Wednesday 28 September 2011
Dear Diary,
It has been great since i have been getting all the support i need form Mrs Careswell and Miss Ballentine. Im glad that some of my friends are learning to accept me for who i am.
3 Reasons why i like being bald.
1. I can take my wig off when it gets hot
2. I can have any type of hair i want
3. It has changed me.
Im scared that i will never get a boyfriend because of my wig. I think that no one…
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Added by Lucky1000 on September 28, 2011 at 12:52am —
5 Comments
So I almost got denied entrance to a club in Russia the other day because of a thing called face control. I've got 3 girls with me, diamonds on my wrist, dressed to the T with a US passport. The bouncer takes one look at me and says sorry buddy I can't let you in because of FACE CONTROL. After he realized the girls weren't coming in without me, and a harsh look from my girlfriend to some other people sitting there, probably the admins. They waved me into the club. What a putz, the bouncer was.…
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Added by Alex on September 27, 2011 at 5:30pm —
5 Comments
hi im new on this site,i came across it by accident while googling alopicia. iv developed alopicia areata while i was halfway through my 3rd pregnancy,the 2 patches fully grew back after a year but now im geting more patches appearing. i have had a pretty stressfull life over the last year or so and im wondering if the patches have came from the stress or if they just hapened to arrive at the same time.
has anyone else had alopicia that they think has arrived from stress directly? any…
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Added by laura on September 27, 2011 at 11:00am —
3 Comments
Hello and WOW! I discovered this site purely by accident and have spent some time reading through so many brave peoples stories. My name is Leon , from Cape Town ,South Africa and am the only person (up and until now) who I knew had this curse/blessing.Well obviously I know others have it but have never heard or read their stories.So thank you for this place to share. I refer to it as both blessing and curse because while it surely did affect me as a child ( since 13) and I had to fight my way…
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Added by LeonJ on September 27, 2011 at 8:30am —
2 Comments
I lost most of my hair end of February beginning of March of this year, 2011. In the past month I have begun to lose my eyebrows. I am losing them at break-neck speed. Its incredible. When I go out,when I have a gig (I'm a musician) I have to beef them up, pencil/draw in.
I'm finding it incredible how fast they're going. Anyone out there have any info on if they grow back? I didn't think I'd lose them because they stayed intact. All part of the disease. I've learned to pencil in well…
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Added by Lili Añel (aka Eulalia) on September 26, 2011 at 2:00pm —
2 Comments
Anyone out there wear a freedom wig or vacuum piece that still has hair to shave? I would love to wear something that I don't have to glue/tape but am worried that regrowth will compromise the vacuum.
Added by Beemarie on September 26, 2011 at 11:00am —
2 Comments
A few days ago, I confided in the members of my fellow worship team at church about my Alopecia, and they could not have been more supportive. What really touched my heart so deeply was how God managed to take care of the things that concerned me the most, people's reactions. The worship leader of the church instructed the members of the choir that if anyone in the church asks what is wrong with me, they should respond, "God is healing her", and that nothing else should be mentioned. Everyone…
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Added by Elizabeth on September 24, 2011 at 11:30pm —
No Comments
Thanks for finally making a wig with some nice length to it in a
PETITE cap size. The Chantel is SO my new favorite hair!! Frames my face well, I think.
Chantel Wig
Added by Laura Adams on September 24, 2011 at 1:09am —
No Comments
A few days ago, as I was combing my hair, tears started to fill my eyes, because I saw the strands of hair again, getting tangled up in my comb, and also littering my bedroom floor. It's hard not to get angry at even my hair strands for falling out. My hair piece gets the best treatment, I lovingly run my fingers through it's strands, while my God given hair, get's tossed around, without any attention. I have realized that I've let Alopecia make me a bitter woman. A friend of mine, while I was…
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Added by Elizabeth on September 23, 2011 at 10:30pm —
8 Comments
It has been several years since I posted. I check in once a month because it reminds me that I am not alone. I have worn wigs or weaves full time for the last two to three years. I finally shaved my head today and that is why I am posting. It feels freeing but I am not ready to let the world see me like this and don't know that I ever will. Even though I have come along way I am not there yet. I must say that I am grateful that there are so many options for women with this condition. I have…
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Added by Diane Holland on September 23, 2011 at 10:00pm —
2 Comments
Do you think support groups are helpful and what do you expect of them?
Added by PC on September 23, 2011 at 1:00am —
2 Comments
Hi, I’m Diane. Well, I’m slowly coming to terms with my Alopecia. I have Alopecia Areata with 3 bald spots. I’ve decided that I will probably never be able to accept going bald and I will never be one of you brave woman that go without a wig. I could never see myself as pretty or beautiful without my hair! My best friends and I used to joke all the time about me being vain and about how my hair always had to look perfect (even in a rainstorm or water park LOL). Now I would be happy to have a…
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Added by FANCY1024 on September 22, 2011 at 10:30pm —
6 Comments
Just when I think I'm getting somewhere - that I'm ok with this losing hair malarky, I'm over being upset, life goes on, I've accepted it now, etc etc - it seems another bout of anguish comes from no where!
I hadn't cried for ages - even when I realised just recently that during my blissful mini break from obsessive daily checking (while I'd happily convinced myself that having just one bald patch meant I must only have a mild case of alopecia, and therefore it would all be over and…
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Added by AJ on September 22, 2011 at 7:30pm —
6 Comments
Today I am bad, both months, a new disease adds in the others, since June it is a sarcoidose and the syndrome of laufgren I have not realized my alopecia, then the other disease yet moreover, I cannot it any more, my morale is in zero, I find help(assistant) or nobody who is in the same situation as me how make you? To have the air(sight) so happy in spite of the disease:-(
Added by coccinelle on September 22, 2011 at 8:16am —
No Comments
I'm a 24 yr old Indian guy with AA. It's been 2.5 months since I discovered and frankly it's been hell.
I'm a part-time writer (besides being a software engineer in Bangalore) and writing about my experience with alopecia has been almost therapeutic.
Here's my blog.. Comments and feedback are very much welcome.. :)
http://alopecia-anonymous.blogspot.com/
Added by Nachiketa Sanyal on September 22, 2011 at 8:06am —
5 Comments
Hello! I have alopecia areata and right now what's left of my hair is a sort of mohawk!
I am curious though, have any other alopecians experienced hair loss like me? It started around my ears and gradually progressed upwards and around the back.
Added by Amy on September 22, 2011 at 5:30am —
3 Comments
THERE was once a bald man who sat down after work on a hot summer's day. A fly came up and kept buzzing about his bald pate, and stinging him from time to time. The man aimed a blow at his little enemy, but — whack — his palm came on his head instead. Again the fly tormented him, but this time the man was wiser and said:
"You will only injure yourself if you take notice of despicable enemies."
SOURCE: Æsop.(Sixth century B.C.)…
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Added by rj, Co-founder on September 22, 2011 at 4:30am —
1 Comment
Today I took a big step, in my battle with self esteem, something that Androgenetic Alopecia has robbed me of having...I went to choir practice and I left my wig( Hannah, I name everything, lol)at home. I did this, because I wanted to give the Devil notice that my wig and my Alopecia, does not dictate the person that I am. Let me explain...Ever since I purchased my wig 2-3 years ago, it has been my life support. I have used it as a crutch. I have allowed the wig to have power over my thoughts…
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Added by Elizabeth on September 22, 2011 at 12:00am —
4 Comments
I am continually impressed by members' willingness to share their struggles, triumphs and insights -- especially since it takes real courage not only to reach out for help, but to also reach back with help.
I see this all the time in Alopecia World and, trust me, I realize as much as anyone that it's this very kind of openness that makes our beloved community so strong and appealing to alopecians from all over the world.
I could never thank each of you enough…
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Added by rj, Co-founder on September 21, 2011 at 8:30pm —
9 Comments
Dear Member,
Thanks to new feature called "Quick Add," you can now update your status and post other new content from any page on Alopecia World.
To do so, you only need to click the plus sign (+) next to the "Share" button in the "Latest Activity" feed that now appears on every page of the site.
You can quickly post status updates as well as new blogs, photos, videos, discussions, events, and music.
Add a check to the Facebook or Twitter box to notify your…
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Added by Alopecia World on September 21, 2011 at 4:30pm —
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