The PSP Association

Working for a world free of PSP

The PSP Association was founded in 1994 and is the only organisation dedicated to helping everyone affected with PSP, their families and carers, and promoting and funding research into causes, treatments and a cure. We provide a range of services to ensure people living with PSP have access to the information, care and support that is vital to quality of life.

We work with medical, health and social care professionals raising awareness of PSP and providing education, training and advice on a diverse range of subjects, from better diagnosis to managing the disease from onset to death. We also work to influence decision makers at national and local levels to raise awareness and improve services.

Visit The PSP Association:
http://www.pspeur.org