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Our Mission
The International Lichen Planus Foundation is dedicated to unraveling the complexities of Lichen Planus by inspiring health and well-being to each patient. We unite patients, clinicians, educators and researchers to foster innovation, reduce diagnostic delays, and provide a voice for those living with chronic mucosal and cutaneous challenges.
What is Lichen Planus?
Lichen Planus is a common skin condition that causes itchy, purple, flat-topped bumps on the skin, as well as white patches in the mouth or on the genitals. It is not contagious, meaning you cannot catch it from someone else or spread it to others.
Read More About Lichen Planus
Educational Resources
Whether it's recognizing your stress triggers or making sure your topical medication is working as hard as it can, the right habits matter. Explore our tips and resources for managing lichen planus day to day.
Explore Educational Resources
Support Groups
Lichen planus is a chronic inflammatory condition that touches every aspect of life — and yet, for many who live with it, finding reliable information and genuine understanding can feel isolating. The International Lichen Planus Foundation was founded to change that.
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About Us
The Foundation is dedicated to connecting patients with knowledgeable healthcare providers, advancing innovative treatment research, and raising awareness of this chronic immune-mediated condition among both the medical community and the general public.
Read About The Foundation
About Our Founders
The International Lichen Planus Foundation was officially founded by Dr. Nancy W. Burkhart and Dr. Donna A. Culton in 2026 in order to advance research, provide patient support, and improve the quality of life for individuals living with Lichen Planus.