Abstract

This needs assessment study aimed to characterize domains of service needs of persons with developmental disabilities (PDD) and their families. Participants were 96 adults with DD (n= 5), their family members (n= 40), and service providers (n= 31). Seventy-six participants completed a survey on needs (education and early intervention, healthcare, and self-advocacy). Another 20 participants completed focus group interviews (family members,n= 14, service providers,n= 6). Following a descriptive analysis of quantitative data and content analysis of qualitative data, results show very high needs for services in the following domains: (a) training for skills in self-advocacy for persons with DD and their families, (b) healthcare access—health insurance and specialty care access, and (c) access to post-secondary education for persons with DD, and disability-specific education/training for service providers. Implications for rehabilitation services include addressing these needs through transition services with self-advocacy training, post-secondary education preparation, and informational service on healthcare access.

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