Mark Berry
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
Mark Berry is acting CEO of the patient charity and online forum Phoenix Rising. He is also secretary, treasurer, and forum moderator, and he contributes to the Phoenix Rising blog. He has been living with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) for over 15 years.[1]
On 7 March 2016, he posted an open letter to Queen Mary University of London on behalf of Phoenix Rising calling for the release of the PACE trial data.[2]
