Hi my name is Rafael. I am 18 and live in Brazil. I have alopecia areata since last year. I would like to add as a friend. can we be friends? Rafael a hug ....
Hi Gina -- I'm a southern Californian (in absentia) transplanted to The Netherlands, a fellow alopecia sufferer, and a member of LGBTS Alopecian family. Hope you're hanging in there!
Thanks for joining. I live in the inland empire. I am married and have 2 children . I have had Alopecia all my life. I don't think you ever get use to it but it dose get a littler easier to deal with. Keep you head up!
I enjoy writing also and now call myself a writer; that isn't published. I notice your comments have attracted a lot of people that like to write and some have said they don't have the time. You must set aside at the very least 10mins or even 30mins to write. Even if what your writing doesn't make sense. I've spent countless days writing what appeared to be jibberish; however, when rereading them, I found bits of pure inspiration and was able to collectively add those bits to essays and poems.
Hi Gina,
Yes it can be sucky, alright!
I've had it for nearly 30 years. AU for 20. I wrote a book to help women (especially girly-girls!) cope with it, and even have fun with it! You can find out more by going to my page, and order by clicking my web site which is on my page. Good luck! I'd like to know how you are doing!
LeslieAnn
If you're interested, ca
Hi Gena..I couldnt help but notice that very cantaigeous smile you have...Its like a giant ray of sunshine..Its nice to meet you,and Holla if you like..Bob : )
I'm doing great. Thanks for asking. Will you ever post your poems on here? I would love to read them! I like to write too. But it seems that being married and having four kids has pushed my writing into oblivion. My dad always asks me "So when is that novel gonna be done?" I just roll my eyes at him. lol
Gina,
Welcome! I know it is tough, but you seem to be a positive person , and have a beautiful smile, so just keep smiling. Yes alopecia sucks but there are worse things in life. I am a published poet also and have written for most of my life. Perhaps we can chat sometime.
Christine
Hi Gina, 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.
Hi Gina! Welcome! I also have Alopecia Totalis. I lost my hair when I was 5. I have been through many struggles in my life because of it. Mostly of self-acceptance. But I can honestly say that I am at peace w/ my condition and am happy in my life. This is a great community! I have recently joined, and have found many new friends.
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Gina's Comments
Comment Wall (23 comments)
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Scott
Sounds like you are having a tough time right now! I'm sorry about that!
Heather
Next years NAAF Conf is in LA.
Jeffrey
Thanks for joining. I live in the inland empire. I am married and have 2 children . I have had Alopecia all my life. I don't think you ever get use to it but it dose get a littler easier to deal with. Keep you head up!
Hope you are having a good day today.
Jeffrey
Yes it can be sucky, alright!
I've had it for nearly 30 years. AU for 20. I wrote a book to help women (especially girly-girls!) cope with it, and even have fun with it! You can find out more by going to my page, and order by clicking my web site which is on my page. Good luck! I'd like to know how you are doing!
LeslieAnn
If you're interested, ca
Welcome! I know it is tough, but you seem to be a positive person , and have a beautiful smile, so just keep smiling. Yes alopecia sucks but there are worse things in life. I am a published poet also and have written for most of my life. Perhaps we can chat sometime.
Christine
Cheryl
co-founder
Welcome to the group. How's So Cal treating you? it's raining in San Francisco tonight.
Looking forward to getting to know you.
Jeff
XOXO
CAR
Roger.
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Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.