Showing results by author "RARE" in All Categories

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.

FENTYNOL- WORLD EPIDEMIC- "FREEING FENTYNOL FEVER" LIFE BEFORE, DURING, AND AFTER FENTYNOL. I WANTED TO SHARE MY STORY AND EXPERIENCES WITH THE WORLD. I have been through so many obstacles, escapes with death, lowest of the low, each episode will focus on a specific time in my addiction, or in my recovery, that I want to share, but I also hope to gain knowledge from you all as well. I want to show everyone there is life after é proof...imi TRUELY believe we can do anything we put our mind to. I will have a guest on the show each week, maybe a Dr, music artist, transient, CEO, Dentist, all ...

Un viaggio nell'economia che conta davvero. Notizie, analisi, previsioni e approfondimenti di economia, mercati, metalli, investimenti, finanza, energia, commodities, lavoro e soldi.

News and information on metals, economy, investments, markets, technology, energy and the most important international rankings of the moment.

The NMOSD Your Way Podcast series features Neuromyelitis Optica Spectrum Disorder (NMOSD) patient ambassador, and host, Lelainia, alongside healthcare professionals, patient advocates, and caregivers. In each episode, participants share some deeply personal experiences about this rare, auto-immune condition. Their candid conversations unpack some of the mystery behind this little known condition and delve into the day-to-day realities of living with NMOSD. Participants also provide insights into living well, offering encouragement and information to others who may find themselves either newly ...

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.

Hip-Hop, Pop Culture & Entertainment!

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).

Transformando pacientes em protagonistas!

🎙️ 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! 🚀

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.