I know Fibro Action has a lot of information on this too. But when you watch this doctor, he made me feel so good,
Apparently this disease's name has changed over the years from lazyitus,sloathfulness, yuppy flu, cfs, me and now we are at fm.
When you cannot sleep have a look through these articles I found trawling the web.
These have made me feel so much better, I am not depressed, I am not in poor physical condition ( well I wasn't until I was given all the different meds to take to fob me off) I need a solution to the problem, not meds that dumb it down, and in fact they are not working that well either
Maybe the DLA should employ some of use to to the assessments and evaluations!
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So what's the answer? ASk for a brain scan or alternatively go to the USA and be treated like a normal human being.??????