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I had been bonding for 3 years and just recently noticed that when I detach/reattach I no longer have to shave the top of my head. I always thought that one day, maybe when I retire I'd stop wearing hair and just cut my hair really short like Annie…
Added by Bridgid Weber on April 28, 2015 at 10:30pm — 1 Comment
Hello,
I live in Phoenix Arizona and I'm searching for an opportunity to become more involved in the Alopecia community here in AZ. I have had a very positive experience growing up with Alopecia and I want to share my experiences with others in my community. I have developed a way of thinking that I think may benefit someone struggling with Alopecia, male or female. I can even share some of my experiences with anyone who wants to hear them. I would love to at least be someone…
ContinueJUST SOME WORDS
Don't wanna be the victim,
Don't wanna play the part,
My false sense of self is tearing me apart.
I'm done telling myself lies
I'm done hearing myself cry,
The way i lived my past wont be the way that I die.
I didn't waste those years for nothing,
I didn't give'em away for free,
the things I've hated about myself,
they aren't really me.
I guess I did it to see how bad it hurt,
I guess I lit it to see how bad it…
Added by Leif Rautenbach Bridgman on April 27, 2015 at 3:34am — 1 Comment
Hi, I am wondering if any of you are using Rogaine 5% foam, or have used it. I am about to start and looking for information on technique, success and possible side effects.
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AW Related Discussions: http://www.alopeciaworld.com/forum/topic/search?q=Rogaine
Added by yukonalopecia on April 24, 2015 at 11:30am — 2 Comments
For women leaving in India, with Aelopecia very much problematic.
there is no awareness about this disease. we want to form some foundation who support n help the aelopecia people. it is need of people like us, who leaving with aelopecia.I request all people here to help us n guide us, what to do???
n i request all Indian with aelopecia who is member of this group, please come together n co operate in this work.
Added by ketaki on April 23, 2015 at 6:16am — No Comments
I am a high school teacher along with running my business. In high school, I teach some tough kids, the kids that don't love school, the ones that have many other issues that make school seem meaningless and the kids that teach me everyday in one way or another. I love both my jobs.
I decided to share my story about my hair loss with my students this year and with my high school volleyball team that I coach. The result was complete understanding and empathy from all of the students.…
ContinueAdded by Jennifer Krahn on April 17, 2015 at 7:30pm — 12 Comments
Added by Alta on April 14, 2015 at 9:09am — 4 Comments
Added by Alta on April 11, 2015 at 11:42am — 6 Comments
Added by Natasha on April 7, 2015 at 3:46pm — 6 Comments
Does anyone know how long they last for, how many years?
Added by sarah bradley on April 7, 2015 at 7:30am — 3 Comments
So I have read the horror stories on here about what happened when someone had informed their significant other about their alopecia. Since 2008, I have been inflicted with AA and having really done much dating until recently. I have been wearing wigs and sometimes it gets rough and frustrating due to some of the constant pain wigs can create
Well now I find myself in a weird and unfamiliar place. I am currently dating a great guy who seems to be genuinely into me. He has questioned…
ContinueAdded by Dedi on April 6, 2015 at 7:30pm — 32 Comments
Hello,my name is Scott,I am the father of a 10 year old girl recently diagnosed with AA. It all started roughly 7-8 months ago. My wife Annabell and I found a small quarter sized bald patch on my daughters head.My daughter,Railyn,already knew of the spot on her head however,she was scare to come to us. She is at the point now,where she has lost almost 50% of her hair,even more possibly.
I'd like to add that Railyn has allergies too milk,eggs and peanuts,among others,milk being a…
ContinueAdded by pippinrox on April 3, 2015 at 11:33am — 5 Comments
A question for those of you that have taken the shots to treat the AA. My personal physician diagnosed my alopecia areta and said one of the possible treatments is shot in the bald patches. I took the shots in the (at that time) area with no hair. That was one of the most painful and unpleasant experiences I have ever had. My question is, when you took the shots was it extremely painful or was that because a primary care physician did the work and not a dermatologist?
Added by Dark Wolf on March 30, 2015 at 7:50am — 16 Comments
I have the glamorous and degrading ALOPECIA AREATA, a condition which causes my hair to fall out in copious amounts when I'm under stress. I've wrestled with this disease since the age of ten, when the boy I like in primary school noted that I have a ,"funny bald patch," on the crown of my head. About the size of a quarter, this was just the beginning of my so far, twelve year battle with my so called, 'Curse.'
Its wrong to call it that and right now in my more mature state I refer to…
ContinueSo I just started a new job about 6 months ago at a popular chain book store and in the first few months of working there I just went as what I think of as "myself" just a shaved head. (androgenous alopecia) In those few months I got numerous women coming up to me and asking if I was going through chemotherapy. Some simply just smiled sympathetically at me and said they would pray for me.
One woman who happens to be a regular customer automatically thought I had cancer and skipped…
ContinueAdded by Nicola on March 22, 2015 at 1:51pm — 8 Comments
My name is Jennifer. My daughter Madison is a happy, joyful, beautiful 5 year old. Right at the end of October, while washing her hair, I noticed two small bald spots, just about the size of erasers. My first though was, maybe it was fungal. We had had a bought of ringworm the month before. But, after using fungal cream for a week, it was getting worse. So off we went to the pediatrician. The doctor looked at it and said almost immediately that it was alopecia. I had that word floating in my…
ContinueAdded by Jenkatie27 on March 21, 2015 at 8:06pm — 4 Comments
I'm not too sure exactly when my hair started falling out. I noticed it around December of 2014. Interestingly enough, much of my hair is also turning white. I'm in my 60s so white is not a problem. Anyway, I realized that both of these issues came about after I had surgery. I've heard that surgery can cause your hair to turn white I'm just curious is anyone's alopecia started after a traumatic event?
Added by Dark Wolf on March 20, 2015 at 5:51am — 3 Comments
Added by Barbara on March 18, 2015 at 10:01pm — 10 Comments
I'm not sure why I was so blindsided by the question. I mean, I know it has been asked before of women who lack hair, and this was just the person to be asking it, a wide-eyed, blonde-bobbed young girl who was also waiting in line to use the bathroom at the campground. I replied a cheery, "Yes, I am," and that was that. Only it really wasn't because I am still upset by it.
I was having a fine weekend, my sense of self confidence bolstered by my 9 year old's birthday party at a…
ContinueAdded by GardenJess on March 15, 2015 at 5:14pm — 3 Comments
Im writing a lot this weekend because I went to the dentist and had two teeth removed and typical, end up with a dry socket. The pain is something else. So im trying to distract myself.
Here goes a recent picture of my hair, well scalp..you can see clearly new hair growth and where it is and isn't coming through.…
ContinueAdded by Mjay on March 14, 2015 at 8:32pm — 2 Comments
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