VITILIGO SUPPORT QUESTIONS, ANSWERS, & UPDATES MEETUP

support group emory

Emory University’s Department of Dermatology will host another vitiligo awareness and support group event September 06, 2014 from 11 a.m. – 12:00 p.m. in the Alperin Auditorium at 1525 Clifton Road. The event is being held in collaboration with Vitiligo Bond Inc., a registered nonprofit organization that seeks to provide support for those living with vitiligo.

Vitiligo is a pigmentation disorder in which the cells that make pigment in the skin are destroyed resulting in white patches that appear on the skin in different parts of the body.

“It is said that vitiligo has no known cause and no known cure. But people with vitiligo and physicians who treat vitiligo cannot help but search for the cause and cure,” says Sulochana Bhandarkar, MD, assistant professor of dermatology at Emory University School of Medicine.  “We want patients with vitiligo to know they are not alone.”

The event will offer information about vitiligo, as well as provide a question & answer forum for participants. Participants can also learn about living with vitiligo, how you can take holistic approaches, how nutrition affects your pigment, learn about new treatments and early interventions in treating kids and adults with vitiligo from Dr. Anantha Holla, Dr. Sulochana Bhandarkar and Vitiligo Bond. (Light refreshments will be served).

To register for the event visit www.vitiligobond.org or you can click the link below to register:

https://docs.google.com/spreadsheet/viewform?formkey=dGwwSjZISUFCaEtHTkRiR0ZlMkxUVXc6MA#gid=0

Contact:

Ms. Henry

404-997-2201

info@vitiligobond.org

About

Natasha Pierre McCarthy is the proud founder of National Vitiligo Bond Inc. Foundation (Vitiligo Bond), a nonprofit organization dedicated to supporting and empowering individuals with vitiligo. Inspired by her work as a Christian business professor and teaching from her pastor, she transformed her vision from God into reality by creating a platform that educates, uplifts, and connects those affected by vitiligo. Vitiligo Bond raises awareness through innovative educational initiatives, including Vitiligo 101 sessions at Emory University with Dr. Holla, community events, social media outreach, partnerships with support groups, and collaborations with public figures and state leaders. By fostering a strong sense of community, Vitiligo Bond ensures that no one living with vitiligo feels alone. Through dedicated advocacy efforts, Vitiligo Bond—alongside passionate advocate volunteers—has played a key role in spearheading and securing Governor Proclamations in multiple states, officially recognizing Vitiligo Awareness in Colorado, Georgia, Florida, Indiana, Louisiana, Maryland, Massachusetts, Mississippi, New Jersey, North Carolina, South Carolina, and West Virginia... The organization has helped start up support groups and nonprofits nationally and internationally. In addition, well known business brands have consulted and used models from the organization to represent their products and to help destigmatize vitiligo. Additionally, the organization has been recognized by Congressman Hank Johnson, who supported efforts to gain national recognition for vitiligo awareness. This advocacy contributed to President Barack Obama acknowledging Vitiligo Awareness during the month of June. Currently, further legislative efforts have been initiated to address bullying. Natasha believes that everyone is created with a purpose and deserves to live a full, vibrant life. “We all have the ability to shine.” Vitiligo Bond remains committed to raising awareness, destigmatizing vitiligo, advocating for youth who experience bullying, and supporting men and women struggling with self-acceptance. Through its platform, the organization also assist in research efforts to uncover the cause and ultimately find a cure for vitiligo.

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