Well it certainly has been a long time since I've been on this site... I guess I'll just do a quick update. I was contacted recently on facebook by the girlfriend off one of my cousins. She just got diagnosed recently- maybe a year ago?- with alopecia. My cousin, having grown up all his life with me having alopecia, referred her to me because shes been having some difficulty adjusting, and doesn't have anyone to talk to about it.
I feel so bad for her. I know how hard it is to deal with this disease, especially at first. I'm glad that I have the opportunity to be there for her to talk to If she needs it-.thats something I never had for the first many years after being diagnosed, and even when I found friends who accepted it, it just wasn't quite the same because they didn't understand how it had affected me. They just saw it as something cool and unique. And while that did really help me grow into myself and come to accept and even occasionally enjoy my alopecia, it isn't the same as having people to talk to that have been where you've been. People that understand ridicule and loneliness the same way.
I'm glad I get the chance to help her cope with alopecia. But I also know that it's only just the beginning for her. Shes on some medications right now, and, just like with everyone else, they only work for her when shes on them. Luckily for her, her hair is still growing back, and I told her that was a good sign.. But I worry she'll get her hopes up too high. I've had alopecia for exactly two thirds off my life, sixteen whole years now, and it took the better part of all that time to finally accept that my hair is never coming back.
I think I'll refer her to this site. I think it would help a lot- it's definitely helped me.

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Comment by Pat on November 10, 2011 at 12:17am

It's great she has you to talk to. It's kind of difficult to predict how others will react to a support group. Denial can make us not want to face the fact our hair may not regrow. I remember when I first started losing my hair there was an interview on the Today show with 2 women who had AU and I was horrified to think I could one day be bald as my derm had told me it would grow back. It was like my worst nightmare seeing those women. I don't condemn myself for that, it's how I thought back then that my life would be a living hell without hair. Well I guess it was the first few years :) All you can do is be there for her Brittany and listen to her fears without trying to make her feel better. You can give her the stats that say most people regrow their hair, and they do, but also a small percent lose it all and only time will tell what her aa will do. Sharing how you handled it [or not] will help her relate as she's probably been told its only hair which will make her feel so much worse when she gets depressed about it. Oh boy, what a journey eh? Hopefully like all of us she'll come out a stronger person for going through this and she's got something you never had...YOU!

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