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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.

VF Welcomes New Members To The Board Of Directors

The Vasculitis Foundation held its annual membership meeting on June 21 in Jacksonville, Florida.  The meeting was held in conjunction with the 2015 International Vasculitis Symposium which drew over 220 more »

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V-PPRN Launches Study On Employment and Income

The Vasculitis Patient-Powered Research Network (V-PPRN) is a team of patients with vasculitis, caregivers, researchers, data specialists, and providers on a daily mission to share and learn from one another more »

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V-PPRN Receives $1.4 Million Award For Research

The Vasculitis Patient-Powered Research Network (V-PPRN) has been approved to receive a three-year $1.4 million award by the Patient-Centered Outcomes Research Institute (PCORI) as part of the second phase of more »

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Clinical Trial for ANCA-Associated Vasculitis – Now Enrolling Patients

Sites throughout the U.S. and Canada are seeking patients with newly diagnosed or relapsed anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis.  This clinical trial is designed to determine whether a new non-steroidal more »

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