well, im a professional business woman that now sells full lace wigs after finding out "officialing" that i had scarring alopecia after it got alot worse all within 1 year. I believe it may have grown dramatically due to stress. But it started when i was 17. But even then I had very, very thick pretty hair. I was know for my "pretty hair", so when the hair loss can no longer be covered up, this became a very big deal for me. Many times I would cry and get upset...even still now to be honest. But came to realize that there is ALOT MORE IMPORTANT things you can be upset with now a days. So I began wearing, applying and selling lace wigs. This may be on a needed basis for some of us or simply a vanity thing for others. never the less these units help us achieve our self confidence back. I sell them as well as apply them. I sell european virgin hair, mongolian, malaysian, chinese virgin or indian virgin or processed hair. These wigs have been a true life saver for being, being as though weaves will not cover up all problems and regular old fashion wigs are so hard, think and heavy and just plain uncomfortable
GROWING UPSCALE HAIR LACE WIGS are airy light very natural looking and best yet affordable!
I'm writing to you because I will be having a program at my school "What is Beautiful" and we'll be discussing the many lengths that women/ men have gone to achieve what is beautiful according to society. We will show quick clips and then have a panel consisting of Rutgers students and people with alopecia. Would be interested in participating or know of anyone that is around the NJ area that would like to participate?
Date: April 21st @9:15pm
Location: Rutgers University, New Brunwsick, NJ 08901
Student Activities Center
Please let me know as soon as you can:)
Bumped into your page, But just wanted to tell you that you look beautiful. Nice to see you took a challenge (alopecia) and turned it into a positive (self-acceptance/bussines venture). Have a blessed holidays.
Hi Shemika, 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
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