Showing results by author "Las Raras" in All Categories

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.

The Non-Monogamy Playbook is the handbook for anyone curious about consensual non-monogamy: polyamory and open relationships. The Non-Monogamy Playbook shows us that there's joy in having multiple people in your life (platonic, sexy, romantic), but with each connection there is added vulnerability. This is the ultimate modern guide to non-monogamy, helping you create confident, healthy relationships.

Written by sex educator and body-positivity advocate Ruby Rare, Sex Ed is the practical and fun guide to sex that you've always wanted - but never known how to ask for. This is the information you should have been taught at school: a no-holds-barred roadmap that covers everything from how the brain is the most important sex organ and how to communicate what you want to yourself and a partner, all the way down to the messy stuff - solo sex, orgasms, touching, kissing, blow jobs, cunnilingus, anal play, lube, toys, kegels.

🎙️ Welcome to the Rare Sats Podcast! 🎙️ Ready to dive into Bitcoin’s hidden treasures? We uncover rare satoshis—unique digital gems within the blockchain. Discover why they’re so valuable, how to find them, and what makes them the next big thing in crypto. Each episode brings you insider stories, expert insights, and market updates that will transform your view of Bitcoin. Whether you're a seasoned collector or just curious, join us in the hunt for Bitcoin’s rarest finds. Subscribe and explore the secrets of Rare Sats! 🚀

キャリアアップのためにと転職した先の社宅。そのお隣には、小学校から大学まで同じ学校、同じ部活の後輩……けれど、今はあなたの上司である女性が住んでいた。

『カフェ×ASMR』理工系の才媛たるリケジョ店員が、持ちうる科学知識を総動員させて、あなたの体を癒し全回復させます。

Radio Rare is a podcast where we share the stories of those in and around the rare and less common cancer community. Being diagnosed with a rare cancer doesn’t mean you’re alone. Radio Rare will dive into the human stories of the rare cancer experience, the innovation and the advocacy. Addressing the feeling of isolation experienced by so many, we look to create a close community of those affected by rare and less common cancers. Produced by Rare Cancers Australia

夢を追うストイック系JK、ASMR部に堂々登場！！あなたの前に現れたのはストイック＆クールなJK「七野宮奈留」。

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.

Transformando pacientes em protagonistas!

Shedding light on underrepresented diseases and the efforts of non-profit foundations working tirelessly to support those affected.

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.

This page features multiple Podcasts for the gem of a text based game, torn.com - The original Torn Underground w/ Ara & TheFelan. Tuesday Talks w/ Paul. Lastly, Women of Torn w/ Jairyll & Glandem!

Marzo de 1943. Agazapados dentro de una habitación secreta, varias personas contienen la respiración mientras aguardan a que el sonido de las botas reforzadas con metal de los soldados alemanes se aleje. En la estación internacional de Canfranc, en el Pirineo, la esvástica ondea sobre la playa de vías. En medio de la oscuridad, Laurent Juste, jefe de la aduana, Jana Belerma, camarera del hotel, y el bandolero Esteve Durandarte arriesgan sus vidas para devolverles la libertad.

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.