Dados Bibliográficos

AUTOR(ES) J. Mendoza , G. Lasco , Maureen L. Seguin , Lia M. Palileo-Villanueva , Alicia Renedo , Martin McKee , Benjamin Palafox , Dina Balabanova
AFILIAÇÃO(ÕES) College of Medicine University of the Philippines Manila Manila Philippines, Development Studies Program Ateneo de Manila University Quezon City Philippines, Centre for Global Chronic Conditions London School of Hygiene and Tropical Medicine London UK, Department of Global Health & Development London School of Hygiene and Tropical Medicine London UK, Department of Social and Environmental Health Research London School of Hygiene and Tropical Medicine London UK
ANO 2022
TIPO Artigo
PERIÓDICO Sociology of Health and Illness
ISSN 0141-9889
E-ISSN 1467-9566
EDITORA Wiley-Blackwell
DOI 10.1111/1467-9566.13503
CITAÇÕES 1
ADICIONADO EM 2025-08-18

Resumo

Patients' embodied experiences do not always correspond to the biomedical concepts of particular diseases. Drawing from year‐long fieldwork in the Philippines that involved semi‐structured interviews, focus group discussions and digital diaries, we examine how individuals 'do' hypertension through their embodied experiences and the knowledge and practice that emerge from them. Drawing inspiration from Annemarie Mol's work on the notion of 'multiplicity' of disease, our analysis was informed by a commitment to privileging patients' embodied experiences and the multiple ontologies of hypertension. We find that for patients diagnosed with hypertension in the Philippines, symptoms enact illness; patients rely on their own embodied knowledge to define their illness' nature (e.g., diagnosis), experience (e.g., frequency of symptoms and non‐chronicity) and praxis (e.g., self‐care practices). We show how this knowledge gained from having embodied experiences of living with the disease interacts in various ways with biomedical knowledge, other diagnostic labels and clinical practices, to shape how hypertension manifests and is managed by patients. Beyond interrogating the relationship between what counts as a 'disease' and what is considered a 'symptom', our findings underscore the need to pay attention instead to the mutually co‐constitutive processes of embodied experiences and disease categories in co‐producing patient knowledge.

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