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Join

The VF is a membership based organization. Our members are the lifeline of this organization and the services we provide.

Resources

The VF supports patients and their families by providing the current information on diagnosis and treatment.

Find a Doctor

Looking for a doctor in your area? Use our new map feature to find a doctor or Vasculitis Foundation chapter near you.

Participate in research

Help find better treatments, improve diagnosis, and advance the understanding of vasculitis by participating in research.

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Upcoming Events

  • Vasculitis - A 30 Year Perspective
  • Coping With Vasculitis
  • One Family - Three Cases of PAN
  • VF Physician Perspectives: Dr. Eric Matteson
  • Cheryl and CNS Vasculitis
  • Carol and Takayasu’s arteritis
  • Victor and GPA Wegeners

Webinar Series 2018 Topic: Dermatology/Skin Involvement in Vasculitis and the ARAMIS Study Guest Speaker: Robert G. Micheletti, Assistant Professor of Dermatology at the Hospital of the University of Pennsylvania Time: 1:00 p.m. EST Register: https://r

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Join Us for a Violin for Vasculitis Concert! Join us on February 25 at 4:00 p.m. a

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The main objective of Rare Disease Day 2018 is to raise awareness with policy makers and the public of rare diseases and of their impact on the lives of patients, and to reinforce their importance as a public health priority. International campaign. Partner with NORD and EURODIS. https://www.rarediseased

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Click here to view full calendar  

Vasculitis Patient-Powered Research Network

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The V-PPRN seeks to transform how clinical research in vasculitis is conducted by directly engaging patients, investigators, care providers, and health systems to develop research methods to electronically collect health records and patient-reported data on a large number of patients with various forms of vasculitis.

Join The Network!

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