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CIDP (Chronic Inflammatory Demyelinating Polyneuropathy)
Autoimmune Diseases | Last Active: 2 days ago | Replies (258)Comment receiving replies
@sherlock, I see that you have met some of the members in the Anyone here dealing with peripheral neuropathy discussion, but have started one specifically on CIDP. I would like to invite @pammy922, @cwallen9, @mayor47, and @jazzy27, to this discussion as they have all mentioned CIDP in the past. I would also like to invite @angelarisstrom, who had IVIG treatments for Guillain-Barre syndrome which is closely related to CIDP.
@sherlock, how are the IVIG infusions helping?
Replies to "@sherlock, I see that you have met some of the members in the Anyone here dealing..."
I am brand new to Mayo Clinic Connect. I did several searches. I tried CIDP; spelling it out; spelling it out with P being Polyradiculaneuropathy--that's my diagnosis, but I don't know what it means. Can anyone help?
Hi Justin, please add me to the CIDP discussion group. I was diagnosed earlier this year. Thanks Tony
Please include I also have been do w/CIDP
Please add me to your CIDP group discussion. I have been diagnoised with CIDP and small fiber Neuropathy and have received two 5 day IVIG treatments wit my third in January.. Looking for answers. Struggling to minimize damage at 69 yoa. Help
I have also been diagnosed with CIDP. I believe that this is because there seems to be no apparent cause?
Anyone have any diet recommendations that would possibly help
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They help with energy and pain. I always know when it's time for my next infusions as pain increases. Is anyone having IVIG just for small fiber neuropathy?