Caring for people with severe myalgic encephalomyelitis: An interpretative phenomenological analysis of parents' experiences.
J Health Psychol
; 21(12): 2824-2837, 2016 12.
Article
em En
| MEDLINE
| ID: mdl-26063209
ABSTRACT
Experiences of parents who care for sons or daughters with severe myalgic encephalomyelitis are rarely discussed within the literature. Narratives of parent-carers in Lost Voices from a Hidden Illness were analyzed using interpretative phenomenological analysis. This study aimed to give voices to those who care for individuals with myalgic encephalomyelitis and are often stigmatized and inform future research supporting parent-carers. Results included themes of identity change, guilt, feeling like outsiders, uncertainty, changing perceptions of time, coping mechanisms, and improvement/symptom management. Findings could inform the development of carer-focused interventions and provide vital information to health professionals about parent-carers' lived experience.
Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Pais
/
Síndrome de Fadiga Crônica
/
Cuidadores
Tipo de estudo:
Qualitative_research
Limite:
Adolescent
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Adult
/
Child
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Child, preschool
/
Female
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Humans
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Male
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Middle aged
Idioma:
En
Ano de publicação:
2016
Tipo de documento:
Article