Hi Everyone! My names Nicole I'm 21 and I live in Tampa,FL. I'm new to this site but not new to Alopecia. I've had AA since i was 3 and i have always felt alone. I just recently found this site and the NAAF site and realized I am NOT alone. my AA has always just been spots here and there never anything I couldn't hide with my own hair. but within the past 6 months it has got to the point where it is impossible to hide it, so 2 months ago I bought my first wig. I'm still getting used to it, I got a wig that looks as close as possible to what my real hair looked like. I don't want anyone to know I wear a wig. My mom tells me I should have fun with it and change my style all the time. but I'm just not ready for that..and I don't know if I ever will be. How do you just accept it and not care what people think? :( if any one has and advice id love to hear it. or if you just wanna talk id like that too. I've found it really helps me to talk to people that know what I'm going through.

Views: 21

Reply to This

Replies to This Discussion

The hardest part about coping is just dealing with the fact that "this may be it, nothing is going to change." Once you can manage that "tomorrow will be the same" and the "day after will be the same," you will be better able to manage with today. But if how you think today and how you deal with it today is just to get to tomorrow, as in just getting by, then the weight of coping will always be heavier. You literally just have to accept and move on, like its not a big deal, and once you do that, it is amazing how the little things that had been bugging you before, just sort of disappear.
Thank you for the advice! I really hope i can get to that point someday. I'm just starting to realize im not alone. and it has helped me alot to talk to other people going through the same thing. so i hope can accept it soon :)
Anytime . . . the best way to manage is simply to talk about it. The forum here allows you to be open and to forget about hiding. Just ask questions; we all have been through it and have sincere advice.
Hi Nicole, i am in exactly the same position you are, have been able to 'hide' spots, but in the past few months it has become increasingly worse. I have bought wigs but the thought of anyone i know finding out what i am dealing with and knowing i have a wig on is something i am just not ready to deal with. It would not be so bad if i did not have to work everyday, then i could hide in my house, but i have to work! I am not at that place that some are with 'bald is beautiful', because a womans hair at least for me was the only thing i had that meant anything to me. I need help with this too like you.
Hi! i know i feel like hair is one of the most important things to a girl. and knowing that there"s a good possibility i could lose it all is really scaring me. but honestly i like my wig i think it looks really pretty and i kinda like not having to fuss with my hair anymore. it use to take me hours to do my hair just the right way to hide my spots. so its nice not having to stress about that anymore. but I'm just so horrified about people finding out and what they will think. Maybe we could help each other :) I'm here to talk anytime. i find it has really helped me to talk to people that are going through the same thing.
Hi Nicole and welcome! You're going to love Alopecia World!

Check out my page for what I've done. It works for me, but I know it's not for everyone.

Take care,
Mary
i been coping since i was five. I t still hard to talk about it wwith other people you dont know well. but iam coming out slowly with this with co workers. I dont rember my true color of my hair since lost it at 5. My momgo out find me wig with different color every time she goes out and i buy the color i like .I go to work and see the reaction my coworker will have. It is always good no matter what i wear. I like to talk to people with the same issues to . this is the first time i get to talk to some one like this.

RSS

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