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Hi Marcia--
I've been diagnosed w/ CPS after a recent visit to a rheumatologist (also dx'd me w/ fibromyalgia and hashi's thyroiditis). I had been previously dx'd by my PCP with Systemic Lupus (SLE) and my symptoms fit SLE quite perfectly, I've just only had a positive ANA labwork wise. I haven't had a stroke, or trauma to my CNS that I can think of whatsoever. Also, I hurt everyday and yes I've had some bad pain but fatigue is my very worst symptom and my pain doesn't seem to "fit" what I read about CPS, only occasionally. I don't think I have this, I think they misdiagnosed me. I just thought I'd see if there was a nerve test or a labtest or anything that could confirm it or rule it out. It sounds terrible and I feel for you, how old are you, if you don't mind my asking. What do you do for your CPS? The only thing I really seem to fit is that when my extremities get cold (hands and feet) they hurt so bad and sometimes I have shooting pains because of it. Thank you so much for the information and for replying to my post!! I hope you are doing as well as possible right now.
Take care!

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