We invite Health Boards and Trusts to submit their clinical data for cohort 7 on the Epilepsy12 data platform.
This interactive tool shares Epilepsy12 performance indicator data in the public domain at frequent intervals.
Our programme ran from 2019 to 2024, supporting paediatric epilepsy service teams in England and Wales to identify and implement local service improvements.
Our impact report details how incremental changes and whole-team training have enhanced patient care, addressed mental health challenges and improved outcomes for children and young people with epilepsy.
This group of epilepsy experienced or interested children, young people and families volunteers to improve care for patients and their families - such as a Clinic Chat Check List.