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.
We have a new chat room if you click on the links on the side of the page to get in JUST TAKE A PEAK, you need to join OASERV PAGE site first the click on join chat and type in (YAHOO CHAT ROOM) that will get you into the chat. (CHAT TIME TO BE DETERMINED)
This is Jeffery Woytowich _ Website for Children's Alopecia Project
www.childrensalopeciaproject.org
We're here to help you through your (JOURNEY OF ALOPECIA)
"Beauty is not what's on your head. It's what's in your heart". SO LET'S NOT FORGET THAT PEOPLE!!!!!
Alopecia Areata is a Overworked Immune System, that makes your Body Attack itself!!
SO GO AHEAD AND POST US!!!!!! WE LISTEN!!!!...AND WE DO CARE!!!!!
Hi I am reasearching wig companies and styles (vacuum ect.) and was wondering what your experiences are with wigs, what you like and don't like, and what you
I have universalis as well ,officially it has not been diagnosed but itsĀ happening They call in non cicatricial non inflammatory Alopecia. I have been
Thanks for your response Carrie. I also have alopecia universalis but have only been dealing with it for a few months. Started seeing signs in Feb. but didn't
I've researched them and they are kind of expensive. You should try to get them to make a claim for you and see if you can have insurance cover it. I went