January 22nd, 2020 by Chassin
Please take action TODAY to make the most of this inspiring moment for all of us living with AA.
Photo Credit: MSNBC
THANK YOU for joining Bald Girls Do Lunch in celebrating Massachusetts Representative Ayanna Pressley. And, expanding our work to support more girls and women living with AA.
It’s a beautiful step forward for awareness, acceptance, and the Bald Girls community.
Posted in 2020, AA Support Network Blog, About BGDL, Action Alert, alopecia areata, diagnosis, Donate, Friends of BGDL, fundraising, How to: talk about alopecia, Massachusetts, media coverage, support, supporters, Talking about alopecia
October 6th, 2018 by Chassin
Posted in 2018, About BGDL, alopecia areata, Awareness
November 27th, 2017 by Chassin
Bald Girls Do Lunch is donor-supported. You can be a Bald Girls donation hero today. Your friendship and support works to stop alopecia areata anxiety and shame.
Posted in 2017, About BGDL, Awareness, Friends of BGDL, fundraising
July 17th, 2014 by Chassin
July is our month! Check out our life-enhancing tips from the BGDL Alopecia Areata Support Network Blog.
Posted in 2014, About BGDL
March 29th, 2014 by Chassin
American Express encourages you to use your AMEX Rewards Points instead of cash to make your 2014 charity donation to Bald Girls Do Lunch.
Click here to find out more.
What We’re Doing Already in 2014:
Launched the popular Alopecia Areata Support Network blog
Completed Phase I of the Women with Alopecia video shoot
Published inspiring personal stories of fabulously positive women
Fostered public understanding of lives affected by alopecia areata
Educated about human hair and scalp prosthetics
…..and much more!
Posted in 2014, AA Support Network Blog, About BGDL
November 26th, 2012 by admin
With some amazing reviews we got from you, we’ve won a 2012 Top–Rated Award from GreatNonprofits.
Check out our profile! Add your review!
http://greatnonprofits.org/reviews/profile2/bald-girls-do-lunch-inc
Posted in 2012, About BGDL
December 13th, 2009 by Chassin
Holiday time for many means friends and family gathering round. This season, you might be new to alopecia. Or, maybe it’s resurfaced. Or, maybe you’ve decided to take a new approach and let others in a bit more about what this condition is and isn’t.
Our BGDL appearance on the TODAY show can help. Just send the link around or click, sit back and enjoy yourself. There are millions of us. Often hiding in plain sight. All around the world.
Posted in 2009, About BGDL, Awareness, Today Show, video