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Negotiating political power and stigma around fragile X Syndrome in a rural village in Cameroon: A tale of a royal family and a community

BACKGROUND: Fragile X Syndrome (FXS) is a neurogenetic condition that significantly impacts the lives of affected individuals and their families due to its association with intellectual disability (ID) and stigma. METHOD: In this paper, we present the findings of an ethnographic study in the communi...

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Autores principales: Kengne Kamga, Karen, Munung, Nchangwi Syntia, Nguefack, Séraphin, Wonkam, Ambroise, De Vries, Jantina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104168/
https://www.ncbi.nlm.nih.gov/pubmed/33544459
http://dx.doi.org/10.1002/mgg3.1615
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author Kengne Kamga, Karen
Munung, Nchangwi Syntia
Nguefack, Séraphin
Wonkam, Ambroise
De Vries, Jantina
author_facet Kengne Kamga, Karen
Munung, Nchangwi Syntia
Nguefack, Séraphin
Wonkam, Ambroise
De Vries, Jantina
author_sort Kengne Kamga, Karen
collection PubMed
description BACKGROUND: Fragile X Syndrome (FXS) is a neurogenetic condition that significantly impacts the lives of affected individuals and their families due to its association with intellectual disability (ID) and stigma. METHOD: In this paper, we present the findings of an ethnographic study in the community of a patient who received a genetic diagnosis for FXS in Cameroon. This study builds on data from 28 participants of a royal family and 58 from the community who participated in 20 in‐depth interviews and nine focus group discussions. RESULTS: We identified two types of stigma in this community: public stigma directed towards the royal family and associative stigma experienced by royal family members. We outline the stereotyping labels used for the family and its children with Fragile X Syndrome and describe the stigma‐power dynamic between the community members and the royal family. First, most villagers use less stigmatizing terms to addressing FXS children from the chieftaincy because of their position in society. Secondly, due to their social position, the royal family uses their status to negotiate marriages with community members. From these observations, we can suggest that the primary role of stigma in this community is to keep people away from FXS and keep them down through domination and exploitation. CONCLUSION: We advocate that other researchers examine if the same pattern exists in other inheritable forms of ID and conduct more qualitative research on FXS in Africa.
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spelling pubmed-81041682021-05-10 Negotiating political power and stigma around fragile X Syndrome in a rural village in Cameroon: A tale of a royal family and a community Kengne Kamga, Karen Munung, Nchangwi Syntia Nguefack, Séraphin Wonkam, Ambroise De Vries, Jantina Mol Genet Genomic Med Original Articles BACKGROUND: Fragile X Syndrome (FXS) is a neurogenetic condition that significantly impacts the lives of affected individuals and their families due to its association with intellectual disability (ID) and stigma. METHOD: In this paper, we present the findings of an ethnographic study in the community of a patient who received a genetic diagnosis for FXS in Cameroon. This study builds on data from 28 participants of a royal family and 58 from the community who participated in 20 in‐depth interviews and nine focus group discussions. RESULTS: We identified two types of stigma in this community: public stigma directed towards the royal family and associative stigma experienced by royal family members. We outline the stereotyping labels used for the family and its children with Fragile X Syndrome and describe the stigma‐power dynamic between the community members and the royal family. First, most villagers use less stigmatizing terms to addressing FXS children from the chieftaincy because of their position in society. Secondly, due to their social position, the royal family uses their status to negotiate marriages with community members. From these observations, we can suggest that the primary role of stigma in this community is to keep people away from FXS and keep them down through domination and exploitation. CONCLUSION: We advocate that other researchers examine if the same pattern exists in other inheritable forms of ID and conduct more qualitative research on FXS in Africa. John Wiley and Sons Inc. 2021-02-05 /pmc/articles/PMC8104168/ /pubmed/33544459 http://dx.doi.org/10.1002/mgg3.1615 Text en © 2021 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Kengne Kamga, Karen
Munung, Nchangwi Syntia
Nguefack, Séraphin
Wonkam, Ambroise
De Vries, Jantina
Negotiating political power and stigma around fragile X Syndrome in a rural village in Cameroon: A tale of a royal family and a community
title Negotiating political power and stigma around fragile X Syndrome in a rural village in Cameroon: A tale of a royal family and a community
title_full Negotiating political power and stigma around fragile X Syndrome in a rural village in Cameroon: A tale of a royal family and a community
title_fullStr Negotiating political power and stigma around fragile X Syndrome in a rural village in Cameroon: A tale of a royal family and a community
title_full_unstemmed Negotiating political power and stigma around fragile X Syndrome in a rural village in Cameroon: A tale of a royal family and a community
title_short Negotiating political power and stigma around fragile X Syndrome in a rural village in Cameroon: A tale of a royal family and a community
title_sort negotiating political power and stigma around fragile x syndrome in a rural village in cameroon: a tale of a royal family and a community
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104168/
https://www.ncbi.nlm.nih.gov/pubmed/33544459
http://dx.doi.org/10.1002/mgg3.1615
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