Welcome

Welcome! My 2 year old daughter has been diagnosed with aa, as well, but it's been known to us for a while, so I think I'm finally past the initial shock and am looking into equpping her as best I can to be 'someone different who makes a difference'. A friend reminded me that although she'll undoubtedly garner attention because this is glaringly obvious, she'll be able to use that ability to do great things. That's a really cool option to have in life.

You picture of your little darling is adorable. I hope you post more!

Hi Jessica!!!

Thank you!! I do scrapbooking... so I thought I'd try jazz up the page a bit!
Great to have you on the site too!!!

Filakia (greek kisses)

Thanks for the add :)

most def im loveing all my new AA friends its amazing....cant wait to meet people

yea im finding some great people on here from all over. i cant wait to go to the confrence

its in louiyville kentucky

Thank you Jessica, just trying to raise awareness and self-esteem.
Jeff

thanks for the add. I started losing hair when i was very young, just like your daughter. the first time i ever lost hair due to alpecia was when i was an infant. It happened several times while i was a young child. i wish you the best of luck with your daughter.

Hi Jessica, I live here too. My son and I have aa my son started at 2 years old and is now 19. He is doing great. Mine started again recently. Would be glad to talk to you.

Best Wishes,
Maureen

Hi Again I live in Medford

Thanks! You too! Next week is my Spring Break. =)

Hi Yes I know West Islip, i grow up in Islip. who is your doctor for your daughter?

Thanks =)

You too.

Roger.

I don't no them. My son had been to Schniders for some stuff also. He was going to Stonybrook Derm. If there is anything I can do to help, please just ask!

Maureen :)

Hi Jessica, I have i chat my my chat name is merrymohern. I just started using it, my step son put it on for me. So how ever you log onto it do so lol!

Bye,
Maureen

Hi again Ihave aim and mac so i put you under both to see if it worked. sry I am not good with all this computer stuff. I know it is simple, but I never used it before. Bye

hi jessica...Sorry I dont know of any support groups in nyc..the nearest one i WAS REFERRED TO WAS CAP.the Chilodrens alopecia project in pennsylvania. How r u doing? It was very hard on my mentally and emotionally when my daughter was diagnosed...Stay strong, please don't let your daughter see u upset..THey understand alot more than they lead us to believe...email me if you feel like venting..when this was happening to my daughter I couldn't explain it or talk about it to anyone without breaking down. Stay strong for yourself and your daughter.

Hello, nice site you have.