I have continued to be impressed with the positive impact that BGDL has had on the alopecia community. Especially in the last several years with their new makeup line. Helping women with alopecia to feel beautiful and pretty with products customized just to their needs has really furthered the organization's cause. I've been lucky enough to continue my involvement volunteering at various events and the experience has been very rewarding.
Bald Girls has been a wonderful experience sharing our thought & feelings about having Alepecia. You find out thru sharing you are not alone. So many have been affected by this autoimmune disease. Thea has brought so many folks together thru her lunches & it is such a good feeling.
Kudos to Thea & all that u have accomplished. I only hope there is a cure around the corner. Mimi M
This is an outstanding example of an organization that has a clearly defined mission and lives up to it on every level. Bald Girls Do Lunch provides public education and support for women living with alopecia areata while also offering practical advice. Thank you, Thea Chassin, for continuing to help so many women!
I am very impressed by the multiple ways Bald Girls Do Lunch reaches out to the community. In addition to organizing special events and serving as an invaluable resource for information and support, BGDL also provides a vital service in educating the general public. The email newsletter is especially informative and well-designed. Thanks to Thea Chassin, countless people have had their lives changed for the better.
Bald Girls is a fantastic non-profit that makes an enormous impact in the lives of so many people. I’ve seen the incredible strength and guidance Thea offers to so many people and I recommend BGDL as a great resource for learning more about alopecia and the resources available to members of the alopecia community.
BGDL is an amazing organization run by wonderful people that make a huge difference in the alopecia community. The kindness and friendship you receive from Thea is extraordinary and provides powerful support In difficult times. There is no other organization like BGDL and it deserves more stars than I can post.
It's not often that a non-profit is able to so clearly deliver on its mission. BGDL is one of the rare organizations that has a clear mission and is able to truly help. Women with alopecia finally have a place where they can get the support and information they need.
I wish you included women with other causes of hair loss, like female pattern. I felt so sad when I learned I was not welcome at these meetings. I know you stick to your mission statement, but couldn't you branch out?
Thanks for your interest in Bald Girls Do Lunch, but I can't help but notice that your disappointment is misdirected. I see that you are very disappointed because our mission helps women with an autoimmune hair loss disease and you don't have an autoimmune hair loss disease. We're very successful and highly respected, so why would you take it out on us publicly with 1 star, as if saying that we are somehow unsuccessful? We're always known to go out of our way to be helpful, so I have an idea I hope you like. Female pattern hair loss is a serious concern as it causes much distress for women world-wide. I have had the honor to get to know ( because I educate them about alopecia areata) some of the most caring and talented specialists from many professional hair replacement centers across the United States. Many of them hold meet-ups specifically for women just like you with female pattern hair loss to meet others with the same concerns. If you need help finding a hair replacement center near you, we will do what we can to help you find one.
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.
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.
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.
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.
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.
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!!
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.
I was so happy to find Bald girls Do Lunch group. I wanted to share my feeling and experiences as an alepecia person. It has always been a feel good time to be among with these gals/ women sharing our feeling & dealing with alepecia. Thea has been so wonderful pulling everyone together all over the states for lunch and comroderie. Thank you Thea...
I have very recently been diagnosed with rare scarring frontal fibrosing Alopecia and am having trouble with the rapid hair loss. My dermatologist has told me that my hair will never come back and has suggested I wear a wig. As a person who hates even wearing a hat in winter I was in shock. I thought I was alone and had no where to turn. My internet search led me to BGDL and thank heavens for that. I look forward to having a community of women who are in the same boat. I will value their help and support as I learn to deal with this affliction. I live near Calgary Alberta Canada and do not know if there is a group in that city but at least I will have the group here to turn to for support.
BGDL is a blessing. They share valid information honestly, promote health physically and psychological. Real information on how society views people with no hair and they are changing the world with awareness and accepting.
Bald Girls Do Lunch is a tremendous organization, and its founder, Thea Chassin, is a force to be reckoned with. The relative rarity of alopecia areata can make the women who suffer from it feel ashamed and alone. Finding out that there are others like them who face the same challenges — and who do so with style, confidence and humor — has been a life-changing experience for many of the women Thea’s helped. I applaud her commitment and wholeheartedly support the Bald Girls organization.
I am a 59 year old woman with Alopecial Universalis. I had suffered with bouts of Alopecial Areata through the years but after completing chemotherapy for breast cancer I went on to lose all the hair on my body. It took me a while to figure out that it was never coming back and I was so self conscious and felt so unattractive. Through Thea and Bald Girls Do Lunch I have been able to connect with others who share the same problems and experience the same emotions. The group is a wonderful source for practical solutions to every day problems, support groups and a source for the latest in research for a cause and cure. I suppport this wonderful effort and am sooo glad it has been there for me and others like me
Bald Girls Do Lunch is a one-of-a-kind organization that meets the needs of specific population - women with alopecia areata - whose needs would otherwise go unanswered. The organization is dynamic, current, and very personalized to allow for every woman coping with the challenges of alopecia areata to find something relevant and helpful for their own personal situation and needs.
Very refreshing to just be able to sit & visit with people that are going thru the same thing you are or have been going thru. Very down to earth & informative. So happy I am a member of this great group! Thank you Thea.