www.alopeciaworld.com
I turned 31 this past summer and it seems like just yesterday I was in 5th grade. 20 years ago was the year that changed my life and set me on a collision course with God!
I was sitting in Mrs. Thorburn’s class in Brookings School. Mrs. Thorburn was an incredible teacher who didn’t put up with nonsense and we got along great because I loved to be the class clown! She was my favorite teacher in 5th grade and that year turned out to be a year I would never forget.
I had semi-long…
ContinueAdded by Alex Gomez on October 4, 2013 at 10:21am — 1 Comment
Hi everyone,
I've just joined and really want to share the things I've found most effective for treating alopecia areata.
1) Go straight to a proper Trichologist. Don't bother with dermatologists as, like G.P's, they tend to just prescribe topical steroids, (which I was uncomfortable using and found to be rubbish)
2) Get your iron level checked. The optimum ferritin level is between 70 and 100, and levels lower than that are associated with fatigue, breathlessness and…
ContinueAdded by Madam mim on October 3, 2013 at 2:30pm — 2 Comments
Hi! I am about to turn 35 years old and after doing some math, realized I have been dealing with AA for 15 years now. It started my freshman year of college - one morning I woke up and most of both my eyebrows had fallen out. I actually didn't really worry too much about it. As time went on, though, the hair on the right side of my head started to recede all along the hairline, along with the right eyebrow. The left side of my head was perfect! This went on for years. I visited doctors and…
ContinueAdded by Mary Anne on October 2, 2013 at 12:00pm — 6 Comments
Hi, everyone,
How do you deal with potential dates? I have tried wearing a wig and hated it, so am now going to try wearing a bandana while trying treatment with Minoxidil.
I believe that one of my potential 'romantic' possibilities has been put off by my alopecia, and I really don't see any future 'possibilities' while my scalp is getting more bald. It annoys me on two counts - (1) - I obviously don't like losing my hair, but (2) on the other hand, I still have more hair than…
ContinueAdded by Anne on October 2, 2013 at 12:22am — 2 Comments
We can live happily without hair if you have someone you love, love is the engine of life, without it we are unhappy even if you have the beauty of Venus and silver Crésus.
Added by Le sage on September 30, 2013 at 8:00am — 1 Comment
Well, one day left in September. Alopecia Awareness Month. Been a good one this year, the Liverpool Alopecia Flashmob went up on Youtube and now over 23K views! Yay!
Added by Laura Adams on September 29, 2013 at 8:30pm — No Comments
Added by VanillaPlum01 on September 29, 2013 at 8:28pm — 6 Comments
Hey, I was just wondering what are some of your favorite sports to watch/play? I myself enjoy playing softball, soccer, volleyball, and football. (With my cousins not legitimate football!!!) I enjoy watching football, wrestling, and baseball.
Added by Jessica Hoschouer on September 29, 2013 at 5:30pm — 3 Comments
Hi There,
I haven't been on hear for ages. What's happening?
Added by Natalie Young on September 28, 2013 at 4:30am — 1 Comment
My daughter is 3yrs old and she has AT, recently she started putting pants on her head pretending its hair and she's telling me that she wants hair- what should I tell her and what is the best way to approach this? I've always told her that some kids have hair and some don't and would show her pictures and videos of kids with Alopecia. I need advice! Help me..
Added by MychildhasAT on September 25, 2013 at 5:30am — 3 Comments
So a few months ago while reading a passage from a gastroenterology textbook, I came across mention of an association between alopecia areata and Celiac's disease. I have had undiagnosed gastrointestinal issues (primarily chronic abdominal pain episodes) and found this interesting. Does anyone here have GI issues as well? Anyone with confirmed diagnosis of Celiac's disease? I just wondered what the actual prevalence of patients with both conditions was.
In my other readings there is…
ContinueI was in the Marine Corps when my first spot appeared it was 1994 so than I thought no big deal I will just shave my head and I did for 18 years I got diagnosed with alopecia in the 90s went through the shots and creams etc. I just recently retired and decided it was time for me to look like a civilian but it wasn't that easy my hair at this point is not falling out yet I just don't have much form the result of being shaved everyday, but my beard on the other hand has patches and circles all…
ContinueAdded by mac on September 24, 2013 at 2:55pm — 4 Comments
My title is actually misleading. My one year anniversary of diagnosis with AA was on Sept 17. But I've stopped letting AA control my life and have been TOO BUSY to post anything! :-) That feels really great to say. A few months ago I would not have been able to say that about myself. I thank the Lord above for giving me strength and confidence to get through this. I don't remember the day I decided to shave my head, but it was the best decision I have made so far. I am hopeful that my hair…
ContinueAdded by Sierra D on September 24, 2013 at 12:00pm — No Comments
Hi,
I thought I would try to order a wig online since I don't have many options for purchasing one at a store in my area. I placed an order with a website and never received the wig. I have been looking at other sites but am hesitant. I am not ready to go for the custom wig yet...still holding out hope that I am going to regrow. Any suggestions for a reputable site where I can find human hair full lace wigs at reasonable prices? Thanks.
Stephanie
Added by Stephanie on September 23, 2013 at 10:37pm — 5 Comments
I am having trouble with posting in the forums section and thought I would try here instead.
My question: Is it possible to successfully color the white regrowth?
In the past I have only tried Henna and it made my white hairs turn yellow, hence looking more obvious than the white regrowth. I have a large patch at the top of my head up front which has been preventing me from cutting bangs since I need every hair on my head to cover up missing patches at the moment. I use…
ContinueAdded by Georgie on September 21, 2013 at 2:51pm — 6 Comments
Added by Mayo on September 20, 2013 at 1:39am — 17 Comments
I have "worn" hair for many years. My pieces are custom made and I use tape to secure them. I take it off every 7-10 days to clean and put on new tape. I want the freedom to wear pretty scarves and to feel the wind on my head again. I went several weeks without wearing hair and was shocked how many people asked me if I was battling cancer. I have not had eye leashes or eyebrows for many years, I suppose this makes me look like I am going through chemo to some folks. I wear trendy clothes,…
ContinueAdded by Vicki V on September 18, 2013 at 5:02pm — 1 Comment
First of all i wanna say that this is my first post on alopeciaworld. I am a part of this community only a few weeks now and while reading lots of posts and responses for the first time i felt like i am not alone.
Since i never met a person with alopecia i always thought than no one can know how i feel and how hard and sometimes frustrating it is to go out in the world with alopecia. Lots of times in these 6 years of battle with alopecia my family and friends told me that it is only…
Added by Jack Sparrow on September 17, 2013 at 6:30pm — 13 Comments
today I woke up with so much more confidence. I went to school and at lunch someone asked me why I don't wear my hair down anymore. I told them the honest reason. After I told them I felt 10 times better. if they have to say something they can this is me and this is who I am nobody can every change that.
Added by Ashley ingordino on September 17, 2013 at 3:00pm — 3 Comments
Added by Ashley ingordino on September 15, 2013 at 6:19pm — 7 Comments
2024
2023
2022
2021
2020
2019
2018
2017
2016
2015
2014
2013
2012
2011
2010
2009
2008
1999
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