Mission: Building upon the collective strength of the vasculitis community, the VF inspires and empowers individuals with vasculitis and their families through a wide range of education, research, clinical, and awareness initiatives.
Subscribe for the VF E-News
HERE
A
A
A
5th Annual Vino
for Vasculitis
+
Vasculitis
Vasculitis
Behcet’s Disease
Central Nervous System (CNS) Vasculitis
Cryoglobulinemia
Eosinophilic Granulomatosis with Polyangiitis (EGPA/Churg-Strauss Syndrome)
Giant Cell Arteritis (Temporal Arteritis)
Granulomatosis with Polyangiitis (GPA, formerly called Wegener’s Granulomatosis)
IgA Vasculitis (Henoch-Schönlein Purpura)
Hypersensitivity Vasculitis (Leukocytoclastic)
Kawasaki Disease
Microscopic Polyangiitis
Polyarteritis Nodosa
Polymyalgia Rheumatica
Takayasu’s Arteritis
Urticarial Vasculitis
Resources
Resources
Educational Webinars
Research and Treatment Institutions
VF Medical Consultants
Educational Articles
Fish’s Focus on Health
Frequently Asked Questions
Patient Advocacy Groups
Pediatrics/Young Adults
Pediatrics/Young Adults
Newly Diagnosed
Education Concerns
Transition Concerns
Educational & Awareness Videos
Find a Physician
Research
Research
Research Program
Our Researchers
VCRC-VF Fellowship Program
Vasculitis Patient-Powered Research Network (V-PPRN)
Vasculitis Clinical Research Consortium (VCRC)
Chemocentryx ADVOCATE trial now enrolling
Participate in Research
Participate in Research
Studies Enrolling Patients
NIH Clinical Trials
Events
About
About
Vasculitis in the News (RSS Feeds)
Our Board
Our Team
Anniversary
Vasculitis Foundation Newsletters
Annual Reports
Press Page
Literature Order Form
Join
Contact Us
VF Bob
Donate
Donate
Support the VF Through the Amazon Smile Program
United Way Giving
Ways to Give
Store
Home
/
Join
Join VF
Donate
