Literature DB >> 21846662

A qualitative study of families of a child with a nut allergy.

Emma Pitchforth1, Simon Weaver, Janet Willars, Emilia Wawrzkowicz, David Luyt, Mary Dixon-Woods.   

Abstract

OBJECTIVES: The aim of this study was to explore, using qualitative methods, the experiences of children and their parents living with nut allergy.
METHODS: Children with a confirmed diagnosis of peanut allergy were identified from a database of patients maintained at an allergy clinic at a large teaching hospital. Interviews with 26 families were conducted involving 11 children, 25 mothers and 12 fathers.
RESULTS: The diagnosis of nut allergy signalled a critical transition-or biographical disruption-in the life of the family. Parents took on the role of 'alert assistant' and sought to create 'safe places' where nuts were not permitted, but often struggled when outside the home environment. The option of 'passing as normal', often used by people with a chronic illness to avoid stigma, was not available to them. Consequently, parents often reported being treated as faddy, demanding, and neurotic, and children suffered from teasing and exclusion. The social consequences of nut allergy were worsened by poor labelling and control of foods and products containing nuts. DISCUSSION: In many ways, nut allergy may be considered a form of disability, because it imposes social barriers on participating fully in society.

Entities:  

Mesh:

Year:  2011        PMID: 21846662     DOI: 10.1177/1742395311411591

Source DB:  PubMed          Journal:  Chronic Illn        ISSN: 1742-3953


  10 in total

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2.  Allergy to Peanuts imPacting Emotions And Life (APPEAL): the impact of peanut allergy on children, adolescents, adults and caregivers in France.

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5.  Factors associated with parental burden among parents of children with food allergies in China: a cross-sectional study.

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6.  Diet and identity: being a good parent in the face of contradictions presented by the ketogenic diet.

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Review 7.  Children's, parents' and other stakeholders' perspectives on early dietary self-management to delay disease progression of chronic disease in children: a protocol for a mixed studies systematic review with a narrative synthesis.

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8.  Parent experiences with paediatric allergy pathways in the West Midlands: A qualitative study.

Authors:  Lavanya Diwakar; Carole Cummins; Scott Hackett; Martyn Rees; Lynette Charles; Caroline Kerrigan; Helen Creed; Tracy Roberts
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9.  The cycle of uncertainty: parents' experiences of childhood epilepsy.

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10.  APPEAL-2: A pan-European qualitative study to explore the burden of peanut-allergic children, teenagers and their caregivers.

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  10 in total

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