IACFS/ME New York Research Conference Report
IACFS/ME New York Research Conference Report Read More »
The ME Association has produced a summary report of the recent M.E. research conference which took place in New York.
Dr Luis Nacal
Potential research into Long-Covid and ME/CFS at the ME Biobank
Potential research into Long-Covid and ME/CFS at the ME Biobank Read More »
The ME Biobank team with Dr William Weir are hoping to conduct research into Post-Covid and ME/CFS. Please register your interest in taking part.
Register Now! The International Association CFS/ME Virtual Conference
Register Now! The International Association CFS/ME Virtual Conference Read More »
The IACFS/ME Virtual Conference is open to all and will be held on Friday 21 August from 3.00PM – 8.30PM UK time.
Meet The Scientist: Professor Chris Ponting – DecodeME
Meet The Scientist: Professor Chris Ponting – DecodeME Read More »
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.
MRC: Largest Genetic Study into ME is Launched!
MRC: Largest Genetic Study into ME is Launched! Read More »
The £3.2 million study is jointly funded by the MRC and hopes to aid development of diagnostic tests and targeted treatments.
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.
ME/CFS Biomedical Partnership PPI Steering Group Update | 02 December 2019
ME/CFS Biomedical Partnership PPI Steering Group Update | 02 December 2019 Read More »
We explain what happened at the recent MRC/NIHR workshop and invite you to complete a survey on research criteria.
MRC/NIHR Workshop: The ME/CFS Biomedical Partnership – Genetics and Biomarkers | 07 November 2019
The MRC will host a workshop to help the CMRC with its major bioresource proposal involving 20,000 samples and data from people with M.E.