How does a small charity tackle the need…
The doctor gave me a diagnosis and then said “there…
Lead Developer
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…
New CEO Appointed
Update on Care Information
Your Personal Guide to PSP We know that many of…
Make a lasting difference
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…
Hampshire Local Group visits Rainbow Centre
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…