Special Needs Child

Jeni Decker is five-foot nothing and one hundred and [redacted] pounds - a self-described roly-poly, forty-something, Reubenesque bon-bon of a gal, often called cute but never sexy. She has two sons with autism on opposite ends of the spectrum (Jake and Jaxson), a husband who prefers hunting to household chores, an Australian Shepherd named Sugar, and an albino frog named Humbert Humbert. This is her story - a brash, personal, and sometimes shocking memoir.

Long ago, in a land by the sea, 12-year-old Aaron lives with his mother in the wooded countryside. Because the boy is mute, he depends on his mother completely. But when a sudden blizzard strands his mother in a distant town, Aaron finds himself alone for the first time in his life. Setting out in the snow to look for his mother, the boy embarks on a perilous, silent journey that will carry him to the eerie Half-a-Moon Inn. There, held captive by the sharp-eyed Miss Grackle, Aaron will discover her wicked powers.

Before Stinkville, Alice didn't think albinism - or the blindness that goes with it - was a big deal. Sure, she uses a magnifier to read books. And a cane keeps her from bruising her hips on tables. Putting on sunscreen and always wearing a hat are just part of life. But life has always been like this for Alice. Until Stinkville.

Spending the summer with his grandparents in the Pennsylvania countryside is pure joy for young Jamie. There, he fills his days with looking up at the sky, watching the clouds make dragons and knights. There, it doesn't matter that he can't read. The special school he attends is far away. But one afternoon, when Jamie sees a man parachute down through the sky, the boy's fantasy world of clouds is shattered. The man is very real - and very dangerous. How can he convince his grandparents that the man is not part of his imagination?

Jillian Benfield was living life in the spotlight as a TV journalist, but after receiving a life-altering diagnosis for her unborn son, she realized no camera-ready outfit could dress up her grief. Overcoming this unexpected circumstance wasn't an option. She would have to undergo it instead. In doing so, she discovered who she was and who God wanted her to become.

You want your child to progress in leaps and bounds, and this book will help you do just that by equipping them with the necessary coping skills to handle any situation. Within this audiobook, you’ll discover detailed coping strategies that will reduce your child’s stress and enable them to take the reins of their own emotions.

Jamie Grimm has finally accomplished his dream of proving himself the Planet's Funniest Kid Comic, and the sky's the limit from there. Enter a couple of TV executives with a huge plan for Jamie: a new show about Jamie and his oddball friends! But when Jamie struggles to learn the acting ropes, will it be an early curtain call for the biggest show of the decade?

Navigating the special education system can be tricky but not impossible. With this guidebook, you'll have all the tools you need to secure top-notch services for your kiddo. Put your game face on and become your child’s fiercest advocate and greatest cheerleader.

La "dyslexie", un mot étrange et impossible à prononcer, pourtant c'est bien ce qu'on m'a diagnostiqué. Moi, Dylan, quatorze ans, j'ai des problèmes de connexion, je suis dys-connecté. Cette particularité ne m'empêche pas de vivre, par contre elle ne me facilite pas les choses, surtout à l'école... "Dylan, arrête de faire le guignol !" "Dylan, tu pourrais t'appliquer !" Personne ne doit découvrir mon secret, c'est ce que je me suis juré !

Stacey Simms' parenting philosophy is "not perfect, but safe and happy." Does that make her the world's worst diabetes mom? Some people on social media thought so. But her stories and the lessons they impart show that diabetes laughs in the face of perfection. Raising a happy and healthy child with type-one diabetes, as well as any siblings, requires flexibility, planning, and a great sense of humor above all else. It's a journey full of challenges, but you are not alone!

Jay reads Braille. Sam uses a wheelchair. Ben has Down syndrome. In this series, young listeners can learn more about how to be a good friend to friends with different capabilities and conditions.

Organized children are raised, not born. That’s the philosophy behind this confidence-building, sanity-saving book. Fostering organized thinking in your child will help with concrete concerns (think a tidier bedroom!) and build critical life skills like learning to plan and grasping the big picture. Dr. Korb’s 5 Steps to Raising an Organized Child apply to all ages. So, whether you have an infant or a teenager, it’s never too late (or too early!) to foster organization in him or her and harmony in your whole family.

ADHD is not the result of ineffective parenting education, and it is not related to the "badness" of the child. ADHD is an attention disorder that if not managed right can become a real problem - for the individual, family, and school - with discomforts and frustration at school and personal level. Very often, the first to suffer from this situation are discouraged and stressed parents because they feel guilty and unable to manage the child's behavior.

Learn about children who are blind, their challenges and adaptations, and their similarities with others.

My friend Darius has a disability called dyslexia. But that doesn’t matter to us. We make our own comics, help each other with our homework, and volunteer at a nearby animal shelter. I’m glad Marius is my friend!

My friend Sarah has a disability called Down Syndrome. But that doesn’t matter to us. We tell jokes and laugh, go to ballet class together, and have a lot of fun. I’m glad Sarah is my friend!

Learn all about kids who are deaf.

Some people are deaf. What does that mean? Listeners learn what deafness is, how it can be caused, and what daily life is like for someone who can't hear.

No one said motherhood would be easy. For Adiba Nelson, the journey to parenthood started with a big bang and continues with a breakdown (or two) and several “why?” questions for God.

Graham Hale Gardner died before turning 23 and never learned to walk or speak due to severe cerebral palsy complicated by epilepsy. Yet he left a legacy of love and compassion that deeply moved scores of people from widely different backgrounds. Graham’s story, written through the eyes of his father, speaks of the enormous legacy left by a boy who never spoke. A story that raises provocative questions about the “invisible lines of connection” that make us human.