If you ever need a shot of motivation, just talk to Brian Kilgarif. Brian is raising money for the VF on behalf of his wife, Steph, who was diagnosed with granulomatosis with polyangiitis (GPA) in 2002, when she was 16. His goals are to raise vasculitis awareness, and to honor…...
Connection at VF Symposium Eases Isolation of Takayasu Arteritis
Loneliness is a common feeling among patients with vasculitis. When you find someone else on a similar path, it can help ease the isolation. That’s what happened to Dedra DeMarco and Devri Velazquez, who met at the 2019 International Vasculitis Symposium in July and discovered they share a lot in…...
VF Research Committee Paving the Way For a New Generation of Investigators
The promise of better treatments for vasculitis has special meaning for Jason Springer, MD, MS, chair of the Vasculitis Foundation (VF) Research Committee and member of the VF Board of Directors. Before he ever started medical training, Dr. Springer’s father was diagnosed with vasculitis, a disease he had never heard…...
Sam and Helen Dodge: Feeling Hope in the Wake of a Vasculitis Diagnosis
Sam Dodge spent much of his working life as an ad cameraman, and he collects antique motion-picture cameras, so it’s not surprising that he thinks in terms of film metaphors. Sam was diagnosed last year with microscopic polyangiitis (MPA), and he describes the experience like this: “Sometimes I feel as…...
