Myalgic Encephalomyelitis by Anonymous

I have just begun medical use of marihuana for myalgic encephalomyelitis/CFS (M.E.). I have more of a sense of well-being, less of that vague pain, less exhaustion, and I seem to sleep better.  It's only been 3 days so far.  It's the only medicine I dont have to remind myself to take...I find i want another dose on a regular basis.  ( the others are nutritional supplements, progesterone cream, and a breathing med).   I don't believe it's a "drug habit" but it’s really helping me, and I'm sensitive to its success.  I also suspect it's not merely numbing sensation of pain, drugging me to sleep etc, but is actually reducing the pathology causing pain, insomnia etc.