www.alopeciaworld.com
I hate the way I look sometimes. I look in the mirror and think ugly. I do wear a wig, and I can't decide if it is the alopecia that is indirectly making me feel bad, or just a natural female thing to do. I sometimes see myself in my wig and think I look like someone in drag, I don't know if I see the wig for what it is, fake, but I see beyond the wig and look at my face and hate it...
I look at my body and this is something I can control yet I seem out of control and just see myself…
ContinueAdded by KFlame on May 11, 2013 at 6:00pm — 11 Comments
Well i have not been on here for a while. Nor have i made one of these for a long time. So lets just start by saying if you do not want to be depressed or feel bad then you might not want to read this. There are many things in one's life that people cant change and Alopecia is one of them. Many people on this site find happiness. Many people on other sites find happiness. What happened to me wasn't because of this site. Ever since i was a kid i had Alopecia. Doctors told my parents that my…
ContinueAdded by T on May 11, 2013 at 3:30pm — 10 Comments
Granddaughter is having a hard time when other people come to her and tell her they are sorry that she is going though cancer. She also had a lady come up to her and say to her "isn't that a wig?" And then she pulled it off her head. It was in a mall! This devastated my 11 yr old gd and she left the mall.
What would you do?
Added by grandma concerns on May 11, 2013 at 12:22pm — 14 Comments
Everytime I talk to mom about my state, she goes like "why are doing this to me? Why are you making me suffer so bad?" But I am not making her suffer, I just don't know why is she thinking like this, ever since my father had died two years ago, she started acting so nervous and putting blame on me having this disease... She has this weird thought that I am making my hair fall on purpose to get her attention and to make her suffer. I just don't see the point in this, instead of feeling less…
ContinueAdded by Yuri Kim on May 8, 2013 at 5:00am — 19 Comments
I had these grand plans to get my hair to grow and I have failed at it.I've watched as these spots have roamed around to different areas. Now \\I'm beginning to see patches on legs and on my arms. Iguess I just have to accept this. My depression in not complete and i have left work, not wanting to venture out of my home.people hear have been so cruel.What do we have left? what do i have left anymore? I am such pit of depression that i acnt get myself out of.
Added by michael on May 8, 2013 at 1:00am — 4 Comments
Today was the first day that I ventured out without a hat or wig. Enjoyed wandering through our local garden store and gift shop and then dining at a Mexican restaurant. I received the courage to do this after reading "Boldly Bald Women" by Pam Fitros. Although I have suffered with Alopecia Areata for many years, I only recently lost all my hair to AU. It has been a tough adjustment but have had wonderful encouragement from family and friends.
New to Alopecia World, but thankful for…
ContinueAdded by Janet on May 8, 2013 at 12:30am — 6 Comments
I have had Alopecia for over 20 years, since I was a little girl. So I consider myself a "seasoned veteran" of this disease. For the most part I'm pretty use to it. The unpredictable nature, wearing wigs, the occasional explanation to someone, etc. However, one thing that had always given me anxiety was dating with my alopecia.
I thought that would never be an issue again once I got married, however I find myself back in the dating world and the anxiety is right there with it. Not…
ContinueAdded by Dame on May 6, 2013 at 11:30am — 42 Comments
Last night on Jay Leno he did a bit about why products at the 99 cent store might be 99 cents. He showed a "fashion doll", somewhat like a Barbie, and after he opened it, showed why it was only 99 cents.
The doll only had long hair around the outline of its scalp, and was otherwise bald. He joked perhaps one could do a Donald Trump comb over...the usual yuks.
Then he stated "Maybe its an Alopecia doll I don't know".
I found this incredibly insensitive and insulting. I…
ContinueAdded by Mary on May 4, 2013 at 2:00pm — 7 Comments
Hi!
I've had AA since I was six but recently I've started losing hair all over my body, including my eyelashes and eyebrows. You can't really notice that my eyelashes are falling yet, I think, and I use eyeshadow to fill in my eyebrows but I'm scared it's going to get worse and won't know what to do... What do those of you who have no eyebrows or eyelashes do to conceal this hair loss? I would love to get some advice :) Thank you!
Added by CMF on May 2, 2013 at 12:22pm — 14 Comments
Added by Adam L on April 27, 2013 at 10:00pm — 3 Comments
Well. I'm not sure where to start. Basically I had AA on and off since I was 4 years old. At 12 I finally decided that the PUVA treatments and the high dosage of steroids were breaking me down so I just lost all of my scalp hair and have been bald ever since! Middle and high school were definitely the worst, the kids were beyond horrible. Which had lead to my major self esteem issues, which I'm sure all of us have battled with.
During my junior year in HS I started having major…
Hi all, Been awhile since I posted, but finally accepted having no hair only took a year....yeah go me, but now I am looking for a new Job as my Job is being made redundant and I have an interview on Monday but don't know how to address the Alopecia thing my current work place was accepting but the idea of having to make new employers understand is hard, Just wondering does anyone have a booklet or a letter they have attached to there resume's or given out that explains it, something that…
ContinueAdded by Cassandra on April 26, 2013 at 6:00am — 13 Comments
Tomorrow I am going to start a new routine of natural vitamin supplements A-E, a shampoo with zinc, daily scalp massages, rogaine twice a day and yoga and meditation classes because i believe that stress plays a major role in this disease. I so tired of my doctor dismissing every alternative as inconsequencial. It's my hair thats falling out not his. I'm not going to take this lying down anymore! I'm not going down without a fight. I'm naturally high strung and vociferous, so that will be a…
ContinueAdded by michael on April 25, 2013 at 11:00pm — 4 Comments
Pleased to discover this fine forum. My male partner began having mild alopecia last fall at the age of 55, starting off with a bare patch on his chin. This spread to make a larger area, then we noticed a few bare patches on the back and sides of his head. He has quite dark, short hair and I have noticed that some small bald areas have been slowly growing back though now grey or very light hair. His regular visit to get his hair trimmed became uncomfortable as he was very conscious of others…
ContinueAdded by Sheila on April 21, 2013 at 7:56pm — No Comments
Added by Trish on April 21, 2013 at 1:34am — 3 Comments
I've been reading about it and I am curious, has anyone here tried this diet and if so, would you recommend it? I am considering ordering the guide and trying it out, but I would hate to waste my money on something that doesn't work.
Added by Braya on April 16, 2013 at 7:00pm — 2 Comments
So I have had alopecia areata since I was two. I have always had somewhat of long thin hair with little patches that nobody ever noticed. I decided to get hair extensions last year which pulled out about 40% percent of my hair but not all of it.Last month I had a fight with my best friend and all my hair fell out.I wear a wig now(im only 13)and its really tough. I have never talked to anyone with this disease who is my age and I hope I can meet someone who does:)thanks
Added by madison on April 15, 2013 at 7:00pm — 19 Comments
To basically start, I was diagnosed with Alopecia when I was 10 years old. At the time I was just a kid and had no idea how rude and mean people could be at the time. Had no friends until High School because kids wanted to poke fun and be ignorant, this was when Alopecia was not as known back then. Long story short some hair came back but never all the way, in High school continuing on to now I have such amazing people in my life and never thought about my hair loss to much. It became who I…
ContinueAdded by Brian40below on April 15, 2013 at 4:30pm — 1 Comment
All my hair fell out whilst on vacation last September,from having a full head of dark brown hair (not great hair mediocre at best but all mine)to nothing and have subsequently found out it ain't coming back.
So after a good cry I decided only to look at the positives of this.
A three minute shower means 20 more minutes of sleep,No misbehaving to sit staring at oneself in salon mirrors whilst having hair styled
(HA) legs & other body parts no longer have to be…
Added by Gemma on April 14, 2013 at 7:34pm — 8 Comments
2024
2023
2022
2020
2017
2016
2015
2013
2012
2011
2010
2009
2008
Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.
© 2024 Created by Alopecia World. Powered by