Research Funding

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.

Patients, Scientists, and Advocates Celebrate £3.2m Funding for DecodeME, the Largest Ever ME/CFS DNA study! Read More »

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.

Myalgic Encephalomyelitis: MEPs call for more funds for research into complex illness | 19 June 2020

“By adopting this resolution, Parliament gives voice to patients’ concerns and supports their legitimate requests for greater awareness and funding for research.”

Myalgic Encephalomyelitis: MEPs call for more funds for research into complex illness | 19 June 2020 Read More »

“By adopting this resolution, Parliament gives voice to patients’ concerns and supports their legitimate requests for greater awareness and funding for research.”

ME Association Research: New study to measure physiological changes in daily activity in people with ME | 12 May 2020

This exciting study will examine the physiology of M.E. and is led by researchers from Leicester, Oxford and Manchester Universities and Physios 4 M.E.

ME Association Research: New study to measure physiological changes in daily activity in people with ME | 12 May 2020 Read More »

This exciting study will examine the physiology of M.E. and is led by researchers from Leicester, Oxford and Manchester Universities and Physios 4 M.E.

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