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Children's Alopecia Project
41, Male
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Children's Alopecia Project
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Children's Alopecia Project's discussions
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Started this discussion. Last reply by Margie Sep 13.
Children's Alopecia Project
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Started this discussion. Last reply by rach Sep 21.
Canadian conference??
Replied Jul 20
Alopecia World Box at the CAP Site
Started Jul 20
Children's Alopecia Project's Events
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Children with Alopecia Day
April 14, 2009 from 12am to 11:45pm – Where ever you may find yourself!
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Alopeciapalooza 2009
August 7, 2009 at 4pm to August 9, 2009 at 12pm – Sheraton Society Hill
Children's Alopecia Project, Inc. - a 501(c)3 Non-Profit
Profile Information
- Relationship Status:
- Married
- About Me:
- I am Jeff Woytovich, the founder of CAP. I started CAP so we could help raise awareness but also the self-esteem in children living with all forms of alopecia. We want them to become stronger teens and productive adults and the advocates of the future!
- Are you 18 or older?
- Yes
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Children's Alopecia Project
Posted on April 17th, 2008 at 10:09pm — 2 Comments
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I am a mother of a young girl with Alopecia and I would be so greatful to learn about these camps. My daughter feels so alone and I would give anything for her to be able to meet other children with Alopecia. She needs to see that she is not alone! Ever so grateful, Cynthia (B.C.,Canada).
Just wanted to say I think this is a wonderful Project you have started. I know it is very rewarding for you. I work with the Wigs for Kids, and the Shiriners Burn Hospital, so I have seen numerous cases of Alopecia in Children as well as Adults.
Warm regards,
Linda Amerson, DT, IIT
www.hairandscalpessentials.com
This camp sounds great! I'm sure the camp has changed many young alopecians lives for the better. I would have loved to be apart of camp like this while growing up with AA.
I recently have been trying to help young ones who suffer from diseases/illnesses. I currently volunteer as a camp counselor at Camp Okizu (childrens cancer camp)....as a matter of fact...I leave again this Saturday wahooo. It's really a special experience because you're not only surrounded by an amazing and inspiring group of kids...but the camp experience is awesome. I would love to be able to help bring this camping experience to young alopecians on the west coast. Is CAP located anywhere on the west coast? If not, then how can one go about starting a new chapter?
-Andrew
Thankyou so much for bringing the CAP crew up from PA to see the show. I can't tell you how moving it was for my cast to meet the kids. What an adorable group!
It would be great to find a way to get us down to Philly for a "run" in the fall. Much love to you guys!
xoxMargaret
It's a really great, what you're doing for children w/ AA. I am interested in being involved. I myself was diagnosed at 10 months, and lost it all at 5 years. I have recently started a support group here in Arizona, and one of my goals is to do something for the children. I have thought about doing a group just for kids. I would love your advice. I will look into the cap website to see how I can get involved. Do you have a directory of your members? Is anyone from Arizona?
If there is anything I can do to help I would love to, just let me know!!
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