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A ball is being organised by the family of a man who lives with Corticobasal Degeneration (CBD) to raise funds to support our work.
Cathy Howarth, from Horsforth, Leeds, and her daughter Charlotte are aiming to sell 170 tickets for an autumn charity ball at Weetwood Hall Hotel, on 17 October.
Continue reading “Charity ball to boost funds” »
Thanks to modern scanning technology, researchers can study detailed pictures of the impact the disease has on the brain and the effect of potential treatments.
That’s why we’ve agreed to fund the PROSPECT-MR research study, led by Cambridge University researcher Professor James Rowe, as part of the new National PSP Research Network.
Continue reading “Support our summer raffle” »
The PSP Association is dedicated to the support of people with Progressive Supranuclear Palsy (PSP) and the related disease Cortico Basal Degeneration (CBD), and those who care for them.
As PSP and CBD are very similar, we often use ‘PSP’ as a shorthand for both.
PSPA is a registered charity in England and Wales (1037087) and in Scotland (SC041199).