We want our research to be shaped in genuine partnership with the people it aims to help, valuing lived experience alongside other forms of expertise. We recognise the historic power imbalance in health research and are committed to sharing power more equally by involving people with lived experience in setting priorities and working with us throughout the process. Their involvement also brings personal benefits, including confidence, new skills, and the satisfaction of helping improve services for children and young people.

You can read our public and patient involvement and engagement strategy here:

Last edited December 2025