Janelle Wiley
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
Janelle Wiley is an American patient advocate for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). She has been involved in "citizen-science" analysis of the PACE trial alongside Graham McPhee and others. She has also testified at several Chronic Fatigue Syndrome Advisory Committee (CFSAC) meetings.[1] She became ill with ME at the age of 19 while she was studying biology at university.[2]
Janelle Wiley was one of the contributors to the ME Analysis: Evaluating PACE project at Phoenix Rising.
