Donate towards PSPA's Better Future Fund to help researchers learn more about PSP & CBD to aid earlier diagnosis and improve care.

Our Mum was diagnosed with PSP in 2018, although we knew something was wrong for several years prior. PSP is a rare neurological condition, estimated to affect only 4,000 people in the UK. The condition develops gradually which is what makes it such terrible Illness, that left Mum wheelchair bound & in the latter months with very little quality of life. In her memory we are asking for donations to help researchers identify the disease quicker in others & learn more about how to improve the care needed.