This report outlines the results of one stage of a larger project being carried out by NatCen on behalf of the DCSF and the Department of Health (DH). The overall aim of the project is to develop a questionnaire and survey design to measure parents’ experience of services for their disabled children.
The survey data would feed into a performance indicator to measure the core offer (information, transparency, assessment, participation and feedback) as well as the general experience of families with disabled children.