The expectations of parents of disabled children

Abstract

Following the diagnosis of a child's disability, parents have to develop new expectations concerning the child, their role as parents and the support services that are designed to meet their needs. Research shows, however, that these needs frequently remain unmet. In this article, Fran Russell, who writes as a parent of a son with a learning disability and as a professional with experience of practice in early years support services, explores parents' perspectives from a different direction. She argues that an investigation into parents' expectations could lead to a greater understanding of how parents of disabled children respond to their new‐found situation. Fran Russell's own research, undertaken as part of her Education Doctorate programme at Leeds University, reveals that little is currently known about parents' expectations and indicates a pressing need for parents to be better informed, at an early stage in their experience of parenthood, in order to interact more effectively with professionals at a range of levels.

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