In the last year with Covid 19 charities have suffered especially research.  I support the PSPA as I lost Ian to PSP 7 years ago,  

Since 2019 have raised over £85,000 taking part in coastal walks, hosting coffee mornings & street parties.  I couldn’t have done it without the help of generous friends & the local community.

Back in 2009  the local doctor’s hadn’t heard of PSP.  Ian was originally diagnosed with Parkinsonism then 6 weeks later a visit to the neurologist confirmed it was Progressive Supranuclear Palsy.  Since then there have been 6 local people diagnosed with PSP. 

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 aim to improve the lives of everyone affected by PSP and CBD. We rely entirely on voluntary donations, and that's why we need your support.