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How does a small charity tackle the need…

The doctor gave me a diagnosis and then said “there…

Remember a charity week 9-15 September

“For Mum leaving money in her will was an obvious…

Exploring physical activity in people with rare neurological…

The PARC (Physical Activity for people with Rare Neurological Conditions)…

Thank you to our 2019 London Marathon runners

Thank you very much to every single one of our…

25th Anniversary Raffle

25th Anniversary Raffle Winners will be announced on Saturday, 1st…

Update on Care Information

Your Personal Guide to PSP We know that many of…

Building our Volunteer Team

On the 1st March we held our first open day…

Update of the Continuing Healthcare Alliance

Since the Continuing to Care report launch in November, over…

Research north of the border: Dr Diane Swallow

Neurology registrar Dr Diane Swallow has recently embarked on a…

PERK up! Early steps on the road to…

The complexity of neurodegenerative diseases like PSP and CBD means…

Unsung heroes

We know that there are many unsung heroes helping out…

MRC make major investment in PSP research at…

We are thrilled to announce a major investment by the…

PSPA-Funded Research Published

We are delighted to announce that PSPA-funded researcher Prof James…

Existing drugs step up in battle against neurodegenerative…

Research published today in the journal ‘Brain’ shows that two…

Pedal power raises funds and awareness

A huge congratulations to Team PSPA for completing the 100…

Crowd Funding the future of research

Many of you will have received our autumn appeal for…

Sara Koe Research Fellowship – Dr Edwin Jabbari

In his latest blog post, Dr Jabbari gives us an…