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

Glenda's Friends

  • LeslieAnn Butler
  • rj, Co-founder
  • Cheryl, Co-founder

Glenda's Discussions


Started this discussion. Last reply by Jemsnixon Mar 21. 3 Replies

Gifts Received


Glenda has not received any gifts yet

Give a Gift


Glenda's Page

Profile Information

Relationship Status:
About Me:
Hello everyone...
Do you have alopecia?
Scarring alopecia
Are you age 18 or older?
Yes - I am 18 or older

Comment Wall (11 comments)

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

Join Alopecia World

At 7:22pm on February 24, 2009, LeslieAnn Butler said…
Keep me posted!
At 5:21pm on February 23, 2009, LeslieAnn Butler said…
Wow, I wish I could help you on this one. I have never ordered a lace front wig online. There are other women here who I'm sure have had both good and bad experiences with online could put the question out to all the women on the site, either via a discussion group or email to your group of friends. And I would love to know what you find out! Okay?
At 6:36pm on February 20, 2009, LeslieAnn Butler said…
Glenda, I'm doing very well. I totally understand why you want to wear your wig. I have had this for over 30 years and I have never gone out in public without one. You are still you, with your wig -- it's part of you, like your clothing or makeup. Don't feel ashamed.
Big hug!
At 4:47pm on January 16, 2009, Cherylnz said…
Hi Glenda
Welcome to Alopecia World
At 8:53pm on January 9, 2009, Eileen Simpson said…
Hi I would like to say that one day you won't feel this way, but it could take some time. Yes I know how people can be I work for a elementary school where children are always making fun of others, and it's really too bad that it continues to adulthood. I try to stop it in it's track here, but it's hard when the support doesn't come from the parents. Or that they learn these terrible things from their parents. It makes me very angry and I just hate that way some people are, but every person who is this way there is at least one other person who cares. I think we have to focus on the people who are possitive and ignore the others. I know first hand that it's hard I wore glasses all my life and was different then others, some of the kids made fun of me and there were others who didn't for those that didn't they became my friends. I don't have many friends now but the ones I do have have wonderful hearts and wouldn't blink to help others.

I am here for you

At 10:21pm on January 8, 2009, Eileen Simpson said…
Welcome I hope you enjoy being here I am new here also and I love it here. There are so many wonderful people here as you will find out. I'm glad you found us.

At 5:26pm on January 8, 2009, LeslieAnn Butler said…
Hi Glenda,
There's nothing wrong with wearing a wig -- nothing at all. I prefer it, and after all these years (30)I have not gone without it.
It can be hard. After I became the spokesperson for the National Alopecia Areata Foundation, a lot of women were needing my help and support, so I wrote a book called, "If Your Hair Falls Out, Keep Dancing!" If you feel like it, you can find out more on my page -- and let me know how else I can help.
At 8:58pm on January 6, 2009, Linda said…
Hi Glenda, welcome to AlopeciaWorld!
At 1:32pm on January 6, 2009, Cheryl, Co-founder said…
Hi Glenda, 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
At 12:53pm on January 6, 2009, rj, Co-founder said…
Hi, Glenda. Welcome to Alopecia World! This is a great place for great people, so be sure to make your positive presence known. :-) - rj, Co-founder


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.

© 2023   Created by Alopecia World.   Powered by

Badges  |  Report an Issue  |  Terms of Service