About Us

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. 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.

 

The International Lichen Planus Foundation functions in several key areas:

 

About Patient Support 

Research on patient support groups has shown positive conclusions about patient recovery rates and has provided insight on the social and psychological benefits to the patient. These programs provide several key functions. Since some disease states, such as lichen planus, are considered to be an “orphan disease state” most patients do not know anyone who has their diagnosis, symptoms or treatment regimen. 

Find out more about our support group here.

 

Get Involved

We welcome patients, caregivers, and medical and dental professionals from around the world. Join us to access resources, connect with others, and be part of a community committed to improving life with lichen planus.  To join us or just reach out, contact us here.