the Last Decade
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In the final episode of 2024, host Meghan Weaver shares her top 10 toy recommendations that have been loved by her daughter Rowan and the entire family over the years. From VTech GoGo Smart Wheels to the Yoto player, these toys not only entertain but also support various developmental milestones and therapeutic needs. Meghan provides detailed insig…
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