Though you may feel alone with your child’s diagnosis, it is important to find out that you are not, and to reach out to others who share your fears, concerns, confusion and experience with alopecia areata. Because of the need for this vital connection between parents of children with alopecia areata, NAAF encourages your involvement in the programs we have designed to help you reach out.

Message Boards
Helping Hearts through Hands
NAAF Annual Patient Conference
NAAF Newsletter

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