Showing results by author "Las Raras" in All Categories

「はいはい、お待ちしてたよー。『ウィッチズ・エルミタージュ』へようこそ！　今日キミを超チルくしてあげる心の友はうち、山の魔女・アズサちんだよー。

「殿下は頑張りすぎです。少しはご自分のことも大切にしてください」誰にでも優しく、周囲の人達から頼られる領主のあなた。

「はい？　魔女？　え、ええ、そうです。 その、お、おそらく……ですけど、 今日お客様のケアをさせて頂く……雷電の魔女・ヘレナ……です」

「……ここで会ったことはお姉ちゃんたちにも妹にも秘密だから、内緒のデート、だね」静かな雨音を聴きながら、ゆっくりと一緒に過ごす夜――

「妾はお主が欲しくなった……世界よりもな」勇者である貴方と対峙する魔王。決戦の直前。彼女は、ある一つの提案をしてきた。

「もうちょっと、ここに――　い、一緒にいてあげても、いいわよ……？」一緒に海を眺めたあとは、２人きりの空間でまったり……

「思えば、こんなに落ち着いたのも百年ほど久しいかもしれぬ」勇者である貴方と対峙する魔王。決戦の直前。彼女は、ある一つの提案をしてきた。

「こうやって一緒にいるの……とってもうれしいんですから……」他に誰もいない浜辺で、波音を聴きながらゆったりお散歩。ちょっともどかしい、２人きりの静かな時間――。

『ああ、お姉ちゃんが欲しい』ついそんな言葉をこぼしてしまった事はありませんか？

「幸い、夜は長ぇしな。あんたの話相手くらいにならなってもいいぜ」深夜00：00。上手く寝つけず、夜風に当たる為に家を出る。扉を開けた先……

Il podcast gMG Your Way è una serie di otto puntate realizzato con il patrocinio e contributo dell’associazione pazienti Associazione italiana miastenia (A.I.M). Romina Gibertoni, segretaria di A.I.M, ci accompagnerà in un percorso di scoperta all’interno del mondo della gMG, ossia la miastenia gravis generalizzata. In ogni episodio, Romina sarà affiancata da persone che vivono e affrontano questa malattia ogni giorno, clinici, caregiver e altri membri attivi della comunità gMG, che, attraverso la condivisione delle loro storie, esperienze e professionalità ci aiuteranno a capire ...

Sejam todos bem vindos ao Talento Raro Podcast, um podcast semanal voltado para a cultura e mundo pop. Todas as novidades, lançamentos e assuntos mais comentados da semana você encontra aqui! Para não perder nada, nos siga no Instagram: @talentoraropodcast

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

Hi, Welcome to the Strong and Rare parenting podcast. My name is Victoria, and I am a special needs momma of two fun loving boys. In this podcast, we will speak about all things Autism, ADHD, and Rare Diseases. This podcast will bring awareness, acceptance, and knowledge on all things we want to learn as parents raising children with special and medical needs. When you join me, I hope that you will walk away with hope and be empowered to be a driver of change for our community. Support this podcast: https://podcasters.spotify.com/pod/show/strongandrareparenting/support

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 ...