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.
…
continue reading
RaRa Raadio toob sinuni saated, mis haaravad endaga kaasa, ärgitavad mõtlema ja kergitavad suunurki ülespoole. Usume, et leiad siit mõtteid, mis teevad sind rikkamaks inimeseks.
…
continue reading
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
…
continue reading
Podcast by Rare Candy
…
continue reading
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.
…
continue reading
We are a thriving church located in the pacific island of Rarotonga. On this podcast, you will find powerful preaching taken right from our church services. We will also be producing bonus content that is designed to help you live a life of breakthrough and make an impact for Christ! Subscribe and become a part of what God is doing!
…
continue reading
Rare Disease Advisor's Rare Care Podcast features exclusive interviews with experts and stakeholders from the rare disease community.
…
continue reading
Bienvenidos al Podcast de Cinoscar & Rarities, espacio del blog de cine Cinoscar & Rarities. Reseñas, estrenos, festivales, noticias, especiales y todas las novedades del séptimo arte. Podcast dirigido por @CinoscaRarities y @CineAmateur http://cachecine.blogspot.com.es/
…
continue reading
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.
…
continue reading
Fighting sarcoidosis as well as other rare diseases.
…
continue reading
Revolutionary War Rarities is fast, fun, and rarely known history on the American Revolution. All PodCasts are 8-10 minutes long and are released every two weeks. Revolutionary War Rarities is the PodCast from the ”Sons of the American Revolution”. Please subscribe and let’s make history fun again. Thank you for joining us. #americanrevolution #revolutionarywarrarities #americanhistory #foundingfathers #revolutionarywar #sonsoftheamericanrevolution #rarehistory #americanrevolution
…
continue reading
Host Josh Mills brings together a wide variety of adult children of celebrities for a fun, funny, bizarre, jaw-dropping, strange and wonderful look behind celebrity, by the people that know them best: their very own children.
…
continue reading
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.
…
continue reading
O podcast Peças Raras foi criado em 2006 pelo professor e radialista Marcelo Abud. Áudios que contam a história do rádio e entrevistas com comunicadores são a base dos episódios. Aqui, vamos publicar alguns conteúdos que valem ser lembrados. Siga na sintonia!
…
continue reading
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
…
continue reading
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.
…
continue reading
A blockchain informational podcast. We produce an annual blockchain convention called Rare Evo.
…
continue reading
Somos un grupo de amigos con diferentes puntos de vistas que vamos a discutir sobre temas diferentes, con una objetividad personal, pero siempre con respeto para emitir un criterio justo y sensato.
…
continue reading
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!
…
continue reading
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
…
continue reading
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.
…
continue reading
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
…
continue reading
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 ...
…
continue reading
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!
…
continue reading
🎙 Welcome to Rarified Air: Stories of Inspired Service, a podcast that takes you on a journey into the DNA of InterSystems. I will be your guide as we explore how our unparalleled commitment to customer service fuels limitless human potential. 🤝 Join us as we dive into the culture of InterSystems and share the stories of the people who make it all possible - our customers, partners, and employees. From helping healthcare providers improve patient outcomes to powering the world’s most importa ...
…
continue reading
Welcome to the new Rare Kidney Disease Show part of the RKD Scientific Network sponsored by Travere Therapeutics. The Rare Kidney Disease Show is your primary source for cutting-edge insights, expert perspectives, and pivotal updates in nephrology. Led by our panel of experts, explore the advances in glomerular nephropathies through compelling conversations, challenging case studies, and discussions tackling hot topics. Join us as we strive to provide you with the ultimate resource to suppor ...
…
continue reading
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!
…
continue reading
siraman rohani ala rarrizi
…
continue reading
Intro,obrolan
…
continue reading
A journal through my 20’s.. for everyone seeking to Live unapologetically. On RaRa, we have weekly laidback and chill conversations about matters affecting the millennial youth, ranging from Faith, Love, Relationships, Sexuality, Career choices and everything in between. Let’s become better versions of ourselves together. Reach out to me via rarathepodcast@gmail.com Instagram @zubbey. Love & Light.
…
continue reading
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.
…
continue reading
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 ...
…
continue reading
Magazine semanal dedicado al apasionante mundo de los libros. Actualidad nacional e internacional sobre novedades editoriales, premios, entrevistas a autores, poesía, libro viejo y ediciones raras o limitadas. Todo esto y más se dan cita en este espacio cultural de Radio Intereconomia, dirigido por Andrés Sánchez-Magro.
…
continue reading
En esta serie mensual entrevistamos a pacientes, familiares, científicos, investigadores y líderes hispanos en el mundo de las enfermedades raras, para que nos compartan sus historias, alegrías, desafíos y aprendizajes. Acompáñanos a compartir estas historias, desde la odisea del diagnóstico (¡hablando un idioma diferente!) a los conceptos erróneos en nuestra comunidad. Hablaremos de la diversidad cultural en los países de habla hispana e intentaremos comprender mejor los diferentes factores ...
…
continue reading
Escape The World Thru MusiQ.
…
continue reading
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 ...
…
continue reading
Rarzclothing - Trending Fashion In the USA. Rarzclothing is a global online store, where people come together to buy and collect unique items at low prices cost. Contact Info: Website: https://rarzclothing.com/ P: (SMS text recommended) +1(951) 236-0707 E: support@rarzclothing.com A: 2880 Stevens Creek Blvd, San Jose, CA 95128, United State Hastags: #rarzclothing
…
continue reading
1
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!
…
continue reading
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!
…
continue reading
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 ...
…
continue reading
We are in an Acura in a park we came to do yoga but it wasn’t here, so we started talking about stuff in the parking lot.
…
continue reading
Welcome to Joslyn Rardon, where amazing things happen.
…
continue reading
Un podcast de adultos que están descubriendo lo que eso significa.
…
continue reading
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 ...
…
continue reading
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 ...
…
continue reading
Caden Rardon Interviewing Chauncey Rardon about his coaching experience
…
continue reading
TIXTO son capsulas de tecnología aplicada a la evangelización, su productor y locutor es Roberto Arias (@bettocr) de RARComputacion.com
…
continue reading
Conversations started by The Whitworth Group
…
continue reading
A series of eclectic mixes from my vinyl record collection- check for regular updates and downloadable classics.
…
continue reading
1
The Israel Palestine “Frat Bro” Reaction Is A Psy-Op & Matt Walsh Notices Something Interesting!
55:39
55:39
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
55:39
God bless you. Have a good weekend! My YouTube, Music & Shop! http://DreamRareLinks.comAn0maly
…
continue reading
1
REPORT: Daily Wire Gag Orders Candace Owens, Nick Fuentes Allowed Back On X & Tucker Carlson, Charlie Kirk & Matt Walsh Speak Out About "The Laws"!
2:55:39
2:55:39
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
2:55:39
Long one! Whoops... :D Sponsors Or Social Media Consulting: http://DreamRareBiz.com My Shop: http://DreamRare.com All My Links: http://DreamRareLinks.comAn0maly
…
continue reading
1
121: An Interview With University of Pennsylvania Neurologist and CIDP Expert Chafic Karam, MD
4:13
Rare Care Podcast
…
continue reading
1
Wisdom Beyond His Years: 17-Year-Old Arjun Khemani on Education, Entrepreneurship and the Beginning of Infinity
1:02:57
1:02:57
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
1:02:57
Get ready for a fascinating conversation with Arjun Khemani, a remarkable 17-year-old who's the youngest guest ever on my podcast! Arjun's journey is anything but conventional - he dropped out of school to pursue his passions, explored various gigs, and landed a job at AirChat, a platform for authentic voice conversations. In this episode, we dive …
…
continue reading
1
La Revolución de la Inteligencia Artificial: Cómo Está Cambiando el Mundo
54:36
54:36
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
54:36
Exploramos el impacto de la inteligencia artificial en nuestra sociedad y cómo está transformando la tecnología, el trabajo y la vida cotidiana. Únete a nosotros para discutir los avances más recientes y sus implicaciones para el futuro.
…
continue reading
1
159: Sharing the Mental Load with Your Partner in Disability Parenting w/ Amanda Griffith-Atkins + Will Atkins
52:10
52:10
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
52:10
Nothing breeds resentment faster than one member of a romantic partnership feeling like they're pulling all the weight in one area of life. And when it comes to the parents of medically complex kids, that resentment can compound even faster, especially as the mental load of navigating medical care often falls onto one partner. (Let’s be real: it’s …
…
continue reading
1
The Role of Patient Experience Data in Drug Development with Pina Haberl and Sam Morrison
34:37
34:37
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
34:37
Welcome to this month's episode of the P4A Let’s Talk Rare podcast by Partners4Acess. Today, Georgie and Owen are joined by their colleagues Pina Haberl, Senior Director, and Sam Morrison, Executive Director at Partners4Access. Join us as we discuss the crucial role of patient experience data in drug development. The conversation explores the need …
…
continue reading
1
Powering Through Adversity: Personal Trainer Shaun Kehoe’s Journey from Brain Surgery to Fitness Advocate
32:21
32:21
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
32:21
The I Care for Rare podcast reveals the challenges faced by the families caring for people who have a rare health condition, In this episode we delve into the challenging world of rare diseases with Sandra Markus, founder of iCare4Rare, and Shaun Kehoe, a certified personal trainer with a remarkable journey of his own. Zach, Sandra’s adult son with…
…
continue reading
1
#293 - Both Of Em? w/Gina LoBue from 50 States of Madness
1:23:36
1:23:36
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
1:23:36
#293 - Gina LoBue from 50 States of Madness podcast joins us for some laughs, as usual!Want to support our show?Patreon.com/RareFormRadio for extra content, bonus episodes & goodies!RareFormRadio.Threadless.com for some rad merch. http://linktr.ee/RareFormRadio --- Support this podcast: https://podcasters.spotify.com/pod/show/rareformradio/support…
…
continue reading
1
Using Directed Evolution to Develop New Vectors for Genetic Medicines
31:08
31:08
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
31:08
Much of the challenge of developing genetic medicines lies in having the right vector to deliver the therapy to the cells within the body where they need to go. 4D Molecular Therapeutics has developed platform technology that generates large numbers of genetically diverse, synthetic adeno-associated viral vectors that have desired characteristics u…
…
continue reading
1
9X56 - ESTRENOS: Rivales, El clan de hierro, Sangre en los labios y Remando como un solo hombre
33:31
33:31
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
33:31
Xavier Vidal reseña 4 estrenos vinculados con el deporte: "RIVALES (CHALLENGERS)", "EL CLAN DE HIERRO", "SANGRE EN LOS LABIOS" y "REMANDO COMO UN SOLO HOMBRE". Sin spoilers. ¡Gracias por darle al play! Redes sociales: @CinoscaRarities Blog: https://cachecine.blogspot.com.es/ Correo: cinoscararities@gmail.com Escúchanos en Spotify, Ivoox y Apple Pod…
…
continue reading
1
Saagar From Breaking Points Joins To Expose Talk Truth About How Biden Admin Wants To Bring In Gaza Refugees & Republicans Won't Tell You Who Else Does!
55:16
55:16
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
55:16
Great chat with Saagar Enjeti of the political podcast "Breaking Points" joins to talk about Biden bringing in more refugees & US troops in Gaza! My Shop: http://DreamRare.com All My Links: http://DreamRareLinks.comAn0maly
…
continue reading
1
Courageously Candid: Living with Addison's Disease and Functional Neurological Disorder - Savannah's Story
55:14
55:14
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
55:14
In the latest installment of the Rare Matters Podcast, we have the honor of sitting down with Savannah, a remarkable individual navigating life with Addison's Disease, Functional Neurological Disorder, and a cluster of yet-to-be-diagnosed conditions. In a candid and courageous conversation, Savannah sheds light on the daily realities of living with…
…
continue reading
1
Finding Purpose in All of It
48:50
48:50
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
48:50
“We have a heartbeat, right?” Josh and Kristin Hoyle knew that life with their new daughter Chloe was going to be different and likely difficult long before she was born. Even in this knowledge, they believed there was a purpose for what they were about to experience. And they leaned into the challenge. Chloe has Bohring-Opitz syndrome and requires…
…
continue reading
1
Mostyn's Story: Mother's Day Special with Zoe Hummel
50:06
50:06
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
50:06
Motherhood is a journey filled with challenges, but every step is worth it for the love and joy it brings. Zoe Hummel joins the show in this special Mother’s Day episode to discuss her son Mostyn’s emotional story to diagnosis, and the unique challenges and triumphs of being a nano-rare mom. Order your Mother's Day card by May 6, 2024! All proceed …
…
continue reading
Glen and Psi talk about Ivy League campus protests, Elvis, Tom Hanks, Bees, Arnold Schwarzenegger, Kendrick Lamar vs. Drake, and much more.For Premium Rare Candy Episodes and Written Content, head to our Substack https://rarecandy.substack.com/Merch Store https://rare-candy-industries.myshopify.com/Rare Candy on Apple, Spotify, Youtube, Rumble, X, …
…
continue reading
In this powerful message, Pastor Jonathan shares about the need for oneness in the church today. The Bible says that the world will know we are Christians by our love for one another. The Lord's house is not to be filled with comparisons or back-biting, but the Lord wants a church filled with grace, mercy, forgiveness and love for one another. We k…
…
continue reading
This will be the last episode until some time next month, I will have some good episodes coming so stay tuned! like, subscribe and follow me for more content! I hope you enjoy another rant session from your favorite lesbian! Intro music Please consider supporting the show! Support the Show.Avee
…
continue reading
1
The TRUTH About Palestine Campus Protests That You WON’T HEAR on Fake Opposition GOP & Dem Media! w/ Clint Russell of Liberty Lockdown.
2:07:12
2:07:12
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
2:07:12
Clint Russell of Liberty Lockdown joins to talk about the angles that people WON'T HEAR on normie GOP & Democrat media! Full video: https://www.youtube.com/live/zyUtsH1qbYI?si=3jOglEv9UTKcgdwZ My Shop: http://DreamRare.com All My Links: http://DreamRareLinks.comAn0maly
…
continue reading
1
EP 11 - Innovation Insights: Adapting to Evolving Customer Expectations with Jeff Fried
22:42
22:42
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
22:42
In this episode, John Palladino welcomes Jeff Fried, Director of Platform Strategy for InterSystems, to discuss customer needs, innovation pace, and InterSystems' strategies. They explore how the company meets evolving needs, including anecdotes from the COVID-19 pandemic and customer-driven innovation instances. Key Takeaways: Innovation pace has …
…
continue reading
1
92. cass’ guide dog is retiring?!
1:15:05
1:15:05
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
1:15:05
hi hello hey, the title says it all: Cassandra’s guide dog, Romana, is retiring Like humans, guide dogs also get to retire from their years of hard work! Romana has worked for nearly 8 wonderful years and has earned a well deserved rest. In this episode, Cass explains what the retirement process entails. She and Case share memories and laughs from …
…
continue reading
1
Episode 180: Jim Meskimen (Marion Ross)
1:23:50
1:23:50
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
1:23:50
Today on another encore edition of the Rarified Heir Podcast, we are talking to actor/impressionist Jim Meskimen, son of actor Marion Ross. We speak to Jim (and his many guises – he really has an amazing ear for voices) about growing up the child of everyone’s favorite TV mum, Mrs. C., Marion Cunningham from the 70s TV juggernaut Happy Days. We als…
…
continue reading
1
Libertarian Debate! Will Javier Milei Be A Good Leader For Argentina? An0maly & Jeremy Kauffman.
1:38:36
1:38:36
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
1:38:36
This guy was hating on my Twitter post & I invited him on the show to debate! My Shop: http://DreamRare.com All My Links: http://DreamRareLinks.comAn0maly
…
continue reading
1
14. Uitvindingen. Wie financierde je startup?
21:10
21:10
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
21:10
Waar gingen de Willie Wortels van de oudheid naar toe met hun uitvindingen? En kon je rijk worden van een slimme uitvinding? Nou dat bepaalde de keizer wel. En Olivier Hekster haalt je ook gelijk uit de droom: muntgeld, cement en boogconstructies lijken misschien typisch Romeins, maar waren dat zeker niet. In de rubriek hebben we het deze week over…
…
continue reading
Karen Martinez, a mother from Eastvale, California, shares her experience with Camp del Corazon, a camp for children with congenital heart defects and lung disease. Her daughter attended camp for the first time at the age of seven and has been going every summer since. The camp offers events throughout the year and fosters lifelong connections amon…
…
continue reading
1
Pierre-Vincent Girardin | Bourgognes rising star?
14:07
14:07
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
14:07
Ambitionsniveauet er gigantisk. Visionen soleklar. Og de fysiske vinrammer futuristiske og topmoderne. Girardin har kørt sig selv i stilling til berømmelse.RareWine Podcast - Viden om vin
…
continue reading
1
Summary of the Song
1:04:37
1:04:37
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
1:04:37
Epilogue "Put me like a seal over your heart, like a seal on your arm. For love is a strong as death, jealousy is as severe as Sheol; Its flashes are flashes of fire, The very flame of the Lord. Many waters cannot quench love, Nor will rivers overflow it; If a man were to give all the riches of his house for love, it would be utterly despised." God…
…
continue reading
1
S2E20 "I Did Not Know That - American Revolution Little-Known Facts"
16:47
16:47
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
16:47
Please click on the picture below and watch the latest episode of Revolutionary War Rarities, the podcast from The Sons of the American Revolution. This episode is entitled “I Did Not Know That” and focuses on numerous little-known facts and people of the American Revolution. Today, we also have a very special guest joining us and his name is Val C…
…
continue reading
1
El Club de los Negocios Raros, “El Juglar", de Antonio Pérez Henares (chani) 28/04/2024
59:59
59:59
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
59:59
Magazine semanal dedicado al apasionante mundo de los libros. Actualidad nacional e internacional sobre novedades editoriales, premios, entrevistas a autores, poesía, libro viejo e ediciones raras o limitadas. En esta ocasión tendremos a Lorena Carbajo, fundadora y directora editorial de Bala Perdida (Madrid); Antonio Pérez Henares “chani”, autor d…
…
continue reading
1
9x55 - SERIES: Mi reno de peluche, El problema de los 3 cuerpos, El régimen, Shogun, Deadloch, Ripley y Extras
55:28
55:28
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
55:28
Reseña sin spoilers de series y miniseries disponibles en plataformas de streaming. Participan Mayra Meza, Xavier Vidal, Raúl Artiaga, Antonio Vuarnet y Norberto Piñar. ¡Gracias por darle al play! Guía del programa: 0' Presentación - 2' SERIE DESTACADA: Mi reno de peluche - 7' SERIES EN SERIE: El problema de los 3 cuerpos, El régimen, Shogun, Bajo …
…
continue reading
1
Trump Calls RFK Jr. A “Fake” For His Stance On The Big Pharma Shot. Huge Mistake!
59:31
59:31
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
59:31
Full episode on YouTube, Facebook & Rumble. My Shop: http://DreamRare.com All My Links: http://DreamRareLinks.comAn0maly
…
continue reading
1
Gain of Fiction - The Friends of Eddie Coyle w/ Max Thrax (Preview)
31:40
31:40
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
31:40
Full Episode is available to paid subscribers of the Rare Candy substack https://rarecandy.substack.com/p/gain-of-fiction-vol-31-the-friendsRare Candy
…
continue reading
1
The MS Poltergeist, feat. Patient Advocate Jennifer Angus
43:48
43:48
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
43:48
In this episode of the podcast we talk with Jennifer Angus, a patient advocate and para dressage competitor who was diagnosed with multiple sclerosis in 2014. Jennifer has long been involved with athletics having a history as a skiing instructor and is a big advocate of horseback riding as a way to heal the body and mind. Connect with Jennifer Rega…
…
continue reading
1
Matt Walsh EXPOSES Speaker Mike Johnson Over BLM & Palestine Hypocrisy & Backs 1A Over Governor Abbott!
1:49:13
1:49:13
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
1:49:13
Watch full episodes on YouTube.com/An0malyhiphop Sponsors Or Social Media Consulting: http://DreamRareBiz.com My Shop: http://DreamRare.com All My Links: http://DreamRareLinks.comAn0maly
…
continue reading
1
Primary Sclerosing Cholangitis,& Trigeminal Neuralgia
1:05:51
1:05:51
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
1:05:51
In this episode I talk with Christina, Who is the host of Speaking in Spoons and a patient with Primary Sclerosing Cholangitis (PSC), Trigeminal Neuralgia and Hemiplegic Migraines. The aim of this podcast is to connect those with similar conditions, educate medical professionals, and hopefully help find treatments and clinical trials. Support the S…
…
continue reading
1
Why "Red Pill Mansophere" Content Like Andrew Tate Is Making A Lot Of Western Men Convert To Islam
55:42
55:42
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
55:42
Watch full episodes at YouTube.com/An0malyhiphop or see all my channels, music & shop at DreamRareLinks.comAn0maly
…
continue reading
1
120: An Interview with Avner Reshef, MD, Top Israeli Expert in Hereditary Angioedema
17:11
17:11
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
17:11
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Israeli expert Avner Reshef, MD, director of the Allergy, Immunology, and Angioedema Center at Barzilai University Medical Center in Ashkelon, only a few miles from the border with war-torn Gaza.Rare Care Podcast
…
continue reading
1
119: An Interview With Pediatric Neurologist Edward Smith, MD, on the FDA Approval of Vamorolone for Boys With Duchenne Muscular Dystrophy
15:58
15:58
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
15:58
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews pediatric neurologist Edward Smith, MD, about the recent approval of vamorolone, a synthetic corticosteroid, in boys with Duchenne muscular dystrophy.Rare Care Podcast
…
continue reading
1
#292 - Wife Swap Life Swap
1:11:44
1:11:44
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
1:11:44
#292 - The real killer has died. Wife Swap/Life Swap. Prosthetic shoes. Shopping list of health. The squatter hunter. 2 faced crying laugher. Nub City, Florida. --- Support this podcast: https://podcasters.spotify.com/pod/show/rareformradio/support
…
continue reading
1
158: Serena’s Story | Disability Advocate Turned Disability Parent, a Degenerative Diagnosis, + the Power of Now
54:07
54:07
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
54:07
Before she had her son, Serena was already a pediatric SLP, business owner, and disability advocate who spent her time empowering families to understand and become more comfortable with their children’s disabilities. So, she was prepared for anything, or so she thought. But as it turns out, no amount of education or experience can prepare you for t…
…
continue reading
1
Addressing a Shortage of Genetic Counselors with AI
35:18
35:18
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
35:18
As genetic testing continues to expand, it is bringing into focus a shortage of genetic counselors who can work with patients to explain results and answer questions. Igentify is helping genetic counselors manage more patients by providing an AI-based platform that can take some of the load off of them by helping onboard patients, obtaining consent…
…
continue reading
Enjoy another rant session from your favorite lesbian! Follow me on all platforms!! You won’t regret it! My new twitter/X account is @ARareBreedPodca Follow me there! Intro music Please consider supporting the show! Support the Show.Avee
…
continue reading
1
Ron Paul’s WARNING To America Over TikTok Ban, Foreign Aid & Surveillance Bill! My Reaction.
59:45
59:45
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
59:45
I did two episodes today! This is one. Will upload the other one in the morning. You can watch it now here: YouTube.com/An0malyhiphop Or find my other channels: DreamRareLinks.comAn0maly
…
continue reading
1
Historias de Borracheras: Curiosidades y Anécdotas Increíbles sobre el Alcohol
59:52
59:52
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
59:52
Escucha nuestras historias más alocadas y curiosidades sobre el alcohol. Desde las anécdotas más divertidas hasta los hechos más sorprendentes. ¡Únete a nosotros para un episodio lleno de humor y conocimiento!
…
continue reading
1
Exploring Medical Gaslighting and Self Advocacy
46:20
46:20
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
46:20
Join us for the second episode of Rare Matters, where we delve into the crucial yet often overlooked topic of medical gaslighting. In this episode, we uncover what medical gaslighting entails, shed light on its subtle manifestations, and equip you with the tools to identify and combat it. Through insightful discussion and a compelling personal narr…
…
continue reading
1
Unmet Needs in IgAN: Burden of Disease & Long-Term Impact on Patients ft. Dr. Jonathan Barratt : 2
15:44
15:44
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
15:44
Overview: In this episode of the Rare Kidney Disease Show, Professor Jonathan Barratt discusses the need to take a long-term approach when managing IgA nephropathy patients. He presents data from the UK National Registry of Rare Kidney Diseases (RaDaR). During this recording you will hear Professor Barratt discussing the continued risk of progressi…
…
continue reading
1
9x54 - Especial 77º FESTIVAL DE CANNES 2024
1:20:30
1:20:30
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
1:20:30
Dionar Hidalgo y Xavier Vidal comentan las películas del FESTIVAL DE CANNES 2024. Repasamos la sección oficial, Una cierta mirada, Quincena de realizadores, Semana de la crítica y proyecciones fuera de concurso. Todo sobre el festival francés, en nuestro pódcast. ¡Gracias por darle al play! Redes sociales: @CinoscaRarities Blog: https://cachecine.b…
…
continue reading
1
Tucker Carlson vs. Ben Shapiro Culture War Heats Up: Why It’s WAY BIGGER Than Just Them.
59:53
59:53
Прослушать позже
Прослушать позже
Списки
Нравится
Нравится
59:53
Watch the video clips on YouTube.com/An0malyhiphop My Shop: http://DreamRare.com All My Links: http://DreamRareLinks.comAn0maly
…
continue reading