10,000 Voices raffle winners confirmed
Thank you to everyone who has been busying buying and…
Communications
Welcome to our communications page for useful updates
PSPA welcomes a new Chair of Trustees
PSPA is pleased to be welcoming a new Chair to…
Helping the 10,000 people living with PSP &…
This Rare Disease Day, 28 February, PSPA is launching a…
Take part in a study to improve Google…
A team of researchers is currently looking for people with…
Ed’s Three Peaks Challenge to raise awareness of…
Ed Warth is currently training to climb the Three Peaks…
Talbot Underwriting selects PSPA to be their 2021-22…
We are pleased to announce Talbot Underwriting has selected PSPA…
Merry Christmas
As we countdown the last few days before Christmas, everyone…
Office and Helpline Christmas Opening Hours
Monday 21 December – office and helpline 9am to 5pm…
New report to bring rare diseases ‘Out of…
Following nine months of consultation, the rare neurological disease report,…
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…