Starting a new support group for kids

Good Morning All,
My wife Holly and I are parents of a 10 year old boy with Alopecia Areata. He was diagnosed about 3 months ago. We live inthe metropolitan Atlanta Ga area.

We intend to start a support group for kids here with Alopecia. We are preparing to do so in conjuction with Childrens Alopecia Project (CAP).

If you are interested, or have any suggestions please let us know.

You can email us as well at the new email address we have created for this project alopeciakidz@yahoo.com

Thanks, Jim

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Replies to This Discussion

Permalink Reply by Cindy on October 14, 2010 at 7:40am
Hi Jim,

Just wanted to wish you great success with your group. I started one in Mass almost 2 yrs ago with CAP.

Cindy
Permalink Reply by jim truglio on October 14, 2010 at 8:38am
Thanks Cindy,

What were the biggest challenges in getting it off the ground? The folks at CAP seem very eager to help.JIm
Permalink Reply by Cindy on October 18, 2010 at 9:58pm
Jim, you can email me offline at cindy@childrensalopeciaproject.org.
Permalink Reply by Sarah Eisenhardt on October 26, 2010 at 9:35am
Good luck CAP is amazing I just started a group here in Michigan with them... Betsy is wonderful and very supportive.
Permalink Reply by Lisa on February 15, 2011 at 11:57pm
Hi, Jim...I am the mother of a 10 year old, Nina, who just got diagnosed in early December...we are in nashville...good luck with things...I'd love to see how things are going, as I was thinking about starting one here...
Lisa :)

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