“…In this process, people without the disease would attribute negative stereotypes to people with Vitiligo (Dovidio et al, 2010;Fiske, 2000), leading to a social comparison used to maintain the positive status of the first group's social identity (Tajfel, 1981) and keep the latter group apart (Phelan et al, 2008). Among the variables observed in studies on Vitiligo and social discrimination, characteristics as the person's skin color, as well as the white patches' exposure (caused by the disease) are determinant in the way that people with Vitiligo represent their self-image and talk about the inconvenience of having the illness Do Bú & Coutinho, 2018Firooz et al, 2004;Szabo & Brandão, 2016). In addition, research that focused on analyzing the quality of life of this group has shown, in different cultures, that people with Black skin and white patches more easily recognized by the society have lower quality-of-life indices compared to people with White skin and spots that are not perceived by the social context (Bonotis et al, 2016;Do Bú et al, 2021;Ezzedine et al, 2019;Karelson et al, 2012;Mattoo et al, 2001;Morales-Sánchez et al, 2017;Sampogna et al, 2008;Sarhan et al, 2016;Simons et al, 2020;Talsania et al, 2010).…”