KK’s mom reached out to us when her daughter was being bullying at school at the age of nine. We visited her school at the request of her mom, to educate the staff about her condition. We were invited to her school to speak to the children in all of KK’s class so that they were aware of being kind and to say know to bullying. At #VitiligoBond, we developed programs aimed at boosting KK’s confidence and self-esteem. During one of our annual photo shoots, a local agency in Georgia discovered KK on our social media page and wanted to…
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On Giving Tuesday, we want to emphasize the importance of raising awareness. As a non-profit organization, we are committed to shedding light on vitiligo, a skin disorder that is often not well understood. Our mission is to empower, inspire, and mentor both youth and adults through a variety of initiatives, including advocacy, education, self-esteem makeovers, entrepreneurship, support group formation, social media celebrations, social events, and much more. By clicking the link below, you can support our programs, enabling us to spread joy and educate others about vitiligo. We believe that knowledge and compassion are essential tools for fostering a more…
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CEO, Mrs. McCarthy coordinated event with South Carolina vitiligo support group CEO, Mrs. Jefferson. Members from Georgia and South Carolina had a great time together. Stay tuned!
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National Vitiligo Bond Inc Foundation will be at Congressman David Scott’s 13th Annual Health Fair Saturday, August 19 at 9 AM – 2 PM Mundy’s Mill High School 9652 Fayetteville Rd, Jonesboro, Georgia 30238. If you are one of our donors or sponsors and will like to be involved, contact support@vitiligobond.org Thank you #Zanderm for sending samples to display on our table. National Vitiligo Bond Inc Foundation will be at Congressman David Scott’s 13th Annual Health Fair Saturday, August 19 at 9 AM – 2 PM Mundy’s Mill High School 9652 Fayetteville Rd, Jonesboro, Georgia 30238. If you are one…
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Ms. Walker was one of our advocates who decided to take it to another level in her state. Ms. Walker consulted and worked with CEO, Mrs. McCarthy remotely to get her group started in her state of Mississippi. Ms. Walker is amazing and passionate about shining a light for people in Mississippi living with vitiligo.
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Mrs. Yarborough was one of our advocates who decided to take it to another level in her state of Virginia. Ms.Yarborough consulted and worked with CEO, Mrs. McCarthy remotely to get her group started in her state of Virginia. Ms. Yarborough planned her first meet and greet. Thank you to the sponsors who helped Mrs. Yarborough with her first meet and greet.
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Macy’s collaborates with Vitiligo Bond Inc. to raise awareness about vitiligo and educate members on how to use Dermablend. The CEO of Vitiligo Bond organized a program that showcased local youth confidently walking the runway, promoting awareness of vitiligo, and performing songs that advocate against bullying. The event was a vibrant celebration of diversity and empowerment. Attendees were moved by the incredible talent and bravery displayed by the youth, who not only embraced their unique skin but also inspired others to accept themselves. The program also featured workshops where participants learned about skincare techniques and the benefits of using Dermablend…
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CEO of National Vitiligo Bond Inc Foundation was honored by MIPO for making the impossible possible. Thank you “Making the Impossible Possible” (MIPO) for the recognition awards from your organization and citations from New York state legislative officials for the advocacy work done by CEO, Mrs. McCarthy at National Vitiligo Bond Inc Foundation. #MIPO #VitiligoBond #VitiligoAwareness