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VF Honors Three Members for Excellence

The Vasculitis Foundation has honored three members for their exceptional work and support towards the mission of the VF.  The more »


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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 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 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 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 more »


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VF Awards $200,000 in Promising New Research

The VF Board of Directors is pleased to announce that it has selected three new research studies for funding this more »


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Test Post – DAY 1

Mechanisms across the continuum, from those who avoid or play victim, to those who fight and communicate to the disease process that it met the wrong person.


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VF Funds Two New EGPA/CSS Research Studies

The Vasculitis Foundation is pleased to announce it has selected two new research studies on EGPA/Churg Strauss for funding in more »


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