Updates

Funding announcement gets a big response

August 26, 2020

We were blown away by the response when we announced funding for the DecodeME study in June. Thousands of people shared and posted on social media, and both The Times (paywall) and the Guardian ran articles. 17,400 people registered their interest on our new DecodeME website, in addition to over 8,000 people who had already…

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DecodeME – Management Team live Q+A webinar

July 9, 2020

Chair of the Management Group Sonya Chowdhury, hosted a live Q+A webinar with Prof Chris Ponting, Prof Eliana Lacerda and Any Devereux-Cooke, to answer some of the questions people have been sending in. Over 1,000 people tuned in live to watch with almost 7,000 watching on Facebook and YouTube since. The questions they didn’t have time…

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Join our webinar Q&A

July 2, 2020

Funding for the world’s largest genetic study into myalgic encephalomyelitis (ME), led by a partnership of patients and scientists, has been announced today.

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Patients, scientists and advocates celebrate £3.2m funding for DecodeME, the largest ever ME/CFS DNA study

June 23, 2020

Funding for the world’s largest genetic study into myalgic encephalomyelitis (ME), led by a partnership of patients and scientists, has been announced today.

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The largest ever DNA study of ME/CFS

A partnership between

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