To all families, friends and anyone suffering with Alopecia who would like to share their experiences with others who have AA, AT or AU or even (AGA), (Female Pattern Hair Lose). A place for us to express our feelings and share our experience with each other who has any kind of alopecia and who are dealing with family members who have it also.

So come on in and join us for support that we all need from one another!! When you join you can post your concerns and post your fears of this disease and ask us questions and I'm sure we'll have an answer.

For chat see links on left side, and add java to get in. Post that your in the CHAT ROOM for anyone to come in. Chat schedule to follow. I've been to five conferences for this condition, all there is, is support.

This is Jeffery Woytowich _ Website for Children's Alopecia Project
www.childrensalopeciaproject.org

"Beauty is not what's on your head. It's what's in your heart". SO LET'S NOT FORGET THAT PEOPLE!!!!! We're here to help you through your (JOURNEY OF ALOPECIA)

Alopecia Areata is a Overworked Immune System, that makes your Body Attack itself!!

PLEASE NO ADVERTISING ON THE MAIN BOARD, THANKS