I am separated with two college age children and work in a hospital.
I first noticed Alopecia Areata 4 years ago which started with loonie size patches mostly on the left side of my head. Since then I have gone on to develop 2 more autoimmune diseases. I am still getting used to this new me and have had regrowth and lost it again. I am in the process of losing my eyebrows now and some new patches appeared recently.
I am happy that I have found this site as it is reassuring at times to know that what I am experiencing (the feeling of a burning scalp etc) is part of this condition.
Thanks
I am not sure myself. I saw it listed on the Bald Ladies Do Lunch website and decided to go, as I live 10 min. from Philly. Now that I look closer, it seems geared toward children. It does have some make-up workshops (which interests me). Will let you all know tonight what happens!
Sharon
Unfortunately, I was only able to go to the Alpocia Palooza on Friday afternoon. I saw only one vendor - Debbie from Fuller Hair. Even Debbie seemed surprised to see me, an adult, at this event for children. The make-up events were scheduled for Saturday and due to a previous committment, I was unable to go. Has anything such as this ever been established for those with alopecia in general?
Sharon Stokes
Sharon
Aug 7, 2009
Sharon Stokes
Aug 9, 2009
Julia McDowell
Love to see you there!
Julia
Jun 3, 2010