The Children's Alopecia Project is having ALOPECIAPALOOZA 2011 outside of Cincinnati, Ohio this year from August 18 to August 21, 2011.

A camp devoted specifically to children with alopecia and their family. We want to help build self-esteem, provide support and raise awareness. It's what we do evey single day, not one a year. It's the reason we are here!

I am Jeff Woytovich and my wife has had Alopecia Areata since 1976 and my 13 year old daughter has had Alopecia Universalis since she was 5 years old. This is why I founded CAP and why I care. I have experience the ups and downs, the snake oil, and everything else you have experienced. I wanted more for my child so she had the tools to be the best. I could not find it, so CAP was born!!

ALOPECIAPALOOZA is FREE to all CAP Kids. (children with alopecia) Heck, everything CAP does is free for the CAP Kids, we never charge them. If you would like information how family members can attend for free please email Betsy at betsywoytovich@yahoo.com, make sure you tell her you want to regisiter on the website too (again, free.)

Check out these sites:

www.ChildrensAlopeciaProject.org
www.facebook.com/ChildrensAlopeciaProject
https://www.youtube.com/watch?v=lhKiNMK-wc8
www.alopeciapalooza2011.charityhappenings.org

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Hi

Have a fab time, what a wonderful thing for all the children and families dealing with this condition. :)

Rosy
We are just deciding whether we are flying or driving. But we are coming, Claudia is insisting how important it is for her to be there.

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