Beth, thanks for adding me. Your story is very similar to mine. Life is what you make of it, email me at chadmidstokke@gmail.com, if you every wanna chat

Hi there,

Thanks for the friend request. I have just read your 'about me', and boy has it hit me. Mine fell out over a couple of months too, and my partner hasn't been the greatest. Always telling me that it's just 'hair'. All of us here on Alopecia World have a similar story and are all struggling—but we are here for each other. You aren't alone, keep smiling and show the world that you don't need hair to be a beautiful person :)

Hey how are you? how are things with you?

Beth your pictures are great. I have had alopecia since 19 3 times bald and never had all my own hair again so I wear wigs all the time except in the house .Lets keep the faith and hope for a cure Pat

Hey beth. How are you?
Ahh your like me, i am glad that someone knows what i delt and what i am dealing with. I was born with it. I was born after the war. But i do get ppl who have alopecia areta. To tell you the truth I Recently Knew What I got. I Found out last year! So I am glad that the 'thing' I have isnt something scary... you know?

You have eyelashes and eye brows like me, even your scalp is like mine but the only difference is i have fine hair but its like a 'v' redcuing hariline... I think some ppl in this site have it as well.... I finally knew that...

My hair doctor, told me " maya what you have is alopecia... " I was like O.O ohhh

I have tried everything, and everything was expensive...So till now i didnt give up but I might be trying chinese herbs.... I dont know if it'll work but its not a crime to try....

Yeah I have suffered, cause where i lived ppl were shit till now they are, they only care about the look... and before i thought this was genetics or i thought i was sick.... but now I dont think that way i know what i got...

Dont worry you have friends in this site... And im with you :)

Your very pretty with and without your wig!!

Sorry to say but your boyfriend needs to get his head out of his ass because what he told you was stupid, and very dumb...! dont worry my partner has his moments.... and i argue with him and tell him " you have no idea what i am feeling right now chris! "


I know how you feel... I sometimes have my sad and depressed off days.... but when i think of you guys i feel that im not alone :) i have ppl like me...


I hope we chat soon!! xoxo hugs!!

Hey how are you?
Its a very good site!
Your really pretty with and without your wig.. its true..
I got the uni alopecia.. check my profile out! :)

Hello and welcome, Beth!
How are you today?
Leslie Ann

ya i have had it since i was 6. either i tell guys right away and they just stop talkin to meor just want to have sex and nothin else or i wait and we are dating and they find out and they dont want to be together any more

Cool ! Maybe sometime this coming summer you and your son can tent camp at my campground. For free of course and you and I can talk hair along with everything else. Your right alopecia blows ! I started losing my hair in my early twentys. I hope to go with out my hats this summer. I'm gonna try. I said that last summer. It's difficult I know. I think it would be easier in a bigger city. When I went home to visit family in Dallas it was easier cause there were more people and blah.blah.blah.... But in this little pretentious valley I get the stares and questions. But, I'm ready .... Dun.dun.dun.dun... We shall see... Keep intouch lady. It's good to meet you ! -K

Hi there Beth !!! You live in Boise ??? That is soo great ! We will have to meet and have lunch together ! I started a alopecia group here last summer and sadly only had 1 person showed. Oh well, I tried to get some of us together.
I live here in Bellevue and manage a RV campground. I love it cause I can work here at home with my adorable 4 month old son Max. I am originally from Dallas, Texas. Have you lived in Idaho long ? Hope to hear from you soon. -K