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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

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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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