melissa
  • Female
  • Rochester, NY
  • United States
Share on Facebook MySpace
  • Blog Posts
  • Discussions
  • Events
  • Groups (1)
  • Photos
  • Photo Albums
  • Videos

Melissa's Friends

  • Angela
  • cindy Babs
  • Karen Smith
  • Joanne S
  • Alicia Duncan
  • Lori Van Decker
  • BTB (John)
  • LeslieAnn Butler

melissa's Groups

Gifts Received

Gift

melissa has not received any gifts yet

Give a Gift

 

melissa's Page

Profile Information

Relationship Status:
Married
About Me:
I have had alopecia sense I was 16. Started with spots, and has now at 31 has gone to totalis after my second child was born. It has been a year now, with sparse re-growth, im not sure if it will lead to anything or not. Im now prego with number 3.
Do you have alopecia?
Alopecia totalis
Are you age 18 or older?
Yes - I am 18 or older

Comment Wall (5 comments)

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

Join Alopecia World

At 6:58pm on April 2, 2012, Angela said…

Melissa, I love the way it looks, feels and how you can curl, that iron, etc. The only thing is the front keeps falling in my face and I have tried everything to have it look like it is suppose to. I'll get my husband to put up a picture tonight if he has time.

At 5:17pm on April 1, 2012, Angela said…

Hi, Melissa. I am new to this site and have few things figured out. I have Androgenetic Alopecia. I have worn wigs for over 5 yrs. Am currently wearing Jon Renau's Haute. I absolutely love your hair. Would you mind telling me about it? Thank You!

At 8:19pm on March 29, 2012, Lori Van Decker said…

Melissa, I also started with alopecia areata at 16 and went totalis in my 30s, and in my late 30s universalis -- and I didn't have any children. This crazy disorder is a mystery!

At 8:10pm on March 28, 2012, LeslieAnn Butler said…

Hello and welcome, Melissa!
How are you today? Congrats on the new member of the family!
Leslie Ann

At 4:43pm on March 23, 2012, BTB (John) said…
Welcome to the AW world of pain and hurt from this lousy disease, it's a great site to express how your feeling. My wife (Pat) has had AA for 25 years tough gig but we have survived. Hope we can share our story with you.
 
 
 

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.

© 2024   Created by Alopecia World.   Powered by

Badges  |  Report an Issue  |  Terms of Service