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...

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Posts


Buy One. We Gift One!

October 13th, 2018 by Chassin

Alopecia Sleep Hat

Purchase one Alopecia Sleep Hat in the month of October for yourself or someone you love with alopecia or going through chemo. We will include your words of encouragement when we gift a sleep hat in our Alopecia Care Kit.

Buy One. We Gift One With Your Wishes.


YouTube Beauty Vlogger Tests BGBrows Liners

May 13th, 2018 by Chassin

Laura Lattimore aka “Hairy Escape” YouTube beauty vlogger puts BG Brows liners head to head. Watch!


Alopecia in Kansas City: What Women Say

April 18th, 2018 by Chassin

Where would you like to attend Bald Girls Do Lunch?

LET US KNOW


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


Drawing on Eyebrows Tutorial with Laura Latti

September 26th, 2017 by Christie Plummer

Alopecia beauty vlogger Laura Latti gives a tutorial on drawing eyebrows using BG Brows Sealant + Dollywink Liquid Eyeliner.


Alopecia Makeup Review with Alopecia Beauty Vlogger Laura Latti

August 31st, 2017 by Chassin



Beauty alopecia vlogger Laura Latti gives BGBrows.com makeup the all-day test.


How to help a friend with alopecia areata find her true beauty

August 8th, 2016 by Chassin

alopecia areata friendship

Heidi showed us the power of her friendship in helping a close friend to live well with alopecia areata. In this follow-up we find out how Heidi does it. In fact, she told us how alopecia areata resonates with her own life, even though she herself has normal hair.

Her insights are very cool. Enjoy! Guest commentary from interview with Heidi S. of New Jersey. Read More

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Friendship Makes the Difference in Alopecia Areata Support

July 12th, 2016 by Chassin

Heidi and Allison

When friendship involves alopecia, it can be an opportunity for strength and support.

That’s what Heidi from New Jersey told us when her best friend, Allison, opened up about having alopecia areata, not something she did often. Read More

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Love and Alopecia Areata Support in Massachusetts

October 8th, 2015 by Chassin

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Follow Laura’s Journey

 

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Read Bob’s Advice