Down Syndrome Across the Life Span

Description

This book promotes a positive message for people with Down syndrome across the world. Living with Down Syndrome is a positive experience for the majority of children and adults with Down syndrome, and for their families. Of course there are difficulties to be faced, but quality of life, from infancy to old age, is determined more by the quality of healthcare, education and social inclusion offered to individuals, than by the developmental difficulties that are associated with Down syndrome. The aim of this book is to bring the latest information on research and good practice to families, practitioners and policy makers in order improve the services available to individuals with Down syndrome in all countries.Content: Chapter 1 Beyond the Myths: Representing People with Down Syndrome (pages 2–15): Jan GothardChapter 2 Learning in Young Children with Down Syndrome: Public Perceptions, Empirical Evidence (pages 18–27): Jennifer G WishartChapter 3 Self?Regulation in Children and Young People with Down Syndrome (pages 28–39): Sheila Glenn and Cliff CunninghamChapter 4 What Matters Most? A Reflection on a Quarter Century of Early Childhood Intervention (pages 41–53): Robin Treloar and Susan CairnsChapter 5 Making Inclusion Work: Improving Educational Outcomes for Students with Down Syndrome in the Regular Classroom (pages 54–63): Loretta R. GlorcelliChapter 6 Cognitive Development and Education: Perspectives on Down Syndrome from a Twenty?Year Research Programme (pages 66–80): Sue Buckley and Gillian BirdChapter 7 Broadening Approaches to Literacy Education for Young Adults with Down Syndrome (pages 81–92): Christina E. van Kraayenoord, Karen B. Moni, Anne Lobling and Kim ZiebarthChapter 8 Numeracy and Money Management Skills in Young Adults with Down Syndrome (pages 93–106): Sandra Bochner, Lynne Outhred, Moira Pieterse and Laaya BashashChapter 9 Life Styles of Adults with Down Syndrome Living at Home (pages 109–120): Anne Jobling and Monica CuskellyChapter 10 Some Studies Involving Individuals with Down Syndrome and their Relevance to a Quality of Life Model (pages 121–138): Verity Bottroff, Roy Brown, Eddie Bullitis, Vicky Duffield, John Grantley, Margaret Kyrkou and Judy ThornleyChapter 11 From Autonomy to Work Placement (pages 139–146): Anna ContardiChapter 12 An Appreciative Inquiry about Adults with Down Syndrome (pages 149–158): Susanne MuirheadChapter 13 Multiple Perspectives of Family Life (pages 159–173): Monica Cuskelly, Anne Jobling, David Chant, Anna Bower and Alan HayesChapter 14 Verbal?Motor Behaviour in Persons with Down Syndrome (pages 175–193): Brian K. V. Maraj, Shannon D. Robertson, Timothy N. Welsh, Daniel J. Weeks, Romeo Chua, Matthew Heath, Eric A. Roy, Dominic A. Simon, Harold Weinberg and Digby ElliottChapter 15 Creating Positive Lifestyles for People with Down Syndrome in Developing Countries (pages 195–209): Roy McConkey