Unsere Gruppe organisiert über 3000 globale Konferenzreihen Jährliche Veranstaltungen in den USA, Europa und anderen Ländern. Asien mit Unterstützung von 1000 weiteren wissenschaftlichen Gesellschaften und veröffentlicht über 700 Open Access Zeitschriften, die über 50.000 bedeutende Persönlichkeiten und renommierte Wissenschaftler als Redaktionsmitglieder enthalten.
Open-Access-Zeitschriften gewinnen mehr Leser und Zitierungen
700 Zeitschriften und 15.000.000 Leser Jede Zeitschrift erhält mehr als 25.000 Leser
Costa Bastos Castro JM
When we hear about Hansen’s disease, commonly known as leprosy, there is an image that is immediately catapulted to our head of limb deformities and skin lesions. Although treatment for the disease is highly effective and able to reduce the symptoms and keep them under control, this disease still brings a lot of suffering to people affected due to the stigma associated. A lot has been done in the research field on this disease which, although fatal a few decades ago, is highly curable nowadays, but whose atrocious effects in the past remain in people’s memories and is the cause of the great level of stigmatization the people affected with leprosy face to this day. Leprosy has faced ostracism for centuries and this has more to do with wrong cultural beliefs and lack of knowledge than with the risks of transmission and the morbid-mortality of the disease. This article is a literature review of what has been studied on the effects of stigmatization in people’s lives, as well as the interventions that can be put in place to minimize them and how to educate society on how to embrace these people. Research shows that the involvement of affected people in stigma-reduction interventions and their empowerment has achieved great results on both how society perceives them and how they perceive themselves. However, there is still a long way to go in terms of social equality for people affected or cured from the disease that involves the community population as a whole.