We are trying to raise money for Alopeciapalooza 2013. Please help us reach our goal!
Sydney is 12 years old and was diagnosed with Alopecia Areata in April 2012. She has struggled with her hairloss and desperately needs to meet other children with Alopecia. This would be a great way for us as a family to meet other families dealing with the same issues. We really wanted to go to Alopeciapalooza last year in Top Sail NC but could not afford to. Please help us!
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906 Penn Avenue
WYOMISSING, PA 19610
CAP is the only 501(c)3 nonprofit devoted specifically to children living with the incurable autoimmune hair loss disease, Alopecia.
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