Thank you Jean for your kind comments. I hope this alopecia experience will make my daughter a stronger person in the long run. How is your son doing? Please fel free to drop by my page with updates any time. We are all in this together.
Tracy

Hi Jean, How are you? I replied to your note to me on the discussion board. Please email if you have any questions. I am happy to share my story. I have pictures posted of various stages of Sam's regrowth. My profile pic is what she currently looks like after a year on a regrowth cycle. Cindy

Hi Jean, We are practically neighbors. I live in Orange. Anyway, my daughter has been OK. She just turned 13 and has been wearing wigs almost 2 years. We are in an unusual situation because she goes to a small private school and has been able to adjust to AU without to many social issues. However, she never goes w/out the wig. I'll be glad to talk to you more on a personal level. I think if we are "friends" I can privately give you my email and phone.

Hi Jean, Yes, I understand the struggle. I also know the struggle that parents have. But has you can see many of these kids grow to be well adjusted adults with careers, relationships, victories and struggles. It is just a matter of find our place of acceptance and going from there. Keep in touch! Cheryl

Hi Jean, I wanted to take this opportunity to welcome you to Alopecia World. I have been living with Alopecia Areata since 1991 and know full well the struggle it can be. I look forward to getting to know you. Cheryl, Co-founder

hi Jean!!
how are you?
thank you for the nice comment!=]
I have had Alopecia Areata since I was 12.
I finally accepted my alopecia after the tyra show.
I enjoy the National Alopecia Areata Foundation Confences because i met alot of people who know what i face with Alopecia.
i'm sad that i can't go the naaf Confence this year because i gradute from high school that same weekend..=[
I also find that Alopecia World is very helpful because you get to talk to people with alopecia.

thanks again
brittany <3