Showing results for "The Rare" in Children's Audiobooks

Welcome to KCNA2 & Rare Epilepsy Podcast, a podcast created for the people living this journey and the people working to understand it. Each episode, hosted by Dr. Nancy Musarra, invites listeners into honest, generous, and sometimes vulnerable conversations with parents, researchers, clinicians, and board members to discuss the daily experiences of living with KCNA2, seizures, and other rare forms of epilepsy. You’ll hear stories, questions, and hopes from people who understand and are living with this disease. Our mission is to raise awareness, build connections and foster hope. This isn...

Dobro došli na podcast! Ovo je naše: “Zašto Rare & Share?”: Tokom lečenja sina od retke bolesti, a posebno nakon izlečenja imali smo prilike da upoznamo sjajne ljude i čujemo vrlo inspirativne priče. Ceo jedan svet sa svojim temama. Ovde ćemo pričati sa onima koji su pokretali lavine događaja, menjali okvire, pomerali granice do tada poznatog. Želimo da razgovaramo o temama koje su važne onima koji se suočavaju sa retkim izazovima kao što su pravni i zakonski okviri, aspekat psihološke podrške, medicinska dostignuća i nove studije. Planiramo razgovarati sa ekspertima, ...

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 ...

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

Zoe and Harvey are amazed to discover a rare baby white buffalo in the park. The animal's presence has to be kept secret to protect it, but when they realize they have accidentally put two poachers on the buffalo's trail, Zoe and Harvey set out to make amends by preventing the scoundrels from capturing it. And to do this, they can always count on their closest ally: Lassie!

L'œuvre essentielle d'Andersen, qui lui valut la célébrité mondiale, est constituée par ses contes. S'inspirant des récits populaires, empruntant ses personnages et ses intrigues à la légende, à l'histoire ou à la vie quotidienne. Il écrivit cent cinquante-six contes de fées entre 1835 et 1873, dont les quatre premiers furent publiés en 1835.

En Un mundo raro existe un mundo que brota en la cabeza de los protagonistas de este libro de relatos y también de sus pies, de sus orejas, de sus oídos. Son niños y niñas que inventan mariposas para adornar sus paseos o que dibujan el sol en medio del invierno, o que siembran letras para inventar cuentos. Niños y niñas con disfuncionalidades que construyen el mundo a su propia medida y bajo su propia mirada: un mundo que rebosa imaginación y poesía. Las ilustraciones a tinta china son de la artista japonesa y titiritera Motoko Toda.

Classic fairy tales and stories are an essential part of children's development. This collection brings together rare fairy tales, stories, myths and legends, to feed the intelligence and imagination of children in their years of development.

Parenting tools and life hacks for raising a child with a rare diagnosis. Let’s get to the meat of it!

Join us on a deeply moving journey as we delve into the remarkable story of a mother's unwavering love for her son, who battles not one, but two rare diseases. Through candid conversations and heartfelt moments, listeners will gain insight into the challenges, triumphs, and resilience of a family navigating the complexities of rare medical conditions. From the initial shock of diagnosis to the daily realities of caregiving, this podcast explores the profound bond between a mother and her child, demonstrating the power of love and determination in the face of adversity. Tune in to be inspired ...

Rare Mamas Rising is a podcast for mothers of children with rare diseases to find strategies, strength, support, and sisterhood! Hosted by Nikki McIntosh, founder of Rare Mamas, author of the book Rare Mamas: Empowering Strategies for Navigating Your Child's Rare Disease, and a rare mom herself, each episode offers heartfelt reflections, practical tools, and empowering strategies to help you rise to the call of rare disease parenting. Catch an episode of Rare Mamas Rising and walk away encouraged, uplifted, and empowered. We rise stronger when we rise together—let's rise!

Nutricia’s Caring for Rare explores what life is like with a rare metabolic disorder – from difficulties at diagnosis to adapting to condition management to thriving in everyday joys. Episodes feature personal experiences with rare inborn errors of metabolism like phenylketonuria (PKU). These stories may not be representative of all rare metabolic disorders, and this podcast in no way replaces the guidance and supervision of metabolic healthcare professionals. Guests on Caring for Rare are compensated for their time. Brought to you by Nutricia North America.

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.

Children may love their older relatives, but it can be a difficult trip when visiting grandparents and older relatives. This book is a playful and touching spin on the anxiety young children feel when visiting elders.

Take a look into Emmas complicated life with multiple chronic illnesses. Sometimes Good, Sometimes Bad, Sometimes funny, Always Honest.

Quelques chansons pour enfants : 12 chansons rares et entrainantes pour petits enfants.

Classic fairy tales and stories are an essential part of children's development. This collection brings together rare fairy tales, stories, myths and legends, to feed the intelligence and imagination of children in their years of development. Here are seven of the rarest and most delightful tales: "How to Tell a True Princess" and "The Darning Needle" by master storyteller Hans Christian Andersen; "Belling the Cat" and "The Wolf and the Fox", taken from Aesop's fables; an English fairy tale, "Master of all Masters"; "Persevere and Prosper", and "The Story of Caliph Stork", two old Arabian tales.

14 chansons et comptines pour enfants...

William F. Hooley (April 16, 1861 - October 12, 1918) was a British-born American bass singer and pioneer recording artist who was popular as a solo singer, as a monologist, and as a member of several of the most successful vocal groups of the early twentieth century, including The Haydn Quartet and The American Quartet.

Parmi les plus beaux contes pour enfants et histoires pour s'endormir se trouvent des perles que leur rareté rend encore plus savoureuse : elles aident les enfants à s'éveiller à la culture littéraire et de développer leur imaginaire, tout en permettant aux parents de partager avec eux le plaisir de la découverte. Ces douze contes rares sont des joyaux de la littérature populaire, difficiles à trouver mais riches d'inspiration.