New report to bring rare diseases ‘Out of…
Following nine months of consultation, the rare neurological disease report,…
Communications
Welcome to our communications page for useful updates
Take part in The Great PSPA Cake Off
Join us this autumn as we launch our first ‘Bake…
Simon Koe steps down as PSPA Chair
Following a five year term as Chair of Trustees, Simon…
Online Summer Raffle Winners
Thank you to everyone who supported PSPA’s specialist information and…
My London Marathon experience: why, how and when.
In December 2012 I turned 40 and started considering what…
Should people living with PSP or CBD wear…
From Friday 24 July, it became a legal requirement for…
Buy your Summer Raffle tickets today
Tickets for our 2020 online Summer Raffle are now available…
PSP & CBD Awareness Week 2020
Our PSP & CBD Awareness Week has been rescheduled to…
Could you help PSPA during the Coronavirus crisis?
We are launching our Coronavirus Emergency Appeal to help protect…
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…
PASSPORT Study Discontinued
At the end of last week pharmaceutical company Biogen announced…
New online interactive resource
We are thrilled to launch our new online interactive resource…