2013
DOI: 10.1111/jhn.12062
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Living with coeliac disease: a grounded theory study

Abstract: Gluten-free living entails a substantial restriction of food choice. The losses and changes entailed impact on the personal and social identities of those living with coeliac disease, and on the behaviour of others towards them. Psychosocial interventions focussed on facilitating coping and adjustment may benefit those experiencing difficulties.

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Cited by 50 publications
(72 citation statements)
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“…We understand that the low number of participants in this research is a strong limitation, nonetheless these results support research done in Europe (21) , Australia (22) , India (23) and in the United States (24) , where studies show a need to care for the biopsychosocial sphere. This way this study hitherto fulfills an existing gap in the literature in Brazil, that thus far had not looked to psychosocial issues and its impacts on CD treatment.…”
Section: Discussionsupporting
confidence: 51%
“…We understand that the low number of participants in this research is a strong limitation, nonetheless these results support research done in Europe (21) , Australia (22) , India (23) and in the United States (24) , where studies show a need to care for the biopsychosocial sphere. This way this study hitherto fulfills an existing gap in the literature in Brazil, that thus far had not looked to psychosocial issues and its impacts on CD treatment.…”
Section: Discussionsupporting
confidence: 51%
“…These themes, and associated subthemes, are presented in order to provide insights into psychosocial issues considered to be specific to older people. Themes like those reported by younger individuals also arose [33][34][35][36][37][38], but are not reported.…”
Section: Resultsmentioning
confidence: 85%
“…Using IPA, participants were invited to describe their lived experiences and an analysis of the data enabled us to draw themes specific to a diagnosis later in life and to issues experienced by older people specifically. Three superordinate themes emerged, each with associated subthemes and although the reported extracts only denote themes deemed relevant to a later life diagnosis, common themes to a CD diagnosis for adults in general were also identified [33][34][35][36][37][38]. Our interaction with the data suggests that the diagnosis and management of CD later in life is complicated, at least in part, by older adult specific considerations, including fears about being diagnosed with a "more serious or life threatening illness" more commonly seen in later life (e.g., cancer), delayed help seeking, poorer engagement with available support systems, and reduced confidence in maintaining adequate self-care if appropriate support were unavailable.…”
Section: Discussionmentioning
confidence: 99%
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