PDF Ebook Count Us In: Growing Up with Down Syndrome (A Harvest Book), by Jason Kingsley, Mitchell Levitz
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Count Us In: Growing Up with Down Syndrome (A Harvest Book), by Jason Kingsley, Mitchell Levitz
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At ages nineteen and twenty-two, respectively, Jason Kingsley and Mitchell Levitz shared their innermost thoughts, feelings, hopes, and dreams, their lifelong friendship—and their experiences growing up with Down syndrome. Their frank discussion of what mattered most in their lives—careers, friendships, school, sex, marriage, finances, politics, and independence—earned Count Us In numerous national awards, including the EDI Award from the National Easter Seal Society. More important, their wit, intelligence, candor, and charm made a powerful and inspirational statement about the full potential of people with developmental disabilities, challenging prevailing stereotypes.
Now, thirteen years later, the authors discuss their lives since then—milestones and challenges, developments expected and unexpected—in a new afterword.
- Sales Rank: #545584 in Books
- Published on: 2007-03-05
- Released on: 2007-03-05
- Original language: English
- Number of items: 1
- Dimensions: 8.00" h x .56" w x 5.00" l, .47 pounds
- Binding: Paperback
- 208 pages
From School Library Journal
YA-Written by two young men with Down's Syndrome, this book will open eyes and touch the heart. The interview style is involving as the authors discuss their friendship, having Down's Syndrome, marriage, children, becoming independent, and their hopes and dreams for the future. They speak openly about how people have treated them differently because of their disorder and how they feel about it. The book is occasionally a challenge to read since the authors speak in unusual syntax. Black-and-white photographs from family albums appear in a center insert. Curious teens and friends and family members of the disabled will feel the emotions of these two remarkable young men and learn how they work to cope and to succeed.
Jacqueline Craig, W.T. Woodson High School, Fairfax, VA
Copyright 1994 Reed Business Information, Inc.
From Booklist
Kingsley and Levitz write about education, employment, ambitions, families, sex and marriage, and their disability--Down syndrome--in a dialogue format. At Jason's birth, the obstetrician said that he'd never learn anything and should be institutionalized. Fortunately, the Kingsleys ignored this advice, and their son has since attended school, written poetry, registered to vote, and memorized scripts for appearances on "Sesame Street" and "The Fall Guy." Mitchell is an equally successful young man whose mother was one of the founders of the Parent Assistance Committee on Down Syndrome. Hearing about Down syndrome directly from these young men has a good deal more impact than reading any guide from a professional or even a parent. Their comments are eye-opening and heartening. Denise Perry Donavin
From Kirkus Reviews
Two young men with Down syndrome celebrate--with the support and word-processing assistance of their mothers--their successful coming of age and hard-won independence. When, three years apart in the early 1970's, Kingsley and Levitz were born and diagnosed with Down syndrome, their respective parents were advised to institutionalize the boys without even taking them home from the hospital. Fortunately, that advice was ignored, and the parents became friends through the Parent Assistance Program on Down Syndrome, founded by the Levitzes; soon, the boys became friends as well. As pioneers in the infant- stimulation program now widely approved, if not widely available, for Down syndrome children, Levitz and Kingsley entered some early special-education programs and went on to be mainstreamed in high school. Bolstered by the unusually rich cultural resources of their families, they passed their New York State Regents exams, graduated, and are now dipping their toes into college and independent living. The text here consists primarily of transcribed conversations (minus difficulties in articulation) between Kingsley and Levitz, along with their parents' occasional interjections and questions, supplemented by some written material from the young men. It's both a celebration of the pair's triumph over expectations (``we should call each other Up syndrome'') and a sometimes painful recitation of their struggles and sorrows. All the usual issues of adolescence are here--sex, girls, God, death, love, war, independence--discussed with both a realistic assessment and an idealistic innocence that typifies ``mainstream'' teenagers. Levitz, who loves politics, wants to be President; Kingsley, with the soul of a performer, wants to be a teacher, newscaster, actor, and spokesperson for the disabled. Each grudgingly accepts that they may never get driver's licenses--but, as Kingsley says, life is ``A Learning Adventure.'' Worthwhile inspiration and insight for Down syndrome children, as well as for their families, teachers, friends, and advocates. (Photographs) -- Copyright ©1993, Kirkus Associates, LP. All rights reserved.
Most helpful customer reviews
35 of 35 people found the following review helpful.
irinaz
By A Customer
I first read this book when my son with Down Syndrome was very young. It was extremely encouraging to me to read the very complex and interesting thoughts of two adult men who have Down Syndrome. I wish all teachers would read this book. I think any parent with a child who has Down Syndrome, especially a very young one, would benefit from reading this book. I really fell in love with Jason and Mitchell.
30 of 30 people found the following review helpful.
Count Us In by Jason Kingsley, & Mitchell Levitz
By A Customer
This is a book written in their own words by two young men who have Down's Syndrome. They share the ups and down's of their lives . Although my son is only nine, I found this book very helpful because it gave me some preview of things to come. Because the book was written in the boys' own words, it gives a unique picture into the minds and lives of older children with Down syndrome. It also gave some insight into familiar problems, as well as some events that were unique to these boys who authored the book. I found myself wishing that my own son had a close friend to help guide him through the ups and downs that await him in his teenage years. Then I realised that I could actively seek out peers for him to become friendly with at my local Down syndrome chapter, and maybe I could find some friends that he could become close with in a similar fashion to the authors of this book. I highly recommend this book to all parents, caregivers, teachers and other professionals who work with children who have disabliities similar to Down Syndrome, because the experiences of these boys could cover a broad spectrum of disabilities, not only Down Syndrome. So many books are written from an outsider's prespective. This book comes straight from the sourcel.
14 of 14 people found the following review helpful.
very educational
By Jessica Green
i think this book should go to individuals to learn about issues that might be dealing with. these two advocates have learned a lot and how their parents has taught them i think i definitively recommend this book to go to many libraries and bookstores so that other men can learn how to do things on their own just like any other men. i am a women and i have down syndrome to i have read this it made me realize that having down syndrome is a celebration
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