
Two Sides of a Kidney
Blog When you’re a nurse and have four kids under the age of seven, feeling tired can be par for the course. But Theresa Caldron’s
Blog When you’re a nurse and have four kids under the age of seven, feeling tired can be par for the course. But Theresa Caldron’s
Blog The John Grube Foundation e.V., based in Hamburg, awards the “John Grube Prize” in honour of its namesake, who died young of granulomatosis with
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