I first developed AA when I was 28. I thought it was a side effect of me having chicken pox, a bad marriage and bad hairdresser! I went through the anthralin oinment turning my skin purple, I went through the cortisone injections and finally I just said forget it! I have hair now 20 years later but it has a mind of its own! Some months I am good, then I feel the burn and voila! A bald spot. Sometimes my children notice the "spots" first, my 7 year old will try and cover it with my hair..she says hold still mommy, I'm hiding your spot!
I have yet to watch your video, but you were right on it when you said the body is healthy but the psyche is what suffers. I still deal with esteem issues...getting tattooed eyesbrows helped with some of that. i wear glasses more than my contact lenses because I went without eyelashes for so long, I learned to hide behind the glasses! Now they are fashionable to wear and I love getting new ones to "change-up"!
I don't expect miracles, I have a loving family who loves me the way I am and when that last strand decides it doesn't want to grow back...I will deal with it like a champ the best I can.
Do you have alopecia?
Alopecia areata
Are you age 18 or older?
Yes - I am 18 or older
Comment Wall (3 comments)
You need to be a member of Alopecia World to add comments!
Hello and welcome, Michelle!
I know how hard alopecia can be; I have had it for about 30 years. 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!" You can find out more on my page -- and it's available on this site under "Bookshelf." Let me know if there's anything else I can do!
LeslieAnn
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 (3 comments)
You need to be a member of Alopecia World to add comments!
Join Alopecia World
Welcome to Alopecia World!
Tracy
I know how hard alopecia can be; I have had it for about 30 years. 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!" You can find out more on my page -- and it's available on this site under "Bookshelf." Let me know if there's anything else I can do!
LeslieAnn