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Helping people living with Progressive Supranuclear Palsy & Corticobasal Degeneration to live the best life they can #TeamPSPA🧠 Sign-up to our Pathway to Progress Challenge here: https://www.pspassociation.org.uk/pathway-to-progress/
The PSP Association









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It's promising interest in #ClinicalTrials for Progressive Supranuclear Palsy has been increasing in recent years. PSPA Trustee, Dr Boyd Ghosh, shares how there are more PSP trials than ever, with more to come. #ClinicalTrialsDay
25d
The PSP Association
Nature Partner Journals are seeking essays from clinicians, researchers & advocates on all forms of Dementia. Help shape “The Human Connection” journal. Find out more & submit your experience: ow.ly/CSNi50YIRfx #NeuroScience #BrainHealth #MedicalJournals
We support @mariecurieuk.bsky.social’s call on the #government to ensure people living with #terminal conditions like PSP & CBD can access #financial support easier. Our recent #survey found 65% of people with PSP & CBD experience new costs they didn’t have before.
Only 1 in 5 people get #NHS Continuing Healthcare (CHC) funding, with postcode lotteries making access unfair. We’re supporting Dementia UK's call to #FIXCHC for fairer assessments and funding. Sign @dementiauk.bsky.social petition: ow.ly/S90x50Z6CJ9 #healthcare
PSPA's CEO James Cusack, and Research Coordinator Megan Hodgson are excited to be at his year's #TauGlobalConference in #Washingston which started yesterday! @alzassociation.bsky.social @curepsp.bsky.social #RainwaterCharitableFoundation #Tau #TauResearch #Tau2026 #Conference
#Healthcare professionals: Join us in #Stirling on 18 June for our #free PSPA Regional #Awareness event! Learn to spot PSP & CBD, understand progression, and improve support. Book now: ow.ly/jmWP50YY2aO #PSP #CBD #Scotland
#Health & social care professionals: Join us in #Aberdare, South #Wales on Fri 3 July for our free PSPA Awareness Event! Learn to spot signs of PSP & CBD, understand progression, and explore support. Hear from our Helpline Care Navigator, Dionne. Book free: ow.ly/yC9x50Z73Go #FreeEvents #Healthcare
1mo
17d
Join us at Neuro2026: The PSP & CBD International #Research Symposium with #CurePSP on 5–6 Nov 2026 at Hilton London Bankside for the latest in PSP & CBD research. Open to all researchers and #medical professionals. More info & tickets: ow.ly/fWsP50YMthA #Neuro2026 #Research
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26d
Today’s #Carers Week’s focus is education. 46% of young carers leave school with five GCSEs, compared to 60-65% of peers without caring responsibilities. Explore the Building Carer Friendly Communities blueprint for ways to inspire action in education. Learn more: https://bit.pulse.ly/zbk3fajufc
The PSP Association
The PSP Association
Our next policy group meeting is taking place tomorrow, 11:00-12:00, on Teams. The meeting will be a chance to discuss the results from Scotland's elections and learn a bit about the make up of the new Scottish Parliament. Thank you to Mark Jackson from @pspassociation.bsky.social for chairing.
The PSP Association
The PSP Association
The PSP Association
The PSP Association
The PSP Association
3d
1mo
Carers Week
Neurological Alliance of Scotland
Video
People living with life-limiting illnesses that will only get worse shouldn’t have to be put through repeated benefits reassessments. They add stress and paperwork at a time when people are already dealing with so much. It has to stop. 🛑 www.independent.co.uk/news/uk/home...
17d
Exclusive: The current system is ‘simply wrong’, more than 30 organisations write
www.independent.co.uk
Stop forcing terminally ill benefit claimants to prove illness, charities urge
Marie Curie UK
Video