Research: New Study to Harmonise Research Definitions in ME/CFS
Research: New Study to Harmonise Research Definitions in ME/CFS Read More »
The ME Association is delighted to announce that it has […]
The ME Association categorically disagrees with the opinions expressed in Science Norway article
***Sharing for information – not a recommendation*** Today, an opinion
Parliamentary questions surrounding the DHSC Delivery Plan on ME/CFS
Parliamentary questions surrounding the DHSC Delivery Plan on ME/CFS Read More »
Ashley Dalton, Parliamentary Under-Secretary of State for Public Health and Prevention
Research: Second-Phase Funding to Advance the Development of a Diagnostic Test for ME/CFS
The ME Association and ME Research UK are excited to
Farming Life: Cumbrian farmer features in unique photography exhibition highlighting ME/CFS
The experiences of Cumbrian farmer, Andrew Jackson (58), who has
Ask your MP to sign the Early Day Motion!
Ask your MP to sign the Early Day Motion! Read More »
Ask your MP to sign the Early Day Motion (EDM)
Disabled people call for an independent PIP review; add your name
Disabled people call for an independent PIP review; add your name Read More »
Disabled people’s organisations have published an open letter calling for
MP John Milne writes to Wes Streeting
MP John Milne writes to Wes Streeting Read More »
Under a heading “Concerns regarding ME/CFS Strategy in the Final
Metro: I thought I had food poisoning – it was far worse
Metro: I thought I had food poisoning – it was far worse Read More »
I couldn’t get out of bed. I felt drained, constantly.
Parliamentary questions on ME/CFS and Long Covid research funding, and the Epsom and St Helier NHS Foundation Trust service
MP Tom Morrison, Liberal Democrats asked Ashley Dalton, Parliamentary Under-Secretary
BBC News: Martha’s rule rolled out to all acute hospitals in England
BBC News: Martha’s rule rolled out to all acute hospitals in England Read More »
Martha’s rule rolled out to all acute hospitals in England
The ME Association awards Decode ME the Howes Goudsmit Award 2025
The ME Association awards Decode ME the Howes Goudsmit Award 2025 Read More »
The ME Association are pleased to announce that we have
BACME: ME/CFS Tube Feeding Survey
BACME: ME/CFS Tube Feeding Survey Read More »
British Association of Clinicians in ME/CFS (BACME) are conducting a
ME Essential: Winter 2022: Men don’t talk about things – or do they?
ME Essential: Winter 2022: Men don’t talk about things – or do they? Read More »
Along with ME/CFS, David, who also suffers with Postural Tachycardia
ME Essential: Summer 2023: There is always hope!
ME Essential: Summer 2023: There is always hope! Read More »
By Rachel White Before I developed Myalgic Encephalomyelitis, I was
The Times: Medical Misogyny and ME/CFS Research: MEA writes to the Times Editor in response to published letters
The Times published the following letters (9th August 2025) in
Sunday Times: Sarah Boothby: As my daughter died of ME, the state met in secret to blame me
**Trigger Warning: Upsetting Content – also discusses the wrongly assumed
BACME Statement on DecodeME study results
BACME Statement on DecodeME study results Read More »
BACME has sent the ME Association the following statement to
The Guardian: Scientists find link between genes and ME/CFS
The Guardian: Scientists find link between genes and ME/CFS Read More »
“These provide the first robust evidence for genetic contributions to
Decode ME release initial DNA results!
Decode ME release initial DNA results! Read More »
The DecodeME team announce results from the analysis of 15,579