Anna’s Alopecia
Anna being positive in front of the entire student body! You Go Girl!
Anna’s Alopecia
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Don’t forget you are not alone. Search “baby let your hair hang down”. Georgia is an amazing woman. They are almost ready to release the film. They just need some more money to finish the distribution deals. If you want to help with the film please think of giving just a few bucks. One less latte from a lot of people and the film is in wide release. Alopecia need not be hidden and shameful. Georgia helps people (especially kids) deal with the disease and understand the problems.
I’ve had alopecia my whole life. I’m proud of you for being so open about it. <3
Hope to see you next year at the conference, anna!
~Emma :)
hi i have alopecia areata and my life is tragic at school because everyone makes fun of me because i am blad. i have had alopecia areata since i was 3. the last time i have had long hair was when i was in kindergarten. i am glad i have alopecia areata because you are speacial. maddi is a lucky girl and so am i. we are special people and i feel her pain.
what age does this usually occur at
Hello how are you friend , i need your help
i am also Alopecia Areta Patient,
am 27 yrs old. and i have lost my all hair and also eyebros
If you can tell me the meaning of your comment, I might approve it…………..???
Please make sure your friend contacts NAAF - National Alopecia Areata Foundation for education and support!!
my best friend found out she had alopecia today , her first bad patch , and her names anna, imagine finding that out on christmas eve :/
i have alopecia also. i have had it for two years and also wear a wig. keep your head up girl. you are strong and beautiful,
good for you! YOu are so awesome!
I’m proud of you, Anna!
I AM SO PROUD OF YOU ANNA!!!! Let’s go Alopecians! By the way, that skirt is cute on you.
Anna, You are one strong lady, I would never have the courage to stand up and speak in front of my whole school. Although i am not ashamed that i have alopecia universall, God only gives dieases to people, who he knows is strong and will copewith it. Anna, i have faith in you and i pray your hair grows back.
very proud of you anna kids used to tease me at school for baldness but i never really cared i stayed strong and im glad anna is staying strong too
Unfortunately I have to disagree with Anna… doctors and scientists are NOT working hard to find a cure…. This disease is not life threatinening, therefore not enough money is spent on finding a cure. I have had Alopecia for almost 25 years now and still no progress has been made in finding a cure.
I was diagnosed at 2 years of age. I have no memory having my own hair. I do not have eyelashes or eyebrows. I was teased as kid in school. I have always worn a wig. I am also a teacher, and I know that kids can be mean. It’s hard today, when we are constantly plagued with ads and commercials about beauty, and so much of that revolves around a woman’s hair.
I have the same type of Alopecia. I was diagnosed with Alopecia at 4 and my mama cried for me. I didn’t know what was wrong until I went to 4-k. I made one friend as a little girl, doctor’s said she would never live to 6th grade and she’s alive and strong, my friend, Nikita. I’m 11 now and I KNOW what it feels like to be the same spot. I’ve been like this for 7 years, going on 8.
wow, I thought I was alone, back 14 yrs ago when I lost my first patch. I now have universalis and worry about my tendons and stuff, connective tissue can be attacked by the immune system too? Anyone with alopecia can message me…
Wow I admire your courage, so many people wouldn’t do this infront of school kids especially.
I’m proud of you, for what it’s worth.
There’s more to a person than their hair. Just be yourself and don’t worry what others think.
I am very proud of youu for standing up for yourself. If i had this diease i would never be able to do something like thiss. You are one strong girl :]]
Ukiah Lions Cheerleaders.
why are you asking for people to “tolerate you” so what, you’ve got no hair, thats okay. people who dress like slobs,.. now thats something we have to try and tolerate. your gorgous hun, try not to let it bug you. i know what it’s like.
I think your beautiful just the way you are. Please don’t ask people to tolerate you. There is nothing about you that needs to be tolerated. People tolerate a bad smell or long walk with a sore toe, you are neither one of those!! Heather & Jeff Clark(Moose’s Parents)
Great speech anna we all love u and support u love ur cheer friend Vicky