Ergebnis für "UP" in Gesundheit von Kindern

In this groundbreaking debut, Charli Clement combines their own experiences alongside unique short profiles from individuals with chronic illness, to provide an intimate and insightful look at the complexities of living as an autistic and chronically ill person. From navigating your diagnosis and healthcare, learning how to manage pain and your own sensory needs to dealing with ableism, medical misogyny and transphobia, Clement offers practical advice and delves into the unique challenges faced by individuals living in this intersection.

Up, Not Down Syndrome is a love letter and a map. Experience how it feels to think your life is over after having an unlovable baby. At first, the loss seems impossible to overcome. Alex becomes the author's greatest teacher. Love is stronger than fear. Everyone has gifts. The book consists of three parts: the story, the lessons that Alex taught the writer and Alex's perspective. Up, Not Down Syndrome is a promise to stay positive, no matter what: up, not down.

The long-awaited follow-up to the million-copy bestseller The Out-of-Sync Child, presenting information and advice for tweens, teens, and young adults living with Sensory Processing Disorder, and their parents. The Out-of-Sync Child Grows Up will be the new bible for the vast...

A diverse collection of autistic voices that highlights how parents can avoid common mistakes and misconceptions, and make their child feel truly accepted, valued, and celebrated for who they are. Most resources available for parents come from psychologists, educators, and doctors, offering...

In But Everyone Feels This Way, Autism acceptance activist and multi-million-follower TikTok influencer Paige Layle shares her deeply personal journey to diagnosis and living life autistically. It all started out pretty normal: Paige lived in the countryside with her parents and brother Graham...

Bloomsbury presents ADHD Unpacked, an essential guide to surviving and thriving with adult ADHD, written and read by Alex Conner and James Brown, the hosts of the hit ADHD podcast, The ADHD Adults. This audiobook features an exclusive bonus episode of The ADHD Adults podcast. 'Essential reading'...

From the author of the bestselling The Reason I Jump, an extraordinary self-portrait of a young adult with autism “Essential reading for parents and teachers of those with autism who remain nonverbal.”—Temple Grandin Naoki Higashida was only thirteen when he wrote The Reason I Jump, a...

Growing Up With Asperger's provides advice, stories, and anecdotes for autistic listeners both young and old, and parents of autistic children. Funny and down-to-earth with an honest look at life from an autistic perspective.

Kimberly Wyse is a blogger, speaker, and Down syndrome advocate, who tells the story of the traumatic birth of her much-anticipated third child, who was diagnosed at birth with trisomy 21 (Down syndrome) and had major medical complications that almost took his life several times. Through the gift of extreme medical intervention and God’s miraculous answers to prayer, this precious boy has exceeded everyone’s expectations and is a joy to his family today.

Kenna was born January 9, 2012, weighing in at a meager 9.6 ounces. She was born 16 weeks too soon. After spending 183 days riding the roller coaster in Club NICU, she is finally home. This is our story of hope, finding happiness in unlikely places, and making the best of the life we have.

The step-by-step guide discusses various aspects of how autism is perceived, explores how best to speak up for individual needs and introduces advocacy for the wider autistic community. Each step outlines one vital aspect of advocacy and allyship, such as emphasizing acceptance, avoiding assumptions and assuming competence. The advice and strategies laid out in this guide center the wisdom and experiences of autistic people and enable the listener to confidently speak up with insight and understanding.

The primary message young children get in stuttering therapy is that they can and should manage their speech — in other words, try to not stutter — by utilizing speech tools and techniques. Is it possible that the anxiety this causes can create an even greater burden? Can that burden lead to excessive silence and disengagement — a far greater handicap than the stuttering itself? Through personal narrative and extensive research, Voice Unearthed answers these questions with a resounding “yes!

When Peter Flom was five years old, his parents were told that he had "minimal brain dysfunction" and "would never go to college". Peter skipped one year of high school, did college in three years, and got his BA at 20. In Screwed Up Somehow but Not Stupid, Peter describes what it's like to live with a learning disability, but also some abilities.

In 1963, Philip Hodges was born, the seventh of eight children, inflicted with Cerebral Palsy. Thanks to the loving devotion of their parents, who saw Philip as a gift and not a burden, the author and his siblings experienced the power of love, devotion, and acceptance that forever changed their lives.

It was a year of challenges big and small, health concerns that had us rushing to the Pediatric ER, another surgery, therapies, doctor's appointments, and a list of goals that Kenna is achieving. If the 183 day hospital stay was about finding happiness in unexpected places and making the best of the life we had, this year was about finding balance, rearranging our priorities, and adjusting our attitudes so that we could enjoy life with the gift we had been given.

The story of Jamie Bérubé’s journey to adulthood and a meditation on disability in American life Published in 1996, Life as We Know It introduced Jamie Bérubé to the world as a sweet, bright, gregarious little boy who loves the Beatles, pizza, and making lists. When he is asked in his...

A mother’s candid and moving account of the challenges and joys of having a Down Syndrome child ‘A searingly honest account of her journey, from heartbreak to joy’ Daily Mail When Sarah Roberts’s son, Oscar, was born, he was unexpectedly diagnosed with Down Syndrome. Sarah had to rapidly...

This is my story. After a lifetime of trying to help everyone else get their lives together, I have finally figured out how to get mine together. I am now 72 years old, semi-retired from a business I created to help young adults with autism function in the world. I live in Mexico with my loving partner. I have fulfilling relationships with my adult children and grandchildren.

For every parent who’s worried about their child’s weight or size, this insightful book offers an approach to health that focuses on the whole child—not just the growth chart. All children deserve a future free of health concerns and one full of self-esteem and wellbeing, no matter their...

Born with a hole in his heart that required invasive surgery when he was only three months old, Quinn Bradlee suffered from a battery of illnesses - seizures, migraines, fevers - from an early age. But it wasn't until he was 14 that Bradlee was correctly diagnosed with Velo-Cardio-Facial Syndrome (VCFS), a widespread, little-understood disorder that is expressed through a wide range of physical ailments and learning disabilities.