I propose to take Questions Nos. 159 to 161, inclusive, together.
The Department of Health and Children is committed, in partnership with other stakeholders, including the Health Research Board, to the development of improved health information systems including data requirements for health and personal social services for people with a disability. The development of information systems must recognise the requirements of the Disability Act 2005 and the current disability databases. I expect the outcome of the Department's Value for Money Expenditure and Policy Review of Disability Services to direct the future information requirements for the provision of health and personal services for people with a disability.
The focus of health service provision for people with a disability is not a medical diagnosis. The Disability Act provides for, among other things, an individual assessment of need, a person centred service statement and the provision of individualised supports. This policy moves away from the provision of segregated, health based, group services for people with a disability.
The National databases provide information in relation to the level of services being provided and current and future needs of people with a disability. The databases do not identify persons with specific disabilities such as Autism or Downs Syndrome.