Official Statement Important Information for the Vasculitis Community Regarding TAVNEOS® (avacopan) April 30, 2026 The Vasculitis Foundation is aware of recent updates from the U.S.
From Advocacy to Impact: Policy Strategies to Accelerate Rare Disease Cures On February 19, the Vasculitis Foundation hosted a virtual rare disease policy briefing that brought
2025 V-Red Winners The Vasculitis Recognizing Excellence in Diagnosis (V-RED) awards celebrate healthcare providers whose insight, persistence, and compassion have profoundly impacted the lives of
Meet VF Young Investigator Audra Horomanski, MD Early Inspiration and Commitment to Vasculitis Research Dr. Horomanski’s journey into vasculitis research began during her residency and
A New Era for Pediatric Vasculitis Research PedsVPPRN: Bridging Pediatric Vasculitis Research and Care Jessica Bloom, MD, MSCS, is a pediatric rheumatologist who has dedicated
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
People living with vasculitis rely on support, research, and connection every day.
Today only, your donation will be matched dollar-for-dollar, helping us reach more patients, fund critical research, and ensure no one faces vasculitis alone.
