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I can really sympatize with you as I have same issues as you do. Having foot...
All they say is that I have CIDP, cause
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Hello @dlcutler, welcome to Mayo Clinic Connect. I'm sorry to hear you are still experiencing pain...
has-anyone-on-this-feed-been-diagnosed-with-cidp-its-very-rare
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I've had CIDP for 4yrs now. I go to the University of Minnesots to Drs. Now...
I've had CIDP for 4yrs now. ... Wednesday they tell me I may not have CIDP
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Hi. A highlight of my recent visit to the neurologist was his saying that I'd posed...
you all the best in tackling your CIDP
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Thank you for asking. My primary autoimmune disease- CIDP (chronic inflammatory demyelinating polyneuropathy) started during the...
My primary autoimmune disease- CIDP ... Accepting that CIDP is a chronic lifelong ... How has CIDP affected me? ... with life changing illnesses like CIDP
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