Wiggin Out is were we had her wig made. The one you like is from there as well as another one from some of the other photos. They are very professional and have great hair, however, they are expensive. It was especially pricey for us due to the blond hair. My daughter goes away for weekends and sleeps over at friends houses and most them don't know she wears a wig, so it's very natural looking. So if you decide on a wig, I would recommend them. Since she is very young and her size will change, be careful with how expensive you go. I would love to hear what the support group was like and if they were helpful. I would think that it would be a greater help for the parent. When my daughter's alopecia started, it was very difficult for me.

If you have any questions, please feel free to ask. Even though my daughter is older, I may be able to be of some help to you.

We live in Orange. May daughter is 15 and has has AU which started at the end of 5th grade (she is now in 9th). Her wig is not a vaccuum. It was custom made and has lace and silicone. I am not sure if you can see on the photos, but we have gone through several wigs, some better then others. We are still kind of working on it as she gets older and wants different things.

We have never gone to a support group and don't really know anyone else with this condition, even though there are many, however we are going to the NAAF convention in LA at the end of June. This will be our first time and the first time my daughter actually wants to go. We thought that it would be a good way for her to see how other people deal with this and also the varous products ect.

Vicktoria

WELCOME!