Comment

Comment by Angie on March 25, 2011 at 9:00pm

Hey Rhonda,
I know the babies in group need to get together too,I've been thinking about a picnic for the members and our families. We don't have many children in the group, but most of our members have children or grandchildren. It will be fun! I'm already excited!

Comment by Rhonda Kelley on March 25, 2011 at 7:41pm

Hey y'all, Please let me know of any get togethers for the kids esp. We are about an hour north of Atlanta but we'd love to be included. Thanks so much!!

Comment by Valerie Hutcherson on March 25, 2011 at 4:00pm

Hi everyone,
I'm looking forward to meeting some of you at breakfast tomorrow @ 10! If you haven't received the details, check your email from Angie.

Comment by Shelly Clark on March 17, 2011 at 5:08pm

We would be interested in getting kids together for sure!

Comment by Angie on March 16, 2011 at 12:27am

Your welcome Zelda, I hope you will find some good information for Sydnie at Team Alopecia. I pray her spirt will continue towards an upbeat direction and you both continue to strengthen each other.

Comment by Angie on March 16, 2011 at 12:18am

Hi Shelly and welcome to Atlantans with Alopecia. I was looking for a children's group on Aw, but I see you found it. "Team Alopecia" is another place to get loads of informaton, they even have a camp for the children to come together.
http://www.teamalopecia.com/content/blogcategory/50/10022/

Comment by Shelly Clark on March 15, 2011 at 3:16am

Hey ATL peeps! I have a 10 year old son with Alopecia. Any kids around ATL who want a friend??

Comment by Angie on March 9, 2011 at 9:56pm

Your welcome. :-)

Comment by Rhonda Kelley on March 9, 2011 at 5:22pm

Im going there now Angie. Thanks so much.

Comment by Angie on March 9, 2011 at 1:38am

It's was a really late night for me, and I'm glad it was. I found a great website" "Team Alopecia" for adults and children with alopecia. I've been thinking about the children with alopecia more. It's really hard for children for various reasons. For our babies in the group there are organizations posted on the website called "loc of love, Hair club for children and children with hair loss. All I can is Wow! check it out, I'm sure you will find some good informaion for the little ones.
http://www.teamalopecia.com/content/blogcategory/50/10022/

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