Revelations: How One Woman is Emerging from her Vasculitis Gloom
January 22, 2024
Blog When I spoke to Lupe on the phone for the first time, I asked her to describe herself in a few words. Colleagues had
Blog When I spoke to Lupe on the phone for the first time, I asked her to describe herself in a few words. Colleagues had
Blog Before Irene Tipton began her journey with (Granulomatosis with Polyangiitis) GPA, she had dedicated her life to helping others learn. First as an elementary
Blog Meet Alex, from Fort Mitchell, KY, who’s living with GPA vasculitis: I was diagnosed in June 2018 when I was 16 years old and in
Blog Samantha SainteMarie was in graduate school, working to get her master’s degree in mental health counseling, when it first happened. She was typing a
Blog Art Diaz was living a full life in Southern California and rarely got sick. He was fit; a runner. Every few years, he’d force
Blog Every morning, Jane would wake up feeling fine. Every afternoon, an intense wave of dizziness would overcome her. She went to a neurologist who
Blog 2022 Vasculitis Foundation Patient Hero, Michael Agathis was diagnosed with Granulomatosis withpolyangiitis (GPA) in 2013.“Strength comes from true belief and faith in God and
Blog Kinanah Yaseen, MD, was awarded the 2020 Vasculitis Clinical Research Consortium (VCRC)-Vasculitis Foundation (VF) Fellowship. She is currently a junior faculty member in the
Blog By Gary Salzman, MD (Edited by Nina Silberstein) A diagnosis of vasculitis changed my life, but I didn’t let it ruin it. Today, I’m
Blog Data From Multicenter Longitudinal Observational Study Prof. Rula Hajj-Ali At the 2022 International Vasculitis and ANCA Workshop, Dr. Rula Hajj-Ali presented on the prevalence
