Abby
  • Female
  • upstate ny
  • United States
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  • Eileen
  • Karen
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Relationship Status:
Single
About Me:
I'm a seven year old girl in first grade who has alopecia areata. I have lost 80% of my hair. I don't want to wear wigs so I just wear hats. I like horses, soccer, smores and picking on my older brother. My mom and I told my class about alopecia areata and now I feel soo much better because I don't have to be afraid of what my friends will say they like me the way I am. (my mom, kim, has typed this up for me.
Are you age 18 or older?
No

Comment Wall (9 comments)

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At 9:44pm on June 17, 2008, Cindy said…
Hi Abby, my daughter Samantha is 6 years old and will be going into 1st grade in the fall. She has had AA for one year now. She started school with hair and lost it all by January. She loves to wear her wig and hairdannas. We live in Massachusetts, but visit NY often. It is nice to hear you had a good experience at school. Cindy
At 9:21pm on June 1, 2008, Alex said…
Hi Abby!
How's school? Are you excited that it's almost over?
From, Alex
At 4:36pm on May 29, 2008, Eileen said…
HI
We initially tried probetesol topically, short term. Kelly hated the oilyness and we decided it was not worth it. Kelly is meds free and continues to have spots that come and go. We do have her take biotin and MSM as well as her multivitamin daily, but that's it.
Where upstate are you?
At 7:07pm on May 28, 2008, Eileen said…
HI Abby
My daughter Kelly is seven and has spotty AA too. We also live upstate NY. And just like you, Kelly and I (her mom) spoke to her class each year to tell them about alopecia You sound like a confident, spunky kid! If your mom wants to contact us, please do so! It would be fun to meet new friends
At 9:27pm on May 27, 2008, Alex said…
Hi Abby!
How are you? Good job on telling your class! I have to do the same thing sometimes in school, and I know it can be hard to do.

Just out of curiosity, have you ever met anyone else with alopecia? My mom and I live in the city (Staten Island) and we have been trying to get some sort of support group/ activity (or something alone those lines) for kids in the New york City area that have never met others with alopecia. We still don't know what, if anything, we are going to do, but it's a work in progress.

Have a good week!
-Alex
At 5:52pm on May 26, 2008, Cool Head said…
Hi Abby and welcome.

I'm glad you are doing well with your alopecia. I hope you attend the conference. There are many other wonderful kids there with alopecia. It always helps to know someone else
At 10:23pm on May 25, 2008, Cheryl, Co-founder said…
Hi Abby, 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 9:08pm on May 25, 2008, Karen said…
Hi Abby,

my daughter is four and she has alopecia as well. I like reading your post because it shows me that you are very brave and confident. I hope my daughter will have your confidence when she is your age.
At 5:09pm on May 25, 2008, LeslieAnn Butler said…
Hi Abby!
You are so brave and wonderful! What you did in class is just exactly the right thing to do!
I had horses when I was seven, too.
LeslieAnn
 
 
 

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