← Return to CIDP (Chronic Inflammatory Demyelinating Polyneuropathy)

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@sb4ca

I also have this though mine is slowly progressing and effects my motor nerves. My balance is only slightly bad. I also have a primary immune deficiency and started IVIG for that. My insurance turned down the infusion for the CIPD because my symptoms weren’t sudden enough. What aspects are the worse for you? I’m sorry you’re having to go through this

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Replies to "I also have this though mine is slowly progressing and effects my motor nerves. My balance..."

IVIG...you too? I was receiving infusions for about a year and then suddenly Medicare also rejected further infusion as there were no clinical trials for my specific condition proving efficacy. My doc appealed three times, all for naught.