I'm 24, living with Alopecia for over 14 years now. I'm lucky to have a supportive family and a loving partner but it's still difficult being bald in this part of Europe.
Welcome to Alopecia World. I've heard that being bald in Europe is particularly not easy. Do you know why this is so? It surprises me as I think of Europe as being so much more forward thinking than other countries. I'm in the US and it's not easy here either. There is a group on this site for Polish people with Alopecia, did you know that? Also, I was just a little older than you when my hair loss started. It was very hard at first--life changing--but now, over the years, it's gotten easier. Good luck to you! :)
Well, that's a universal problem it seems. Many people here and I guess everywhere don't know what Alopecia is. On the other hand, when I do tell people I have it more than half the time they'll tell me that they also know someone else who has it. Spreading awareness is important. That's why feel doubly better when I tell people I have it (something I never used to do until recently). It's helping me heal and I'm educating people about Alopecia. The National Alopecia Areata Foundation (naaf.org) is a very helpful resource if you want to check it out. :)
Maryanne
Hi, Hanna
Welcome to Alopecia World. I've heard that being bald in Europe is particularly not easy. Do you know why this is so? It surprises me as I think of Europe as being so much more forward thinking than other countries. I'm in the US and it's not easy here either. There is a group on this site for Polish people with Alopecia, did you know that? Also, I was just a little older than you when my hair loss started. It was very hard at first--life changing--but now, over the years, it's gotten easier. Good luck to you! :)
Sep 17, 2012
Maryanne
Hi, Hanna
Well, that's a universal problem it seems. Many people here and I guess everywhere don't know what Alopecia is. On the other hand, when I do tell people I have it more than half the time they'll tell me that they also know someone else who has it. Spreading awareness is important. That's why feel doubly better when I tell people I have it (something I never used to do until recently). It's helping me heal and I'm educating people about Alopecia. The National Alopecia Areata Foundation (naaf.org) is a very helpful resource if you want to check it out. :)
Sep 18, 2012
LeslieAnn Butler
Hello and welcome, Hanna!
How are you today? I have AU, too.
Leslie Ann
Oct 2, 2012