Bald Girls Do Lunch, Inc., P O Box 9122, Scarborough, NY 10510
Alopecia Areata: The shame and embarrassment of this disease devastates the lives of too many women and girls when treatments do not work. Since 2007 Bald Girls Do Lunch has connected with over 3,000 to restore self-confidence and conquer isolation. With requests for meet-ups in every state and beyond the USA, Bald Girls is answering the plea for women to find others for community and support. From intimate groups to style workshops to restoring her looks, BGDL puts women on the track to normalcy and living well with this disease. Learn more...
BGDL Fact Sheet
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As part of our Bald Girls community, you know firsthand the impacts of alopecia areata. That’s also what the FDA wants to learn. They held an AA patient-focused meeting in September 2017 attended by Bald Girls Do Lunch CEO, Thea Chassin.
You may enter your comments through 11:59 pm eastern, November 13, 2017 directly to the FDA here.
Thinking something? Say something! Thea Chassin reviews the meeting.
FDA’s taking patient and family comments until November 13, 2017.
Alopecia Areata Slated for FDA Hearings http://bgdl.org/1LeuyGa
Bald Girls Do Lunch Announces FDA Hearings on #AlopeciaAreata #alopecia
The FDA has been holding public meetings on 20 different disease areas, one disease per area over the last year or so to continue through 2017. Alopecia Areata is on a preliminary list to be chosen as a disease in the FDA’s process for patient-focused input for the 2016-2017 disease-specific meetings. The FDA is currently inviting commentary on this preliminary list.
