This article describes a project that explored the views, experiences and aspirations of young people with Down's Syndrome and their family carers. Each young person had gone or was going through the transition to adulthood. Following a scoping study, young people who were leading the lives of their choice, for example through use of person‐centred planning or direct payments, were interviewed, and their stories were published in a booklet. The next phase brought other young people and their families together in workshops to support them in planning for their future, based on the information from the booklet. Interviews with the young people and their families dispelled the myth that parents are obstacles to progress and change. All families actively supported their son or daughter to achieve their aspirations and had high expectations for them.
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9 November 2010
Review Article|
November 09 2010
What kind of a future for young people with Down's Syndrome? The views and aspirations of young people and families Available to Purchase
Jill Davies;
Jill Davies
Foundation for People with Learning Disabilities, UK
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Hazel Morgan
Hazel Morgan
Foundation for People with Learning Disabilities, UK
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Publisher: Emerald Publishing
Online ISSN: 2042-8782
Print ISSN: 1359-5474
© Emerald Group Publishing Limited
2010
Tizard Learning Disability Review (2010) 15 (4): 22–29.
Citation
Davies J, Morgan H (2010), "What kind of a future for young people with Down's Syndrome? The views and aspirations of young people and families". Tizard Learning Disability Review, Vol. 15 No. 4 pp. 22–29, doi: https://doi.org/10.5042/tldr.2010.0590
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