Showing results for "Rara" in Children's Audiobooks

Dive into the vibrant and mysterious world of the coral reef with this enchanting educational book! "Rare Creatures of the Coral Reef" takes children on an unforgettable journey through the depths of the ocean to uncover the fascinating inhabitants of one of Earth's most biodiverse ecosystems. Be inspired to explore the wonders of the natural world and become stewards of the ocean.

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

The Rare Remix is a podcast for families navigating rare disease, disability, caregiving, accessibility, developmental differences, and life after a diagnosis changes the rhythm of everything.Hosted by Bryan and Lindsey, The Rare Remix features real conversations with parents, caregivers, advocates, experts, and anyone on a remixed journey. Together, we explore the everyday realities that families quietly learn to navigate, and discuss potential solutions based on first-hand experiences.This may not be the life you imagined. It’s a remix.

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.

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, ...

Join host Juniper Snout as she explores rare exotic pets, from regenerating axolotls to ghost snakes and capybaras. Each episode reveals jaw-dropping adaptations, specialized care requirements, and legal complexities behind keeping nature's most unusual creatures as companions. For more content like this, visit QuietPlease.ai This content was created in partnership and with the help of Artificial Intelligence AI.

This is the Roadmap to Rare. Hosted by OCNDS parent Eric Finn, this podcast explores the reality of the rare-disease journey—sharing hope through real stories, real challenges, and research. This is our rare disease roadmap.Every rare disease journey is different, but no family should have to navigate it alone.On Roadmap to Rare, Eric sits down with parents, advocates, clinicians, researchers, and leaders in the rare disease community to talk about what the path really looks like—from diagnosis to advocacy, research breakthroughs, and everything in between.Together, these conversations ...

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

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...

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!

Leo es un niño de once años de lo más normal. Excepto por el tema de los portales para cruzar a otros mundos, claro. Leo tiene un superpoder muy extraño. Se enteró una noche, al ir al frigorífico (según él, solo para mirar. En ningún caso para comerse la tarta de chocolate). Descubrió una grieta que lo podía llevar a otros mundos, mundos de duendes y hadas. No se lo podía creer, pero los tenía delante de él y la evidencia es la evidencia. En cierta ocasión, huyendo de Ricky, un abusón que le hacía la vida imposible, se cruzó con unos niños muy extraños.

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

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.

This story is a gem representing the delightful stories from the Indian subcontinent which capture the simple essence of everyday life in India. The simple pleasures of life indicate a time gone by before the advent of cellphones and Facebook, a time which almost stood still, a time when children could revel in the rain, make paper boats and race them down a drain, play marbles, and generally pass time.

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!

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.

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 ...

When Churchills, London’s finest department store, places an order for their best-selling toys from the Jade Emperor Toy Company in China, they get more than they bargained for. A broody and mischievous factory worker inadvertently starts a chain of events that leads to Thomas, a recently orphaned, disabled boy, having the magical adventure of a lifetime. When a hamper arrives from an eccentric aunt at Pendle Farm containing a Churchills’ Doggie Bear called Harry, life will never be the same again for the Shuttleworth family. Can Tom help Harry find what he is looking for?

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.