Kimberly’s Story – a Wegener’s Granulomatosis patient

The last couple of years The Vasculitis Foundation has been trying to put a human face on Vasculitis diseases. I have been in contact with Kimberly for the last few years. Most of us live far apart and in different countries even. These words from Kimberly are heartbreaking.

You can read her part of her story here.

I have asked the same questions that she has written. It is very hard to have a disease that is not understood enough to find what could trigger such a horrendous disease.


About Cyn Bagley

My life is a mixture of travel, jobs, and disease. You can find some of my novels on under the name Cyn Bagley.
This entry was posted in Vasculitis, Vasculitis Foundation, Wegener's Granulomatosis. Bookmark the permalink.

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