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...
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Heidi showed us the power of her friendship in helping a close friend to live well with alopecia areata. In this follow-up we find out how Heidi does it. In fact, she told us how alopecia areata resonates with her own life, even though she herself has normal hair.
Her insights are very cool. Enjoy! Guest commentary from interview with Heidi S. of New Jersey. Read More
When friendship involves alopecia, it can be an opportunity for strength and support.
That’s what Heidi from New Jersey told us when her best friend, Allison, opened up about having alopecia areata, not something she did often. Read More
Fortune Wigs, BGDL Sponsor and Business Friend, provided an exclusive interview for our new Alopecia Areata Support Network Blog. Sign up for blog updates.
To tell us if your company will be a BGDL Sponsor or Business Friend, email: info@BaldGirlsDolunch.org
