The right care at the right time means people can stay healthy and live well for longer, whether this is completing day-to-day tasks, being able to socialize, or staying in education & work. Ask your next MP to become a #NeuroChampion now: bit.ly/NeuroChampion #GE2024🗳️

It’s #PSPCBDAwarenessWeek this week - a huge thank you to Morden Station for sharing and showing #WeCare 💜🧡

Out of office 🥂

Signing up to donate brain tissues is an individual choice. However, such donations can be valuable to researchers, to learn more about PSP & CBD. Learn more about Brain Donation here: pspassociation.org.uk/research/get-i… #BrainDonation #MedicalResearch #PSPAware #CBDAware #RaisingAwareness

Speaker needed for research info session 🧠 I’m looking for AHP’s conducting research that will improve care and QoL for people with PSP/CBD or other progressive neurological conditions! Please share and get in touch if you know anyone who might be interested! The PSP Association

#MyNeuroSurvey by The Neurological Alliance launched on 22nd July. Share your experiences of living with or caring for someone with PSP & CBD today to help improve services. Complete here: …alingreality.welcomesyourfeedback.net/s/lf7qci #NeurologicalAlliance #NeurologicalCondition #RaiseAwareness

Breaking News: Eating about two servings per week of processed red meat—like bacon, bologna and salami—could raise dementia risk by 14% compared to those who eat less than approximately three servings a month, according to research presented at #AAIC24. aaic.alz.org/releases-2024/…

I have loved representing The PSP Association in this clinical studies group and learning about other research projects going on in the UK into PD and APS. Looking forward to August’s meeting!

TGIF 🐾

Earlier this month, Damien was one of the first patients at Sherwood Forest Hospitals NHS FT to receive a new portable pump that gradually releases treatment and helps control symptoms of Parkinson's disease. Taken just days apart, these clips show what Damien's life was like before and after treatment.

Very cool new research published today which reveals the benefits of adaptive deep brain stimulation (DBS) for #Parkinsons 👇 theguardian.com/society/articl…

Dr Kat Bowles (Bowles Lab) spoke to BioTechniques about her new project, funded by The Rainwater Charitable Foundation, investigating how the buildup of tau affects astrocytes, and the role of astrocytes in the development and progression of progressive supranuclear palsy⬇️ buff.ly/3Xn18BQ

Nominations for the WiNUK: Women in Neuroscience UK 🧠 Awards 2024 are now open until 13 September! 🏆 Nominate/vote here👉buff.ly/3X3IGOq The event will be held on 29 November in person and online! #WiNUK #WiNUKAwards2024

Grateful to Robert B. Weide for taking the time & for trusting CurePSP w/ your and Linda's story. We need to amplify the voice of our community ... It's not easy but it's fundamental to our mission. THANK YOU, Bob, for helping us launch #TheCollectiveMind podcasts.apple.com/us/podcast/car…

"To live a healthy life, is something we all deserve, we need every type of person represented in health research” We're proud to have partnered on this film showing why we need better representation in health research.

Congrats Dan! It’s been brilliant to see the progress of this project - can’t wait to see the outputs!

These research information sessions have been a joy to organise! Brilliant speakers, incredible engagement and thought provoking questions from the PSPA community 🧡🧠💜

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

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