Blog

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 of May the VF would like to highlight the people 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 the diseases’ causes and improved therapies. Where are we now 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 your picture to vf@vasculitisfoundation.org  and we will feature your picture on more »


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Lynn’s Story

My Churg Strauss (EGPA) Life I never feel why me? I feel why not me? CSS (Churg Strauss Syndrome/Vasculitis), now known as EGPA – Eosinophilic granulomatosis with polyangiitis – is 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 thing she knew to do: Make lifestyle changes to help more »


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AAV Patients and Volunteers Needed for a Clinical Trial in Vasculitis

Patients with anti-neutrophil cytoplasm antibody (ANCA)-associated Vasculitis (AAV) are at risk of disease relapse and so are often kept on long-term medication that suppresses their immune system. These medications may more »


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2014 Vasculitis Foundation Fellowship Recipient

The Vasculitis Foundation is pleased to announce the selection of Dr. Rennie Rhee, University of Pennsylvania, as the 2014 Vasculitis Foundation Fellowship Recipient. The Vasculitis Fellowship Program is made possible more »


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Rally Events Are Being Held Around the United States. Find One Near You!

The Rally in the Alley events are volunteer-led bowling events held around the country at a community bowling alley. The goal of the events are to raise Friends and Funds more »


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