Lord Hunt of Kings Heath – 2014 Parliamentary Question to the Department of Health
The below Parliamentary question was asked by Lord Hunt of Kings Heath on 2014-06-04.
To ask Her Majesty’s Government what steps they are taking to improve support for children and adults with dyspraxia, a form of developmental co-ordination disorder.
Earl Howe
It is for local clinical commissioning groups (CCGs) to assess the needs of the local populations they serve. CCGs work with their local providers to gain an understanding of the nature of local provision, and the part it should play in their future commissioning plans.
The Children and Families Act has introduced new arrangements for supporting young people with a special educational need and disability, including dyspraxia, and their families. A single assessment involving professionals and commissioners, and the child’s family, will identify the care needs for the child or young person (from ages 0 to 25) to inform an individual Education, Health and Care Plan focusing on outcomes and the integrated services to deliver them.
The Government is committed to ensuring all children and young people should be supported to achieve their best, regardless of their disability or circumstances. The new special educational needs and disability (SEND) Code of Practice due to come into force in September, sets out clear guidance for educational settings on the process for appropriate identifying, assessing and securing further support for children with SEND which can include those with dyspraxia. Through the Code we are ensuring all educational settings have arrangements in place for monitoring the progress of all pupils and responding quickly to their needs.
Chapter 6 of the draft Code of Practice makes specific reference to dyspraxia amongst examples of conditions that educational settings should be aware of when planning SEND provisions.
