Championing Vasculitis Victories: Art Diaz’s Choice to Advocate
July 16, 2023
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 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
Blog The American College of Rheumatology (ACR) and European Alliance of Associations for Rheumatology (EULAR) endorsed the ACR/EULAR classification criteria for ANCA-associated vasculitis (EGPA, GPA and MPA).The classification criteria
Blog Dr. Berti began his work in vasculitis while he was a medical student at Vita-Salute San Raffaele University in Milan, Italy. At the time,
Blog Formerly called Wegener’s granulomatosis, granulomatosis with polyangiitis (GPA) is a form of vasculitis—a family of rare disorders characterized by inflammation of the blood vessels,
Blog (May 2021) Adam Maass, MD, is the first-place winner in the Vasculitis Foundation’s (VFs) 2021 Recognizing Excellence in Diagnostics (V-RED) award program. Now in
