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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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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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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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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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In rarity we unite, connect and find our way to purpose.
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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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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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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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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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Rare and newly discovered interviews with cultural icons featuring Amy Winehouse, Beyoncé, Oasis, Bob Marley, David Bowie, Adele, Courtney Love and many more.
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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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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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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 blockchain informational podcast. We produce an annual blockchain convention called Rare Evo.
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Resilient | Rare | Unstoppable
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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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Unsettled is a podcast about Israel-Palestine and the Jewish diaspora. We're here to provide a space for the difficult conversations and diverse viewpoints that are all too rare in institutional American Jewish communities.
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This is CoRDS Cast, a rare disease podcast created by the team at Sanford Research. Our rare disease registry, CoRDS, connects patients and researchers everywhere. Here, you'll hear interviews with patients, patient advocates, physicians, and researchers to raise awareness about the 7,000 rare conditions affecting 1 in 10 people worldwide.
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Discover the extraordinary journey of living with an undiagnosed rare disease on Rare Matters Podcast. Join us as we empower, educate, and uplift each other.
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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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Intimate, personal portraits of both known and long-forgotten champions, heroes, and witnesses to history brought to you from rare archival interviews.
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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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Funk, Soul, Jazz, Latin, r&b, Brazil, rare groove, world music
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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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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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Hosted by Dave Dameshek, Minus Three 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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Offering up the best in New Wave, Goth, Post-Punk and Ska from the 80's, including rare and hard to find music you forgot you've missed!
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Popular & rare vintage radio programs with brief commentary. Posted weekly.
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Rare Insights: Uncovering The Future Of Rare Disease Treatments
Know Rare (Taren Grom, Liz Kay, Kaitlyn Taylor, Nina Wachsman, and DNA Today’s Kira Dineen)
On “Rare Insights” we bridge the gap between those living with rare diseases and the biopharmaceutical industry. Know Rare amplifies the voices of individuals with rare conditions, providing invaluable perspectives to accelerate therapeutic solutions. Join us as we dive deep into the complexities of rare diseases, exploring real-world insights from passionate industry leaders. Together, we navigate the unknowns and unlock the potential for groundbreaking treatments. Because in this journey, ...
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Buchholz & Buchholz Nursery is a wholesale nursery providing rare, unusual and high-end Japanese Maples, Conifers, and rare plants to wholesale growers. A wide range of specimen plant material is supplied to the better garden centers and landscapers across the United States and Canada. https://www.buchholznursery.com
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Star Wars & Scotch is a podcast hosted by 2 friends (Darkness429 & kmagic101) who are huge fans of a galaxy far, far away and who also happen to enjoy a nice glass of scotch. Join the community and the conversation and May The Force Be With You....Always!
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The Archive of the Funky16Corners Radio Show
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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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Your destination feed for medical, health care and clinical science podcasts courtesy of HCPLive—featuring our shows DocTalk, Rare Disease Report, Heart Team, Overdrive, and Derm Discussions. Music Courtesy of BenSound
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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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Exploring Music History with Professor Robert Greenberg one Monday at a time. Every Monday Robert Greenberg explores some timely, perhaps intriguing and even, if we are lucky, salacious chunk of musical information relevant to that date, or to … whatever. If on (rare) occasion these features appear a tad irreverent, well, that’s okay: we would do well to remember that cultural icons do not create and make music but rather, people do, and people can do and say the darndest things.
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Hard to find rare and obscure tracks, stories, interviews
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an audio-only podcast. released every Monday at 12:01am mst. rare Conversations with a compelling group of guests, on a wide range of relevant topics. nowherefast.substack.com
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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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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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Muddy Boots wanders where sneakers never will, moving on the back roads through the backwoods and to the forgotten cracks of our imagination. Tune in to hear a patchwork of sound, snippet, and song; field recordings from wherever, the random whimsical, and the rare, and not-so-rare. Learn more at muddybootsradio.org/
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DJ, Producer, Funky Promoter, Radio Show Host on Mother Russia's territory and beyond. Funk and Beyond parties and RHYTHMS Radio Shows celebrating 17th anniversary in 2024. Check anatolyice.ru and beyondfunk.ru for more info
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Conversations started by The Whitworth Group
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127: An Interview With Omer Abdul Hamid, MD, of Nemours Children's Hospital in Orlando, Florida
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Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Omer Abdul Hamid, MD, a neurologist at Nemours Children's Hospital in Orlando, Florida, on gene therapy's potential to treat Duchenne muscular dystrophy.By Rare Care Podcast
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Ask Jared Anything w/ Jared Klickstein
1:20:55
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Author Jared Klickstein returns to the show to talk about his new book Crooked Smile (https://www.amazon.com/Crooked-Smile-Escape-Homelessness-Addiction/dp/B0CWZ1GHLW), Fentanyl, Hunter Biden, and answers questions from listeners about harm reduction and Meth + Sex. Follow Jared on Twitter https://x.com/JaredKlicksteinFor Premium Rare Candy Episode…
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Jack Black Endorses Joe Biden, Kansas AG Sues Pfizer & Chuck Schumer Flips Burgers!
1:59:43
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20% All DreamRare.com merch for a week with code: SUMMER ! Most products are selling out DreamRare.comBy An0maly
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Alvin Rocha is a nurse care manager and pulmonary hypertension coordinator at Children's Hospital Los Angeles. He manages PH patients from birth to early adulthood. His main goal is to prepare these patients for the transition into the adult world. He is excited about the advancements in therapies and clinical trials and looks forward to attending …
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My daughter, GraceAnna, and her children met me at my mom's farm for a quick overnight trip this past week! We packed so much in two days and one of the things I did was grab time to record a short podcast with two more of the next generation of Rare but Real girls, AudreyKate and Evangeline. We talk about many things - growing in faith, a study th…
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Send us a Text Message. Meet Joel Cofounder of Endurant Health. Endurant Health has developed an AI tool to help diagnose rare disease patients. Joel's mother was diagnosed with a rare genetic metabolic condition called Homocystinuria. (HCU). Together with friends who are undergoing similar battles finding proper diagnosis they founded Endurant Hea…
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50 Years of Supporting the TSC Community, feat. TSC Alliance President and CEO Kari Rosbeck
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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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#300 - The Big 300!!! w/Lisa Rieffel & Zach Tinker
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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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Summer Mini #3: A Close Call, Feelings of Regret + Embracing Second Chances | Suzi’s Catch-Up
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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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Best of the 2023 Nano-rare Patient Colloquium
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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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Cass + Case in their homes, 2022/2024By Casey Greer and Cassandra Mendez
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“Rare Insights” is a podcast series interviewing industry and organizational leaders about the development of future therapies for rare diseases. On “Rare Insights” we bridge the gap between those living with rare diseases and the biopharmaceutical industry. Know Rare amplifies the voices of individuals with rare conditions, providing invaluable pe…
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Send us a Text Message. Here is another rant session from your favorite lesbian! I talk about the show on Netflix called Designated Survivor. These are just my opinions. Intro music Please consider supporting the show! Support the Show.By Avee
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When Cancer Affects More Than Just Your Body, with Michele Molnar, Founder of Cancer Chicks.
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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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Episode 115 | Sarc Fighter Andrea Maione has both sarcoidosis and long COVID. It's no party.
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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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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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The Unsung Heroes: Siblings Caring for Loved Ones with Rare Diseases
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I Care for Rare is a podcast for parents and families of people living with rare diseases. It’s co-hosted by Sherrilynne Starkie and Sandra Markus, the visionary behind the I Care for Rare campaign and its mission to create a collective voice for individuals, families, and caregivers living with rare diseases, inspired by her experience caring for …
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