Sickle cell and the social sciences: health, racism and disablement
Sickle cell disease (SCD) is a severe chronic illness and one of the world's most common genetic conditions, with 400,000 children born annually with the disorder, mainly in Sub-Saharan Africa, India, Brazil, the Middle East and in diasporic African populations in North America and Europe. Biom...
Gespeichert in:
| 1. Verfasser: | |
|---|---|
| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Abingdon, Oxon
Routledge
2019
|
| Schriftenreihe: | Routledge studies in the sociology of health and illness
Routledge studies in the sociology of health and illness |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Zusammenfassung: | Sickle cell disease (SCD) is a severe chronic illness and one of the world's most common genetic conditions, with 400,000 children born annually with the disorder, mainly in Sub-Saharan Africa, India, Brazil, the Middle East and in diasporic African populations in North America and Europe. Biomedical treatments for SCD are increasingly available to the world's affluent populations, while such medical care is available only in attenuated forms in Africa, India and to socio-economically disadvantaged groups in North America and Europe. Often a condition rendered invisible in policy terms because of its problematic association with politically marginalized groups, the social study of sickle cell has been neglected. This illuminating volume explores the challenges and possibilities for developing a social view of sickle cell, and for improving the quality of lives of those living with SCD. Tackling the controversial role of screening and genetics in SCD, the book offers a brief thematic history of approaches to the condition, queries the role of ethnicity and includes a discussion of how the social model of disability can be applied, as well as featuring chapters focusing on athletics, prisons and schools. Bringing together a wide range of original research conducted in the USA, the UK, Ghana and Nigeria, Sickle Cell and the Social Sciences is anchored in the discipline of sociology, but draws upon a diverse range of fields, including public health, anthropology, social policy and disability studies |
| Beschreibung: | 1 online resource (ix, 241 pages) |
| ISBN: | 9781351580847 1351580841 9781315098685 1315098687 9781351580854 135158085X 9781351580830 1351580833 |
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| 520 | |a Sickle cell disease (SCD) is a severe chronic illness and one of the world's most common genetic conditions, with 400,000 children born annually with the disorder, mainly in Sub-Saharan Africa, India, Brazil, the Middle East and in diasporic African populations in North America and Europe. Biomedical treatments for SCD are increasingly available to the world's affluent populations, while such medical care is available only in attenuated forms in Africa, India and to socio-economically disadvantaged groups in North America and Europe. Often a condition rendered invisible in policy terms because of its problematic association with politically marginalized groups, the social study of sickle cell has been neglected. This illuminating volume explores the challenges and possibilities for developing a social view of sickle cell, and for improving the quality of lives of those living with SCD. Tackling the controversial role of screening and genetics in SCD, the book offers a brief thematic history of approaches to the condition, queries the role of ethnicity and includes a discussion of how the social model of disability can be applied, as well as featuring chapters focusing on athletics, prisons and schools. Bringing together a wide range of original research conducted in the USA, the UK, Ghana and Nigeria, Sickle Cell and the Social Sciences is anchored in the discipline of sociology, but draws upon a diverse range of fields, including public health, anthropology, social policy and disability studies | ||
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| dewey-raw | 616.1/527 |
| dewey-search | 616.1/527 |
| dewey-sort | 3616.1 3527 |
| dewey-tens | 610 - Medicine and health |
| discipline | Medizin |
| discipline_str_mv | Medizin |
| format | Electronic eBook |
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| illustrated | Not Illustrated |
| index_date | 2024-07-03T15:58:08Z |
| indexdate | 2024-07-10T09:00:03Z |
| institution | BVB |
| isbn | 9781351580847 1351580841 9781315098685 1315098687 9781351580854 135158085X 9781351580830 1351580833 |
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| series2 | Routledge studies in the sociology of health and illness |
| spelling | Dyson, Simon Verfasser aut Sickle cell and the social sciences health, racism and disablement Simon Dyson Abingdon, Oxon Routledge 2019 1 online resource (ix, 241 pages) txt rdacontent c rdamedia cr rdacarrier Routledge studies in the sociology of health and illness Sickle cell disease (SCD) is a severe chronic illness and one of the world's most common genetic conditions, with 400,000 children born annually with the disorder, mainly in Sub-Saharan Africa, India, Brazil, the Middle East and in diasporic African populations in North America and Europe. Biomedical treatments for SCD are increasingly available to the world's affluent populations, while such medical care is available only in attenuated forms in Africa, India and to socio-economically disadvantaged groups in North America and Europe. Often a condition rendered invisible in policy terms because of its problematic association with politically marginalized groups, the social study of sickle cell has been neglected. This illuminating volume explores the challenges and possibilities for developing a social view of sickle cell, and for improving the quality of lives of those living with SCD. Tackling the controversial role of screening and genetics in SCD, the book offers a brief thematic history of approaches to the condition, queries the role of ethnicity and includes a discussion of how the social model of disability can be applied, as well as featuring chapters focusing on athletics, prisons and schools. Bringing together a wide range of original research conducted in the USA, the UK, Ghana and Nigeria, Sickle Cell and the Social Sciences is anchored in the discipline of sociology, but draws upon a diverse range of fields, including public health, anthropology, social policy and disability studies Anemia, Sickle Cell / ethnology Sickle cell anemia https://www.taylorfrancis.com/books/9781315098685 Verlag URL des Erstveroeffentlichers Volltext |
| spellingShingle | Dyson, Simon Sickle cell and the social sciences health, racism and disablement Anemia, Sickle Cell / ethnology Sickle cell anemia |
| title | Sickle cell and the social sciences health, racism and disablement |
| title_auth | Sickle cell and the social sciences health, racism and disablement |
| title_exact_search | Sickle cell and the social sciences health, racism and disablement |
| title_exact_search_txtP | Sickle cell and the social sciences health, racism and disablement |
| title_full | Sickle cell and the social sciences health, racism and disablement Simon Dyson |
| title_fullStr | Sickle cell and the social sciences health, racism and disablement Simon Dyson |
| title_full_unstemmed | Sickle cell and the social sciences health, racism and disablement Simon Dyson |
| title_short | Sickle cell and the social sciences |
| title_sort | sickle cell and the social sciences health racism and disablement |
| title_sub | health, racism and disablement |
| topic | Anemia, Sickle Cell / ethnology Sickle cell anemia |
| topic_facet | Anemia, Sickle Cell / ethnology Sickle cell anemia |
| url | https://www.taylorfrancis.com/books/9781315098685 |
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