Living With Vitiligo

For many, the emotional toll of living with vitiligo is substantial. Individuals frequently report feelings of anxiety, depression and reduced self-esteem, often stemming from societal misconceptions about the condition. False beliefs, such as the idea that vitiligo is contagious or caused by poor hygiene, compound the psychological burden. Children and adolescents are particularly vulnerable, as they may face bullying or difficulty with self-acceptance.

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Managing vitiligo is often about addressing the emotional and social dimensions. Support networks, public education and advocacy are essential in creating environments where those with vitiligo feel empowered to live confidently and thrive, while patient support groups provide a safe space for shared experiences, guidance, and encouragement.

GLOVA’s Commitment to Change

At GLOVA, we recognize that understanding and addressing the medical, psychological, and societal aspects of vitiligo is critical to improving the lives of those affected by the condition. Our mission extends beyond research; we aim to foster acceptance, reduce stigma, and advocate for equitable care for everyone living with vitiligo worldwide.

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Through the Global Vitiligo Atlas, we provide comprehensive resources, support cutting-edge research, and work to amplify the voices of individuals with vitiligo. Together, we can break down barriers, build understanding, and create a world where no one with vitiligo feels marginalized or misunderstood.

By focusing on education, advocacy, and support, GLOVA strives to help individuals with vitiligo embrace their uniqueness and lead fulfilling lives, free from discrimination and stigma.