Objective To understand how the narrative and conversational experience of arterial hypertension is configured in the relationships established among patients, family members, physicians and researchers-auditors, placing the illness in a care context to facilitate the dissemination of wellbeing narratives. Method Qualitative research with reflective and contextual conversational-narrative design, which involveda patient diagnosed with hypertension, his family and two doctors. The methods of constructing information was semi structured interviews, reflective observation and literature review. The systematization of information was carried out using frameworks designed for that purpose. For the interpretation of results, narrative and conversational analyses were used. Results In the process of constructing the experience of hypertension by family members or the physician, important aspects are not taken into account such as: the listening request, a demand for bonding, the experience of illness and in this case, the daily experience of old age. In this context, these kinds of relationships can lead to discomfort and suffering in the patient's experience of the illness. The conversation generated by all stakeholders enables the construction of dialogic-reflexive spaces that provide an opportunity to reshape relationships and experience of illness Conclusions The construction of contexts of care where one can talk and hear about issues without families and doctors facilitates the reconfiguration of the experience of illness, allowing for the inclusion of family and physicians in the generation of conversational-narrative positions. This implies personal and collective agency in order to mobilize and organize the resources they have, consistent with the patient's age and diagnosis.
The paper arises from a reflection about the concept of well-being from different knowledge domains in order to articulate its emergence in chronical diseases. In principle, this article gathers epistemologic and disciplinary perspectives in relation to well-being and comprehensions about the process of health-disease. In pursuance of advancing in the proposed articulation of understanding and contributing to the emergence of well-being in the relationship of people in chronic disease, their families and health professionals. The task consists in going beyond predictions and determinisms that define the disease and its intervention from the perspective of the biomedical model, and convening professional interlocutions from diverse disciplinary fields with people experiencing illness and their families; where the experience of disease and well-being are emergent of the joint construction between them, and benefits them in an exercise of collaboration and co-responsability. It is expected to enrich the comprehension and approach of health-disease situations with the actors directly involved in these processes; at the same time, it seeks to contribute in the generation of political frameworks and to society in its relation with the healthcare system, intending to fulfill the purpose of constructing welfare for all human beings.
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