You need information and resources at your fingertips so your questions aren’t left to guesswork and assumptions. As the first non-profit support organization devoting all its resources to the emotional and practical needs of women with alopecia areata, count on us as your go-to resource.
The Bald Girls Do Lunch Blog
We have written over 100 blog posts that cover everything from stories of women with alopecia areata to medical news to wigs for bald women to beauty and style tips—and more! You will find a wealth of information there.
Medical and Scientific Resources
American Academy of Dermatology: Alopecia Areata Patient Information
User-friendly and informative knowledge base.
Questions and Anwers about Alopecia Areata from the National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institutes of Health
Publication # 09-5143, www.niams.nih.gov
Informative, free booklet from the NIH.
Fast Facts About Alopecia Areata from the National Institute of Arthritis and Musculoskeletal and Skin Diseases (National Institute of Health)
Articles, personal stories and inspiration.
Nonprofit organization helps you communicate personally and privately. Journal your emotional process through the critical phases of alopecia. You post once so friends and family can all follow your journey. For children and families affected by alopecia and other conditions.
The only non-profit devoted exclusively to children with alopecia areata.