PEM: Running out of battery & feeling intensely unwell: a carer’s perspective I guess you’ve probably heard of Myalgic Encephalomyelitis – by its abbreviation ‘ME’. Maybe you’ve got an…
Do you have a diagnosis of ME or CFS from the NHS? For decades many people with suspected ME have not been able to find an NHS professional to…
DecodeME Study blog: From DNA to drug development. Five success stories show the potential of DecodeME How do you find treatments for a disease like ME/CFS, where nothing is…
Why we need a study like DecodeME – scientific paper published, by the ME/CFS Biomedical Partnership, 26 Jan 2021 Today, we know almost nothing for sure about what causes ME/CFS….
Dear DecodeME Friend, We have been blown away by the response we have had since we announced funding for the study. Over 25,000 people have signed up to receive updates,…
Genetic risk factors of ME/CFS: a critical review, by in Human Molecular Genetics, ddaa169, 3 Aug 2020 [doi.org/10.1093/hmg/ddaa169] Review abstract: Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a complex multisystem…