ALOPECIAPALOOZA 2012 Is Announced! Nothing could be finer then to be in Carolina!!!





Together, our first three ALOPECIAPALOOZA'S saw just under 600 CAP Kids, adult volunteers with alopecia, siblings and parents! CAP does not charge the child with alopecia and we are proud that we are alone in this way of thinking. It's all about the kids and getting them to their future with the best possible self-esteem level. Yes, it's that simple! www.Facebook.com/ChildrensAlopeciaProject

Visit our Facebook page often to keep up to date and please, always feel free to share what CAP does to others!

Thanks and take care!!

Jeff Woytovich, Founder
Children's Alopecia Project
Post Office Box 6036
Wyomissing, PA 19610
www.ChildrensAlopeciaProject.org
A 501(c)3 Non-Profit helping grow self-esteem because we can't grow hair, provide support and raise awareness of the incurable autoimmune hair loss disease, Alopecia

Tags: ALOPECIA, ALOPECIAPALOOZA, AREATA, CAMP, CAP, LOCKS, LOVE, NAAF, OF, SURF, More…TOTALIS, UNIVERSALIS, WB, WORLD, WOYTOVICH

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Hi Jeff

Wishing you and your great organisation well. Looks like it is going to be another resounding success!

Rosy

I hope more people see this and consider going!!!! Alopeciapalooza last year was AMAZING not only for our daughter who has alopecia universalis but for our whole family! You know it must be good when no one wants to leave!!! CAP kids has given us a whole other family that we are proud to say is ours!!!

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