Who we are


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...





Global Skin Logo - International Alliance of Dermatology Patient Organizations

BGDL Facebook Page




Contact Us

Bald Girls Do Lunch, Inc.
P O Box 9122
Scarborough, NY 10510
info@baldgirlsdolunch.org

We welcome your feedback about our site, our events and ways we can educate you about alopecia areata. Whether you are a parent and wonder what it’s like to grow up with alopecia or you’ve got an adult onset, we’re here to help by email or with our Quick Contact Form.

Join the conversation when a featured topic strikes your interest at blog.baldgirlsdolunch.org

To make an event inquiry or reservation contact
rsvp@baldgirlsdolunch.org
800.578.5332
914.945.0245

Thea Chassin, President and Founder
thea@baldgirlsdolunch.org

Public Affairs
PublicAffairs@baldgirlsdolunch.org
800.578.5332
914.945.0245

Click here to join our list for newsletters and event updates.

Click here for a BGDL fact sheet.

Follow us:
@alopecia
facebook.com/baldgirlsdolunch

Website Inquiries

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webmaster@baldgirlsdolunch.org