Provide help and support for those living with Progressive Supranuclear Palsy and Cortico Basal Degeneration

The PSP Association (PSPA) is the only national charity offering support and information to people living with PSP and CBD. They fund research to help them understand the development of PSP and CBD, improve diagnosis and discover effective treatments and, ultimately a cure. They provide information and support for families and help them access assistance from statutory and other public or voluntary bodies.

Back to all members