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Vasculitis Foundation

The Vasculitis Foundation is the international organization for patients with vasculitis, their families, friends and the health care professionals who care for them.

Kimberly’s Story

My name is Kimberly. Though I hated swallowing the medicines, I did with a ritual and timing that was determined to get rid of this thing.  Each time I took more »

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VF Introduces Vasculitis Fellowship Program

VF Introduces Vasculitis Fellowship Program June 5, 2012 Applications for the Vasculitis Foundation Fellowship are being accepted through October 1, 2012. The $100,000 award, the first for the Vasculitis Foundation, more »

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VF Loses Dedicated Friend and Supporter

Longtime VF Member Passes Away May 2012 The North Carolina chapter lost a dear friend in May when Shirley Ferguson, the mother of Danette Anderson, a Granulomatosis with polyangiitis (GPA, more »

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Raising Awareness in Texas

Jean and Nicole, longtime members of the Vasculitis Foundation, distribute information on vasculitis during the 2012 Dallas/Fort Worth Walkabout and Autoimmune Disease Health Fair on May 12 in Grapevine, Texas. more »

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