How does a small charity tackle the need…
The doctor gave me a diagnosis and then said “there…
Lead Developer
The doctor gave me a diagnosis and then said “there…
“For Mum leaving money in her will was an obvious…
The PARC (Physical Activity for people with Rare Neurological Conditions)…
Thank you very much to every single one of our…
25th Anniversary Raffle Winners will be announced on Saturday, 1st…
Your Personal Guide to PSP We know that many of…
On the 1st March we held our first open day…
Since the Continuing to Care report launch in November, over…
Neurology registrar Dr Diane Swallow has recently embarked on a…
The complexity of neurodegenerative diseases like PSP and CBD means…
We know that there are many unsung heroes helping out…
We are thrilled to announce a major investment by the…
We are delighted to announce that PSPA-funded researcher Prof James…
Research published today in the journal ‘Brain’ shows that two…
A huge congratulations to Team PSPA for completing the 100…
Many of you will have received our autumn appeal for…
In his latest blog post, Dr Jabbari gives us an…