Abstract Vitiligo has been linked with multiple myths and misconceptions, which impacts the diagnosis, treatment, and reporting of the condition. We live in a society where the stigma of vitiligo impairs the quality of life of the affected person. Owing to the stigma to which persons diagnosed with vitiligo are subjected for years together in different settings and across different phases of life, affected individuals may develop a feeling of being unattractive or defective, resulting in having low self-worth and poor self-esteem. Acknowledging the high prevalence of vitiligo, the associated myths and misconceptions about the condition, the surrounding stigma, and the adverse consequences of the same, there is an urgent need to implement targeted public health interventions to reduce the existing stigma. In conclusion, vitiligo is linked with a wide range of misconceptions and stigma, which interfere with the social life, growth opportunities, and quality of life of the affected person. A holistic package of services to reduce the stigma, clarify the myths, and help the individuals lead a dignified and respectful life is needed.
Shrivastava et al. (Tue,) studied this question.