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An international survey of experiences and attitudes towards Pacing using a heart rate monitor for people with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome

In October 2021 we collaborated with the Facebook Group “ME/CFS pacing with a HR monitor #2" to conduct a survey to explore the experiences of and attitudes towards pacing with a heart rate monitor in people with ME.

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The write-up of this survey was published in the journal "Work" in March 2023, and is available as open access here.

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You can read a brief summary of survey results here.

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You can download our poster here, which was presented at the ME/CFS International Conference in November 2021

HR monitor survey pstr_edited.jpg
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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

Contact

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We want to link with physiotherapists or people with ME.

Contact us at physiotherapyforme@gmail.com 

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