• Female
  • Evanston, IL
  • United States

Ava's Friends

  • wendizzle
  • Nathalie27
  • Emily Naples
  • Nicole
  • Ms. S
  • Donna DeHoog
  • Jill Casaldi
  • Tracy and Amanda
  • ashlee
  • Rahela
  • Renee
  • Fox
  • Kelsey O'Ree
  • Ally
  • Kimberly

Gifts Received


Ava has not received any gifts yet

Give a Gift


Ava's Page

Profile Information

Relationship Status:
In a Relationship
About Me:
My name is Ava, I am a social woker in Chicago. I Have had Alpoecia since I was about 3 years old. It started out as AA, then progressed to AU. when I was younger I tried hats and wigs, then I decided to just go for the gold. I went out without anything on, and I loved it. I recently tried a hair system a couple of years ago, and that is what I wear now. If you would like to know anything else, just ask. I love photography, funny people, chocolate and the color green!
Do you have alopecia?
Alopecia universalis
Are you age 18 or older?
Yes - I am 18 or older
Your Website (Leave blank if you don't have one):

Ava's Photos

  • Add Photos
  • View All

Comment Wall (6 comments)

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

Join Alopecia World

At 6:30am on June 8, 2009, Fox said…
Hi Ava,i was wondering what kind of wig you are wearing and where did you purchase it ?

I'm doing some reasurch for myself and looking around,your hair looks great
At 7:46pm on April 26, 2009, ashlee said…
hey hun is your wig a lace front? do you find it easy and fun to do different styles? did you ever try a vacuum fit wig?
At 3:19pm on April 4, 2009, Fox said…
thanks I've added you to my friendslist,most of the people here look so good with their wig on,I actually don't feel so bady anymore hahaha :-)))
At 7:17pm on March 4, 2009, LeslieAnn Butler said…
Hello and welcome, Ava! How are you doing today?
I have universalis, too!
At 8:04pm on March 3, 2009, JeffreySF said…
Hi Ava,

Welcome to Alopecia World.

At 2:42am on March 3, 2009, Roger said…



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.

© 2020   Created by Alopecia World.   Powered by

Badges  |  Report an Issue  |  Terms of Service