Ethnicity and Caring for a Disabled Child: The Case of Children with Sickle Cell or Thalassaemia

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dc.contributor.authorAhmad, Waqar
dc.contributor.authorAtkin, Karl
dc.date.accessioned2018-03-06T18:26:34Z
dc.date.accessioned2023-08-19T09:07:57Z
dc.date.available2018-03-06T18:26:34Z
dc.date.available2023-08-19T09:07:57Z
dc.date.issued1996-12-01
dc.descriptionAhmad, W. I., & Atkin, K. (1996). Ethnicity and caring for a disabled child: the case of children with sickle cell or thalassaemia. The British Journal of Social Work, 26(6), 755-775.
dc.description.abstractServices for haemoglobinopathies have been a major site of struggles for the black communities, yet the social research literature on haemoglobinopathies remains patchy and fragmented. We provide an overview of the literature on sickle cell disorders and thalassaemia major in the broader context of debates on childhood disability and chronic illness, and on ethnicity, racism and health care.en_US
dc.identifier.doihttps://doi.org/10.1093/oxfordjournals.bjsw.a011158
dc.identifier.urihttps://edms.wexl.in/handle/1/535
dc.language.isoenen_US
dc.publisherThe British Association of Social Workersen_US
dc.subjectEthnicityen_US
dc.subjectDisabled Childen_US
dc.subjectCareen_US
dc.titleEthnicity and Caring for a Disabled Child: The Case of Children with Sickle Cell or Thalassaemiaen_US
dc.typeArticleen_US
dcterms.subjectDisabled

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