The Referral Center Group I, Rare Systemic Diseases and Autoimmune Diseases, Necrotizing Vasculitides and Systemic Sclerosis coordinates and manages patients with vasculitis in France, in cooperation with the other centers comprising Group I. Visit their website.
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Building upon the collective strength of the vasculitis community, the Foundation supports, inspires and empowers individuals with vasculitis and their families through a wide range of education, research, clinical, and awareness initiatives.
The Vasculitis Foundation is a registered 501 (c) (3) non-profit organization. All contributions are 100% tax-deductible.
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Vasculitis Foundation
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