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Kayla Martell, Bald Miss Delaware Talks Alopecia: 'We're Just Normal People Without Hair!'

by Grace Gold (Subscribe to Grace Gold's posts)
Posted Jun 30th 2010 at 9:00AM  
19 Comments
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Miss Delaware Kayla Martell, wearing a wig. Courtesy Photo

It's no secret that beauty queens are known for sporting some big ol' Texas pageant hair on stage. So when 21 year-old Kayla Martell captured the Miss Delaware crown and then appeared bald on the CBS Early Show, people stopped and took notice.

Martell has alopecia areata, a condition that sparks hair loss and affects nearly 4.7 million Americans, according to studies conducted by the National Alopecia Areata Foundation.

Most alopecia patients experience patchy round spots of hair loss that may eventually progress into total baldness on the scalp and even body. Fall-out and regrowth cycles can happen at any time, though some patients never do go through regrowth.

While not contagious, doctors today think it may be an autoimmune disease, in which the body attacks its own hair follicles and slows down or stops hair growth.

Martell first began experiencing the symptoms of a receding part at the young age of ten, which then evolved into the more dramatic hair loss she sports today. But the pageant queen wants to make it clear that there is nothing 'wrong' with people who have alopecia.

"We're just normal people without hair! We are otherwise healthy human beings; our bodies are just allergic to our hair. But, it is also important to understand the stigma associated with baldness and the emotional stress that comes from the unpredictable nature of the hair loss," Martell tells StyleList.


Watch CBS News Videos Online


Unwavered by the condition, Martell competed on the Miss Delaware stage five times before finally capturing the crown. Two of those times, the Marymount University senior even appeared without a wig.

We had to know: was it scary competing in front of judges on a beauty pageant stage, without the security blanket of wearing a wig?

"Not at all! The Miss American Organization puts emphasis on recognizing talented, dynamic and passionate women and encourages us to be ourselves. Hair or no hair, Miss America has the power to change someone's life forever. If I have changed a child's life already by being open about my hair loss, then I have been successful!" says Martell.

Martell's persistance in coming back multiple years to compete for the Miss Delaware title wasn't all her own doing, though. It was a special fellow alopecia friend who urged Martell to give the pageant one more go -- which ultimately led to victory.

"This past year, a five year-old girl named Liliana Hakim has inspired me more than any other person. Thinking about her just makes me smile. For a five year-old girl to walk around without a wig and disregard the stares and whispers with a huge grin says so much about her personality. Adults could learn a lot from her! She is a beautiful and strong girl, and I am blessed to be her mentor," says Martell.

Not surprisingly, Martell's pageant platform involves raising funds and spreading awareness for the National Alopecia Areata Foundation, and we hear the talent she'll be showcasing at the national pageant in Las Vegas in January will involve some pretty smooth dance moves.

But the memory that sticks with Martell is not one of winning the crown, but rather the hope her experience has spread to other young patients.

"Just last week, I volunteered at NAAF's International Conference and spent time with children who have alopecia. They all tried on my crown and were able to see that it is possible for a bald woman to become Miss America!"

And for another story about a woman who refused to let a physical condition stop her from a successful career in beauty, read our feature on America's Next Top Model winner Caridee English's battle with severe psoriasis.
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Filed under: Hair Care, Beauty, Hair, News, Skin & Body
Tags: alopecia, bald, baldness, Kayla Martell, KaylaMartell, miss america pageant, Miss Delaware, MissAmericaPageant, MissDelaware, National Alopecia Areata Foundation, NationalAlopeciaAreataFoundation
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READER COMMENTS

(19)Add A Comment

sue, 7-05-2010, 10:25PM

2.5 stars vote downvote upReport
sue

Thank you so much for a great article about a brave woman. My daughter( 21 yrs old) also has alopecia areata and has been caught up in the stress of the condition. Her condition started about 3 yrs ago. I love how Kayla she says that I'm just a normal person without hair. I'm so glad she is a spokesperson for the cause.

Reply »

Concerned Mom, 1-14-2011, 2:08PM

2 stars vote downvote upReport
Concerned Mom

This is a really inspirational story. My daughter has recently been diagnosed with alopecia and we are struggling with what to say and do. So far only have had two bald spots. The first has grown back but as a mom I am dreading the day it gets worse. Having something like this hit you when you are in your teens is devastating. Can't believe there is nothing we can do. I would trade spots with her in a minute. Any advise would be greatly appreciated.

»

noreenarshad, 6-30-2010, 11:22AM

Half a star vote downvote upReport
noreenarshad

Who the hell cares? Okay, the part about having a disease and overcoming it is worthy of attention, but why do I care that the worst side effect is going bald and that may have hindered her and ultimately, she out on top? If it's really that much of a damn detterent that almost got you down, how about doing something useful like becoming a scientist or doctor to stop or help that type of thing? I was afraid it was some poor, sweet girl who's life could be hanging in the balance who got to honstly come up on top by honest inner beauty- oh no, wait, forget stuff like that! The story of a girl without hair and still winning a beauty pageant is much more inspirational! Who cares! By basing her win on the outcome that it was her looks-"OMG, she's bald and she won!"- that still could have deterred her from her win, this only supports the fact that the stupid thing is based on looks anyway, regardless if she won or not. If it wasn't, we wouldn't be talking about this crap in the frist place. So shut up unless you see something to write about an actual girl who's overcoming something that's actually serious, yet has a definate hope, courage, and willpower to help herself and others through an actual intellectual and knowlegdable pursuit!

Reply »

Cherie Corey, 1-15-2011, 6:52PM

2 stars vote downvote upReport
Cherie Corey

Let me tell you what, you may not care, but my little 4 year old grandaughter was just diagnosed. And for her to find out that a "Real Live Princess" in Her words, is just like Her... That big smile that it brought to Her face is one of the best medicines around. Having MS myself, and knowing there is no cure, all I have to deal with it is my attitude. So when Kayla has the ability to not be so caught up in the "pretty people" syndrome, it helps people of all ages in their ability to cope. So, yes it would be so much greater to post that they had found a cure, I get upset at times myself with my own afliction, but finding a way to deal with it is all we can do. I am sure by now you have thought about things. But I understand some of your frustation.. Good luck to you

»

DONNA KOOKEN, 3-01-2011, 3:54AM

2 stars vote downvote upReport
DONNA KOOKEN

What are you sayimg.....the person came out with their short commings? What do you want? Who are ypu? Do you think hair loss is a joke? I dont even know who you are, Do you have hair? Do you know what it is like to be without hair. I am a mom and a grandma with two grandsons. Domt you think I want hair...I was a professional. Now...... no hair... I am a wife,mom, grandmother, sister ,friend, co-worker,neighbor and person in line behind you at grocery store, person at the mailbox, post office , in line at subway I am here. This is not something we Alopecia People ask for..it is not a side effect...we dont have hair!

»

C. Smith, 7-08-2010, 1:19PM

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C. Smith

Great story!

Reply »

gemmaortez, 6-30-2010, 2:27PM

3 stars vote downvote upReport
gemmaortez

wow, some people are filled with so much negativity and angst! I thought this was a great story.

It sounds like miss delaware is leading a very active life filled with lots of community service and is a great role model for young girls. I can imagine how hard it must be to walk around bald as a woman. There are a lot of mean people out there, as evidenced by the previous poster's rampage.

Reply »

s, 6-30-2010, 6:38PM

2.5 stars vote downvote upReport
s

i am 17 and i have alopecia...its hard because i am completely bald now and i wear a wig..props to her for doing what she does!

Reply »

Kaylafan, 7-01-2010, 8:35AM

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Kaylafan

Kayla is a positive role model who has volunteered thousands of hours of community service and recently received the "TEN OUTSTANDING YOUNG AMERICAN AWARD" that many presidents including JFK and even Elvis have received. Her wearing a wig doesn't make it any different than when I put on a hat, wear makeup or even wear hair extensions, color or highlight my hair. It is all enhancing my natural beauty. Keep up the great work Kayla. Hope to see you win on that Miss America stage.

Reply »

Donna Hakim, 7-01-2010, 8:19PM

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Donna Hakim

To noreenarshad - you are completely ill-informed. I have a 5 year old daughter with alopecia areata. Why don't you try shaving your head totally bald and walk around like that for a month and see how "insignificant" being bald is about. This young woman will go farther in one day than you will in your entire life. If you understood what she was doing, you would see this is breaking through so many stereotypes. Sorry if a pageant offends you. You are such an ugly person inside. Get educated about her and her platform of alopecia areata before you decide what is "news worthy". Oh and just remember, she is young - maybe she will decide to be a doctor or scientist. And for that matter, why don't you do something that makes an impact in life instead of spending your time commenting on news online. This is not your only post. Get a life.

Reply »

donna kooken, 3-01-2011, 3:57AM

2 stars vote downvote upReport
donna kooken

Thank You Ms Donna

»

carolyn dobbins, 7-02-2010, 8:45PM

2.5 stars vote downvote upReport
carolyn dobbins

Kayla,
I wrote you a note on Twitter, but I am not sure that you received it...I am 70 years old and mine is Alopecia Universalis.
My first bald spot started at age 16 and loss of hair when I was a sophomore in College. It was devastating then as prople had never heard of it. After many Doctors, I found that it is hereditary. You reach a point with the disease to accept it and live every day as it comes. I wear ball caps a lot and a sweatband when I play tennis. Yes, Bald is Beautiful and I have had a lot of fun with it in my lifetime. I love my short blond wig called ABBY and I told my children that they better not ever put a grey wig on my head. God meant for this to happen to me and I have helped many people going through Chemo and shared my eyelet caps and ball caps with them. I admire you so much for how you have come out into the public eye regarding this autoimmune disease and I will be watching for you during the Miss American pageant. Ignore the ones who are negative with you, as until it has happened to them, they cannot judge you.
Noone but us knows what it is like until they have experienced it. You keep on doing what you are doing, as you are an inspiration to many, many people. If I had you mailing address, I would send you a picture of me. People like me being bald, as it is me.
Love you, girl, keep at it.

Reply »

Karen Briggs, 7-02-2010, 10:59PM

2 stars vote downvote upReport
Karen Briggs

My 13 year old daughter has had alopecia since third grade-she lost all of her hair on her head. She has never let that stop her from being herself. She is cheerleader and class president-and only wears bandanas. She has wigs and wears them when she wants to dress up- I think it is amazing that you have decided to compete and win the pageant. You have been an inspiration to more than you will ever know. Would love for my daughter to be able to talk to you. Also, does anyone know of a tatoo like the breast cancer sign has for alopecia awareness? My family wants to get one in honor of our daughter..

Reply »

noreenarshad, 7-03-2010, 2:05PM

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noreenarshad

Damnit, I'm not trying to be negative! Are you people too inconsiderate and bash happy to read what I wrote PROPERLY? I'm being called negative because people (obviously) misunderstood that I simply wrote that it's not surprising that a girl won a contest so under her, regardless of her lack of hair. You don't need hair to be beautiful. Only your soul and natural aura can determine that. You all need to get off your high horses and stop bullying someone who wrote something you thought you were above rethinking, and instead, immediately found a problem with it instead of giving second thought on what I meant. Why would I say something negative about this young lady? I'm only 16 myself and you don't know the pressures I have to take myself! This girl has something most americans have, and in case your wondering, I'm showing signs of premature balding myself, and my own mother is disgusted by my head every time she offers to brush my hair, and insults me! You people are so quick to judge instead of trying to see the good that humans are bestowed with, simply corrupted by thier life experiances! So you don't know me, and you're to inconsiderate and lazy to appreciate the intellectual pursuit of my first post, doesn't mean that I'm negative for trying to clear up what you obviously neglected to check.

Reply »

21Carlos, 7-08-2010, 5:47PM

2.5 stars vote downvote upReport
21Carlos

@noreenarshad.

Buddy, it's time to grow up. The world is an ugly place. Life is hard. And you know what? Life's like a Nintendo game; it gets harder and harder until you die. I read your original post three times to try and understand it. It sounded exactly the same the third time then when I read it the first.

Reply »

Althea, 7-18-2010, 5:31PM

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Althea

To Noreenarshad. You may say that you were not trying to be negative in your first post. But, it sure seemed that way. To me it seems that you are angry. and maybe you are angry at your mother. and not that you want to be. But, maybe writing that post was a way of venting out your angry toward your mom, that you say your mom insults you., She should not be doing that either. It is not your fault for your premature balding. She should be there to help you through this.
I myself starting lossing my hair when I was in 5th grade, completly lost it all in 6th. I am now 38 yrs old. It was in a span of about 3 months. I only wore a sailor cap then. Started wearing wigs after that. Things got harder in high school. Had kids trying to pull off my wig. They just didn't know anything about what was wrong. I really didn't either. Cause doctors really didn't have clue as to why or how this condition happened. Had different treatments from shots to the head to creams. i have never had my hair grow back. I am now Alopecia universalis.
I didn't even know about Kayla Martell until recently.
I just the other week went out of my house hold property in to public with just wearing a bandanna or scarf. Which for me was a big step. But, wearing a wig is my safe haven. Which maybe some day I will brake.
But, please try to talk to your mother about your feelings to toward everything that is going on. Or talk to someone that could help you with your mom. Cause have family support through all this is a big help.

Reply »

noreenarshad, 7-25-2010, 4:55PM

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noreenarshad

Thanks for trying to understand, but that wasn't the point. Mentioning that was to show fellow commentators that she's no different than you and I. If it's so common, why the huge fuss? No one in this world is above the other. I apologize for my passionate writing. But it makes me sick that pagaents are all about beauty. This article makes it sound more like it depended on her looks instead of her inner ebauty, and that's whta upset me the most. That she COULD'VE lost. All because of her exterior. And that shouldn't happen. If only people were like souls without any physical bodies to hold them back, but the human is a jealous and greedy creature, looking for the weak points of his fellow on which his demise will be based on. And we live in this world. There upstanding people who try to be more noble and wary in thier ways, but to the majority, they are simply moths fluttering near an unreachable light. But they are the masses, still in the shadows, idling thier time away. Remember when I said that we're not special? My favorite chorus teacher once said to the entire class, "You're not special. To the world. You are to your parents, and your friends, but for the rest of the room,no one's going to beg you to come up on stage for the Spring concert. If you recieve a failing grade, that's for your own action." And to this day, I understand that being an individual means I have the responsibility to help influence others in a positive way. And just because I barely have enough hair to make a braid anymore, doesn't mean I can be beautiful. I don't have to become involved in a stupid beauty pagaent and have to win. What does that affect? Only my own egotism (which I'm honest enough to point out). I can change anything in the subtlest action, like the guy who found out about Watergate by taking tape off of the doors. The butterfly effect is as fluid as the moon affects the tides. Just one inch, one poke, one scratch can lead to something. Anything. We live in an unfortunate world where the lower senses dominate until the sun shines and we look at our hands saying "What happened last night?". Until then, I'll still stay in the shadows, with my fingers reaching for the sun. I guess I'm just another moth. But I'm happy.

»

jayne, 8-08-2010, 8:42AM

2 stars vote downvote upReport
jayne

check out shmuel-gonen hair treatment on facebook. i have written to him about my alopecia and am awaiting a response its worth a try

Reply »

Miss DE Fan, 12-29-2010, 8:03AM

2 stars vote downvote upReport
Miss DE Fan

Please help Kayla make it into the top 15 at Miss America! Please vote the following ways (4 different ways)



1. Click vote next to Miss Delawares Video at:

http://www.missamerica.org videocontest/contestants/delaware.aspx



2. Text word MADE to 24470



3. go to http://facebook.com/MissAmericaOrganization and put your login and password or sign up if you don't have one. Then click like on Miss America Organization Page, then click Video Contest up top and then scroll down to Miss Delaware, watch video and click "like" Miss Delawares video.



4. go to http://www.youtube.com/missamericaorg Sign into your youtube account or if you don't have one sign up for a free account. Go to search box and type in VOTE FOR MISS DELAWARE 2010 KAYLA MARTELL click on video of Kayla and then double click "Like" (Thumbs up) to vote for her video.



You can vote 1 time per voting method and unlimited text messages.



Thanks for your support!!!!



Miss De Fan

Reply »

 
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