| The Foundation's newsletter is published four times a year, providing a forum for people with alopecia areata and their friends and families to interact and receive the latest information on all aspects of the disease. It enables people with alopecia areata to speak out about the problems associated with the disease and how to deal with them. It contains news about research and treatments, personal stories, cosmetic tips, information on support groups, and a special children's section called KidNet. |
