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An international survey exploring the experiences of healthcare professionals living with Long COVID (with post-exertional malaise) and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)

The aim of this study is to explore the experiences of healthcare professionals who develop Long
COVID (with post-exertional malaise) and/or Myalgic Encephalomyelitis /Chronic Fatigue Syndrome (ME/CFS).

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To check if you are eligible and find out more about the survey, please download this participant information sheet. The link to the survey itself is at the end of the sheet.

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The survey will remain open until 6pm 31st December 2025.

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Physios for ME

© 2020 by 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

Contact

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Contact us at physiotherapyforme@gmail.com 

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