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PSPA News

Read below all of the latest news and views regarding PSPA

Help us identify the priority research questions for…

This month PSPA launched its first study to identify the…

New online interactive resource

We are thrilled to launch our new online interactive resource…

Christmas Bauble Appeal 2019

Dedicate a Bauble to someone special this Christmas. Your Christmas…

Remember a charity week 9-15 September

“For Mum leaving money in her will was an obvious…

Exploring physical activity in people with rare neurological…

The PARC (Physical Activity for people with Rare Neurological Conditions)…

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…

Office & Helpline Christmas Opening Hours

Monday 23 December – office & helpline 9am – 5pm…

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…