Kristen M
  • Female
  • Hebron, IN
  • United States
Share on Facebook MySpace
  • Blog Posts
  • Discussions
  • Events
  • Groups (2)
  • Photos
  • Photo Albums
  • Videos

Kristen M's Friends

  • Tracy and Amanda

Kristen M's Groups

Gifts Received

Gift

Kristen M has not received any gifts yet

Give a Gift

 

Kristen M's Page

Profile Information

Relationship Status:
Married
About Me:
Hello, I am mom to the most wonderful little girl. She is 12, but was diagnosed with AT around the age of 5. I am actively searching for other children in our general area for her to meet. We live in a small town, and her condition is not accepted by the children at her school. She deals with them well enough, but all children need friends they can talk to. My hope is to find other children with alopecia for her to bond with. I would like to thank many of the people that have posted here. I have read many helpful things such as, permanent lashes. I have been struggling with that decision for some time. I am afraid to put anything permanent on her, when she is still growing, and her face is still changing. I am now considering getting it done "lightly", so it can be added to or not as she gets older and can make that decision herself.
Do you have alopecia?
I do not have alopecia
Are you age 18 or older?
Yes - I am 18 or older

Comment Wall (5 comments)

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

Join Alopecia World

At 8:05am on October 11, 2009, Susan - Jon's Mum said…
Hi Kristen
How are you and Nicole going?
Susan
At 3:14pm on September 24, 2009, LeslieAnn Butler said…
Hello and welcome, Kristen! How are you and your daughter doing today?
I read what you said about "permanent lashes." Do you mean tattooed eyeliner?
LeslieAnn
At 7:49am on September 19, 2009, Susan - Jon's Mum said…
Hi Kirsten,
My son, just turned 13 (had AA from age 6 just developed into AT) is in a similar situation to your Nicole. He doesn't mix much with other children at school. He used to be involved in sports after school but he has dropped that. He has isolated himself. I know how you feel. As a parent it is hard to have to watch your child suffer in any way. I am just hoping that my Jon will gain friends who will appreciate him for the way he is - his uniqueness.
If you can get Nicole involved in out of school activities this does help with their self esteem as well as helps them to communicate with other kids.
Susan
At 11:54am on September 18, 2009, Cheryl, Co-founder said…
Hi Kristen, 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
At 10:21pm on September 16, 2009, Tracy and Amanda said…
Hi Kristen,
How are you and your daughter?
Tracy
 
 
 

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