Living with Chronic Inflammatory Demyelinating Polyneuropathy This is real life for me. It's not always fun. It takes a village. My mom has the boys while I am here for 3 days getting IVIG treatment for my CIDP. She drove me here, and will pick me up when I'm done. My kids don't understand why I have a needle in my arm. Or why I'm at the doctor for so long. Or ...

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