← Return to CIDP (Chronic Inflammatory Demyelinating Polyneuropathy)

Discussion
Comment receiving replies
@becsbuddy

@jshdma I found this information from the National Institutes of Health that mention symptoms of CIDP.
https://www.ninds.nih.gov/health-information/disorders/chronic-inflammatory-demyelinating-polyneuropathy-cidp
Did any of these symptoms lead you to the doctor for a diagnosis?

Jump to this post


Replies to "@jshdma I found this information from the National Institutes of Health that mention symptoms of CIDP...."

@becsbuddy - Thank you for this reference. Actually 2 separate neurologists told me very definitely I do NOT have CIDP. But after numerous tests, they cannot tell me the cause of my symptoms. These are: very gradually increasing sense of electrical current starting at the bottom of legs and over years rising to the rest of my body. My legs getting weaker. I can still walk a few miles, but every step feels like I could fall, especially going downhill. The only diagnosis I have is OLP, an auto-immune inflammation in my mouth. Any ideas from anyone would be much appreciated. A pharma. company suggested that symptoms fit CIDP.