日本ハンセン病学会雑誌
Online ISSN : 1884-314X
Print ISSN : 1342-3681
ISSN-L : 1342-3681
最新号
選択された号の論文の2件中1~2を表示しています
原著
  • Hiroyuki Watanabe, Vu Tuan Anh, Huynh Cong Ai, Tran Xuan Vy, Tran ...
    2024 年 93 巻 2 号 p. 39-47
    発行日: 2024年
    公開日: 2024/10/10
    ジャーナル フリー

      Children of recovered leprosy patients (CRLPs) may experience a significantly lower quality of life (QoL). This study analyzed the QoL of CRLPs in Vietnam by examining their physical and mental health, self-esteem, family, friends, and school using the Kid-KINDLR health scale (Vietnamese version) between 2016 and 2019. A self-administered questionnaire was distributed to CRLPs (n = 58) and a control group (n = 47). The results were subjected to statistical tests and factor analysis. A comparison of both groups revealed CRLPs reported a significantly lower QoL and significantly diminished outcomes for physical health- and family-related items. Factor analysis was performed assuming the latent factor of vulnerability for the inferior QoL group. CRLPs exhibited a different QoL structure as vulnerability potentially influenced the decline of QoL on physical health. Traditional health measures such as the Kid-KINDLR cannot easily verify latent factors affecting QoL; hence, future analyses should assume the existence of underlying influences.

ミニレビュー
  • 近藤 剛
    2024 年 93 巻 2 号 p. 49-56
    発行日: 2024年
    公開日: 2024/10/10
    ジャーナル フリー

      I first visited Nagashima in 1999, and in my involvement with the Hansen’s disease issue to this day, I have learnt that the history of human rights has been advanced by those who have fought for human rights under the wrong Hansen’s disease segregation policy of the state, and I had the valuable experience of visiting the Kalaupapa sanatoria in Hawaii, as well as in Korea and Taiwan, which were established during the Japanese colonial period.

      I learned three important things from the Hansen’s disease issue; (1) the history of the victims who fought for human rights with human dignity under the state’s Hansen’s disease segregation policy; (2) the strength, kindness and richness of the victims’ hearts; and (3) in order to build a symbiotic society where the human rights of all people are respected and not discriminated against, it is important not to forget the inhuman facts that have taken place over the years under the wrong Hansen’s disease segregation policy and to fulfil our responsibility to pass on the story to the next generation, thereby making a step forward in the history of human rights in Japan.

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