Résultats de "RaRo" dans Toutes les catégories

Join Cam, Tymo, JPW & the rest of the Bolts Gaming Team each week as they talk NHL, hockey, esports & more!

Rare Disease Advisor's Rare Care Podcast features exclusive interviews with experts and stakeholders from the rare disease community.

関西住み80年代生まれ一般女性のラジオです。 エンタメ、アイドル、90年代多め 性愛、友人関係、不登校、発達障害、お笑い、社会問題など 気になる話題を話してます。 ライブ配信:平日13-14時の間多め　不定期 もしくは休み前の夜 Twitter:＠rara3ra #なっとうラジオ Apple https://podcasts.apple.com/jp/podcast/%E3%81%AA%E3%81%A3%E3%81%A8%E3%81%86%E3%83%A9%E3%82%B8%E3%82%AA-%E5%87%BA%E5%BC%B5%E7%89%88/id1573841216 spotify https://open.spotify.com/show/7JZ1sw2ow5a29A3NY6ZbtY?si=M0OJsmRXSPqGt5wlITqfeA 前の...

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 prognosis is completely unknown. They were alone. They were scared. And then they went into action. And now ...

En 1875, Mauricio Sargal, un millonario antillano retornado a España, libertino y bon vivant, se ve obligado a regresar a Cuba cuando le comunican que su hermana Dulce ha desaparecido de su hacienda en Siboney. Para saber de ella tendrá que enfrentarse a su cuñado, Bartolomé Gormaz, quien fuera prófugo de la justicia y que, con el olvido de cualquier escrúpulo, ha conseguido reunir una de las mayores fortunas de todos los territorios españoles, peninsulares y de ultramar. En su búsqueda, Mauricio encontrará también el amor en la enigmática Deva.

Silent farts, squeaky farts, smelly farts, thunderous farts, and hilarious dinosaurs! Charlie is having a day full of mysterious farts at school. No one else knows who is causing all the smells. Charlie is too embarrassed to admit he is the source of the farts, until one class...when a massive fart reveals Charlie as the culprit.

A blockchain informational podcast. We produce an annual blockchain convention called Rare Evo.

Comment poser le bon diagnostic sur ces nouveau-nés et enfants atteints par des pathologies rares, des malformations de la tête, du cou et des dents ? Vers qui diriger les familles ? Comment parler de ces maladies, les comprendre et les affronter ? Les différents spécialistes de la Filière TETECOU apportent des réponses. Dans « Mots de têtes », le podcast proposé par la Filière de Santé Maladies Rares TETECOU, nous découvrons l’existence de tout un réseau spécialisé dans des pathologies rares, des malformations de la tête, du cou et des dents présentes à la naissance ...

A Starfield Podcast hosted by Ara and Lyr

Have you ever wondered what an up and coming, independent, rock band does every day? Welcome to the Screw Loose Juice - a podcast from the members of the band, Rare Americans, an award winning Canadian rock band known for their viral animated music videos! Meet the creators behind RA, with in-depth discussions about songwriting, production, touring, creating, marketing, the fans, animation, and their general view of the world and current events. Get behind the scenes with the day-to-day of a modern rock band!

Join James Priestner, lead singer of the viral band 'Rare Americans', as he takes you behind the scenes interviewing the artists you love. Learn what actually goes on inside the music industry straight from the artist's perspective.

The Your way Podcast series features Neuromyelitis optica spectrum disorder (NMOSD) patient ambassador Debbie Leticq, alongside healthcare professionals including neurologist Dr Lesley-Ann Hall, Specialist Nurse and Research Fellow, Dr Therese Burke, and psychologist, Dr Sally Shaw, who all share some deeply personal experiences about this rare, auto-immune condition. Their candid conversations shine a light on the day-to-day reality of living with NMOSD, provide some insights and advice to those who may find themselves either newly diagnosed or learning to live with NMOSD. If you would like ...

Canfranc, 1944. La joven Valentina Báguena, colaboradora de la Resistencia contra las fuerzas de ocupación nazis en el sur de Francia, descubre que la guerra cambia por completo la forma de vivir, de pensar y, sobre todo, de amar cuando conoce al paracaidista alemán Franz Geist el mismo día en que un incendio destruye el pueblo de Canfranc. Tras la devastación producida por el fuego, los habitantes de este lugar serán víctimas, además, de una de las mayores estafas de la historia de España. Un hecho de dimensiones extraordinarias, pero casi desconocido hasta ahora.

ABCs of NMOSD brings together the latest information and research about all things NMOSD, from diagnosis and treatment to quality of life and what it’s like to live with NMOSD. We invite medical experts and researchers, to share the latest up-to-date research and clinical knowledge. We have conversations with individuals who have been diagnosed with NMOSD, their caregivers, and allied health professionals. We give tips on how to advocate at school and at work, where to find help and support, navigate health insurance, and work with a team of medical experts.

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 sending an email to info@wearesrna.org and please use SRNA Podcast in the subject.

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

Hunt and Pie talk about adventures as delivery workers, real stories, total knuckleheads

Advanced spoken Latin podcast by Irene Regini. In each season I interview some "rarae aves", incredibly talented persons who achieved amazing results in the field of the Latin language. You'll learn how they started, how their daily Latin routine looks like and how they grew their projects from scratch. The interviews in full video format are available on my YouTube channel. Your very special journey to becoming a "rara avis" starts here: https://pages.saturalanx.eu/yplc-waitlist/ This is a Satura Lanx production (listen to my other podcasts: Satura Lanx, Litterae Latinae Simplices).

Un podcast sobre gente poco común en el que hablamos de Lifestyle y Negocios Online. Reflexiones, puntos de fuga e historias de creadores, de hacedores que se arriesgan en lo cotidiano para transitar su deseo. Gente rara es un espacio para pensarse, dudar, divertirse, proyectar y lo que sea que te provoque.

How would you like to be given a new identity to live by and then removed from your sisters and brothers—never to be legally permitted to contact them again—even upon your deathbed? This is just one of many examples of red tape adoptees are forced to contend with. This book reveals the making of the current child welfare system. The pioneers who built and profited from the industry continue to deny adoptees access to documents that could lead them back to their families. This book protects you against adoption profiteers and traffickers who profess God is on their side.