Our vision
We aim to improve the lives of everyone affected by PSP and CBD, while funding research to seek a cure.
About us
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.
Our mission
We promote and fund research to understand the causes of PSP and CBD, improve diagnosis, develop new treatments and ultimately find a cure.
We provide everyone affected by PSP and CBD with information and support to enable them to lead the best life they can.
We raise awareness of PSP and CBD, particularly with decision-makers and health professionals, so that they recognise the conditions and have the skills and knowledge to help those affected access the right services at the right time.
The difference we make
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 trustees
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.
25 years of PSPA
Driven by their own devastating experience, they decided to set up a charity from their kitchen table with three aims: promote and sponsor research into the cause, treatment and cure of PSP; raise awareness among the general public; and provide information and support across the UK for families affected. Michael explained how the Charity began and how it helped give him a focus after Sara died.
Work with us
We employ around 20 staff in a range of roles in the regions and at our head office in Milton Keynes, Buckinghamshire.
International Organisations
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.
Contact us
PSPA Margaret Powell House, 415a Midsummer Boulevard, Milton Keynes, MK9 3BN