@efg4me welcome to the “wonderful world” of Polyarteritis Nodosa! I was diagnosed in 2016 with Cutaneous PAN. We are rare indeed, and it’s so hard to find anyone, including doctors who have seen it.

I learned as much as I could about this disease and was able to teach my PCP and others about it.

Last year I had another biopsy and there was no evidence of CPAN. I guess I have recovered. I’m not sure…
Best wishes.

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