Hi Cheryl. Thanks for the welcome. Only had a chance to have a quick look at the website so far but I can see that it looks a great support network. Good to know that you are not on your own, and that others are going through the same experinces. For a while I felt as though I had given up given in to this awful condition, but after reading other peoples comments, it has given me new determination to try to do all I can to stop my condition progressing.
Thank you for your welcome, Cheryl! I appreciate it. I am happy to find a site where I can interact with people who know what it is like to be bald, and all of the emotions that can go along with it. My goal is to throw away my wig and hats and just be free to be me. I want it so badly, but I'm just not there yet. I have so much respect for those who accept themselves fully and are confident in themselves despite their lack of hair. I hope to join in on some conversations more as I understand how the site works. THanks!
Thank you Cheryl for this site, I am newly diagnosed with AA, this month in April 2014. I cannot say how overwhelming, helpless, hopeless, it was to find out there is no cure for this, just steroids in one form or another, with all the side effects. So reading these comments, ideas,things others have tried,helping with the beginning confusion, its been a godsend. Thank you for this site!!!
Thanks for your welcome and for letting me start my day with a photo of a beautiful bald woman with a radiant smile. I'm just a sorry case shoveling cereal into my mouth as I sit at the computer and running out of time to get dressed, get my two year old dressed, and get the other two off to school. And somewhere in there I have to pull a wig over my bald head so I can volunteer in the kindergarten without attracting attention (although I am increasingly feeling bald feels right, and even suggested my son could bring me in for sharing to tell the kids about alopecia). And, hey, the two year old dressed herself!
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