Hi! My name is Lolin and I am 30 years old. I am currently living in the St. Paul area here in Minnesota. About 22 years ago while my mother was brushing my long, curly, dark brown hair, she noticed small clumps of hair from the back of my head falling out. That happened a couple more times after that and before you knew it I had 3 small bald spots on the back of my head. And it stayed that way until 5 years ago. My hair started to slowly thin out. Then suddenly like a thief in the night Alopecia had completely taken what little hair I did have. I wear a wig everyday, everywhere. I am still having a very hard time talking about it or admitting that I even Alopecia. Last September, I decided, during Alopecia Awareness Month that I would actually walk out of the house and go shopping with just a baseball hat on. I felt the eyes on me and could only imagine what people may have been whispering to each other. The funny thing is, I was completely embarrassed. I think nothing of it if I see someone who has lost their hair walking around the mall or at the beach. So why do I care???
Anyway, I am looking for people that I can be me with. I don’t know too many people with Alopecia personally but would love to! Message me anytime! And i've got myspace too! www.myspace.com/lolin78
Hi Lolin, I wanted to welcome you to Alopecia World. I can honestly say that we are a great community here and I hope you enjoy the time you spend with us. Cheryl, co-founder
Bonjour Lolin,
I've been dealing with alopecia for almost all my life.... but I've been with others alopecians only twice.... this site is great: you'll meet a lot of new people... for me, meeting others have done more good than any of the treatments have tried and belive me, I've tried everything!
Looking forward to read you,
Diane
hi there, i would love to email you my story. i would post it here, but it is pretty long. i think it would help you and inspire you. i felt exactly like you did. it has been almost 2 years and i am just now accepting it.
idk.. my friends are really cool about it, and i guess everyone kinds knows, but sometimes i get little comments like... why are you wearing fake eyelashes and stuff like that. that kinda stuff really bugs me.. but other than that i havent really just wipped off my wig and been like "hey look at me im bald" .. haha.
Hi Lolin,
Do you need a support group? You might be able to find out about one close by -- go to the National Alopecia Areata Foundation web site: www.naaf.org and ask for some help.
Hugs, LeslieAnn
Hi Lolin, would you like to connect up with the local suport group? It really helps being face to face with others who are in the same situation. I live in Minneapolis. Let me know. Heidi ...
Hi Lolin. I live 10 mins from Farmington. It's too bad you don't live here anymore. I'm sure though that Minnesota is more exciting. I did find a group in Rochester, just wish I found more people to meet with it. I think it's cool that you wrote about still being mad about having Alopecia. I still get mad from time to time. I think we all do, but don't always say it. Hope all is well in St Paul. Allie
I read your blog and I loved it. I know exactly where you are coming from. I have had alopecia for 36 years and have never gotten used to and I doubt I ever will.
Hi Lolin, how are you doing? I have a women's hair loss social you may be interested. But you need to email me so I can forward the info. My email is hodmark@comcast.net. Then I can add you to the local support group email list and keep you updated on stuff. Q's? Heidi ...
I just read your profile and I'm amazed about how people feel so different about alopecia.
I need to say that I also ALWAYS wear a wig. Everywhere and always except when I'm at home. I've had AT for only a few months. In march my hair was already thinner but I was still able to have a ponytail and to go out even without a hat. Now, all my hair is gone and I really don't mind. Hair, to me, has never been anything special. I've never been that kind of person who was able to style it in great and different way. Now I can wear different wigs and I look different and I feel great.
Hi Lolin
People will judge, we all do it and we always will. Unfortunately, judging and gossiping are two different things and people who gossip are not usually very intelligent. When I was very little my father used to read this poem to me about a wise old owl who spoke less and heard more. I try to remember that all the time and to always be considerate of others. If someone needs their eyes and ears opened then we all have to act together and make them realize how foolish they're being. I see myself as a teacher and role model and try to practise what I preach and I would hope that if you were in a similar situation that you would stand up for yourself too. Have a nice day!
Hey Lolin!
How are you? I love your name ive never heard it before its very pretty!
anyways just wanted to introduce myself. im pretty new to Alopecia World and wanted to meet others like me! If you ever wanna chat I would love too!
Have a great night!
CASEY
Cheryl, Co-founder
May 9, 2008
Diane
I've been dealing with alopecia for almost all my life.... but I've been with others alopecians only twice.... this site is great: you'll meet a lot of new people... for me, meeting others have done more good than any of the treatments have tried and belive me, I've tried everything!
Looking forward to read you,
Diane
May 9, 2008
jennifer
May 16, 2008
jennifer
May 18, 2008
Amanda
May 25, 2008
LeslieAnn Butler
Do you need a support group? You might be able to find out about one close by -- go to the National Alopecia Areata Foundation web site: www.naaf.org and ask for some help.
Hugs, LeslieAnn
May 25, 2008
Heidi
Jun 2, 2008
Allie
Jun 8, 2008
Billie
Jun 9, 2008
Sherry Schaefer
Jun 11, 2008
Denise
Jun 12, 2008
Billie
I LOVE the pic you have posted above... I may have to borrow it from you.
Have a great weekend!
Jun 13, 2008
Heidi
Jun 14, 2008
Zoe
I just read your profile and I'm amazed about how people feel so different about alopecia.
I need to say that I also ALWAYS wear a wig. Everywhere and always except when I'm at home. I've had AT for only a few months. In march my hair was already thinner but I was still able to have a ponytail and to go out even without a hat. Now, all my hair is gone and I really don't mind. Hair, to me, has never been anything special. I've never been that kind of person who was able to style it in great and different way. Now I can wear different wigs and I look different and I feel great.
Jun 25, 2008
Roger
Hows life in Minnesota?
Roger.
Jul 9, 2008
Mandy
Jul 10, 2008
Mandy
Jul 10, 2008
Carol
People will judge, we all do it and we always will. Unfortunately, judging and gossiping are two different things and people who gossip are not usually very intelligent. When I was very little my father used to read this poem to me about a wise old owl who spoke less and heard more. I try to remember that all the time and to always be considerate of others. If someone needs their eyes and ears opened then we all have to act together and make them realize how foolish they're being. I see myself as a teacher and role model and try to practise what I preach and I would hope that if you were in a similar situation that you would stand up for yourself too. Have a nice day!
Jul 16, 2008
Casey
How are you? I love your name ive never heard it before its very pretty!
anyways just wanted to introduce myself. im pretty new to Alopecia World and wanted to meet others like me! If you ever wanna chat I would love too!
Have a great night!
CASEY
Aug 14, 2008