Who we are


Alopecia Areata: The shame and embarrassment of this disease devastates the lives of too many women and girls when treatments do not work. Since 2007 Bald Girls Do Lunch has connected with over 3,000 to restore self-confidence and conquer isolation. With requests for meet-ups in every state and beyond the USA, Bald Girls is answering the plea for women to find others for community and support. From intimate groups to style workshops to restoring her looks, BGDL puts women on the track to normalcy and living well with this disease. Learn more...





Global Skin Logo - International Alliance of Dermatology Patient Organizations

BGDL Facebook Page




Posts


Alopecia Care Kit Video

October 6th, 2018 by Chassin

Buy Your Alopecia Sleep Hat

Posted in 2018, About BGDL, alopecia areata, Awareness


Concert Pharma Tweet Keen on Importance of Our Alopecia Support

September 18th, 2018 by Chassin

I Want to Give Women Support and Smiles

Posted in 2018, alopecia areata, Awareness, support, supporters, Talking about alopecia


Alopecia Areata Support that Works!

June 23rd, 2018 by Chassin

Spring In The City from Bald Girls Do Lunch on Vimeo.

Posted in 2018, AA Support Network Blog, About BGDL, alopecia areata, Alopecia Lifestyle, Awareness, beauty event, event, How to: talk about alopecia


We’re Top-Rated Again!

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.

DONATE

Posted in 2017, About BGDL, Awareness, Friends of BGDL, fundraising


Your Gifts Help More than Ever

April 6th, 2017 by Chassin

DONATE

Posted in 2017, Awareness, Donate, support


Alopecia Beauty in North Carolina

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


#UnboxMe: Bald Girls Do Lunch

March 25th, 2017 by Chassin



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.

Posted in 2017, Awareness, beauty, event, support, Talking about alopecia, Videos


Bald is Beautiful in Buffalo: April 29

February 6th, 2017 by Chassin

Bald is Beautiful in Buffalo
Buffalo News tells Katrina’s story

Katrina R. has never met another girl with alopecia. That’s about to change!

BGDL presents our first Buffalo, NY regional event at J.P’s Pub in Lakeview, NY on April 29, 2017.

Click HERE to RSVP or DONATE to the cause in support of Katrina!

DONATE

RSVP For Lunch Event

Posted in 2017, Awareness, Donate, New York


#AlopeciaAwarenessMonth

September 8th, 2016 by Chassin

As part of #AlopeciaAwarenessMonth I thought I would give some of my thoughts on wigs. For me wearing wigs gives me back the control that Alopecia took away from me. I love being able to have the choice and that in itself gives me confidence as I am in control again. In general I try to focus my thoughts on the areas of my life I can control, rather than things outside of my control. I love hair and make up and love to get glammed up – I see it as a way to express myself rather than as a way to fit in with other people. For anybody with #alopecia I would say wear or don’t wear whatever you feel comfortable with and don’t be pressured either way by anyone. #AlopeciaAwarenessMonth 📷 @chelseashoesmithphotos

A photo posted by Joanna Rowsell Shand (@joannarowsellshand) on

Posted in 2016, Awareness, wigs

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