We reached a major milestone this summer when Alexis Cheviet hit the recrutiment target for our The Dunhill Medical Trust project on attention & memory in people with PSP. Thanks to our colleagues at The PSP Association and in the #NHS trusts! motorbiasproject.com/psp-recruitmen…

We have updated our 'What is PSP' web page to help you fully understand what PSP is and the support available to you and your family. pspassociation.org.uk/information-an… #WhatIsPSP #PSPAInformation #PSPASupport #ProgressiveSupranuclearPalsy #UpdatedInformation #SupportForFamilies

Congrats, Kristen! Your work on #tau #psp #stemcell is inspirational. #WomeninSTEM The PSP Association CurePSP The Rainwater Charitable Foundation

What better way to show your support for PSPA than purchasing your Christmas tree decorations and Christmas cards from our PSPA shop? Visit the PSPA shop: pspassociation.org.uk/fundraising/sh… #CharityChristmas #Christmasshop #PSPAware #SupportPSPA #ChristmasCards #CharityChristmasCards

Let’s goooo The PSP Association Great Run

What’s a 13.1 mile long hill between friends? Maybe see you next year Great North Run! The PSP Association

Today’s #MondayMotivation is Florence Bate & friends. Florence, Louis Aric, Miranda and Liam, set out on 20 July to climb Ben Nevis, Scafell Pike and Snowdon in just 24 hours to raise money for PSPA. They raised £8,872! Thank you! #ClimbingChallenge #RaiseAwareness #PSPAware

Today marks the start of #RememberACharity Week. Families who benefit from PSPA support often wish to leave a legacy in their Wills to show thanks. Download the Gift in Wills Guide here: pspassociation.org.uk/wp-content/upl… #Legacy #GiftinWill #SupportPSPA #SupportForFamilies #PSP

The PSPA Bauble Appeal 2024 has launched! Dedicate a bauble in honour of someone with PSP or CBD on our digital Christmas tree and help support PSPA services such as the Helpline. pspassociation.org.uk/christmas/ #PSPASupport #BaubleAppeal #CharityChristmas #ChristmasAppeal

Pspa have been our only charity who has fully supported our family and supported and trained the professionals who are part of our brothers team. We would be navigating our way in the dark without them! Please support their #baubleappeal

Fill out My Neuro Survey today: …alingreality.welcomesyourfeedback.net/s/qbnvt and make a real difference to people living with PSP & CBD. It takes approx 20 minutes and is completely anonymous and secure. #MyNeuroSurvey #NeurologicalAlliance #NeurologicalCondition #ImproveServices #PSP #CBD

Have your family ever talked you into doing something wild? Florence Bate recently embarked on an epic adventure to climb the three highest peaks in Scotland, Wales & England, raising money and awareness for The PSP Association. CHAOS Radio 🔊 mixcloud.com/chaosradiouk/i… #SupportPSPA

The PSPA Shop has the most beautiful Christmas card range to send to your loved ones. Get organised for Christmas and support PSPA at the same time! Shop here: pspassociation.org.uk/fundraising/sh… #CharityChristmasCards #PSPASupport #CharityFundraising #CharityChristmas

On Saturday 7 September the PSPA Norwich Support Group hosted an Autumn Fair at Poringland Village Hall. There was a steady footfall during the fayre helping the group raise more than £700 plus Christmas card sales in addition. Thanks to everyone who supported the event.

If you’re a physio supporting patients with PSP & CBD, refer them to our online exercise classes. Delivered by Neuro Heroes who are Specialist Neuro Physiotherapists, these sessions will show how being active can help manage common symptoms. Signup here: ow.ly/GI4250TlPBW

Thank you to everyone who participated in the Great North Run! Our 21 runners raised £10,064. If you’ve been inspired by our runners, you can enter the September ballot for the 2025 race. You must enter before Friday 13 September 2024 at 12pm. Apply here: greatrun.org/north.

The latest PSPA Podcast episode with Dr Ed Jabbari shining a light on his latest research is now available to listen to. Listen to the podcast here: pspassociation.org.uk/wp-content/upl… #PSPAPodcast #ClinicalResearch #ClinicalTrials #ProgressiveSupranuclear#Palsy

Great to catch up with Meg Palmer from The PSP Association about past and present research developments.

Was great to catch up with Ed Jabbari about his research projects! Very excited to see what the future holds for tau seed amplification assays! The PSP Association