Our Story

Vitiligo International Patient Organisations Committee is the worldwide alliance of vitiligo patient organizations build in 2018 during the first Vitiligo International Patient Organizations Conference and is now an official NGO based in Paris.
Vitiligo International Patient Organisations Conference 2020: 3rd to 6th December 2020 more than 25 nations are forecasted to take part in this conference. Patient leaders and scientists will be sharing views, expertise, projects, etc. during 3 days with researchers, dermatologists, pharma industries representatives.

Our Objective

Our purpose is to improve the daily life of vitiligo patients, provide them with the support and information they need, promote understanding, recognition, work on cures and care for vitiligo by the medical community and society.
VIPOC, the community and support organization for vitiligo patients’ groups, was created in 2018 after multiple patient organizations had discussed the idea of banding together to improve the awareness and the lives of people with vitiligo.

The Board

Steering comittee

Are you a Vitiligo Patient Leader? Join now to become a member.

Our purpose is to improve the daily life of vitiligo patients, provide them with the support and information they need, and promote understanding, recognition, work on cure and care for vitiligo by the medical community and society.