- Paperback: 496 pages
- Publisher: Wiley-Blackwell (15 Aug 2002)
- Language English
- ISBN-10: 0471418153
- ISBN-13: 978-0471418153
- Product Dimensions: 23.6 x 15.3 x 2.7 cm
- Average Customer Review: 5.0 out of 5 stars See all reviews (1 customer review)
- Amazon Bestsellers Rank: 1,212,021 in Books (See Top 100 in Books)
- See Complete Table of Contents
Down Syndrome: Visions for the 21st Century
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Review
"This volume is a comprehensive collection of articles representing a wide range of disciplines…it will be a valuable addition to the bookshelves of families, medical staff, educators, and researchers." (American Journal of Medical Genetics, August 15, 2004)
“...a comprehensive compilation of the myriad issues facing individuals with Down syndrome and their families across the lifespan...this book, compared to other tomes of highlights from various conferences, seems to contain more bang for the buck as the issues it covers are extremely pertinent and could stand alone apart from the conferences...this book will stay on my shelf.” (Journal of Genetic Counseling, Vol. 13, No. 1, February 2004)
"This book will be of great interest to anyone wanting to have the latest information about this genetic disorder..." (family2000.org.uk, 9 September 2002)
"...puts foward some of the visions and thoughts in an optimistic way and is therefore recommended..." (Int Jnl of Adolescent Medical Health)
"...puts forward some of the visions and thoughts in an optimistic way and is therefore recommended..." (Int Jnl of Adolescent Medical Health, Vol.15, No.1, 2003)
"I...consider a copy of this book a must for every institutional and personal library." (Journal of the National Medical Association, March 2003)
"...exceedingly valuable for a wide spectrum of individuals: parents, professionals, caregivers, and researchers..." (American Journal of Human Genetics, Vol. 72, 2003)
"...exceedingly valuable for a wide spectrum of individuals: parents, professionals, caregivers, and researchers..." (American Journal of Human Genetics, Vol. 72, 2003)
"...a terrific compendium of the wide array of topics...whatever the challenges that lie ahead...we are much better prepared by the information and vision provided by this excellent book." (Archives of Pediatrics and Adolescent Medicine, May 2003)
"...a useful reference tool for families and service providers." (Human Genetics, No.113, 2003)
"This volume is a comprehensive collection of articles representing a wide range of disciplines…it will be a valuable addition to the bookshelves of families, medical staff, educators, and researchers." (American Journal of Medical Genetics, August 15, 2004)
"This book will be of great interest to anyone wanting to have the latest information about this genetic disorder..." (www.family2000.org.uk, 9 September 2002)
"...puts foward some of the visions and thoughts in an optimistic way and is therefore recommended..." (Int Jnl of Adolescent Medical Health)
"...puts forward some of the visions and thoughts in an optimistic way and is therefore recommended..." (Int Jnl of Adolescent Medical Health, Vol.15, No.1, 2003)
"I...consider a copy of this book a must for every institutional and personal library." (Journal of the National Medical Association, March 2003)
"...exceedingly valuable for a wide spectrum of individuals: parents, professionals, caregivers, and researchers..." (American Journal of Human Genetics, Vol. 72, 2003)
"...exceedingly valuable for a wide spectrum of individuals: parents, professionals, caregivers, and researchers..." (American Journal of Human Genetics, Vol. 72, 2003)
"...a terrific compendium of the wide array of topics...whatever the challenges that lie ahead...we are much better prepared by the information and vision provided by this excellent book." (Archives of Pediatrics and Adolescent Medicine, May 2003)
"...a useful reference tool for families and service providers." (Human Genetics, No.113, 2003)
Int Jnl of Adolescent Medical Health, Vol.15, No.1, 2003
"...puts foward some of the visions and thoughts in an optimistic way and is therefore recommended..."
Inside This Book
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Front Cover | Copyright | Table of Contents | Excerpt | Index | Back Cover
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Customer Reviews
Most Helpful Customer Reviews
10 of 10 people found the following review helpful
Format:Paperback
At the NDSS annual conference in Washington, DC in 2000, the sponsors asked the participants to share their ideas. This book is a result of that request. Many of the names will be familiar to those who live in the world of Down syndrome. There are articles by Martha Beck Ph.D. and Siegfried Pueschel M.D. on the role of the family; Len Leshin M.D., Pat Winders P.T., and William Cohen M.D. on health issues; George Capone M.D. and Joan Medlen R.D. on psycho-social issues; and Chris Burke on living with Down syndrome; as well as a host of others. The book also features articles on communication, inclusion, advocacy, research, and self-determination. There is a wealth of very useful information in this book. David Patterson Ph.D. writes about the human genome project and what impact it may have on understanding Down syndrome. Libby Kumin, Ph.D. writes about maximizing communication and language skills in infants, toddlers, children, and adolescents. Patricia Logan Oelwein, M.Ed. writes about math and reading skills in children with Down syndrome. There are also a few lesser known names in here such as John Peter Illarramendi, Jeffrey Mattson, Mia Peterson, and Joshua G. O'Neill, all people with Down syndrome who write about their lives, hopes, and dreams. They remind us that people with Down syndrome can achieve a great deal and can live wonderfully fulfilling lives. This isn't a book for a new parent and it certainly shouldn't be your first book on Down syndrome. There are other books such as "Babies with Down Syndrome," that would be a better choice as a first book. But this book does provide a lot of very useful and interesting information. Anyone interested in finding out what is going on in the world of Down syndrome will want to get a copy.
Most Helpful Customer Reviews on Amazon.com (beta)
Amazon.com:
7 reviews
22 of 22 people found the following review helpful
A collection of very interesting articles
22 Nov 2002
Format:Paperback
At the NDSS annual conference in Washington, DC in 2000, the sponsors asked the participants to share their ideas. This book is a result of that request. Many of the names will be familiar to those who live in the world of Down syndrome. There are articles by Martha Beck Ph.D. and Siegfried Pueschel M.D. on the role of the family; Len Leshin M.D., Pat Winders P.T., and William Cohen M.D. on health issues; George Capone M.D. and Joan Medlen R.D. on psycho-social issues; and Chris Burke on living with Down syndrome; as well as a host of others. The book also features articles on communication, inclusion, advocacy, research, and self-determination. There is a wealth of very useful information in this book. David Patterson Ph.D. writes about the human genome project and what impact it may have on understanding Down syndrome. Libby Kumin, Ph.D. writes about maximizing communication and language skills in infants, toddlers, children, and adolescents. Patricia Logan Oelwein, M.Ed. writes about math and reading skills in children with Down syndrome. There are also a few lesser known names in here such as John Peter Illarramendi, Jeffrey Mattson, Mia Peterson, and Joshua G. O'Neill, all people with Down syndrome who write about their lives, hopes, and dreams. They remind us that people with Down syndrome can achieve a great deal and can live wonderfully fulfilling lives. This isn't a book for a new parent and it certainly shouldn't be your first book on Down syndrome. There are other books such as "Babies with Down Syndrome," that would be a better choice as a first book. But this book does provide a lot of very useful and interesting information. Anyone interested in finding out what is going on in the world of Down syndrome will want to get a copy.
18 of 19 people found the following review helpful
Down syndrome
25 Sep 2002
Format:Paperback
Down syndrome have existed for thousands of years. 3,500 years ago the Olmecs tribe, who lived around the Golf of Mexico made wall reliefs, sculptures and other artefacts that showed handicapped people with Down syndrome features around their temples that seemed to represent a mystical attitude or religious significance. They believed that children with Down syndrome were the result of mating between senior women of the tribe with the jaguar, the sacred totem of the Olmecs and therefore the child with Down syndrome was regarded as a god-human hybrid, the "natural" offspring of this close union with the gods. A number of cave paintings describe sexual relationship between a jaguar and a human and it seems that these children were singled out for special treatment. As they were more frequently born to older and therefore more senior members of the tribe and only a few of the children would survive, gave them a rarity value. Persons with Down syndrome at that time were looked upon as sacred and having religious or superhuman significance.
John Langdon Haydon Down (1828-96) was the first physician to describe in detail the syndrome that came to bear his name. In 1866 he tried to classify the various forms of " feeblemindedness" and concluded that individuals with mental disabilities belonged to different ethnic varieties, such as Ethiopian, Malay and Mongolian. We have learned much since and this book edited by Willian I Cohen, Lynn Nadel and Myra E Madnick in association with the US National Down Syndrome Society (NDSS) will give us more thoughts as we enter the new century.
The book has 42, all American, contributors with a multidisciplinary background, who participated in a conference created to try and look into aspects for the next century concerning persons with Down syndrome (DS). There are 32 chapters devided into ten sections: Self-determination, self-advocacy, advocacy, role of the family, health and clinical care, research, psycho-social issues, education and inclusion, communication, math and language skills, and turning the vision into reality.
The vision for persons with DS is that they will be included in all aspects of family, school, work, social, recreational and community life with equal opportunities and rights. Much has been achived, but there is still a long way to go, not only the the United States, but also world wide.
This book puts forward some of the visions and thoughts in an optimistic way and is therefore recommended reading for both family members, caregivers and profesionals working with person with Down syndrome.
John Langdon Haydon Down (1828-96) was the first physician to describe in detail the syndrome that came to bear his name. In 1866 he tried to classify the various forms of " feeblemindedness" and concluded that individuals with mental disabilities belonged to different ethnic varieties, such as Ethiopian, Malay and Mongolian. We have learned much since and this book edited by Willian I Cohen, Lynn Nadel and Myra E Madnick in association with the US National Down Syndrome Society (NDSS) will give us more thoughts as we enter the new century.
The book has 42, all American, contributors with a multidisciplinary background, who participated in a conference created to try and look into aspects for the next century concerning persons with Down syndrome (DS). There are 32 chapters devided into ten sections: Self-determination, self-advocacy, advocacy, role of the family, health and clinical care, research, psycho-social issues, education and inclusion, communication, math and language skills, and turning the vision into reality.
The vision for persons with DS is that they will be included in all aspects of family, school, work, social, recreational and community life with equal opportunities and rights. Much has been achived, but there is still a long way to go, not only the the United States, but also world wide.
This book puts forward some of the visions and thoughts in an optimistic way and is therefore recommended reading for both family members, caregivers and profesionals working with person with Down syndrome.
6 of 12 people found the following review helpful
Stunning vision of the next century of research
15 Sep 2004
Format:Paperback
The case of down syndrome is one that is complex yet simple, and challenging yet easy. To understand the complexities that must occur to result in an affected patient is beyond most human comprehension. This book does a great job at highlighting the past milestones in research, yet focusing primarily on the future of study in this subject. Bill optomistically creates a nurturing sense of hope in all patients currently affected by this raveging disease, and instills hope for a better life, living life to the fullest
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