Blog

The Kansas City Patient Vasculitis Symposium

The University of Kansas Medical Center and the Vasculitis Foundation are pleased to announce that registration is now open for more »


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Coping With Your Child’s Illness

There may be no worse news for a parent than to learn that their child has been diagnosed with a more »


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Introducing the 2014 Vasculitis Awareness Video

We are pleased to introduce the 2014 Vasculitis Awareness Video, which celebrates the Vasculitis Foundation’s outreach efforts worldwide.  We hope more »


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The VF Wall of Awareness

  The Vasculitis Foundation is dedicated to supporting our community through education, awareness, and research year-round but during the month more »


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New Webinar Announced: The Science of Vasculitis Research Webinar – May 14, 2014

May is Vasculitis Awareness Month, and vasculitis patients and families are keenly aware of the continued need for research into more »


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Send Us Your Selfie

Take a photo of yourself wearing a VF tee shirt, or holding a VF Awareness Poster (Download the poster.) Submit more »


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Literature Order Form


Lynn’s Story

My Churg Strauss (EGPA) Life I never feel why me? I feel why not me? CSS (Churg Strauss Syndrome/Vasculitis), now more »


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Carrie’s Story

Carrie Gallagher is a wellness professional. So after being diagnosed with granulomatosis polyangiitis (Wegener’s) in 2012, she did the only more »


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