Female Pattern Baldness

Join today to meet, support and share information with others who are living with female pattern baldness.

Introducing myself, and interested in stories of your hair loss.

Hi ladies. I wanted to write and introduce myself in hopes of making some new friends and finding some support. I am new to this FPB diagnosis and to participating in forums, and I still feel a bit shy about being open with my feeling about hair loss, but I thought I would give this a shot.

The recent official diagnosis of my androgenic alopecia has thrown me for a loop and there have been bouts of crying, depression, and lots of self pity over the past couple of months, but otherwise I would consider myself a happy and generally upbeat person. I love to cook, eat, and sew vintage dresses. I work in fundraising. I am married to a wonderful man and together we travel and explore when and where we can. More than a great head of hair, someday I would like a dog, a house with a cozy kitchen, lots of vintage clothing, and time to bake every day.

My hair loss story began when I was 21. I studied abroad in Ireland, where I boldly got a very short haircut (think Felicity) with my curly locks. Well, being abroad was lonely for me and by the time it was over I had developed my first and only severe bout of depression in my life. With the sadness, I started worrying about my short haircut because I could see my scalp and worried my hair was thinning. But... of course everyone (including myself) thought this fixation on thinning hair was a byproduct of my depression and anxiety.

Well, the anxiety and depression self corrected after a few months back home, but the fear about my thinning hair has never entirely dissipated. During times of stress I always ended up at the bathroom mirror inspecting my hairline, and I swear finding evidence of thinning. However, my loved ones and husband always saw my concern as a remnant of that sad period of my life and assured me I was stone cold crazy to worry. "You're fine" they would say. "You have plenty of hair" was the common response. And so I would put the worry to rest, temporarily.

But this summer a hairdresser in my hometown was styling my hair for the first time in four or five years, and she gently asked me if I had noticed the change in hair texture on the top and sides of my head. My heart sunk, and upon further inspection with a hand mirror I realized that indeed, my hair is thinning all over and especially on top. Yikes!

Now, 7 years after my official worries about thin hair, I have been officially diagnosed with androgenic alopecia (the dreaded female pattern baldness!) by two dermatologists, and the loss is visible even to those loved ones who always denied my worries. In some ways it is a bit of a relief to hear the diagnosis, as now I know I was not crazy with anxiety all these years. And in trying to find the bright side, I admit that if I had to choose between a chemical imbalance in my brain or a chemical imbalance in my hair follicles, I choose the follicles every time!

I am in the first months of the official diagnosis and just starting to come to terms with the full realization that my head of hair is a temporal state. I find myself wavering between feeling comfortable and confident in my ability to handle this situation with grace, and absolutely sick to my stomach and stricken with fear about the ways this condition might affect my life and my dreams and my relationships and my overall happiness.

As I mentioned, I feel shy and a bit awkward with this right now, but I look forward to easing myself into the forum and the FPB group. I plan on learning from others' experiences, sharing my own, and hopefully becoming more and more confident in my own strength, beauty, and worth with or without hair.

I would love to hear from some of you, just to know your stories and where you are at with your diagnosis (I don't know, for us with FPB do we consider it a "condition" or a "disease" or just a "cosmetic inconvenience"...? I have no idea!). I have lots of questions to bring to discussion and the forum and I look forward to getting to know you. Thanks!
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    Marie

    Hi. Thanks for sharing. Sharing and support are what we are all about at Alopecia World. Everyone ages differently, and for many women Androgenic Alopecia is just one of those things that come as they get older. Although it changes how a person looks and feels, and it can be horribly devastating, it's no more "unnatural" than deep wrinkles and sagging butts. In my early 40s, I realized my hair was more than just a little thin when I saw a photo taken with a flash. The light reflected off my scalp and I saw how truly exposed I was. I was shocked!!! No one else thought it was a problem, but I was horrified. I became depressed and obsessed. But, eventually, in order to stop the madness and get my life back, I had to accept it, so I started wearing wigs. Do people know I wear wigs? Sure they do; I tell everyone! I figure that since I don't pretend that my stilettos are part of my feet, my earrings are part of my ears, or my glasses are part of my face., I won't pretend that my wigs are part of my head. Since they are as visible as my clothing, I consider them just another fashion accessory. Do what it takes to feel good again.
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      JOANNE SMITH

      Welcome Kate - It is very difficult to talk to people about this for sure.It is a million times easier to talk to people with hair loss themselves and as you can see there are plently of us.
      I also have AGA since I was 23years old when I was told this and burst into tears and spent years trying to find a cure. I never spoke to anyone and felt I was the only one! My emotions would change all the times sometimes ok and other times obsessed and depressed about it.
      Since speaking to others accepting it and dealing with it it has become soo much easier to bear.
      Welcome and well done - wish I had done this tears ago!!

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        Kate

        I just wanted to stop in and comment on my own post from 18 months ago, and say what an absolute assistance this site has been over the past year and a half. Access to a community of people who experience similar challenges and emotions - and who share their experiences so candidly and honestly - has made ALL the difference in me finding a comfort level with my alopecia. The members on this site have give me perspective, ideas, advice, and self-assurance that my hair loss is not an all consuming event. I feel a million times better about myself and my future today than I did when I wrote this introduction for myself back in August 2012. For that I want to say thank you, and also hope that my experience can be shared by others like me who start here scared and alone and transform into those who can offer support and hope. Thank you!