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Helpline: phone0300 0110 122

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 vision

We aim to improve the lives of everyone affected by PSP and CBD, while funding research to seek a cure.

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.

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