BALD GIRLS DO LUNCH INC via Crowdrise
October 19, 2014
Sandra's Story: Our 30-second video tells it all. Listen to the real impact of Bald Girls Do Lunch. That's why Jenna's Fund makes a difference. There are so many Jennas and many Sandras.
Team Thea/BGDL is aiming to match Jenna's first $1,000 milestone with another $2,000. Every donor on Team Thea/BGDL will receive a beautiful new scarf donated to BGDL.
Whether your gift is anonymous or you choose to honor someone, ALL size gifts are awesome support to expand the work and reach of Bald Girls Do Lunch in person and online.
Bald Girls Do Lunch is the only non-profit specifically created for women with alopecia areata – the autoimmune skin disease which stops the normal growth of hair on the scalp, brows, lashes and body.
I have Alopecia Universalis, and have had it for over 12 years. I was diagnosed when I was 11, in the sixth grade, and have been bald ever since. Until a couple years ago, I had never met someone with Alopecia, which makes it a lonely road. This organization brings together women and girls with Alopecia and helps you realize you're not alone. When I finally met someone with Alopecia, it changed my life, literally. I finally met people who knew exactly what I was feeling, the struggles and challenges I face, and just how it feels to be bald and try to live a normal life. I really loved meeting people with Alopecia. And for a lot of women, these lunches are the only place they see, or meet others with Alopecia.
Help me raise funds to build the strongest base of support for BGDL, especially in Utah and beyond.