The Virtual Alopeciapalooza Family Challenge Since we can’t be together this year in Maine for Alopeciapalooza, we thought it would be fun to do a virtual camp experience. We focused on our great speakers with
Visit www.Facebook.com/ChildrensAlopeciaProject at the time you want to watch live! Listen to the presentation and then you can type your questions for your speaker. Be sure to share with other families living with alopecia.
Every year since 2009 Alopeciapalooza has been the premiere camp in the entire world for children with alopecia and their family. We have been successful in letting all attendees feel normal because they are. They're
The Annual CAP Kid Appeal CAP is here to build self-esteem, provide support and raise awareness. It's that simple! Thank you….We are so grateful for the incredible generosity of our supporters, both local and national.
People you see as broken records will continue to promote their passions and purpose on earth because sometimes people hear it and react but mostly, they don't. It's at these times when people with purpose