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Malawian mothers’ experiences of raising children living with albinism: A qualitative descriptive study

BACKGROUND: Albinism in humans is characterised by a reduced amount of pigment (melanin) present in the skin, hair follicles and the eye; approximately 7000–10 000 Malawians of all ages are affected. Children with these features face extreme forms of human rights abuses, even death. OBJECTIVES: This...

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Autores principales: Likumbo, Naomi, de Villiers, Tania, Kyriacos, Una
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AOSIS 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063528/
https://www.ncbi.nlm.nih.gov/pubmed/33937005
http://dx.doi.org/10.4102/ajod.v10i0.693
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author Likumbo, Naomi
de Villiers, Tania
Kyriacos, Una
author_facet Likumbo, Naomi
de Villiers, Tania
Kyriacos, Una
author_sort Likumbo, Naomi
collection PubMed
description BACKGROUND: Albinism in humans is characterised by a reduced amount of pigment (melanin) present in the skin, hair follicles and the eye; approximately 7000–10 000 Malawians of all ages are affected. Children with these features face extreme forms of human rights abuses, even death. OBJECTIVES: This study aims to describe Malawian mothers’ experiences, perceptions and understanding of raising children with albinism (CWA). METHODS: The study was conducted in 2018 using a qualitative descriptive design, with purposive sampling and voluntary participation. Mothers, 18 years and older, who had given birth to a CWA and who attended the dermatology clinic of a local public hospital participated. An interview guide used during standardised, open-ended interviews was translated from English to Chichewa using forward and backward translation. Interviews were conducted in Chichewa, audio recorded, transcribed and forward and back translated from English to Chichewa. Thematic data analysis was employed. RESULTS: The mean age of participants (N = 10) was 33 years; two had albinism. Emerging themes confirmed the existence of myths and stereotypes regarding albinism but from the mothers’ perspectives. Mothers reported: (1) some experiences of emotional pain, initially, but also love and acceptance of their children, despite adverse reactions of others; (2) their experiences of stigmatisation of their children and themselves, and of intended harm to their children, and (3) their own lack of knowledge and understanding of albinism. CONCLUSION: In our limited study, mothers’ self-reported experiences of raising CWA in Malawi highlight the need for educational programmes on albinism at national level, particularly for families with a CWA, health professionals and educators.
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spelling pubmed-80635282021-04-29 Malawian mothers’ experiences of raising children living with albinism: A qualitative descriptive study Likumbo, Naomi de Villiers, Tania Kyriacos, Una Afr J Disabil Original Research BACKGROUND: Albinism in humans is characterised by a reduced amount of pigment (melanin) present in the skin, hair follicles and the eye; approximately 7000–10 000 Malawians of all ages are affected. Children with these features face extreme forms of human rights abuses, even death. OBJECTIVES: This study aims to describe Malawian mothers’ experiences, perceptions and understanding of raising children with albinism (CWA). METHODS: The study was conducted in 2018 using a qualitative descriptive design, with purposive sampling and voluntary participation. Mothers, 18 years and older, who had given birth to a CWA and who attended the dermatology clinic of a local public hospital participated. An interview guide used during standardised, open-ended interviews was translated from English to Chichewa using forward and backward translation. Interviews were conducted in Chichewa, audio recorded, transcribed and forward and back translated from English to Chichewa. Thematic data analysis was employed. RESULTS: The mean age of participants (N = 10) was 33 years; two had albinism. Emerging themes confirmed the existence of myths and stereotypes regarding albinism but from the mothers’ perspectives. Mothers reported: (1) some experiences of emotional pain, initially, but also love and acceptance of their children, despite adverse reactions of others; (2) their experiences of stigmatisation of their children and themselves, and of intended harm to their children, and (3) their own lack of knowledge and understanding of albinism. CONCLUSION: In our limited study, mothers’ self-reported experiences of raising CWA in Malawi highlight the need for educational programmes on albinism at national level, particularly for families with a CWA, health professionals and educators. AOSIS 2021-04-20 /pmc/articles/PMC8063528/ /pubmed/33937005 http://dx.doi.org/10.4102/ajod.v10i0.693 Text en © 2021. The Authors https://creativecommons.org/licenses/by/4.0/Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License.
spellingShingle Original Research
Likumbo, Naomi
de Villiers, Tania
Kyriacos, Una
Malawian mothers’ experiences of raising children living with albinism: A qualitative descriptive study
title Malawian mothers’ experiences of raising children living with albinism: A qualitative descriptive study
title_full Malawian mothers’ experiences of raising children living with albinism: A qualitative descriptive study
title_fullStr Malawian mothers’ experiences of raising children living with albinism: A qualitative descriptive study
title_full_unstemmed Malawian mothers’ experiences of raising children living with albinism: A qualitative descriptive study
title_short Malawian mothers’ experiences of raising children living with albinism: A qualitative descriptive study
title_sort malawian mothers’ experiences of raising children living with albinism: a qualitative descriptive study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063528/
https://www.ncbi.nlm.nih.gov/pubmed/33937005
http://dx.doi.org/10.4102/ajod.v10i0.693
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