The latest meeting including an excellent discussion with Sean O’Niell about ways in which ME might feature more often in the media.
Tag: DecodeME
The ME Association End of Week Research Round-up
This week we feature three new research studies including a critical review of genetic research ahead of the DecodeME study.
Meet The Scientist: Professor Chris Ponting – DecodeME
Chris Ponting talks about the DecodeME study that seeks to understand the causes of M.E. and could help advance the discovery of effective treatments.
Forward-ME Group | Minutes of the meeting held on 10 July 2020
Complete lowdown on almost everything that’s happening in the ME/CFS world right now!
Out Now! The Summer Issue of ME Essential Magazine!
The Summer Magazine is a bumper 68-page issue with news, research, DecodeME, interviews, stories, recipes and much, much more. Become a member today!
Free Leaflet: DecodeME – The Largest Ever Genetics Study!
A free leaflet all about the exciting DecodeME research study. It’s the largest ever study examining DNA in people with ME.
MRC: Largest Genetic Study into ME is Launched!
The £3.2 million study is jointly funded by the MRC and hopes to aid development of diagnostic tests and targeted treatments.
The DecodeME Genetics Study: Letters to The Times
Published letters in response to the DecodeME research announcement and recent articles. With Jeremy Hunt and Carol Monaghan.
Patients, Scientists, and Advocates Celebrate £3.2m Funding for DecodeME, the Largest Ever ME/CFS DNA study!
Funding for the world’s largest genetic study into myalgic encephalomyelitis (M.E.), led by a partnership of patients and scientists, has been announced today.
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