Shay and my girl Kaleigh :)'s Comments

Comment Wall (10 comments)

You need to be a member of Alopecia World to add comments!

Join Alopecia World

At 6:02pm on December 22, 2009, Samantha said…
Hi , Sorry Ive not been talking to you guys I men it . But Ive been doing good in school . Samantha
At 2:51pm on November 17, 2009, Angie, Gracie's mom said…
Hey Shay, wondering how you and Kaleigh are doing these days? How are the pagents going? We are doing well, gearing up for the holidays.Gracie is going through a frustrating stage where she does not understand "later" and does not agree with "no!" Can't wait for her to really start talking and reasoning to kick it!! :) Angie
At 2:17pm on August 24, 2009, Angie, Gracie's mom said…
Welcome to the site! My daugter is almost 20 mo old, and has had AA since she was 13 mo old. I guess I've been dealing w/ this for awhile--I'm at the point where its not so raw anymore. Friends and family are helpful, but I found the commonality of this site to be the most helpful. Let me know if you have any questions or want to chat! Angie
At 5:10pm on August 22, 2009, LeslieAnn Butler said…
Yes! Go to this link for the children's video and they'll send it, free.
http://www.naaf.org/temp/childrenvideo.html
At 3:27pm on August 22, 2009, LeslieAnn Butler said…
Hello and welcome, Shay!
There is also a lot of good information on the National Alopecia Areata Foundation web site. When she is ready for school, you can get a free school pack which includes a video that the teachers can play for the school to help everyone understand the condition.
Go to www.naaf.org.
LeslieAnn
At 8:35am on August 22, 2009, Cindy said…
Hi Shay, this is Cindy, Samantha's mom..I did not realize it, but I wrote you an note from Sam's page...I am glad I could help..write anytime..Cindy
At 5:31pm on August 21, 2009, Samantha said…
I want to add, that you should contact the childrens alopecia project. They maybe able to help you locate a family in your area for local support. They are great..www.childrensalopeicaproject.org..Your daughter is cute no matter what!!
At 5:29pm on August 21, 2009, Samantha said…
Hi Shay, your daughter is the cutest thing? This condition can take a toll on us as parents emotionally. Once you have time to absorb it all things will get better. How are you and your daughter doing? I hope you find the comfort in this site that we do..Cindy
At 3:36pm on August 21, 2009, Tracy and Amanda said…
Hello and Welcome,

How are you and your daughter. I also have a daughter with alopecia. This is a great site for support. Hope to be talking with you soon.

Tracy
At 1:32am on August 21, 2009, Cheryl, Co-founder said…
Hi, I wanted to welcome you to Alopecia World. I can honestly say that we are a great community here and I hope you enjoy the time you spend with us.

Cheryl
co-founder

Disclaimer

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.

© 2024   Created by Alopecia World.   Powered by

Badges  |  Report an Issue  |  Terms of Service