Research Illuminates Information Needs of Patients with Vasculitis Jodi Hall, Senior Patient Support Associate at the Vasculitis Foundation, recently presented her study, “Information Needs of
Vinay Kamath, 15, Wants More Vasculitis Research So He Started a Fundraiser When Vinay Kamath, 15, found out his grandmother had ANCA negative vasculitis with
Young Adults Connect at Nashville Conference, Offer Hope to One Another Young adults between 18 and 30 came from all across the United States and
Dr. Catherine Sims Leads Team Researching Pregnancy and Vasculitis Pregnancy can be complicated, even for healthy women. But for someone with a rare autoimmune disease,
Rare Disease Day is All About Sharing Information Get ready to show your support for everyone who has been diagnosed with a rare disease. Rare
Veterans Affairs is Working to Give Its Patients Greater Access to Vasculitis Care, No Matter Where They Live Dr. Paul Monach, chief of the rheumatology
Lack of Vasculitis Expertise Leads to Devastating End Karen Miller has joined her local hospital’s patient advisory board after her mother, Lynn Johnston, died from
Blog “It was the best of times, it was the worst of times, it was the season of Light, it was the season of Darkness,
Eliza Johnstone’s Vasculitis Diagnosis Came Late, She Now Champions Early Diagnosis for Others Eliza Johnstone, a 19-year-old living in the United Kingdom, feels like she
Late Vasculitis Diagnosis Steals Nearly One Decade Christine Gerchow was in her final semester at Villanova University in 2002 and planning for a promising career,
