You’ve heard first hand how disruptive an alopecia areata diagnosis can be. The shock, anxiety and shame can send women into hiding from social activities, even some types of work. Like Shirley…
— CoNCERT (@ConcertPharma) September 17, 2018
Take the survey before August 2nd and you’ll be be entered into random daily drawing for one of five $25 Amazon gift cards.
Privacy: Providing your email is optional. No answers will be saved or associated with your email by the survey creator, Foresite Capital. No individually identifiable responses will be saved.
Eligibility: take the survey if you have alopecia areata yourself or on behalf of any other person who has AA.
Ages: open to all ages, gender and orientations
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
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.
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.”
Because bald is just one more way to be a normal woman.
From the PRStylista Group: #UnBoxMe video clip featuring Thea Chassin and the wisdom of Bald Girls Do Lunch.