Can we safely write about ME anymore ?
It doesn't look like the situation is going to change anytime soon.
The agenda, clinican rather then patient-driven, as always, remains firmly focused on fatigue; which is not even a defining feature of ME.
Can any of us even safely write about "ME" anymore, or claim to have it, given the domination of CFS and the dilution of the name to mean anything you want it to ?
I am not sure we can.