June 4th, 2018 by Chassin

Handfuls of hair coming out in your hands? Jada Pinkett Smith gives her own first-hand account of this shocking experience. We’re inspired by Jada’s colorful choices to rock the headwrap.
This is how we do it at Bald Girls Do Lunch events.

Posted in 2018, alopecia areata, beauty, diagnosis, headwear
April 30th, 2018 by Chassin

Got alopecia? Join Bald Girls Do Lunch CEO, Thea Chassin, for friendship, camaraderie and her Live Well with Alopecia™ tips.
- • Meet locals like yourself who understand the challenges of alopecia.
- • Get answers to questions about living with alopecia and treatment regimens.
- • Need eyebrow help? We’ve got you covered with our BGBrows demo.
- • Be comfy. Be yourself. We love all options: wear your wigs, hair, hats or bald look.
Posted in 2018, alopecia areata, Alopecia Lifestyle, brows, event, How to: talk about alopecia, Make-up, Seattle, support, Treatments, wigs, workshops
April 22nd, 2018 by Chassin
Posted in 2018, alopecia areata, beauty, hair, Wig alternatives
March 18th, 2018 by Chassin

We’ve got a seat for you! Friendship, research news, beauty and more with Thea Chassin: Live Well with Alopecia™ tips for Spring 2018.
- • Who understands alopecia? Women like you!
- • Learn fashion tips and tricks for your wigs, hairstyles and head wraps
- • We’ve got you covered: best brow shapes, faking a lash line and makeup demo
- • Be comfy. Be yourself. We love all options: wear your wigs, hair, hats or bald look
Posted in 2018, alopecia areata, Alopecia Lifestyle, brows, How to: talk about alopecia, Talking about alopecia, wigs, workshops
March 17th, 2018 by Chassin

Got alopecia? Join Bald Girls Do Lunch CEO, Thea Chassin, for friendship, camaraderie and her Live Well with Alopecia™ Spring 2018 tips.
- • Meet locals like yourself who understand the challenges of alopecia.
- • Get answers to questions about living with alopecia and treatment regimens.
- • Need eyebrow help? We’ve got you covered with our BGBrows demo.
- • Be comfy. Be yourself. We love all options: wear your wigs, hair, hats or bald look.
Posted in 2018, alopecia areata, Alopecia Lifestyle, brows, event, How to: talk about alopecia, Make-up, support, Treatments, wigs, workshops
March 11th, 2018 by Chassin

As part of our Bald Girls community, you know firsthand the impacts of alopecia areata. That’s also what the FDA wants to learn. They held an AA patient-focused meeting in September 2017 attended by Bald Girls Do Lunch CEO, Thea Chassin.
Posted in 2018, AA Support Network Blog, Action Alert, alopecia areata, FDA, research, Talking about alopecia
November 12th, 2017 by Chassin

Our submissions page to Talk to the FDA via the Bald Girls Do Lunch impact statement is now closed.
You may enter your comments through 11:59 pm eastern, November 13, 2017 directly to the FDA here.
Posted in 2017, AA Support Network Blog, Action Alert, alopecia areata, FDA
March 29th, 2017 by Chassin
Sandra met us in Raleigh, NC a few years ago. This inspiring motivational speaker and singer continues to spread her message of self-acceptance to boost more women with alopecia.
“Bald Girls Do Lunch in Raleigh was a blessed event. Thea has a wealth of knowledge and a heart of gold. It takes great strength and courage to walk boldly and confidently as a bald women in this society. Not only does Thea live her song, but she inspires women all over the world to do the same.”
Posted in 2017, alopecia areata, Awareness, support, Talking about alopecia, Videos