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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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but it does define me?
I would agree BUT it depends on :
1 How you react to other people.
2 How you react to your Alopecia.
I ham 52 and have been AU for 10 years. how quick it has gone!. I too had lovely hair and i would like it back BUT there is no cure or treatment.
Most women eventually go down the semi permanent makeup and wig route.
Forget about cures or treatments.
Start looking at the above route.
I had semi permanent eyebrows done. Should have done it years ago and i use a black liner on my lower lid (not very well....lol
I'm an ordinary bloke and it makes me feel better.
DO THE SAME!
Instead of cures, treatments ( none) tears, staying in, moping, self pity.
Get planning wigs and makeup. Most people come around to this after some time.
Don't waste your time...
Columbia University is presently doing a study with an oral medication that seems promising. You should try to get into the study. I know they are looking for people like you. There are no major side effects and I know its worth a try. The breakthrough on Fox News with that man who grew hair after 7 years was taking the same drug as the study medication!
Hi Kat,
I live in Houston, can you tell me who I need to contact to submit my DNA and get things started to be on the list for the trials. You mentioned a few names, but i am not sure which one to contact.
Thank you
Ruthie
Alopecia does not define you don't let those stupid and cruel people define you. Please. I know its difficult. Even at age 67, Alopecia universalis almost 20 years, I face the daily decision of to wig or not to wig. If I don't wear wig inevitably someone is commiserating with me about my "cancer" treatment. It's awkward to say the least. We need MORE EDUCATION, less bullying.
Yes, it does define us! I am 42 years old. I lost my hair totally when I was 4. I went through every grade of school thinking next year I'll have hair. By the time I get to High School I've have hair then by the time I am married and then maybe when I have kids... I do not have hair. It does define us. I have to tell you it makes you stronger! I know how devastating to not have hair, a teenage girl. You have to know you are beautiful. I have never gone without a wig and found lots that were really nice throughout the years. It is a personal thing but I would not go without mine. Makeup does a lot too. There are so many things out there to help you. I don't know where you live but insurance pays for many hairpieces (prosthesis) also. Talk to friends and family you will find I am sure that you have lots of love and support. This community is a great place also. Happy to talk more to you.
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