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@harley22 I see you have been visiting the neuropathy support group, also. Sometimes our medical team...
Do the doctors attribute your CIDP diagnosis
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@bjbates53 Have you had this severe fatigue since you were first diagnosed? Has it gotten worse?...
severe fatigue since you were first diagnosed ... There is an ongoing CIDP support group ... /connect.mayoclinic.org/discussion/cidp-chronic-inflammatory-demylinating-polyneuropathy
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The symptoms described in this post sound very much the same as what I have. I...
little over a year ago that I have CIDP ... After months without a firm diagnosis ... sought doctor who is interested in CIDP ... but she questioned diagnosis because
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Ok, here goes...my husband after seeing 4 neurologist was given the diagnosis of Distal axonal sensory...
seeing 4 neurologist was given the diagnosis ... had him taking IVIG infusions for a CIDP
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Oh my god. Are you me lol? I have one of the exact same theories and...
still semi convinced I have MS or CIDP ... something but my MRIs didn't support a diagnosis
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