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A Christmas update from Physios for ME

Before we take a short break over the holidays, we thought we’d share a few updates on our work over the last few months.   Research This remains one of our main focuses and there’s a lot going on, driven by our research lead Dr Nicola Clague-Baker. In October we had another publication success with “ Pacing with a heart rate monitor for people with myalgic encephalomyelitis/chronic fatigue syndrome and long COVID: a feasibility study” which is available as open access here A

New survey: The experiences of health professionals with ME/CFS and/or Long Covid (with PEM)

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.

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Physios for ME

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The information provided on this website is meant to inform and signpost helpful resources. Any treatment for a person with ME should always be individualised, monitored and regularly evaluated

We do not provide clinical services, individual medical advice, or recommendations for private therapists

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Contact us at physiotherapyforme@gmail.com 

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