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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.
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 »
My name is Sue. I believed that my vasculitis was virally induced. The first months back at work were rocky, as the prednisone, blood pressure medicine and minor brain damage more »