Dear Peyton:
Hi, I'm Cynthia and my daughter is Taylor-Jean. It has been a very long time since we have been active on Alopecia world so I've just read your comment from Oct. 28th. Anyways, my daughter began her trip with alopecia when she was 2. She is now 1 month away from 9 years old and she is still having a hard time. She is very hard to talk to. She keeps everything inside but we know that her heart is breaking inside. There seems to be so much in the States, but here in Canada, she hasn't even been able to see another child with alopecia. I really wish we lived in the states sometimes so that i could take her to all the functions that take place and she could meet other kids....such as yourself. As I'm sitting here typing and listening to your music, I feel like I'm sitting with Taylor-Jean as she spends ALOT of time listening to music and all the same stuff that you have playing on your page. COOL! Anyways, I'd love to have her send a note to you and maybe she might have some questions for you...if that's ok. Take care, Cynthia
Hello Peyton: You might not remember me but I am Jeff Woytovich, my wife Betsy and I started the Children's Alopecia Project. Our daughter is Madison and we came to one of your families meetings when you were 9 and Maddie was just 5. You look so grown up I don't think Maddie would even know it was you when she sees your pictures here. Please take care of your self and keep up the good work. Say hi to your Mom and family from CAP.
Hey Peyton! Once I get the ball rolling with the walkathon I'll give your mom a ring! How is school going?? I hope you and your family are doing well :) KIT
Really?
I saw them last Wednesday... the 20th!!
and you're right.. THEY WERE AMAZING!!
I absolutely love them!
My best friend kind of instilled this obsession of them in me lol!
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.
Peyton's Comments
Comment Wall (66 comments)
You need to be a member of Alopecia World to add comments!
Join Alopecia World
Just let me know in what way I can help :)
my e-mail address is: kristin@smartisinc.com
Enjoy Spring break.
Kristin
Hi, I'm Cynthia and my daughter is Taylor-Jean. It has been a very long time since we have been active on Alopecia world so I've just read your comment from Oct. 28th. Anyways, my daughter began her trip with alopecia when she was 2. She is now 1 month away from 9 years old and she is still having a hard time. She is very hard to talk to. She keeps everything inside but we know that her heart is breaking inside. There seems to be so much in the States, but here in Canada, she hasn't even been able to see another child with alopecia. I really wish we lived in the states sometimes so that i could take her to all the functions that take place and she could meet other kids....such as yourself. As I'm sitting here typing and listening to your music, I feel like I'm sitting with Taylor-Jean as she spends ALOT of time listening to music and all the same stuff that you have playing on your page. COOL! Anyways, I'd love to have her send a note to you and maybe she might have some questions for you...if that's ok. Take care, Cynthia
sorry about that
thats really cool that your friend knows her!!
and after you hook up with Nick you will tell Kevin about me and me and him will fall in love
lol
that's so cool!
:)
I saw them last Wednesday... the 20th!!
and you're right.. THEY WERE AMAZING!!
I absolutely love them!
My best friend kind of instilled this obsession of them in me lol!
i cant believe someone would do that.
its horrible
but i bet they are adorable!
I was wondering if that is your natural hair in these pictures...because it looks really nice
Welcome to
Alopecia World
Sign Up
or Sign In
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.