Saw this on IiME FB:
http://www.ncbi.nlm.nih.gov/pubmed/26063209
http://www.ncbi.nlm.nih.gov/pubmed/26063209
PubMed said:J Health Psychol. 2015 Jun 10. pii: 1359105315587137. [Epub ahead of print]
Caring for people with severe myalgic encephalomyelitis: An interpretative phenomenological analysis of parents' experiences.
Mihelicova M1, Siegel Z2, Evans M2, Brown A2, Jason L2.
Author information
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.