The Vasculitis Foundation (VF) advocates for early diagnosis, leading-edge treatment, research, and ultimately a cure for all types of vasculitis.  The foundation supports and empowers patients through education and awareness. 

Through the VF's detailed website, bimonthly newsletter, medical consultants, symposiums, webinars, chapters, support groups and contacts, the VF educates patients, their families and health care professionals about vasculitis. 

Vasculitis is a family of rare autoimmune diseases that can affect people of all ages. The term vasculitis means inflammation of the blood vessels, arteries, veins or capillaries. When such inflammation occurs, it causes changes in the walls of blood vessels, such as weakening and narrowing that can progress to the point of blood vessel blockage to organs. This blockage can cause serious organ damage and without proper treatment may even result in death.

Health Care

Health Diagnostics

Therapeutics

Vasculitis Foundation

Vasculitis Foundation's headquarters in Kansas City, United States

This department oversees and coordinates the planning and execution of various programs and initiatives.

Program Development

This department is responsible for managing internal and external communications, ensuring messaging aligns with organizational goals.

Communications Department

This department focuses on providing support and guidance to patients while advocating for their needs and preferences.

Patient Advocacy and Support

This department oversees the strategic direction and governance of the organization through its board members.

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Other teams

Communications Department

Patient Advocacy and Support

Board Governance