Vitiligo Support International Inc. (VSI) is a patient driven 501(c)(3) nonprofit organization offering a comprehensive resource of vitiligo education, research and awareness for those whose lives have been affected by vitiligo.

We are here to address your questions and concerns and help you connect with our community. You will find the hope, support and healing that can only be offered by those who understand best - those who have walked in your shoes.

Advocacy

If you are a citizen of the United States, Vitiligo Support International encourages you to join our advocacy team. From time to time we offer opportunities for concerned individuals to join together and help shape public policy as it affects vitiligo. You can spend as much or as little time as you choose in this effort. By joining the VSI Advocacy Team, you will have the opportunity to educate members of Congress about vitiligo, autoimmunity and skin disease in an effort to increase funding and develop policies to benefit those with vitiligo.

To find your legislator's contact information, check these sites.

United States Senate -
  http://www.senate.gov/general/contact_information/senators_cfm.cfm

United States House of Representatives -
  http://www.house.gov/writerep/

If you are willing to help on occasion; please fill in the contact form below so that we can notify you of opportunities to voice the needs of vitiligo patients.

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