Blog

A new survey has been launched with the aim to explore the experiences of healthcare professionals who develop LongCOVID (with post-exertional malaise) and/or Myalgic Encephalomyelitis /Chronic Fatigue Syndrome (ME/CFS). ​ To check if you are eligible and find out more about the survey, please head over to our website for more information. ​ The survey will remain open until 6pm 31st December 2025.

We’re excited to report another of our research projects has been published. "Pacing with a heart rate monitor for people with myalgic...

Karen photo-bombs the team It is now six years since the formation of Physios for ME, when four physiotherapists with a shared goal – to...