PSPA

PSPA is the only national charity offering support and information to people living with PSP & CBD, while supporting research into treatments and ultimately, a cure.

PSPA provides information and support for families and helps them access assistance from statutory and other public or voluntary bodies. They do this via a national helpline, regional support groups, carers groups and a wealth of guides and leaflets for families as well as health professionals.

It funds research to help us understand the development of PSP & CBD, improve diagnosis and discover effective treatments. It is determined to make health professionals more aware of these devastating diseases, because with early and accurate diagnosis, people can get the support they need, when they need it.