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New survey released: hyperbaric oxygen / oxygen therapy

A new survey has been released, looking for the experiences of people with ME and Long Covid with hyperbaric oxygen or oxygen therapy. If you have experience with this intervention we'd love to know more - for more information and the link to the survey please see the official study page here .

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

Contact

Contact us at physiotherapyforme@gmail.com 

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