Video: “It’s Only Hair”
June 21st, 2018 by ChassinVideo: “It’s Only Hair”
From the Department of Anthropology at Goldsmith’s College in London – Life experiences with alopecia areata.
Posts
Bald Girls Loves the Alopecia Areata style of Jada Pinkett Smith
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.
Seattle, Washington Event: May 12
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.
Little Rock Alopecia Events: RSVP by 3/27
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
Little Rock, Arkansas Event: April 29
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.
Bald Girls’ Alopecia Areata Voices for the FDA
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.
Talk to the FDA! Alopecia Areata Patient Views Needed
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.
