Replies to This Discussion

Permalink Reply by rj, Co-founder on October 24, 2008 at 12:06pm

Hi, Jose. The Children's Alopecia Project may be able to assist you as well as members of this group. It would also be a good idea to contact the National Alopecia Areata Foundation (NAAF).

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Permalink Reply by JOSE CHARQUENO on October 24, 2008 at 12:31pm

HEY THANK YOU I FOUND THE CHILDRENS ALOPECIA PROJECT YESTERDAY AND I AM TRYING TO SET UP A FUND RAISER AT THE SCHOOL THAT I TEACH AT. THANKS FOR YOUR RESPONSE I APPRECIATE IT
JOSE'S MOM ANGELA

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Permalink Reply by theantichick (Shannon's Mom) on November 13, 2008 at 8:07pm

I'm just starting to get up to speed with all of this too. My 11 year old daughter has AA (we just got the official diagnosis today, have been dealing with the hair loss for several months now). I have contacted CAP and NAAF and have been given a contact person in the D/FW area but have been swamped with work & other issues and haven't been able to make a phone call yet. We're in Arlington.

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Permalink Reply by Shanea Matthews Mobile 4 Beauty on November 19, 2008 at 8:56am

Hi Jose,

You should definately try the National Alopecia Foundation. My company had participate with the foundation for the first time this year. They had so many seminars and workshops it was very informative. The conference will be coming up next year you should really think about attending.

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