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
Posts
Very recently while speaking with one of my cherished childhood friends, she told me about a friend of hers that she suspects has the condition. I wanted to hear her advice for men and women like her friend who have never mentioned why they look the way they do.
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As we approach the holiday season when folks are gathering ’round, we want to help this be a better year for women with alopecia areata.
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We’ve recently focused on the latest medicines and research in the alopecia areata field. Interested in the latest science and findings?
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This is our second in a 2-part series about a relatively new class of immuno-suppressant drugs called Janus kinase inhibitors, which sure have received a lot of media attention lately.
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Physician Takeaways from Alopecia Drug Treatment Case Study
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When headlines hit the media with word combinations like alopecia, research, clinical trials and drugs, we want to help you understand them and keep them in perspective.
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Physicians Note That Alopecia Drug Treatments Require Further Testing
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Click through to read Candace’s story, learn from the coping strategies that were most helpful for her, and hear her personal opinions on the media and hair-growth news.
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How to Effectively Cope with your Child’s Alopecia: Candace’s Story
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We have noticed there has been a recent uptick in the number of mentions of alopecia areata and clinical trials in the news. After some research we are writing this week to share some basic information about clinical trials and important things to keep in mind if you are thinking of participating in one. We even had a chance to catch up with Sydney from our previous post to hear her weigh in with her reaction to current news of clinical trials related to alopecia areata.
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What to Know About Clinical Trials and Alopecia
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Recently I had the pleasure of speaking with Sydney Olson, a 21 year old college student who has had alopecia areata for over 10 years. Sydney is currently a biology major and chemistry minor at Concordia University in Nebraska. She was kind enough to share her story and many tips from her experiences with the condition. Those tips include opening up about AA to your family and friends, understanding how those around you cope, and how to be confident as a young woman with severe hair loss.
21-year old’s sage advice for #alopecia coping: Sydney’s Story http://t.co/ZfSL6tBP0Z #alopeciablog pic.twitter.com/7yvZ1pBlBF
— Bald Girls Do Lunch (@alopecia) September 18, 2014
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Self-Confidence Restored after Alopecia: Sydney’s Story
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We here at Bald Girls Do Lunch would like to do our part to spread awareness about Alopecia Areata by sharing with you the story of our newest Ambassador, Jenna Baker. Read Jenna’s inspiring story about her experience with Alopecia and how you can help Jenna reach her goal of raising $3,000 to fund Bald Girls Do Lunch.
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Introducing our New Ambassador, Jenna Baker
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