Covid-19 Vaccinations

The ME Association regularly updates its information on all aspects of COVID vaccination and collects feedback on adverse reactions.

The latest update, which was published on Sunday 16th May 2021, can be found HERE.

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International ME Awareness Day 2021

To coincide with International ME Awareness Day 2021 (12th May), ME Research UK (SCIO Charity no SC036942) with the financial support of The Gordon Parish Charitable Trust (SCIO Charity no SC045752) announces a £400,000 joint initiative to fund biomedical research into the role of viruses in ME/CFS (Myalgic Encephalomyelitis/Chronic fatigue syndrome) globally.

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Stepping Aside

Margaret Mar decides that the time has come to step aside from the chairmanship of the Group.

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NICE - Consultation on draft guideline - December 2020

Myalgic encephalomyelitis (or encephalopathy)/chronic fatigue syndrome: diagnosis and management. Consultation on draft guideline – deadline for comments 5pm on 22/12/20 email: cfs@nice.org.uk

We would like to hear your views on the draft recommendations presented in the guideline, and any comments you may have on the rationale and impact sections in the guideline and the evidence presented in the evidence reviews documents. We would also welcome views on the Equality Impact Assessment. In addition to your comments on our guideline documents, we would like to hear your views...

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NEW Statement on long COVID and ME - December 2020

Statement on long COVID and ME/CFS by the International Alliance for Myalgic Encephalomyelitis, December 2020. IAFME is a formal collaboration between national organizations representing patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS).

SARS-CoV-2 (COVID-19) continues to affect millions of people globally. While some people recover, other people have a delayed recovery...

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