Parental Experience of Services for Disabled Children

BMRB was commissioned by the Department for Children, Schools and Families to undertake qualitative research with parents of disabled children aged 0-19 years. This research consisted of two phases exploring parents’ experiences and views of the range of services they use in relation to their disabled child. This research explored the service issues beyond the core offer; parents’ perceptions of difficulties accessing services; lack of service availability; poor communication and information about services; and, what constitutes a good service. Leadership Briefings Issue 4.06 (42)

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