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Bald Girls Do Lunch Inc

Rating: 4.88 stars   52 reviews 2,118

Address:

PO Box 9122 c/o Thea Chassin Scarborough NY 10510 USA

Mission:

Bald Girls Do Lunch (BGDL) helps women with alopecia areata live full and fulfilling lives, and it’s all centered around the idea of getting together for “lunch.” Our lunches and other events are fun, friendly, educational, relaxing and, most of all, totally empowering. By being with people who experience the same things you, your self-esteem improves and you gain confidence, camaraderie and a powerful sense of community. Since 2007, we’ve brought lunches, workshops and demonstrations to 60 cities in 25 states, and are connecting more women all the time. BGDL is the only non-profit specifically created specifically for women with alopecia areata, the autoimmune skin disease that stops the normal growth of hair on the scalp, brows, lashes and body. Alopecia can have a devastating effect on a woman’s self-image — but sitting around and wishing for a cure or treatment is NOT what we’re about! In addition to our lunches and events, we have an active blog and newsletter, and cosmetic line called Signature Collection. You can check them out at www.baldgirlsdolunch.org.

Results:

Over 2000 women with alopecia areata receiving e-newsletter..... One-on-One makeup sessions with professional artists at BGDL Beauty Workshops in NY, IL, CT and RI...... Infographic: "Understanding the Lives of Women with Alopecia Areata"..... 3-time Gold Triangle Award winner from the American Academy of Dermatology..... "Virtual Lunch" - the only e-newsletter created for women with alopecia areata with outstanding open rates!..... Comprehensive weekly educational blog at blog.baldgirlsdolunch.org

Target demographics:

Women and teen girls with any type and any duration of the autoimmune skin disorder, alopecia areata. We also assist women with scarring alopecias.

Geographic areas served:

Nationwide USA, Canada and global

Programs:

In-person workshops, meet-ups , social and educational activities to conquer the isolation experienced by women with alopecia areata. Our global communications, superb e-newsletter and in-person events for women bring true life changes. Care packages for the newly diagnosed include our very own Sleep-hat.....both a real and a virtual hug from the women in our network to our newly diagnosed "sisters".

2015 Top-Rated Nonprofit
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More Info

800.578.5332
http://www.baldgirlsdolunch.org

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Reviews for Bald Girls Do Lunch Inc

Rating: 5 stars   Featured Review

1 person found this review helpful

I was referred to Bald Girls Do Lunch from a blog, as I was researching top products for creating eyebrows, as mine have basically become invisible over the years. I wanted make up products that would allow me to draw the brows on and keep them on. I ordered the brow powder, sealer and brush. Once my order was placed, I received an email asking questions about my hair coloring and skin tone, as there was a brow powder color that did not show up on the order form and may be a better match. After answering and asking a few questions it was determined that Dark Blonde would most likely be a better choice so my order color was changed. Thea, at Bald Girls Do Lunch, and I exchanged a few emails, and I felt like I had just made a new friend. She truly provided the absolute best Customer Service I have experienced probably ever in my life (and I am no spring chicken). Thea seemed to actually care about my satisfaction with the products and that I received the right products for me. I have since reordered and again, Thea, the true definition of Customer Service, sent me a personal email, thanking me for reordering from Bald Girls Do Lunch. I will continue to order, which supports medical hair loss issues. Here's to you, Thea, you are the best, Thank you again.

 
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(Nonprofit Staff) wrote:

Thank you madgranmom for sharing your experience with our BGBrows.com alopecia makeup shop. Any time we can add a human touch, we're delighted to make alopecia that much easier to manage.

Role: General Member of the Public
Rating: 4 stars  

1 person found this review helpful

I've had alopecia areata for 43 years, and this is the first event I've ever attended. I just wish groups and support like this were around when I was growing up with this disease. Although we had a small group, it was great to talk with other women about their experiences, as well as getting great tips on makeup and headwear from Thea, the founder of BGDL. I loved the relaxed setting of dinner and drinks, and the fact that Thea travels so you don't have to go too far to attend an event. This group finally made me feel like I'm not alone.

 
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(Nonprofit Staff) wrote:

We're so glad you were there! When you said " This group finally made me feel like I'm not alone" we're delighted to know that. Conquering the isolation of alopecia is one of our reasons for being the women's network for alopecia. Thank you for telling us the difference we're making for women.

Rating: 5 stars  

2 people found this review helpful

So responsive! When my 12 year-old daughter, Rachel, was recently diagnosed with alopecia areata my wife and I got online to learn as much as we could as quickly as possible. We found Bald Girls Do Lunch to go above and beyond our expectations. We talked to Thea at Bald Girls Do Lunch who answered all our questions the same day. We just knew talking to her that we were in good hands and that she was all about getting us sorted out and on the right path.
We feel so relieved to know there is this is resource for parents of girls. Thea got us connected with a young woman in her phone support list because she knew that this particular person got her alopecia the same age as our Rachel.

 
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Rating: 5 stars  

1 person found this review helpful

This is such an amazing nonprofit. The stories and advice are great and it really brings people together.

 
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Role: General Member of the Public
Rating: 5 stars  

2 people found this review helpful

BDGL helps so many women with alopecia all across the country with their content and events. Women with alopecia are underserved by all of the existing organizations, so it is great to see BGDL stepping up to help them in a very specific way.

 
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Role: General Member of the Public
Rating: 5 stars  

1 person found this review helpful

I am always amazed by the wonderful impact Bald Girls Do Lunch manages to have on so many people. There is no other organization like it and therefore, it has such an important role in the lives of all the people (most importantly the women with alopecia) that it serves. It is truly inspiring to see BGDL's phenomenal growth in regards to the number of people served as well as the international reach. Wishing Thea and BGDL continued success!!

 
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Rating: 5 stars  

1 person found this review helpful

I think Bald Girls Do Lunch is a wonderful organization. Thea Chassin, the thoroughly dedicated and creative founder of BGDL, has empowered and united women and girls with alopecia through casual meet-ups, fun events and informative newsletters. She started the organization with the desire to share all her first-hand knowledge and experience with the various issues that affected her along her journey with alopecia. Women no longer need to feel alone, afraid and ashamed. There is a supportive community of women out there for you!

 
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Rating: 5 stars  

1 person found this review helpful

Thea is awesome. I only wish I knew about Bald Girls years ago.

 
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Role: General Member of the Public
Rating: 5 stars  

1 person found this review helpful

Bald Girls do Lunch is a great organization. We took my daughter to an event shortly after her alopecia diagnosis. It helped her to see that she was not the only one. It really helped her.

We follow the Bald Girls do Lunch blog. It has all kinds of information and tips about alopecia. It is a great resource if you have alopecia or want to help someone with alopecia.

 
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Role: Professional with expertise in this field
Rating: 5 stars  

2 people found this review helpful

As a clinical social worker and someone who has had alopecia since age 5 (I'm now 63), I feel very grateful for BGDL. I wish organizations like BGDL, Alopecia World and NAAF had been around when I was younger. It is incredibly important
for individuals and families to have knowledge, support and caring as they live with and learn to accept and managing the effects of Alopecia.

Thea has an incredible and positive spirit, great sensitivity to others and has made a great contribution.

 
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