Hey Heather! Its Taylors mom (Shana) How have you been? Sorry we didn't make it on March 10, hope it went well! Are you still working with kids and going to school?
You'll have to tell my how you like Amy's Presence wigs -- I've heard that CyberHair is better than other synthetics because it doesn't frizz up.
LeslieAnn
You asked about my hair -- I get my wigs from Brenda Kay Hair Specialties in Portland, OR. She cuts and styles them and they are fabulous. She works with people all over the world, so if you're interested I can give you her contact information...
L.A.
Hi Heather!
You can get my book by clicking the link at the bottom of my page: www.leslieannbutler.npauthors.com! You get a discount if you get it this way. Otherwise you can also get it online at Amazon and Barnes & Noble.
LeslieAnn
Hi Heather,
I have AU too. Hooray for you that you have a positive attitude! That is the only way. I've written a book about it and I'm hoping it will help a lot of women with this...
LeslieAnn
Hi Heather
My daughter Taylor who is 10yo was diagnosed with AA about 3 months ago with 1 patch. Just in the last 2 weeks she developed about 7 new patched and now they are meshing together and her hairline in the front and the back are receding. Have you heard of biomatrix wigs. She will be getting one of those soon. But in the meantime we are having a hard time accepting things. We are trying to be positive. Any help to try to cope would be great.
Shana (mom) and Taylor
Hi Heather. I am so glad to hear what you said about not letting this disease get you down. I have finally come to terms with it myself and am really and truly happy. I just don't CARE anymore....I LOVE the fact that I no longer have to shave......and my friends have all responded to the "new me" so well. It's awesome to be at peace with it all! Take care, Daria
Welcome to Alopecia World! I was just diagnosed with AA at the beginning of this month. This website is such a great place for finding others to talk to. ;)
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.
Heather's Comments
Comment Wall (17 comments)
You need to be a member of Alopecia World to add comments!
Join Alopecia World
hey whats up??? I haven't heard from u in awhile so hi!!!!
Love
Taylor
-Taylor
I am glad we met and YES, hopefully we will go do it again with the other girl. Who is she? How old is she?
Love
Taylor
Love
Taylor and Shana
LeslieAnn
L.A.
You can get my book by clicking the link at the bottom of my page: www.leslieannbutler.npauthors.com! You get a discount if you get it this way. Otherwise you can also get it online at Amazon and Barnes & Noble.
LeslieAnn
I have AU too. Hooray for you that you have a positive attitude! That is the only way. I've written a book about it and I'm hoping it will help a lot of women with this...
LeslieAnn
My daughter Taylor who is 10yo was diagnosed with AA about 3 months ago with 1 patch. Just in the last 2 weeks she developed about 7 new patched and now they are meshing together and her hairline in the front and the back are receding. Have you heard of biomatrix wigs. She will be getting one of those soon. But in the meantime we are having a hard time accepting things. We are trying to be positive. Any help to try to cope would be great.
Shana (mom) and Taylor
XOXO
CAR
Roger.
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.