Team Superstar: Gail Porter

gailGail Porter has always been a beautiful young woman and a very popular celebrity in Britain and Europe.  Now she is also a hero and an inspiration to millions of alopecians around the world for the brave way she handled her very public experience as a newly diagnosed alopecia patient last year.  You can Google Gail and find thousands of articles and fan sites about her.  Go ahead and try it!  Here are a few to get you started: Daily Mail, The Guardian, BiggestStars.com.

Team Superstar: Margaret Baker

margaretbeauty1Margaret is a formidable quadruple threat- Model/Actress/Playwright/Motivational Speaker.  She has also had alopecia since she was two and a half.  Ms. Baker is obviously gorgeous, but she fought hard for the inner strength to be the confident, successful woman she is today.  Take a few minutes to discover more about this multi-talented young woman.  And be sure to keep an eye out for her in the stage play "My Life As A Bald Soprano"

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Featured Article

For Kids & Parents
Being a kid is hard enough, but being a kid with alopecia can be down-right difficult.  Fortunately there are some fantastic organizations that offer support, friendships, and fun to kids who are dealing with this disease.  There is the Children's Alopecia Project (the photo at left is from their camp), the I'm a Kid Foundation, and Locks of Love.  There are cool dolls for kids of all ages, as well as web sites and coloring books.
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Young Alopecian Finds Comfort in a Doll That Looks Like Her Print E-mail

Lots of kids like dolls that look like them.  One need only look at the great success of companies like American Girl to see that.  But kids who are dealing with hair loss find that there options are pretty limited.  One enterprising mom in Colorado  went out of her way to see that her daughter had a doll that she could relate to.  This excerpt was originally printed in The Gazette, in Colorado Springs:

A doll is being specially made for Maddie Werner -- one that will look a lot like the second-grader. It will have pale skin, a few freckles and will wear either jammies or a soccer uniform. And like Maddie, it won't have hair.

Maddie, 7, has lost her curly goldenbrown locks -- her "princess hair," as she called it. She's also lost her brows and lashes because of a condition called alopecia areata, an autoimmune disease that attacks hair follicles.

The condition isn't contagious, isn't lifethreatening and isn't painful. Maddie is otherwise healthy. Still, her mother, Lisa Werner, worries about her.

"I think that girls or women have a lot of identity tied up in hair," Lisa Werner said.

Click here to read the rest of this really nice article.

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