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Cricket is great if you're into things like wasted youth, failed relationships, sun damage and broken dreams. A weekly show featuring news, views and interviews with major names from across the cricket scene.
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Get a rare glimpse into the minds and methods of sadistic murderers. From notorious names like Jeffrey Dahmer and John Wayne Gacy to lesser-known killers like “Death House Landlady” Dorothea Puente, what turns a regular person into a predator? Serial Killers is a Spotify Original. New episodes Mondays.
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Podcast by Rare Candy
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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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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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Fighting sarcoidosis as well as other rare diseases.
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Rarely Reserved is a Star Wars: Shatterpoint podcast hosted by Omnus and Syn.
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Not just another bad movie podcast, Blank Check reviews directors' complete filmographies episode to episode. Specifically, the auteurs whose early successes afforded them the rare ‘blank check’ from Hollywood to produce passion projects. Each new miniseries, hosts Griffin Newman and David Sims delve into the works of film’s most outsized personalities in painstakingly hilarious detail. Produced by Ben Hosley.
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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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Hosted by Dan Cleary, RFR is a comedy podcast that aims to be just that; in rare form. Sex, race, religion, conspiracy, controversy... nothing is off limits! The faint of heart need not apply. Follow us on Instagram & Twitter: @RareFormRadio - subscribe wherever you get your podcasts - Give us a rating & review if you'd be so kind.
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Young women have been growing up with an indoctrination of what womanhood is and what it should be. They've been taught everything that is in direct opposition to the Word of God. Young women who want to be different from the world are rare but they are real. Audrey Broggi will often be joined by her daughter and her daughters-in-law who desire to be discerning in a day when everything seems to go against God's design.
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Rare 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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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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Based on the iconic, Emmy-nominated series on A&E, this show explores some of the most difficult-to-solve murders, which stymied investigators and went cold, sometimes for decades. In fact, one-third of all murders in America remain open. But thanks to dogged investigators and breakthroughs in forensic technology, these cases become part of the rare 1% of cold cases that are ever solved. Cold Case Files is hosted by Paula Barros.
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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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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 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 the rare book t ...
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Popular & rare vintage radio programs with brief commentary. Posted weekly.
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Left Right & Center is for listeners who feel like people on the other side of the political divide are on Mars. David Greene pieces together the big picture by inviting people from the left and the right to unpack their ideological differences, not to smooth them over, and look at what’s truly at stake. The show offers a rare kind of clarity. It doesn’t ask you to agree. It asks you to look more closely at what’s happening and to challenge your assumptions. You might not always agree – you ...
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A podcast dedicated to the rare coin market, providing education and insights to collectors and new dealers in the hobby.
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Hosted by Dave Dameshek, Shek Show provides you with the hometown edge, informed counsel and rare access to the best bets every week on the sports calendar. You’ll also get unique listener games and an unyielding focus on the Game of Life. Is Shek a homer? No. Is he aware of the built-in advantages of being at home? You bet.
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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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*The Bureau of Lost Culture broadcast rare, countercultural stories, oral testimonies and tales from the underground. *Join host Stephen Coates and a wide range of guests including musicians, artists, writers, activists and commentators in conversation. *Listen live on London’s premier independent station Soho Radio or via all major podcast providers. The Bureau is collected at The British Library Sound Archive
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The official HorrorBabble podcast: a home for horror classics and rare weird tales. Our Teespring Store for all your HorrorBabble Merchandise https://horrorbabble-merch.creator-spring.com/ Support us on Patreon https://www.patreon.com/horrorbabble Visit the HorrorBabble YouTube Channel https://www.youtube.com/HorrorBabble
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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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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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an interview podcast. released every Monday at 12:01 am mountain standard time. rare conversations with a compelling group of guests, on a wide range of relevant topics.
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Host Mitch Goldman and his musician-guest explore rare archival recordings of one of the guest’s favorite artists.
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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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2 Shows in 1. 1 - Jazz, Latin Jazz, Jazz-funk, Rare Groove, Steely Dan 2- acidjazz, nujazz, house and more
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The goal of our “Ask the Expert” podcast series is to share the latest research and information on rare neuroimmune disorders and provide an avenue for individuals diagnosed with these disorders and their family members to ask questions to experts who specialize in these disorders. The podcasts are moderated based on questions submitted by our community. We would like to hear from you. If there are topics that you would like us to address in our podcasts, you can share your thoughts by sendi ...
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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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Under the Influence gives listeners a rare backstage pass into the hallways, boardrooms and recording studios of the ad industry.Join host and adman Terry O’Reilly for fascinating (and humorous) stories that connect the dots between pop culture, marketing and human nature. Hosted on Acast. See acast.com/privacy for more information.
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The Mises Institute, founded in 1982, is an educational institution devoted to advancing Austrian economics, freedom, and peace in the classical-liberal tradition. Our website offers many thousands of free books and thousands of hours of audio and video, along with the full run of rare journals, biographies, and bibliographies of great economists.
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Conversations started by The Whitworth Group
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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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‘All Things Adrenal’ is a monthly podcast from NADF dedicated to education, awareness, and stories from individuals living with adrenal disease.
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The Take 5 is a music podcast where the people you love, share five songs they love. Each guest has a different theme, and the memories attached to their most beloved songs flip them to fan mode, often giving a rare insight into their creative heart. Hosted by Zan Rowe.
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Twice a week, the Guardian brings you the latest science and environment news
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Hydro Heroes Unite is a podcast for parents and caregivers of children with hydrocephalus. Hosted by Taisha Cameron, Season One shares stories from families navigating pediatric hydrocephalus and insights from medical professionals. New episodes every other Wednesday. Created in partnership with the Hydrocephalus Association.
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Welcome to Music to Move You!, the show that moves your feet, moves your body, and moves your soul. We play Rare Soul, Northern Soul, Classic Soul, and other dance genres from the late 1950's to the mid 1970’s. Let’s get you on dance floor! New episodes premiere Tuesdays at 4pm (Central) and replay on Thursdays at 5pm (Central) on www.workingclassradio.com. New episodes are released as a podcast on Fridays. Playlists and extended archives are found at www.mixcloud.com/djmodmyke. Hosted on Ac ...
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Beyond the Count is a podcast about life with Immune Thrombocytopenia (ITP). Through personal stories, expert interviews and practical advice, each episode explores the everyday challenges and small wins of living with a rare autoimmune condition. Whether you’re newly diagnosed, supporting someone, or just looking to learn more, this podcast is here to inform, support and connect.
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Funk, Soul, Jazz, Latin, r&b, Brazil, rare groove, world music
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Patient Empowerment Program: A Rare Disease Podcast
n-Lorem Foundation (Dr. Stan Crooke, Amy Williford, Kim Butler, Andrew Serrano, Jon Magnuson, and Kira Dineen)
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Join the nano-rare disease community! Interviews features leading physicians, scientists, biotech experts, and patient advocates. Lessons teach core concepts about drugs. Our host Dr. Crooke has led the creation of antisense technology and his foundation, n-Lorem, is using this powerful technology to discover, develop, and provide personalized experimental antisense oligonucleotide medicines to nano-rare patients for free, for life. n-Lorem is a non-profit organization established to apply t ...
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Podcast by rarebirdlit
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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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Every beginning carries within it the seed of its own destruction.
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We’re back with Season 2 of our podcast PNRI Science–this time recorded live at PNRI’s 2025 Rare Disease Day symposium. It was a day full of energy, insight, and shared purpose, as scientists, clinicians, advocates, and industry leaders came together to accelerate rare disease research and treatment. Hosted by Jack Faris, CEO of the Pacific Northwest Research Institute, and his daughter, actor and producer Anna Faris, this season captures personal stories and fresh perspectives from across t ...
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Palliative care with a=Ann Front LMFT from California
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Send us a text What’s the difference between palliative care and hospice? Why is palliative care still misunderstood—and how can it support people with cancer, rare diseases, and other serious conditions long before end-of-life? In this powerful episode of Rare Connection, host Joanna Ball welcomes Ann, a licensed psychotherapist, breast cancer sur…
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We decided to talk about how we me express ourselves through list selection, or hobby projects and what we do at the table. This is certainly a topic that is a little abstract but we felt understanding ourselves and fellow players will only lead to enjoying the game even more. You can support us by leaving a review or subscribing on Patreon.…
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Glen and Psi talk about Ireland, Stephen Colbert, Therapy/Mental Health, Coldplay Kiss Cam Incident, and more For premium episodes and written content, check out our substack. Free and Paid options https://rarecandy.substack.com/ Follow Rare Candy on All Platforms https://beacons.ai/rarecandy
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Dr. John Granton, a critical care and transplant physician at Toronto General Hospital, shares his journey in pulmonary hypertension and lung transplantation, detailing the groundbreaking advancements in transplant technology. He discusses the evolution of lung preservation methods, the challenges of chronic rejection, and the hope for longer-lasti…
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Claire and her brothers went to Guatemala with their church on her first mission trip! We sat down to talk about all she learned and all she did while she was there. I know you will be encouraged as you listen!
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Get ready to shake, shimmy, and sleuth your way through an hour of explosive 1960s dancefloor grooves with a spy twist! From soul and surf to garage rock and jazz, this show uncovers the secret agents of sound—featuring Nancy Sinatra, Luther Ingram, and Barbara Feldon. Whether you're dodging lasers or decoding love letters, these tracks capture the…
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183: An Interview With Dr. Richard Nowak, Director of the Yale Myasthenia Gravis Clinic
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Richard Nowak, MD, director of the Myasthenia Gravis Clinic at Yale School of Medicine in New Haven, Connecticut.By Rare Care Podcast
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#364 - Perverted Taco w/Todd Newman
1:07:46
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#364 - Jumbotron disaster. Saving your friend's family. Taco Truck Surprise. Scummy streets. So blind. Epstein LOL. Killer dolls.
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Nelk Boys Netanyahu Interview ROASTED By Comments & Exposed Randomly By UFC Fighter Ilia Topuria!
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Hope you enjoy this episode! My YouTube channel is: YouTube.com/An0malyhiphopBy An0maly
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Mixed Feelings When Your Child’s Health Stabilizes w/ Jessica Loey
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When your child’s health stabilizes, it should feel like a win. But about when it just feels...complicated? In this episode, Jessica Loey joins Madeline to talk about the messy reality of “after.” They explore what it’s like to go from survival mode to something that looks more stable, and how this can bring up guilt, grief, and a strange sense of …
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This episode is all about maniacs! Bibliomaniacs, that is.... They may be extreme, they may be passionate, and, ignoring some unsavory criminal activity, they may even have served to preserve culture over the years. If you have a story about a bibliomaniac - or perhaps you are a bibliomaniac! - please drop us a note at [email protected] Enjoy!…
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New Insights into Genetically Caused Developmental Delays
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Emerging observations from our work at n-Lorem suggest that not all developmental delays are permanent. In the absence of structural damage—such as microcephaly, congenital deformities of the skull or bones, or organ malformations—there appears to be potential for improvement in movement disorders, cognition, autistic features, and more. These insi…
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124. we’ve changed our minds?: our 5 year podaversary
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hi hello hey, happy FIVE YEARS of Rare with Flair! As wild as it feels to say, it’s true: we’ve changed in the five years since we started this podcast. To celebrate our fifth podaversary (!!!), we’re reflecting on the ways we’ve grown. Some shifts are small, and others are in how we approach big things like disclosing, advocating, and accepting he…
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This season, you probably have heard Everleigh’s voice a little more often. It was this story that gave us the idea. In this short episode, we hear about one of the unexpected struggles that Brittany had to deal with earlier this year. Usually, Evie is the one in the hospital but this time, Brittany’s son Maverick was the patient. The remarkable th…
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Episode 143 | Why Sarc patients MUST exercise and the New FSR Patient Registry explained
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On Episode 143 of the FSR Sarc Fighter Podcast, I have two guests. Taylor Harwood, Senior Research Coordinator for FSR, joins me to explain the new and improved patient registry. Even if you've already registered, there is a small step you need to take to ensure researchers can find and use your valuable information. Also joining me is physical the…
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Mark McConnell, "Publishing in the Renaissance: Christophe Plantin's Business Strategy"
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Mark McConnell, "Publishing in the Renaissance: Christophe Plantin's Business Strategy" by Rare Book School LecturesBy Rare Book School Lectures
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Part 2 of James Bond Sidecars: Daniel Craig Its a special milestone episode of Rare Cuts Media Society! In this 50th installment, your hosts gather to celebrate by diving into the 2004 British crime thriller, Layer Cake, starring a pre-Bond Daniel Craig. This episode is all about uncovering hidden gems, and the team brings their signature humor and…
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OST-HER2 and the Fight Against Osteosarcoma: A New Hope After 40 Years
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Join us as we sit down with Paul Romness of OS Therapies to explore an exciting breakthrough in OST-HER2 targeted therapies for osteosarcoma—a rare and aggressive bone cancer. Learn how this innovative approach is offering new hope to patients, advancing precision medicine, and pushing the boundaries of rare disease treatment, not just for humans b…
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In this week of Rare Treasures we are having mini episodes where we talk about characters with disabilities. We investigate to see if they are a good representation of disability. In this episode we are talking about Dory from Disney's Finding Nemo (2003) and Finding Dory (2016) and if she is an accurate representation of disability. Research and R…
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