About the Vitiligo Society
The Vitiligo Society is a UK‑based charity dedicated to supporting people affected by vitiligo. We provide trusted information, support, and advocacy, and work to improve understanding of vitiligo through education, research support, and collaboration.
Our work is guided by the experiences of people living with vitiligo, informed by clinical expertise, and underpinned by strong governance and transparency.
What we do
We support individuals and families affected by vitiligo by:
- Providing accurate, accessible information about vitiligo
- Offering emotional support and opportunities for peer connection
- Raising awareness and challenging misconceptions
- Supporting research and evidence‑based care
- Working with healthcare professionals, researchers, and partner organisations
Our aim is to ensure that everyone affected by vitiligo can access reliable information, feel supported, and be treated with understanding and respect.
Our mission and strategy
The Vitiligo Society operates with a clear mission and strategic direction, shaped by the needs of our community and informed by evidence and lived experience.
Governance and accountability
We are committed to openness and accountability in how we work.
Trustees and staff
The charity is overseen by a Board of Trustees, supported by staff and volunteers who deliver our services and activities.
Governance and policies
Our governance framework and policies set out how we operate responsibly, ethically, and in line with charity law and best practice.
Annual reports
We publish annual reports detailing our activities, impact, and finances.
Clinical expertise and guidance
Clinical insight plays an important role in ensuring our information and activities are safe, reliable, and evidence‑based.
Medical Advisory Board
The Vitiligo Society is supported by an independent Medical Advisory Board made up of experienced healthcare professionals.
Clinical guidance and research
We engage with research, clinical guidance, and emerging evidence to support better understanding and care for vitiligo.
Partnerships and collaboration
We work with a range of organisations, including charities, professional bodies, researchers, and healthcare partners, to strengthen our impact and extend our reach.
Get in touch
If you would like to contact the Vitiligo Society, ask a question, or find out more about our work, we’d be pleased to hear from you.
Our commitment
The Vitiligo Society exists to serve the vitiligo community. We aim to work with integrity, empathy, and respect, and to ensure the voices of people affected by vitiligo are at the heart of what we do.