Vanessa Pereira Lima, Valéria De Araujo Soares, Jaqueline D' `Paula Ribeiro Vieira Torres, Luana Souza Torres, Gabriel Duarte Paulino, Ticiane Dias Prado, Henrique De Castro Reis, Josiane Steil Siewert, Manuele Miranda Mafra Oliveira, Ana Luiza Silva, Mirela Lopes de Figueiredo, Anáira Gisser de Souza Ribeiro, Ana Paula Ferreira Maciel, Marlete Scremin, Mateus Sena Lima, Daniela Fagundes Souto, Diego Edson de Oliveira, Taysa Cristina Cardoso Freitas, Nayara Jane Ferreira Soares
{"title":"LIVING WITH HANSENÍASE","authors":"Vanessa Pereira Lima, Valéria De Araujo Soares, Jaqueline D' `Paula Ribeiro Vieira Torres, Luana Souza Torres, Gabriel Duarte Paulino, Ticiane Dias Prado, Henrique De Castro Reis, Josiane Steil Siewert, Manuele Miranda Mafra Oliveira, Ana Luiza Silva, Mirela Lopes de Figueiredo, Anáira Gisser de Souza Ribeiro, Ana Paula Ferreira Maciel, Marlete Scremin, Mateus Sena Lima, Daniela Fagundes Souto, Diego Edson de Oliveira, Taysa Cristina Cardoso Freitas, Nayara Jane Ferreira Soares","doi":"10.51249/hs.v4i01.1841","DOIUrl":null,"url":null,"abstract":"The present study aimed to know the experiences, meanings and perceptions of patients with leprosy. This is a descriptive study, exploratory qualitative approach. The study was a polyclinic, located in minas gerais, reference in the treatment of leprosy. The data were produced through individual interviews with a screenwriter, semi-structured data analysis made it possible to identify four thematic categories: perceptions about the knowledge about leprosy; the discovery of leprosy; living with leprosy and live with leprosy in society. Identified that the perception of patients about the meaning and knowledge about leprosy is superficial and limited, however, the knowledge deficit did not interfere in the belief of the treatment and cure of disease resolutivo. One can understand that late diagnosis is still present in the discovery of leprosy and psychological issues, emotional, physical and social feature direct impact in the lives of patients.","PeriodicalId":507713,"journal":{"name":"Health and Society","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Health and Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.51249/hs.v4i01.1841","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The present study aimed to know the experiences, meanings and perceptions of patients with leprosy. This is a descriptive study, exploratory qualitative approach. The study was a polyclinic, located in minas gerais, reference in the treatment of leprosy. The data were produced through individual interviews with a screenwriter, semi-structured data analysis made it possible to identify four thematic categories: perceptions about the knowledge about leprosy; the discovery of leprosy; living with leprosy and live with leprosy in society. Identified that the perception of patients about the meaning and knowledge about leprosy is superficial and limited, however, the knowledge deficit did not interfere in the belief of the treatment and cure of disease resolutivo. One can understand that late diagnosis is still present in the discovery of leprosy and psychological issues, emotional, physical and social feature direct impact in the lives of patients.
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