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I wonder if MD and ME/CFS and FIBRO could have similar pathologic functioning. What do you think about it?
It would not surprise me - but, fwiw, I do not have pain and I'm a rapamune responder.
Do you know of any ME researchers looking into this?
Tangentially, I have a suspected neuroendocrine tumour (NET) and have read that rapamycin is one of the treatments for the tumour.
Because NET's are slow growing, I wonder if rapamune has been inhibiting tumour growth for the last 2 years I've been taking it.
And I wonder if my ME symptoms are a manifestation of the tumour as exertion can trigger NET symptoms.