Kalen Young

VPPRN Rising Above Expectations

  The Impact of Participation Thank you for your support and participation with the Vasculitis Patient-Powered Research Network! In three years our Network has grown to over 2,000 participant in 29 different countries representing 13 of the vasculitides.  There is strength in numbers.  Every participant in the VPPRN helps to…...

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24-Hour Twitter Event

Vasculitis Awareness Month 2018: Making the Invisible Visible May is Vasculitis Awareness Month and we would like to help spread awareness about the patient experience. Ever wish others understood what it is like living with a chronic and invisible disease like vasculitis? To shed light on this issue, the Vasculitis…...

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Jason’s Message

2016 marks the Vasculitis Foundation’s 30th anniversary. As board president and a vasculitis survivor, I’d like to take the time to share a few thoughts with you. When I was diagnosed in 2011, the first place I turned for information was the Vasculitis Foundation. From that moment to today, I…...

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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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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 and programing that foster positive change. The Wall of Awareness features ‘selfies’ of VF members, physicians and VF staff who…...

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