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!!!!!
Fake, fraud and guilt... interesting concepts mentioned by several people recently. Women with alopecia often behave like they live at the end of the lens:
I've gotten so used to the cancer looks that at this point I just smile and let it go. I do feel guilty about some of the advantages - no one makes me wait in
sally, If Kaity decides she's going to wear the wig for the wedding, it's a good idea for her to wear it for at least a week (but longer is better!) before
i guess i kinda feel like it's my fault that my daughter has AA, but only in the regard that it's my fault that she is here at all. if i accept guilt for her
Good for your daughter! We rely too much on what society thinks of us, hence the feeling of guilty because I cannot relate to the questions of cancer. We