Thank you for visiting the Children's Alopecia Project's Alopeciapalooza registration/donation page!

Alopeciapalooza is the only international convention devoted specifically to children with alopecia and their families.

We want this to be an event where the CAP Kids learn about how their self-esteem today effects the rest of their lives, we want the parents and the family unit to learn what is and is not important in the day to day activities of a CAP Kid. We want this to be an event where much is learned and fun is not an alternative route, it is the destination!

With your registration, participation and or generous donation we will continue to make Alopeciapalooza an annual reality. It all started with Alopeciapalooza 2009 in Philadelphia, August 7-9, 2009 where 65 alopecians and their families came together to help build self-esteem and learn more about who they are and others who live with the same life altering hair loss disease.

ALOPECIAPALOOZA - Camp Edition - Poconos, August 20-22, 2010

Notable speakers   

Staciana and Brett Winfield, Margaret Baker, Katie Batson, Laura Hudson, Jen Oney, Mike Pannula, Annette Thompson, Christine Cieplinski, M.Ed., Mike Kuczala and Jeffrey Miller, MD.  

 

Enjoy the video on the left. Images of last years ALOPECIAPALOOZA.

Visit www.childrensalopeciaproject.org and email Betsy Woytovich at betsywoytovich@yahoo.com for more information.