Utilize este identificador para referenciar este registo: http://hdl.handle.net/10071/13945
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Campo DCValorIdioma
dc.contributor.authorOliveira, A.-
dc.contributor.authorSá, C.-
dc.contributor.authorFreitas, A.-
dc.date.accessioned2017-07-11T15:16:11Z-
dc.date.available2017-07-11T15:16:11Z-
dc.date.issued2013-
dc.identifier.issn2281-3993por
dc.identifier.urihttps://ciencia.iscte-iul.pt/id/ci-pub-15438-
dc.identifier.urihttp://hdl.handle.net/10071/13945-
dc.description.abstractChronic diseases are characterized by continuous pain and suffering, affecting the personal well-being, emotional, family and social. Patients experience moments of disruption, in face of alterations or deformations in their body image, and the need to change their habits and social roles. Some patients accept their situation, having good practices of self-care, adapting to their limitations and seeing the future with hope, while others represent the disease with sadness, negativity, fear and worry. The suffering but particularly death, emerges as a possibility that they prefer to ignore. This study aims to contribute to the understanding of how patients perceive their chronic disease, as well as life and death. Data were collected through a focus-group conducted with the consent of ten participants - adult and aging patients with rheumatoid arthritis. Among the various questions discussed, we highlight these: 'How do you envisage your illness?', 'How do you feel towards life?', 'How does illness affect your life?', ' How do you envisage death?' All participants recognize the disease as incurable, associating it with suffering, loneliness and grief. Women complain especially of the limitations imposed by the disease, which hinder the achievement of household tasks, while men emphasize the constraints they experience at a professional level. Patients reveal resignation or intention to learn to live with a persistent pain, but they all tend to ignore death. They believe in therapy, although they see it as excessive and with a temporary effect. The most important thing they consider is to be alive, hoping to get better.por
dc.language.isoengpor
dc.publisherMediterranean Center of Social and Educational Researchpor
dc.rightsopenAccesspor
dc.subjectChronic illnesspor
dc.subjectRheumatic diseasespor
dc.subjectPainpor
dc.subjectBodypor
dc.subjectLifepor
dc.subjectDeathpor
dc.titleLearning to live with a chronic illness, without thinking about deathpor
dc.typearticleen_US
dc.pagination326-334por
dc.publicationstatusPublicadopor
dc.peerreviewedyespor
dc.relation.publisherversionThe definitive version is available at: http://dx.doi.org/10.5901/ajis.2013.v2n9p326por
dc.journalAcademic Journal of Interdisciplinary Studiespor
dc.distributionInternacionalpor
dc.volume2por
dc.number9por
degois.publication.firstPage326por
degois.publication.lastPage334por
degois.publication.issue9por
degois.publication.titleAcademic Journal of Interdisciplinary Studiespor
dc.date.updated2017-07-11T15:15:27Z-
dc.identifier.doi10.5901/ajis.2013.v2n9p326-
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