Vincent Napier, family & friends Strikeback, by raising Funds and Awareness for PSPA
Vincent Napier has been living with PSP since his diagnosis at Christmas in 2017.
PSP is a progressive neurological condition, for which there is no cure: but there is HOPE! Vincent is actively engaging in vital research at Addenbrookes Hospital which will help others in the future. Vincent is an inspiration to his family, which is why they are creating a fund and awareness raising team, to Strikeback against PSP & CBD, in support of PSPA.
PSPA is a national charity providing support and information to people living with Progressive Supranuclear Palsy (PSP) and Corticobasal Degeneration (CBD), while funding research into treatments and ultimately a cure.
PSPA rely entirely on voluntary donations, and truly appreciate your support.
PSP is a progressive neurological condition, for which there is no cure: but there is HOPE! Vincent is actively engaging in vital research at Addenbrookes Hospital which will help others in the future. Vincent is an inspiration to his family, which is why they are creating a fund and awareness raising team, to Strikeback against PSP & CBD, in support of PSPA.
PSPA is a national charity providing support and information to people living with Progressive Supranuclear Palsy (PSP) and Corticobasal Degeneration (CBD), while funding research into treatments and ultimately a cure.
PSPA rely entirely on voluntary donations, and truly appreciate your support.
Contribute
Help grow Team's Tribute by adding messages or memories you'd like to share.
