www.alopeciaworld.com
I discuss a brief outline of my newfound struggle with my appearance.
Tags:
You have to do what is right for you. I think that life is easier wearing a wig, but that is me. No one is staring and people are easy to talk to... I guess I'm approachable. Is it fair? No. Am I hiding who I really am? Maybe. But I'm more than just my hair. Good luck to you. There is no wrong answer.
Thanks, Sue!
I wear a wig, but My mom wore wigs when I was a kid and she didn't have alopecia. A wig is like an accessory...I HATE going out with earrings... I feel naked. Am I really naked? No, but that's how I feel about it. Am I hiding my true self for wearing earrings... No...I just love wearing earrings. Do my earrings make me and others feel better? Yes... I get compliments on my great earrings all the time. Do you love having hair? Most of us would say,YES! Alopecia just coaxes us into wearing someone elses. I don't see anything wrong with that! But YOU have to find your own peace. Know what you love and follow your heart. (I know this analogy is pretty simple, but you get my point)
Hi!
As a mom of an eight year old with alopecia, she's totally bald but still has eyebrows and eyelashes, I can say that Olivia is very comfortable without a wig and uncomfortable with a wig.
As an adult who lost your hair in adulthood rather than in childhood I can understand your termoil.
You have to do what is comfortable for you and not for what is comfortable for others. If they can't accept you for who you are, especially your mom..then that is their problem.
What makes YOU comfortable? Yes, people will stare and think you have cancer. Some may even ask, but don't let it stop you from being you. After a while you won't see the stares. We don't and neither does my daughter. This is who she is and this is who you are.
Just get out there and be yourself, whatever you choose :)
Sybil
For me there is no struggle, I will always wear a wig, have for more than 41 years now. The only people who have ever seen me without one, is my kids and when they move out that will stop. It is how I am comfortable. I don't to spend the rest of my life explaining my lack of hair to anyone, ever. My husband accepted me, but I do not anticipate other will be so understanding. I had hair when we married and 6 months later it was gone. Now that he has passed, I simply do not want to put myself in a position of rejection, so my lack of hair is my little secret and it will stay that way. That is me, you have to look inside you and determine how much you want to expose yourself to questions from well meaning strangers.
To wear or not to wear? I try to keep my life as normal as possible, I want to continue working and living as I did when I had hair. My hair didn't define me then, and it doesn't define me now. I say wear a wig! I think people may feel bad for me if I go out socially without my wig. I want to keep my life normal in-spite of this alopecia.
You do what is best for you. I choose hair. ;-)
Try not to dwell on this so much. You seem to be making a mountain out of a mole hill. No one who is anyone in your life really cares one way or another. Do what ever. Find something to keep you occupied. Volunteer with those less fortunate-nursing homes need visitors. Make your life meaningful, you will see that this issue fades away as it should.
Hey Nicola,
Great questions! I have alopecia universalis, have had no hair for 11 years, and don't (won't!) wear a wig. I have lots of great hats to keep my head warm and/or shaded, but mostly I prefer to go bald. I wrote an essay about my journey to come to terms with being a bald girl - that has my answers to several of your questions. It is at: http://cedarmoon.us/baldnbold.html I encourage you to read it - and to be your authentic self, whatever that means for you.
bald & proud, Brenna
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
You need to be a member of Alopecia World to add comments!
Join Alopecia World