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. This little non-profit that started in my spare bedroom has grown into an international organization that helps children with alopecia around the world. Without the ongoing support from donors like you, we would not be where we are today, helping thousands of children through 50 support groups in the United States and in 5 countries, Regional CAP Kid Camps in California, Washington State, North Carolina, Colorado, Ohio and of course our big camp, Alopeciapalooza, which is attended by up to 500 people each year and will be held annually in Maine. Yes, CAP Kids and their siblings under 5 are still free for all our camps.
Alopecia is an autoimmune disease that is not life-threatening but is life-altering. It is not contagious. You can’t catch it and it does not hurt. It is almost like your body is allergic to hair, which causes it to fall out. That’s the good part of Alopecia. The bad part is being teased, made fun of, laughed at and ignored. Emotionally, it could be devastating. Luckily, because of your support, CAP is here!!
Please donate at https://donate2cap.eventzilla.net
Sincerely and with much gratitude,