Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

Hello, I'm a new member.

I am both an M.E patient and advocate. I also own an online training company that teaches about M.E./C.F.S.

I would be interested to hear from any OT who has looked after M.E./C.F.S patients. How did they respond to your support? What support did you offer and did the support have positive patient outcomes?

Thanks!