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


Clinical Trial for Adults with Alopecia Areata

August 27th, 2021 by Chassin
THRIVE-AA2

A clinical research study is currently recruiting adults

Ages 18-65 with a diagnosis of alopecia areata
Who have lost 50% or more of the hair on their head
To participate in a study of an oral investigational drug.

For more details visit the U.S. National Library of Medicine’s Clinical Trials website.

Bald Girls Do Lunch is providing this announcement for informational purposes only. Bald Girls Do Lunch does not imply endorsement.  The decision to participate is voluntary and wholly the responsibility of the individual person.


Now recruiting Alopecia Areata Clinical Trial: THRIVE-AA1

March 24th, 2021 by Chassin

THRIVE-AA1

A clinical research study is currently recruiting adults in the US and Canada.

The preliminary requirements to participate in this study of an oral investigational drug are:

  • • Adults ages 18-65
  • • A diagnosis of alopecia areata
  • • 50% or greater scalp hair loss

For more detailed clinical information visit https://bgdl.org/THRIVE-AA1.

Bald Girls Do Lunch is providing this announcement for informational purposes only. Bald Girls Do Lunch does not imply endorsement.  The decision to participate is voluntary and wholly the responsibility of the individual person.

Click for All Details


New Alopecia Research Opportunity. Thank you, participants! Recruitment is now closed.

June 1st, 2020 by Chassin

Do you have or know someone with alopecia? Interested in taking part in psychological research?

Ms. Paige Clarke-Jeffers announces the enrollment of Black women with all forms of alopecia areata in her research project: “Black Women’s Experiences of Living with Alopecia” at Birmingham City University, United Kingdom. The study is for her Masters of Health Psychology dissertation.

Aim your smart camera at this QR code for the Participant Information Sheet

Continue Reading


Alopecia support is here.

November 2nd, 2019 by Chassin

Shannon’s Story from Concert Pharmaceuticals, Inc on Vimeo.

You’re not alone if you’re wondering how do I cope with alopecia areata knowing there’s no alopecia cure? One way to feel supported is right here: watching and reading personal stories  — people like yourself living with alopecia.

Watch Shannon’s heartfelt story: how she talks to herself and to others.

We thank Concert Pharmaceuticals for including our Bald Girls ambassador, Shannon, in their patient web portal for alopecia areata at ConcertPharma.com/patients/

Read Shannon’s Interview


Bald Girls’ Alopecia Areata Voices for the FDA

March 11th, 2018 by Chassin

FDA

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.

Join the Conversation


Got Alopecia? Take Self-Help Research Survey!

January 18th, 2017 by Chassin

Logo University of Sheffield

Researchers at the University of Sheffield’s Department of Psychology want to hear from you!

Will a self-help program aid patients with visible skin differences?

Be part of the survey this week. You might win a very nice Amazon Gift card chosen from all participants.  Register  HERE  Learn more HERE.


Alopecia Areata Research Update from Mount Sinai

August 9th, 2016 by Chassin

Guttamn Staff
Dept of Dermatology Researchers, Icahn School of Medicine, Mount Sinai Health System

Here at Mount Sinai School of Medicine, it is an exciting time for treatment in alopecia areata. Currently we have three trials going on: an injectable, a topical and an oral. Read More

Read More


Clinical Trials Got Your Interest?

April 23rd, 2016 by Chassin

Dr. Emma Gutman

Mount Sinai ( New York ) has options for alopecia areata patients

Mount SinaiIs there a cure for alopecia areata? No, there is no cure, but researchers are doing clinical trials in search of safe and effective alopecia treatments. Dr. Emma Guttman, in New York is conducting several studies including a pilot study with Tralokinumab for moderate to severe alopecia areata.

Follow along with our interview so you can talk to your friends and family about new studies for alopecia treatment… Read More


Clinical Trials Underway at Mount Sinai Department of Dermatology

March 18th, 2016 by Chassin

Icahn School of Medicine at Mount Sinai (New York)

Alopecia Areata research is of great interest to people with this autoimmune skin disorder. This Bald Girls Do Lunch blog informs you with patient-friendly posts on alopecia areata news, clinical trials and popular posts like our features on Tofacitinib and Ruxolitinib. In 2016…Read More

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