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I am in the 9th grade and I was diagnosed with alopecia universalis. I got it when I was in the 5th grade when my strands of hair that i thought where just split ends. 7th grade was when it really started to come out in patches until around 8th grade it was all out and I was completely bald. Not only did my hair fall out on my head but I have hairless parts on my arms and legs. I have no eyebrows and I have to draw them on. My eyelashes have recently started coming out and i dont know what to do. Im a teenage girl and how society is one of the things that is so important to me is being taken away. I had long thick black hair its so hard to look in the mirror because I feel so ugly. Its easy to say things like dont let alopecia define you but it does. It affects how you feel about yourself. It is so hard going to school constantly being asked if my hair was a wig and people asking to touch it. In my 7th grade year I once got chased down the hall to my next class because 2 boys where trying to pull it. It has been hard and I cant get out of this dark hole. I try to smile and be happy but it just is not working. I want to feel pretty I want to be confident but I just cant. Im so sad and I just dont know what to do. Like im still a child I shouldnt have to be worrying about this im supposed to be worrying about school and education and friends not hair loss. im completely bald and I feel like im drowning.
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I am so sorry this has happened--it totally stinks. BUT, while alopecia is part of your life right now, no, it does not have to define you. You can also be the girl who is beautiful writer or a great runner or fast skier or a budding artist. Do not let hair define all of you--it is yet one piece of who you are. There was a wonderful article on a young man who has Vitiligo inthe DC area who is a champion runner. If you watch "America's Got Talent"you will see that recently a young woman with alopecia did an amazing dance--and told the judges at the end about her alopecia and then the camera video-taped her with no hair and you know what? She looked great. Trust me--this is not easy and I am not saying to say it is. But it is only life-aftering if YOU let it be.
Maybe go volunteer at a pediatric cancer ward one day and see what those kids are going thru as when I get down about this issue, it makes me feel better to realize that while Alopecia sucks, you can/will still have a great life.!!! good luck and write back when you can. Big hug to you. And yes, the Yale study is promising although it may take a while.
My name is Mark and I live on the east side of Milw. I am 58 now, singl, nvr married. I got alopecia when I was in 4th grade and it turned into alopecia Univsrealis by age 15. Part of that was no doubt due to the fact that some of my patches of hair that I did still have on my head were ripped out by bullies. My parents bought me a wig when I was 15. I didnt expect to but I wore one for 40+ yrs. I finally took it off about 10 years ago. And now I wear a baseball cap every where bec I am so used to having something on my head. And with univsrealis we cant hide the fact that we dont have eye brows or eye lashes either. But the wig did not help my social life at all. Instead of it giving me confidence to approach women at college bars etc, I just didnt bec I thought that if I introduced myself that evetually I would have to tell them that I was bald and they would scare away. To this day I have never had a girl friend of relationship in mmy whole life. I dont know what to tell you except to be open about this condition to pep when you can because ignorance is the worst symptom of this condition. Take chances in life, if you lose, or if she runs away, get up and try again. Its easy for me to say. I already went through 7-9th grade prob the two worst years of my life. But hang in there guy. Mark S Hansen I'm also on twitter and facebook.
You are absolutely correct...it DOES define you. But you give it the definition. I am stronger, more confident, more free that ever before, because of it! You will get there too. Because there is so much more to living this life than our hair...!!!! Good luck
OMGOSH!!! I totally understand your story I myself will be going into the eighth grade. I though found it easier to deal with after I found all of my good friends. I think it helps when you have people that are almost always around you so that they can protect you in one way or another.
I was diagnosed when I was 14, and I understand how you feel, even now at 35. I still struggle with some of the same fears and insecurities every now and then. I am so sorry that you are having to go through this, particularly at this time in your life. I know firsthand how it can feel as though your femininity is being stolen away from you, and how friends and family making assurances doesn't really make a difference in how you feel about yourself.
The kicker is that no one can make you feel good about yourself. Only you can do it. You must look for ways to make it work for you.
Also, you need to allow yourself some time to grieve! Your hair loss is an actual loss. People who haven't been there don't get this---it's not just hair... it's a piece of yourself. It's an identity you are no longer able to truly embrace because it is no longer you. You don't have to smile about it right now. You have every right to get mad about it, to cry about it... whatever you need to do to get yourself to a point where you can accept yourself exactly as you are. And you're right, it does define you... sort of... in the same way that experience defines each of us. As you get older, you will find that you have a unique perspective on human nature, on kindness, cruelty, love, and so much more... It's okay to allow it to shape you, just allow it to shape you for the better.
THERE IS NOTHING WRONG WITH YOU. YOU ARE BEAUTIFUL.
So sorry for you to have to go through this so young. I'm so grateful for this site... it puts you with a group that understands! I pray that you find your peace. I rebuke the sadness and fully expect that God will lead you to your place of beauty and satisfaction and that virtual and actual arms cradle you in love! In the precious name of JESUS. Amen.
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