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The Vasculitis Foundation is the international organization for patients with vasculitis, their families, friends and the health care professionals who care for them.
Caregivers are a vital part of a vasculitis patient’s life. And yet, there are not many resources for this dedicated group. Dr. Lesha Carpenter has published on this important topic more »
In my last article, I wrote about the feelings of loneliness a patient often experiences after a diagnosis of diseases like vasculitis. This article will focus on the caregivers of more »
During 2014, we at the Vasculitis Foundation have been especially proud of the programs and services we have been able to offer our community. Planning for the 2015 International Vasculitis more »
The Vasculitis Foundation is pleased to announce the creation of theVasculitis Clinical Research Consortium (VCRC) – Vasculitis Foundation (VF) Fellowship Program in Clinical Investigation. The VCRC is an integrated group of more »