“While there are now fresh moves to revise NICE guidelines on CFS/ME in the United Kingdom, these advances are likely to have been hindered by the scale of epistemic injustices experienced by patients with ME/CFS (NICE 2017). Of the valuable participants in the ongoing discourse about ME/CFS, it is patients who are not only the most vulnerable but have the most to lose.” InjusticeBiasAuthoritarianismChronic Fatigue SyndromeMyalgic EncephalomyelitisMe CfsHealth ServiceStigna Author:Charlotte Blease