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