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I was diagnosed with CIDP in 2020 and I had 16 IVIG infusions And that was...
I was diagnosed with CIDP in 2020 and ... Surgeon was completely aware of my CIDP ... My CIDP affects my right foot and my
Support Group: Autoimmune Diseases
Posted: Sep 20 6:13am
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Hi everyone! My name is Susan and I have lived with chronic pain for a number...
paralyzed by an autoimmune disorder (CIDP ... CIDP is a rare neuromuscular disorder ... neurologist thinks that I possibly developed CIDP ... Right now I am taking nothing for my CIDP
Support Group: Chronic Pain
Posted: Nov 5, 2020