2011
DOI: 10.1590/s0034-71672011000500002
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Embodying 'health citizenship' in health knowledge to fight health inequalities

Abstract: This paper wishes to contribute to the debate around citizen participation in health system decision-making that has been present internationally for the last 30 years. I argue that if we aim to change health inequalities, health professionals and planners need to understand the illness and health service experience of citizens. The concept of 'health citizenship' introduced here refers to health knowledge that integrates the lay knowledge of patients and that this integration is translated into health actions… Show more

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Cited by 9 publications
(8 citation statements)
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References 9 publications
(12 reference statements)
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“…To strategically maximize its impact on factual knowledge acquisition but also motivation and behavioural skills, NAFLD health communication initiatives should be designed to cater to the information needs and skills of individuals and communities. For this population, the construction of NAFLD knowledge around the cultural model for liver physiology as a blood filter as well as the shared explanatory models and popular theories used to explain cirrhosis and fatty liver could be of benefit [69][70][71][72].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…To strategically maximize its impact on factual knowledge acquisition but also motivation and behavioural skills, NAFLD health communication initiatives should be designed to cater to the information needs and skills of individuals and communities. For this population, the construction of NAFLD knowledge around the cultural model for liver physiology as a blood filter as well as the shared explanatory models and popular theories used to explain cirrhosis and fatty liver could be of benefit [69][70][71][72].…”
Section: Discussionmentioning
confidence: 99%
“…Low formal education is associated with low health literacy and worse health outcomes. These populations are the most burdened by chronic illnesses and the hardest to engage in adherence and prevention programs [ 71 , 77 80 ]. Moreover, not only do the participants of this study represent a very small portion of total consultations at APDP, but they also differ considerably on their degree of experience with the disease, as their T2DM history ranges from 0 to 48 years.…”
Section: Discussionmentioning
confidence: 99%
“…Rather, preferences were actively co-constructed through discussions of non-medical arguments, particularly by exploring patients’ previous experiences or the inconvenience of staying in the hospital for treatment. Previous work about illness narratives demonstrates the complexity of patient experiences and the need to value their cultural knowledge regarding illnesses (Groleau, 2011; Groleau, Young, & Kirmayer, 2006). Direct prompts for patients’ opinions were observed in most of the consultations during the field research.…”
Section: Discussionmentioning
confidence: 99%
“…In this context, digital citizenship is becoming a fundamental right to enable individuals to participate in the governance of health services, which remains particularly challenging for vulnerable and marginalised groups (Groleau, 2011). Social media generates social worlds that shift the location of health from inside the body to distributed environments, in which technical objects, infrastructures, stories and allegories mark what becomes relevant to health as an experience, contrasting ways of living with the acuteness of diagnostic interventions (Dumit, 2006;Manderson & Smith-Morris, 2010).…”
Section: Health Experience and Mediationmentioning
confidence: 99%