Our vision
We aim to improve the lives of everyone affected by PSP and CBD, while funding research to seek a cure.
PSPA is a national charity providing support and information to people living with PSP and CBD, while funding research into treatments and ultimately a cure. We rely entirely on voluntary donations.
We aim to improve the lives of everyone affected by PSP and CBD, while funding research to seek a cure.
PSPA provides support and information to people living with PSP and CBD, while funding research into treatments and ultimately a cure for these conditions.
Our Board of Trustees is responsible for overseeing the Chief Executive and Senior Management Team to ensure the charity is run well and remains solvent.
A Sub-Committee reporting to the Board of Trustees, PSPA’s Research Committee makes recommendations in relation to PSPA’s research programme.
We employ around 20 staff in a range of roles in the regions and at our head office in Milton Keynes, Buckinghamshire.
PSPA covers the United Kingdom and works very closely with other PSP organisations across the world working together supporting research and the provision of information and support into PSP and CBD.
PSPA Margaret Powell House, 415a Midsummer Boulevard, Milton Keynes, MK9 3BN