I grew up never knowing what it was like to have hair or look like everyone else. I was diagnosed with AU when I was a baby and lost all my hair as a young child. I work now as a model in NYC trying to spread awareness about Alopecia and be some kind help to the community. I think visibility is very important because growing up, I never saw anyone like me. It wasn't until I was in my teens before I ever met anyone else with my condition.
Alopecian Beauty Mixer (Charity Event)
(STRICTLY ENFORCED DRESSCODE NAVY BLUE & WHITE /CREAM ONLY) September is Alopecia Awareness Month thier ribbon color is navy blue so September 30, 2017, We'll be launching a fundraising campaign to support individuals who suffer from the diseases Alopecia Areata & Cancer. This is a family friendly event that will include networking, food, drinks, special guest, custom wig give aways/demos, complementary massages, makeovers and A lot more. Including a bartender for 21+ participants! We also will have live performances/Celebrity photographers are going to be in the building for personal and group shoots. Why not have a amazing time while supporting a positive cause? Lets come together as a community and show support, love, while giving back to one another! See you there...
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