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My London Marathon Experience: It’s great being part of #TeamPSPA Blog Fundraising

My London Marathon Experience: It’s great being part of #TeamPSPA

My wonderful Auntie, Moira Catherall passed away in 2018 after experiencing many challenges with PSP.…

PSPA Admin8th September 2020

My London Marathon experience: why, how and when. Blog Communications Fundraising

My London Marathon experience: why, how and when.

In December 2012 I turned 40 and started considering what challenges I could set myself.…

PSPA Admin2nd September 2020

Research north of the border: Dr Diane Swallow Blog Research

Research north of the border: Dr Diane Swallow

Neurology registrar Dr Diane Swallow has recently embarked on a three year research fellowship in…

PSPA Admin5th June 2018

Sara Koe Research Fellowship – Dr Edwin Jabbari Blog Research

Sara Koe Research Fellowship – Dr Edwin Jabbari

Dr Edwin Jabbari has recently finishing his general medical training. To kick start his career…

PSPA Admin5th June 2018

Working on Prof James Rowe’s PSPA -funded project – Patricia Vazquez Rodriguez Blog

Working on Prof James Rowe’s PSPA -funded project – Patricia Vazquez Rodriguez

Patricia Vazquez Rodriguez is working on Prof James Rowe’s PSPA -funded project, carrying out special brain…

PSPA Admin5th June 2018

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PSPA is the only UK charity dedicated to creating a better future for people living with Progressive Supranuclear Palsy (PSP) and Corticobasal Degeneration (CBD). We work to ensure the 10,000 people living with PSP or CBD receive support and care that is co-ordinated, has continuity and is compassionate. We rely entirely on voluntary donations. PSPA is a registered charity in England and Wales (1037087) and in Scotland (SC041199).