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Hi Christy, thanks for your friend request. Hope, things are good for your today
Welcome to the International Alopecia Day Group, Christy!
Mary
Thanks for the friend request. I don't get on here very often anymore because I'm still in denial after 16 years of this balding process. I am completely bald now in fact my head looks a lot like yours only my fine hairs are completely white. Even when I first started losing my hair and new little growths grew back they were white. Part of it they say. Good to see your dark hair! Love your cute, stylish wig!!
You just inspired me to get on here more often and communicate with people who know exactly what I am going through. Have a great week!
All the best,
Mary
Some people have a photo of themselves taken and send me that and I include it in my slide show. ( Watch last year's video to see what I mean.) Other people organize a small picnic, walk, social gathering, with friends including others who have hair loss. It can be a very small gathering, or a big event.
The idea is to have fun and to let people know about Alopecia Areata and hair loss. Someone with Female Pattern Baldness like yourself is welcome.
My original idea was for ONE day when people who hadn't tried going out in public bald would do that - sort of a coming out day, and a chance to take that first step. That idea is still part of IAD, but now it's about simply celebrating and raising awareness. (You can be wearing a wig - being wigless is optional, but that's awesome if you do.)
Have A Great weekend if I don't talk with you!
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