Confused? Scared? Concerned?

We know that you are 1 to 9 per 100,000 people who have CIDP.

We’re Here. And we’ve Been Where You Are.
The majority of the Foundation’s volunteers are intimate with the range of emotions that come with a recent diagnosis of CIDP – a nerve disorder so rare that you probably have never heard of it.
Fortunately, There Is Help And There Is Hope.

While the “c” does stand for “chronic,” there are treatments today that can improve and may cure the disorder if caught early and managed appropriately.

Within our community of CIDP survivors support—the kind that comes from experience—is readily available for you.

You do not have to go through this alone. We’re here.