Great project. Hope that many children gain self-esteem and confidence and feel very normal, accepted and beautiful the way they are. Your photos are great witness to this. Best wishes!
I love what you have done with CAP. Here in NZ we are starting to organise a NZ network, support and events and I am just about to complete our first website. Do you mind if I link CAP on it and an introduction. We dont have anything here at the moment and I'd love to see people read about what you have done and inspire them to make the same thing here.
Hey, I saw that you are going to be in Pittsburgh for the marathon I was just wondering if you knew were you would be set up, if in oakland I definatly will stop by and say Hi!
I just learned about AA in March 2009. In 1 month by daughter lost all her hair and to this day she is still totally bald. I need help and advice. I live in Nassau, and down here alopecia is very rare in kids. She is 7 yrs old and I'm trying to be strong for her.
Thanks for the info! I would definitely be interested in attending your monthly meetings and helping out with the kids! Can I find information on the CAP website regarding meeting times and locations? Can I just show up, do I need to bring anything?? I now live in Exeter Township with my husband, but I grew up in Whitfield and graudated from Wilson. We are basically neighbors!
I just recently joined this website and have become aware of your organization. I live in the Reading area and was wondering if you were aware of any alopecia support groups in the area of adults? Any info you have would be great! Thanks!
Jeff, I think some time ago I saw your post on another board about expanding CAP meeting to other areas of the country. Is that something that still interests you?
Hi! I guess I have grown up a lot and I'm so grateful that my hair has grown back too! Of course, I still have a few patches here and there but I can't complain about that! How is Madison? Tell her I said Hi!
At 2:23am on September 10, 2008, Taylor-Jean said…
Dear CAP:
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).
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What a great example of pro-active parenting I am in awe, just great to see!!!!!!!!!!!
I love what you have done with CAP. Here in NZ we are starting to organise a NZ network, support and events and I am just about to complete our first website. Do you mind if I link CAP on it and an introduction. We dont have anything here at the moment and I'd love to see people read about what you have done and inspire them to make the same thing here.
Cheers
Paul
Roger.
I was talking with Carol tonight and she told me she had an awesome time in Philly for Alopeciapalooza.
Hope all is going good with you and yours!!!
Jeffrey
how do i go about registering for the event in philadelphia?
thx
I just recently joined this website and have become aware of your organization. I live in the Reading area and was wondering if you were aware of any alopecia support groups in the area of adults? Any info you have would be great! Thanks!
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).
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Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.