Wear Ed’s Lace to raise awareness of PSP & CBD
Wear Ed's Lace to raise awareness of PSP & CBD.
PSPA Admin23rd May 2022
Share your story for Rare Disease Day 2022
This year, Rare Disease Day is taking place on 28 February. The themes of the…
PSPA Admin7th February 2022
Make Some Noise for people living with PSP & CBD
We are pleased to confirm PSPA has been selected to be part of the 2021…
PSPA Admin30th September 2021
PSPA Podcast launches with support from Pavers
PSPA has launched a podcast for carers thank to the kind support of The Pavers…
PSPA Admin10th June 2021
Funding partnership with SpeakUnique
PSPA are excited to be offering funding for voice banking through a partnership with SpeakUnique.…
PSPA Admin15th April 2021
PSPA welcomes a new Chair of Trustees
PSPA is pleased to be welcoming a new Chair to lead its Board of Trustees.…
PSPA Admin31st March 2021
Helping the 10,000 people living with PSP & CBD be heard
This Rare Disease Day, 28 February, PSPA is launching a new campaign to help people…
PSPA Admin28th February 2021
PSPA awarded funding for delivery against Scotland’s Neurological Care and Support Framework
PSPA is delighted to have successfully bid for a round 1 funded project for delivery…
PSPA Admin16th October 2020
Ask the Helpline – Live Q&A Session
On Wednesday 10 June, to help mark Carers Week, PSPA is launching the first of…
PSPA Admin4th June 2020
PSPA Funded Research Update
Since the lockdown began, many medical researchers who also usually hold clinical posts such as…
PSPA Admin20th May 2020
Initial findings from the PROSPECT Study
Research estimates that up to 10,000 people may be living with PSP & CBD in…
PSPA Admin20th December 2019
25 years of PSPA – interview with our founder Michael Koe
“We were so upset that no one seemed to know or care about PSP.” When…
PSPA Admin5th April 2019
