About Us
Vitiligo International Patient Organizations 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.
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Connecting the Global Vitiligo Community
- 40+ member organizations
- 30+ countries represented
- One Voice for Vitiligo
VIPOC connects patient leaders, researchers, and advocates across continents to strengthen vitiligo research, policy, and awareness worldwide.
Latest in Scientific Research
Skin and Digital–The 2024 Narrative
Dominique du Crest, MBEa ducrest@skinaid.eu ∙ Monisha Madhumita, MDb ∙ Wendemagegn Enbiale, MD, MPH, PhDc ∙ Alexander Zink, MD, MPH, PhDd ∙ Art Papier, MDe ∙ Gaone Matewa, BBAf ∙ Harvey Castro, MD, MBAg ∙ Hector Perandones, MDh ∙ Josef De Guzman, OD-OPSi ∙ Misha Rosenbach, MDj ∙ Tu-Anh Duong, MD, PhDk ∙ Yu-Chuan Jack Li, MD,…
Racial and Ethnic Diversity in Vitiligo Clinical Trials: A Retrospective Cross-Sectional Study Assessing Demographic Reporting of Participants
Racial and Ethnic Diversity in Vitiligo Clinical Trials: A Retrospective Cross-Sectional Study Assessing Demographic Reporting of Participants
July 2024 | Volume 23 | Issue 7 | e164…
Quality of life of adult vitiligo patients using camouflage: A survey in a Chinese vitiligo community
Quality of life of adult vitiligo patients using camouflage: A survey in a Chinese vitiligo community
Abstract Background Vitiligo is an acquired depigmented skin disease…
Mental Health and Psychosocial Quality-of-Life Burden Among Patients With Vitiligo Findings From the Global VALIANT Study
Mental Health and Psychosocial Quality-of-Life Burden Among Patients With Vitiligo Findings From the Global VALIANT Study
Kristen Bibeau, PhD, MSPH; Khaled Ezzedine,MD, PhD; John E. Harris,…
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