PSP & CBD and Coronavirus
We are aware that many of you will be concerned…
Information & Support
Welcome to our information & support page
#JointheFight to help raise awareness of PSP &…
Could you #JointheFight against the misdiagnosis of PSP & CBD…
Initial findings from the PROSPECT Study
Research estimates that up to 10,000 people may be living…
New online interactive resource
We are thrilled to launch our new online interactive resource…
Exploring physical activity in people with rare neurological…
The PARC (Physical Activity for people with Rare Neurological Conditions)…
Georgie runs the 2019 London Marathon for PSPA
Georgie Irwin is running the London Marathon for PSPA in…
25 years of PSPA – interview with our…
“We were so upset that no one seemed to know…
The Neurological Alliance Patient Experience Survey
This questionnaire is about your care and treatment for your…
Improving our support to you – our vital…
Volunteers are the lifeblood of PSPA. It is directly because…
New post to support people in Scotland with…
The Scottish Government will provide £25,000 in funding to PSPA…
Awareness Week 15 – 21 May 2017
For people with PSP getting a correct diagnosis is challenging,…
Reorganisation of our Information & Support Services
You just need one number for support – our Helpline