Our History and Mission
The Cicatricial Alopecia Research Foundation (CARF) was formed as a result of one person's experience with scarring alopecia (cicatricial means scarring). When the patient realized that little is known about such disorders, she decided, with the help of her doctor, to initiate a grassroots effort to raise funds to study these problems.
CARF began raising money with the following mission in mind:
- to provide funds for research to find effective treatments and a cure
- to support education and advocacy
- to raise public awareness
CARF funds are available to support research that will enhance our knowledge about this difficult group of diseases. Please see our Research Grants page for more information.
This website has been created to provide information about the cicatricial alopecias for patients, their families and physicians, as well as the public.
CARF is International
CARF has grown from a group of seven patients to include more than 1,800 patients who have received information through our patient support and educational work–newsletters, support groups, conferences, and website.
CARF has patients subscribed in 91 countries, all 50 states, Washington DC and Puerto Rico.
When you join CARF you'll be able to join local support groups, receive newsletters, be notified about upcoming patient-doctor conferences and other pertinent information.
Click here to join CARF.
CARF is the world's only voice for patients with cicatricial alopecia. We hope you will make a donation to support patients and our research to find better treatments and a cure. CARF needs your contribution and support.
Click here to Donate