Our programs of lunches and dinners finds women in the same communities across the country and makes it possible for them to find each other. For five years, Chassin, who lives in New York, has been a support-group leader for alopecia areata, dealing with women, men and children of all ages. Jennifer Izatt will tell you she's vain, so she's not quite sure why having her hair fall out in huge clumps didn't bother her too much. Izatt struggles a bit with her partial eyebrows and eyelashes. That's great, she says.
She found the most successful ones were those that were purely social, where people with the condition could mix and mingle. They expand the circle of friends, and who couldn't use another friend? Now I'm doing that," Izatt says. The point is to get women with alopecia areata together to talk and laugh and realize they're anything but alone with the condition. And she was familiar with the condition, which her little brother has had for seven years. Our programs of lunches and dinners finds women in the same communities across the country and makes it possible for them to find each other. He, too, copes well and talks readily about the condition. Chassin had a couple of bouts of partial balding before, but in her hair started thinning and disappearing entirely at the lower back of her head. I hadn't realized how alone with it I felt. Mission Statement To improve the quality of life for women of all ages living with alopecia areata by enhancing their self-esteem and self-confidence and by increasing their capacity to manage all aspects of their lives with alopecia. And it's a natural way to bring together women who might otherwise never meet each other. Our special Beauty Events raise public awarenss that all women who are bald do not have cancer. I am determined to do my part to mainstream acceptance. That's great, she says. And some who are choose to wear wigs or scarves. Jennifer Izatt will tell you she's vain, so she's not quite sure why having her hair fall out in huge clumps didn't bother her too much. For five years, Chassin, who lives in New York, has been a support-group leader for alopecia areata, dealing with women, men and children of all ages. And there's still time for women who are interested to contact her and join the fun, although she needs a head count. She's made peace with the condition, called alopecia areata, which first appeared when she was in her 20s, in the form of a quarter-sized bald patch on the back of her head, surrounded by otherwise long, thick hair. We don't just say " this is a psychologically difficult conditoon for women," Chassin's programs give women the confidence and tools for better coping and greater self-acceptance. Despite the name, not all the women who come to the lunches are bald, like Chassin. Her eyelashes "come and go. Izatt struggles a bit with her partial eyebrows and eyelashes. Many women have developed alopecia in childhood and have never met another woman like herself. Description We are the only nonprofit created specifically for the needs of women with autoimmune hairloss disease.
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