Jeff, the founder of CAP has been the first to introduce me to other individual who have aloepcia and live regular normal lives. He is a real special man, with a real special family, who run a real special organization!!!!
It's a safe place where they only care about self-esteem and how the family is handling everything. Very great!!
Nothing but support for families. CAP makes sense out of a disease that makes none. It's about the children, not their hair.
I am the founder, so I am bias. Please visit www.childrensalopeciaproject.org and see if you think we try to help build self-esteem, provide support and raise awareness. Thank you and take care. Founder, Jeff Woytovich Children's Alopecia Project, Inc.
When my daughter began losing her hair, she felt alone and did not know anyone like her. Children's Alopecia Project has changed her life and my life, too! She met other kids that were just like her and knew what she was feeling and I met other parents that knew what I was going through. My daughter is self confident and CAP played a huge role in that. I will forever be thankful for Jeff and his mission to encourage and help all kids facing the challenges, physically and emotionally, with hair loss. It's our CAP, we all wear it.
When my daughter lost her hair at 8yo, so also lost her confidence and happiness. She got bullied and she was devastated and we were heartbroken for her. Ever since we got involved with CAP, things changed for the better. CAP is definitely life changing & even life saving. CAP is supportive, uplifting, accepting & totally awesome beyond words!
CAP is all about the children with alopecia not the alopecia in a child. They focus on self-esteem and confidence and not treatments and cures. They try to let kids know that everyone is different and that is normal!
Children's Alopecia project helped my daughter see she was not alone and the only little girl like her. She struggled with bullies and the groups at one of the summer activities helped her to learn to cope. She was given this opportunity free because of the love and hard work put in to making these camps free for the kids with alopecia.
CAP is a wonderful organization that helps children with any form of Alopecia. It allows these children to meet others that have the same incurable condition, which causes them to lose their hair. The focus is to help the children grow self-esteem and to spread awareness. To see these kids interact with each other is just amazing!
This is an organisation that is what all organisations should aspire to....its about the kids. Building lifelong friendships, self esteem, and a level of confidence someone with our without Alopecia of any brand would want to achieve. It has done wonders for our son, who i turn, instills confidence around the world, with a condition he is not afraid of or worries about, but loves and owns.
Childrens Alopecia Project is an amazing, life changing, self esteem boosting, loving organization! I lost all my hair at the age of two and started volunteering with CAP 6 years ago and it's been the best 6 years to be able to meet, learn from, grow with and be apart of the family! I've never felt as accepted and loved in my entire life until I joined CAP! I'm thankful everyday for this organization, the people it's blessed me with as well as all the opportunities! CAP truly is life changing and I can't say enough about all of the great work and events it does!