I was diagnosed with AA when I was only two years old. When I hit third grade, we realized it was time for my first wig. As devastating as it was we knew I had no other choice because I was sick of being bullied at school. From third grade until almost 11th grade I wore a wig. My hair ended up coming back and staying (for the most part) up until about three months ago. I now have lost almost 85% of my hair and am having an extremely hard time coping with this considering I am only 23 and have my entire life ahead of me still. I joined this website looking for more of an understanding as well as support from others who suffer with the same auto-immune disease I do.
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.
Comment Wall (4 comments)
You need to be a member of Alopecia World to add comments!
Join Alopecia World
Thank you for you comment, it warmed my heart <3
Hello Sarah Elizabeth, and welcome to AW!
How are you today?