About Vitiligo Association of Uganda

Founded in 2015, the Vitiligo Association Uganda (VAU) is a pioneering organization committed to advocating for the rights and well-being of people living with vitiligo across Uganda. With a strong focus on mainstreaming vitiligo within the government health system, VAU works tirelessly to ensure that the condition receives the recognition, resources, and support it deserves at both policy and community levels.

VAU’s multifaceted approach includes raising public awareness about vitiligo to combat stigma and misinformation, empowering individuals through education, and providing much-needed psychosocial support to help patients and their families cope with the emotional and social challenges associated with the condition. The association recognizes that understanding and acceptance are key to improving the quality of life for people affected by vitiligo.

In addition to advocacy and support, VAU prioritizes research and data collection to deepen knowledge about vitiligo in Uganda and inform effective strategies for care and treatment. By gathering and analyzing relevant data, VAU aims to influence healthcare policies and promote evidence-based interventions that benefit the vitiligo community.

The organization’s collaborative efforts extend to partnerships with healthcare providers, government bodies, and international organizations, all aligned toward the common goal of advancing vitiligo awareness, acceptance, and patient rights.

Through its comprehensive programs and passionate commitment, Vitiligo Association Uganda stands as a vital champion for vitiligo patients, helping to shape a future where they can live with dignity, support, and hope.