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Comment by Children's Alopecia Project on January 3, 2012 at 7:17pm

The Children's Alopecia Project is based outside of Reading, PA. If you have not done so yet, check us out on Facebook and on our website at www.ChildrensAlopeciaProject.org

Comment by lauren on December 6, 2011 at 12:30pm

Hey sarah and lily my names lauren and I'm 18, i have had alopecia for almost my entire life and I know everything that you guys are going through so if you ever need to talk or anything just let me know.

Comment by Lily on November 28, 2011 at 10:06pm

Hi I'm Liy and I'm 10 years old. I have alopecia.

Comment by Sarah:) on April 27, 2011 at 6:49pm

Hello! My name is Sarah, i am 14 and from indiana. I'm struggling with alopecia even though i've had since i was 8. Having alopecia in middle school really sucks! I wear a wig and all, but 8th grade gossip still leaves wounds on my heart. People always come up to me and ask me if i wear a wig, i haven't yet had the courage to tell everyone at my school. I don't have much confidence so i like to keep my alopecia a secret (which probably isn't good). I tell my closest friends and that is all. So i really don't have a lot of people to talk about it with, i usually just end up crying my emotions out instead:( I would love to get to know some more people who struggle as well! Thanks everyone

Comment by vellyvel on April 27, 2011 at 8:56am

Hi my names velvet i an 16 from england please add me as i would love to talk to people x

Comment by Lisa on February 28, 2011 at 11:54pm

... oh, I also wanted to ask what the best way to meet others ANYWHERE near us??? (Nashville) it seems like she's the only person in the world with aa. I wish there were more kids to talk to. :)

Comment by Lisa on February 28, 2011 at 11:53pm

HI, girls...I'm a mom of an amazing, beautiful 10 year old girl who just got diagnosed in Dec...she hasn't lost it all yet, and we're praying for the best...i just wanted to say how incredible you all are here...I was reading and thought my girl could be as brave soon and post some on here, not to mention start to look into a wig or a headband with hair...it's all so new to her and God bless her, she's such a trooper and so brave but I know people are starting to notice and I pray for her to be strong. Any tips from you older girls? :) lisa

Comment by Shanice Snyder on December 28, 2010 at 5:34pm

Hiya! I'm 16, I live in Washington and I've had Alopecia totalis since I was about 8 years old. When I go to school I wear wigs and when Im not I wear bandanas and hats. I'm hoping to be able to walk around outside without a wig or anything on my head. But I still need to build up self-esteem and confidence :) I hope to make new friends! <3 Feel free to chat with me :D

Comment by Rita on August 19, 2010 at 8:31pm

hey everyone!! I'm 17 and i have alopecia totalis and i've had it since i was 4 years old.. it's been up and down with my hair loss since the past 5 years. but this time it is just staying at "fuzz" and hasn't grown past that since december. but anyways, lately i've been a lot better with not having my hair probably because i'm now wearing a wig. but i'd love to walk around without having it on all the time but i guess i'm just not ready for it. I'm hoping to make some new friends!!

Comment by Mia on May 23, 2010 at 12:41pm

Hey :)
I´m Mia, a 17 year old girl from Germany. I´m having AT but my hair just starts to grow a little bit. I´m so excited to see what will happen. I´m sorry for my English - its not my mother tongue :)
I hope I can get to know some people here who have the same :D

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