Featured Blog Posts – February 2011 Archive (59)

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New to Alopecia World...first blog ever :-)

Hello to everyone out there. I am a very new member of Alopecia world, I can't believe I only just discovered this place! I have had Alopecia since I was three years old, just small patches that would grow back and then fall out somewhere else.

I guess its been getting slowly worse over a few years, but particularly so in the last 9months. I've gone from having some large patches of hair loss, to only having a few patches of hair left. This was winter last year, so I just wore beannies… Continue

Added by Sarah Peters on February 9, 2011 at 2:22am — 3 Comments

Great month!

I am super excited! I started treatment for my Alopecia about a week ago. There isn't a gaurntee that it will work but just thinking about having braids again makes me so happy I have tears in my eyes. There are many friends that tell me they like what I look like without my hair but I I had thick red curls and looked like I was actually my grandmothers child because she has the same red hair. The shots are somewhat bothersome but I hope in the end it is worth it.



Something else… Continue

Added by Natasha Gehrke on February 8, 2011 at 11:49pm — 1 Comment

Rough Day

I saw this on postsecret.com. Pretty much describes my day. Some days you just can't win, but this made me feel a little better. (And for anyone who doesn't know what Post Secret is, I would strongly suggest you check out the website and see what it's all about.)…



Continue

Added by Alex on February 8, 2011 at 5:22pm — 1 Comment

Who is this bald woman singing and dancing with Prince at Madison Square Garden?

Beginning at about 1:30 in this video (after Prince kicks Kim Kardashian off stage), there appears to be a bald woman in a costume singing and dancing with him. Does anyone know who the heck she is, if this is indeed a woman?

https://www.youtube.com/watch?v=6-Wrs5Whx6w&feature=player_embedded#

Added by Mary on February 8, 2011 at 3:45pm — 11 Comments

Well, that wasn't very nice

So as I said in my past blog, my hair is gone again. People at my job for the most part all know I have Alopecia, I can't give it to them, and I don't hide my head under scarves and hats and wigs, its just not me. I'm comfortable with myself and the way I look...so anyways I work in the mailroom of a large government building, so I see lots of people a day. This guy from our IT department, that I see a LOT since hes 2 offices down from me and is always shipping computer equipment, came in and… Continue

Added by Tamara on February 8, 2011 at 1:00pm — 17 Comments

Some people are sooo rude and ignorant!

I have had alopecia for 13 years. This weekend I went out with some friends and this "lady" was like "Where is all of your hair?", from across the bar so everyone could hear her. I was really embarrassed because in 13 years I've never had anyone be so blatantly rude. Even the people sitting next to her looked at her like she should shut the !.&@ up.

The worst part is she went on to talk about how she was married to a guy who hand alopecia for ten years. I can only assume he left her… Continue

Added by Paul DeMars on February 7, 2011 at 1:59pm — 13 Comments

Bald again...Bald again

So if you saw my last blog post, I had this lovely re-growth going on, only 1 or 2 bald spots, I was quite excited. WELL...fast forward to last week and I found a few more. I was kind of upset, but said 'Oh well, luckily my hair is only an inch long, not to the middle of my back like last time'. It was all different lengths, and it looked like I let my 1 year old niece cut my hair. So I pulled out the buzzers and did the 1/2 inch guard. BIG mistake! I found so many more bald spots that were… Continue

Added by Tamara on February 7, 2011 at 10:23am — 7 Comments

Je suis chauve :D

For one of my school subjects, I do french. The course is by distance, so I've never seen my teacher, though we talk on the phone. One of the units, we learn how to discribe people, or ourselves, in french. For the last year I have written "mes cheveux sont teints en rouge" - my hair is dyed red, which my wig is. The other day I finally did it. My workbook now says "Je suis chauve. Je vais l'alopecia." It seems a silly thing to be so excited about, but it feels really great. Something about… Continue

Added by Georgia Gardner on February 6, 2011 at 2:45am — 1 Comment

The 24 month update

Well its been almost 2 years since i spotted my first patch (on my beard), still havent come to terms with it, still wearing a hat everyday, still staying indoors as much as possible, and still praying someone will find a cure for this awfull disease.



i have had some regrowth over the last 6 months but still getting new patches, although i do have more hair than i did 6 months ago. i know cos ive took 100s of photos and im constantly comparing them!



i feel like ive wasted… Continue

Added by Shane Beard on February 5, 2011 at 9:51pm — 7 Comments

First wig consultation today

Well,

It didn't go exactly as planned.

I absolutely loved this place, the guy helping me, and hair he had...but definitely not his prices. He measured me, got the color I wanted, I was actually feeling ok for once about all this...then slapped me with a $4,000 bill. I caught my breath, then told him I had to hold off. I couldn't even sell my car for that if I wanted. =/

My insurance offered to pay for $100 worth of it which really doesn't help. As discouraged as it made me, I… Continue

Added by Lindsay on February 5, 2011 at 9:20pm — 8 Comments

My Hairstory

Once I had this head of hair.

It had curls and waves

And required no care.



“How Lucky you are,” I was often told.

To have such hair,

Lovely to behold.



One day my thick hair felt thinner and light.

On closer look there were patches,

With no hair in sight.



My hair! My hair!

Where did it go? What did I do?

This is not fair!



I tried to stop it, to keep there.

I had shots and treatments.

I’d do anything to… Continue

Added by Brenda B on February 5, 2011 at 10:35am — 2 Comments

Recently diagnosed with AA and depressed

Hi ladies and gentlemen I'm Sarah I'm a 24 y/o single mum of one. I've been recently been diagnosed with AA so far I've found 2 patches on my head I've not come to terms with AA yet and like many of you might say it may take some time in getting use to. I've been so depressed since Tuesday(when my doc said I've got AA) I don't know if I'm coming or going I have told my friends on Facebook and I've had some good words my daughter's dad has been helping me to come to terms with it and he's the… Continue

Added by Sarah Niker-Fleming on February 5, 2011 at 6:45am — 7 Comments

Trying to get a grip on AA

Hi everyone, I am new to the Alopecia world and was diagnosied last June with Alopecia Areata. It was such a shock when my daughter noticed the patch about the size of a quarter on the left side of my head...there were tears and alot of fears. Some weeks later after batteling with my GP I got to see a derm, within minutes he had me diagnosed with AA, but by this time that small quarter patch was nearly the left side of my head...and a few other small patches. I did the basic treatment with… Continue

Added by Jill Wolfe on February 3, 2011 at 2:17pm — 3 Comments

A turning point?

I wore my hair down (as in not in a ponytail with tons of hairspray and grips) to the office the other day, and with no hair piece. I had to scrape back the top a bit and grip that back so it offered a bit more cover on the back. I was really worried as it felt so thin on the back, but my colleague (who has seen my hairloss from the worst period) assured me it was fine.



I've also booked in to a normal hair salon to have my haircut before my holiday to Tenerife, rather than going and… Continue

Added by Rachel on February 3, 2011 at 1:25pm — No Comments

New, scared and need YOUR opinion

Hi Ladies (and men)-



My name is Jennifer and I’ve recently been diagnosed with androgenic alopecia. I just turned 30, I’m single, and horrified. I’ve noticed my hair falling out off and on for about 5 years now. I figured it was stress since the shedding seemed to coincide with major stressors in my life (several moves to different states, grad school, family problems etc). The last 6 months it’s gotten significantly worse, my scalp is showing and I’m obsessed with wearing my hair in… Continue

Added by Jennifer Schlueter on February 3, 2011 at 1:42am — 5 Comments

Love

I have been in several realtinships since my alopecia took all my hair. I was always worried that no one would love me because of how I looked. Many of the relationships I was in left me feeling less than confident. No man ever really made me feel beautiful. For the longest time I thought that my alopecia would stop me from finding true love, a man I could stay with and who would make me feel beautiful when he looked at me. My mother was in the hospital and her nurse has alopecia. I never met… Continue

Added by Natasha Gehrke on February 2, 2011 at 1:52am — 10 Comments

Hardest thing I've ever been through

Alopecia started for me last year,at the age of 31. I had long blond hair and it started to fall out. I found handfuls of it on my clothes,on my hands when i washed it, cloged up drains,and i had bald spots that were getting bigger and bigger.Eventually i started wearing a hat cuz of the spots and hair started growing back while the other was falling out so i had new hair when the last bit fell out. So now i wear a knit hat but i have some new hair on the back , top and sides. I have lost my… Continue

Added by Amanda kay o'neal on February 1, 2011 at 12:30pm — 11 Comments

Questions!

hey everyone my name is Kaeleigh and i've been with my boyfriend Joe for 4 years now and he lives with me. This July he turned 21 and has never had or heard of anyone in his family with alopecia, to be honest we both have never even heard of it. Come November.. December 2010 his beard had a bold spot right in the middle of his chin and then come January 2011 he got his hair cut and it looked like the barber butchered the back of his head but as the days went on the top of his head started… Continue

Added by Kaeleigh Bialko on February 1, 2011 at 11:00am — 5 Comments

May I tell your stories?

Students in their final year of high school in Australia sit the HSC. Drama students are required to present an individual project In my case, a performance.

I've never really publicly dealt with my alopecia and am in the process of designing a dramatic piece to deal about my own feelings and what it is to be an alopecian.

As part of this, I was wondering if anyone would be willing to tell me their alopecia story, or a story from their life relating to their alopecia. I wish to… Continue

Added by Georgia Gardner on February 1, 2011 at 12:00am — 6 Comments

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