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Family expectations and transition experiences for young adults with severe disabilities: does syndrome matter?

Jan Blacher (University of California, Riverside, USA)
Bonnie Kraemer (San Diego State University, USA)
Erica Howell (University of California, Riverside, USA)

Advances in Mental Health and Learning Disabilities

ISSN: 1753-0180

Article publication date: 15 March 2010

809

Abstract

The differential impact of young adult diagnosis on families during the period of transition from school to adult life was examined. Participants were parents of 246 young adults with severe learning disability aged 18‐26. Young adults were classified into four diagnostic groups: autism (N = 30), Down's syndrome (N = 68), cerebral palsy (N = 95) and an undifferentiated learning disability group (N = 53). Research questions pertained to parent expectations about their young adults' transition to living and working environments post high school. Parental satisfaction and worries were also assessed. The results indicated more community expectations of work for young adults with Down's syndrome, and more restrictive expectations for young adults with autism, including more expectations that young adults with autism would move out of the family home into a residential environment. Parents of young adults with autism also worried significantly more about various aspects of transition than other parent groups.

Keywords

Citation

Blacher, J., Kraemer, B. and Howell, E. (2010), "Family expectations and transition experiences for young adults with severe disabilities: does syndrome matter?", Advances in Mental Health and Learning Disabilities, Vol. 4 No. 1, pp. 3-16. https://doi.org/10.5042/amhld.2010.0052

Publisher

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Emerald Group Publishing Limited

Copyright © 2010, Emerald Group Publishing Limited

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