Helping the 10,000 people living with PSP &…
This Rare Disease Day, 28 February, PSPA is launching a…
Information & Support
Welcome to our information & support page
Coronavirus vaccine and PSP & CBD
At the beginning of December, the UK became the first…
Office and Helpline Christmas Opening Hours
Monday 21 December – office and helpline 9am to 5pm…
PSPA awarded funding for delivery against Scotland’s Neurological…
PSPA is delighted to have successfully bid for a round…
PSPA Youth Support Group
We are pleased to be launching a new Youth Support…
PSPA Support Grants now available
Following the fantastic response to our Coronavirus Emergency Appeal, we…
Should people living with PSP or CBD wear…
From Friday 24 July, it became a legal requirement for…
PSP & CBD Awareness Week 2020
Our PSP & CBD Awareness Week has been rescheduled to…
Ask the Helpline – Live Q&A Session
On Wednesday 10 June, to help mark Carers Week, PSPA…
PSPA Funded Research Update
Since the lockdown began, many medical researchers who also usually…
Nominate PSPA for a £1000 donation
Help PSPA be in with a chance of receiving a…
Join the #TwoPointSixChallenge to support PSPA
On 26 April the nation is coming together for an…
Volunteer support during the coronavirus
In support of the NHS Volunteering initiative, PSPA volunteers will…
Message from the CEO
The developing Coronavirus pandemic is currently at the forefront of…
PSP & CBD and Coronavirus
We are aware that many of you will be concerned…
#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…