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
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D’Lyric Inspired is excited to join forces with Vitiligo Bond Inc., (VBI), which was founded in November 2010 by Natasha Pierre-McCarthy, who is also a Vitiligan (a person with Vitiligo). VBI is a registered nonprofit 501c(3) organization based out of Atlanta, GA. that aims to provide support for those living with Vitiligo. Currently, Vitiligo Bond Inc. is in collaboration with Congress to make Vitiligo an official observance day in the United States. VBI has grown into a worldwide support group, through its Facebook and social media presence. Together, D’Lyric Inspired and VBI plan to increase awareness about Vitiligo using an…
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A National Vitiligo Bill was introduced March 20th 2017 to bring about awareness to vitiligo. See press release links below. Press Release We would also like to thank Rowdy, Ava, Carter & Stella for bringing awareness to vitiligo this week. We would also like to thank Ava’s Mom Julie for always sharing Ava’s photos every year to help us spread awareness about vitiligo. This recent photo from Ava’s Mom, Julie speaks volumes. The National Vitiligo Bill will help children like Ava, Carter and many more ease the stigma for people living with vitiligo. Please help support organizations…
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On March 22nd, 2017, a number of our new members of Vitiligo Bond, Inc. (VBI) was a part of a photo-op with our Governor, at the Capitol in Atlanta, GA. Featured in the photo is one of our youngest members Jhori who met Governor Nathan Deal for the first time. Small acts of kindness like this can empower a child and have a lasting impact. Vitiligo is a non-contagious auto-immune skin disorder that strips pigment from a person’s skin leaving it patchy. Every year, our Governor takes pride in standing with us. This is the 7th year of this activity. VBI encourages…
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Vitiligo Bond’s Vitiligo Awareness Face 2 Face Meetups Welcome to Vitiligo Bond’s Vitiligo Awareness Face-to-Face Meetups Network! Vitiligo Bond is the leading organization in Georgia focused on the unique challenges faced by youth and adults with vitiligo. We offer resources, connections, and outreach to ensure that everyone feels supported, empowered, and hopeful. Our mission is to guarantee that no one experiences vitiligo in isolation. Keep an eye on our social media for information about upcoming monthly meetups. If you’re interested in sponsoring our event, please reach out to us via email at support@vitiligobond.org.
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We currently have a t-shirt fundraiser and online social outreach campaigns going on our Facebook page. Come by and check it out at ww.facebook.com/vitiligobondinc! We would also like to give a huge shout out to #4Imprit for making our vitiligo awareness campaigns possible.
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Thank you to our Georgia community partners for your continued support. Vitiligo Bond, Inc and MEG Enterprises, LLC “Be The True You” Vitiligo Awareness Press Conference was a huge success.
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#NOMAKEUP
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Please join Vitiligo Bond Inc., (VBI) and MEG Enterprises, LLC (MEG) at their press conference on Thursday, November 17th, 2016 at the Atlanta Sheraton Hotel, 165 Courtland Street, NE, Atlanta, GA 30303 from 6:00 to 10:00PM. The press conference will shed light on the concerns and challenges of people with vitiligo. Medical doctors, legislative officials, celebrities, and members of the Vitiligo community will join this event. The press conference will introduce the “Escape Colorism: Be the True You” tour, which will raise visibility and awareness of Vitiligo to cities around the USA. The tour will be launched from Atlanta, Georgia.…
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During the summer month through fall from 2013-present, Vitiligo Bond’s outreach education team met with hundreds of people in the public to share outreach information about vitiligo. We credit this to NIAMS partners who support our outreach education programs by providing our organization with the resource handout materials we need to share with the public. We also have had the opportunity to go to schools to reach out to administrators about vitiligo and educate them about it. Below are some photos of some of our past and present outreach efforts. We hope to grow our outreach efforts with help from our sponsors and kinds…