Accessibility links



The PSP Association is the only UK organisation dedicated to funding research which aims to:

    • develop a better understanding of the causes of PSP

    • establish the best ways of caring for people with PSP

    • develop an effective treatment for PSP

    • find a cure for PSP.

    The PSP Association supports both Progressive Supranuclear Palsy (PSP) and Cortico Basal Degeneration (CBD). References to PSP in this section should be read, where appropriate, as PSP and CBD.

    Following consultation with people with PSP and CBD, their carers, health care professionals, researchers and other interested parties, we have published our new Research Strategy which sets out the broad focus for the charity's research for the five-year period from January 2011 to December 2015. 

    For Researchers

    For Researchers

    For grant holders and those wishing to apply for funding.

    Read More...

    Funded Research

    Funded Research

    Find out more about research we fund

    Read More...

    Medical Advisory Panel

    Medical Advisory Panel

    Find out more about our Medical Advisory Panel.

    Read More...

    Medical Workshops

    Medical Workshops

    Learn more about our International Medical Workshops.

    Read More...