i have had cfs/me since i was about 11/12 years old, but i was only diagnosed by process of elimination 3 years later (18 months ago) and since then the only treatments i've been made aware of are physio, a small meeting once every month or so with 4 other kids who can still run around all the time:( and a counciller for my parents and i (which has only ended up with me on prozac:mad:)
every docter i've spoken to has said they're the only treatments available in my area and that really, there aren't treatments at all.
it's got me wondering, is it only in only in hampshire, england that this happens or is it differant elswhere in the uk AND is there a test or other treatments available abroad? (i've heard rumours that there are)
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