About The Vitiligo Society

Founded in 1985, The Vitiligo Society is a leading charitable organization based in the United Kingdom, dedicated to supporting people living with vitiligo both nationally and internationally. With over 850 members and a global online community of more than 10,000 followers, the Society is committed to reducing the psychological, social, and physical impact of vitiligo while advancing the search for effective treatments and, ultimately, a cure.

The organization’s mission is built around five interconnected priorities: providing up-to-date and reliable information on vitiligo; informing the community about the latest scientific research and contributing to its advancement; developing and investing in high-quality support services; advocating as a strong voice for those affected; and reaching out to ensure no one faces vitiligo alone.

Through these efforts, The Vitiligo Society offers a trusted platform where individuals can access expert knowledge, connect with peers, and find practical and emotional support. The Society organizes educational resources, public awareness campaigns, and collaborative projects with researchers, medical professionals, and other patient organizations. By combining lived experience with scientific expertise, it ensures that the needs of the vitiligo community are both heard and addressed at every level.

Beyond direct support, the Society actively works to dismantle the stigma surrounding visible differences, promoting greater understanding in workplaces, schools, and wider society. Its advocacy extends to influencing policy, funding research initiatives, and creating opportunities for people with vitiligo to share their stories and shape the public narrative.

Guided by compassion, determination, and a global perspective, The Vitiligo Society continues to build a future in which vitiligo no longer limits opportunities, confidence, or quality of life and where those affected can thrive with pride and visibility.