For people that have had it, have it now,suspect they might have it or have friends or family that have it and want more information (show your friends if they are curious or you don't have the energy to explain how you are feeling)
This experience is personal to us, your experience may be different. We are not medical practitioners, just two people discussing our experience of M.E.- Myalgic encephalomyelitis or as it is known in USA Chronic Fatigue Syndrome
Would have loved to hear more on how the women got better
jordan2252 8 months ago
Revelatory dialogue.
xyzllii 10 months ago