
Physios For ME
@physiosforme
A group of physiotherapists with a special interest in Myalgic Encephalomyelitis (ME) with the aim to improve physiotherapy management for people with ME
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http://www.physiosforme.com 27-06-2019 12:27:12
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Last year, following the inquest into my daughter's death from ME a minister said the govt was “committed to funding high-quality research”. Since then? Nothing. No more research funding. No sign of the NHS delivery plan. Today is World ME Day. Time for Wes Streeting to step up.


Published today! Victoria Bastos, Kerrie Greene et al found two distinct immunotypes of ME/CFS based on the cerebrospinal fluid analysis. Great collaboration with Michael VanElzakker Amy Proal, PhD and the Bragée clinic in Sweden. (1/) academic.oup.com/jimmunol/artic…


Congratulations to "M.E. Awareness and Reform" from The Times and The Sunday Times for being awarded winner of Campaign of the Year at The Press Awards 2025!


Pleased to have 3 abstracts accepted for the Chartered Society of Physiotherapy conference in Nov. Thanks Chartered Society of Physiotherapy (CSP) Physios For ME



Well that's a wrap. 40 follow-up measurements (across Liverpool and Manchester) completed for our #tvns study. Thank you to all #ME participants. KarenLesliePhysio now to complete the interviews and your PhD! Time for a short break by the sea for me. Physios For ME


‼️Michelle Bull Dr Michelle Bull 💙 Physios For ME Living with ME/CFS and Long Covid: Managing symptoms Norsk tekst Evening lecture #MECFS & #LongCovid Conference #DiggingDeeper Stavanger, Norway 8May2025 @ Norges ME-forening - Rogaland Fylkeslag Sissel Sunde 🇳🇴 Per Oddvar Navestad #PEM #LifeMatters youtube.com/watch?v=vv0pUw…

Just saw this in the physio frontline journal! All advocacy is important however small! Thanks Chartered Society of Physiotherapy (CSP) Physios For ME



