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Hence, the problem with AA is no one knows where it ends up. In my daughters case it did shed till it was all gone in 4 months. Everyone is different. There is no real answer to your question, unfortunately it is a wait and see. What I did when I saw this happening to my daughter knowing that her hair was a big part of her identity too was start to look at wigs that were as close to her own hair as possible. This is when I started to study what makes up the best wigs for those with medical hair loss. I am a phone support person for the National Alopecia Areata Foundation. You might want to look up their website and learn more about the condition and what research etc is going on. They are a top notch organization. If you want to reach out to me for more information on wigs or any other topic related to AA you can friend me. All my best and you came to a great website to learn.
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