Hi, I was diagnosed with M.E in 2009, and medically dismissed as a civil servant not long after. Over the last 8 months I have found the pain levels have increased, so I am now thinking it's fibro instead. I also suffer with RLS for years. I take several medications which have balanced my symptoms to a certain degree, along with pacing myself etc. But the pain is increasing, will be returning to GP for further diagnosis. I expect several others have had this as a misdiagnosis, but wonder how seriously I will be taken and even if the GP will bother to change my notes.....
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