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PSPA News

Read below all of the latest news and views regarding PSPA

Check out our new Tea Party Pack!

A Tea Party or Bakesale is a great way to…

PSPA London Marathon Volunteers Required for 2020

We are looking for volunteers to make our runners experience…

London Marathon 2019

Thank you very much to every single one of our…

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…

Why you should ‘Ride London’!

A dear relative of mine has PSP and I’ve seen…

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…

25th Anniversary Raffle

25th Anniversary Raffle Winners will be announced on Saturday, 1st…

Understanding disease progression: PSPA researcher publishes results

We are delighted that our Sara Koe Clinical Research Fellow,…

Update on Care Information

Your Personal Guide to PSP We know that many of…

Building our Volunteer Team

On the 1st March we held our first open day…

Update of the Continuing Healthcare Alliance

Since the Continuing to Care report launch in November, over…

Research north of the border: Dr Diane Swallow

Neurology registrar Dr Diane Swallow has recently embarked on a…

PERK up! Early steps on the road to…

The complexity of neurodegenerative diseases like PSP and CBD means…

Unsung heroes

We know that there are many unsung heroes helping out…