• Chat with Arash Mostaghimi, MD, MPH, FAAD

    Arash is an assistant professor of dermatology, director of the inpatient dermatology consult service, and co-director of the Complex Medical Dermatology Fellowship at Brigham & Women’s Hospital. As…

    Wednesday, November 1, 2023 7:00 pm – 8:00 pm Online Through Zoom
  • Chat with Brett King, MD, PhD

    Dr. Brett King is an Associate Professor of Dermatology, specializing in skin diseases recalcitrant to first-line therapies. He has pioneered the use of Janus kinase…

    Tuesday, November 28, 2023 7:00 pm – 8:00 pm Online via Zoom

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What does Susie have to say about BGDL events?

“Awareness about alopecia areata means a lot to me because it represents my reputation and who I am. It has molded my personality and changed my lifestyle. 

I want my friends to know about my alopecia areata because it is a part of me that I currently cannot change. It should be understood and accepted. 

The difference between reading about alopecia online and talking to other people in person at a BGDL meet-up is that you get to speak to people that have similar experiences as you. You realize that you are not the only one struggling. 

I’m involved with Bald Girls Do lunch because this group is about making people feel comfortable and know that they always have someone to talk and relate to.”