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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)

This survey closed in January 2026 with 170 responses.

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Thank you so much to everyone who took the time to respond. We will now analyse and write up at a later date.

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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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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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