My Nonprofit Reviews
Review for Alopecia Areata Support - Bald Girls Do Lunch Inc, Scarborough, NY, USA
I have very recently been diagnosed with rare scarring frontal fibrosing Alopecia and am having trouble with the rapid hair loss. My dermatologist has told me that my hair will never come back and has suggested I wear a wig. As a person who hates even wearing a hat in winter I was in shock. I thought I was alone and had no where to turn. My internet search led me to BGDL and thank heavens for that. I look forward to having a community of women who are in the same boat. I will value their help and support as I learn to deal with this affliction. I live near Calgary Alberta Canada and do not know if there is a group in that city but at least I will have the group here to turn to for support.