Caring for people with severe myalgic encephalomyelitis: An interpretative phenomenological analysis of parents experiences

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.
Source: Journal of Health Psychology - Category: Psychiatry & Psychology Authors: Tags: Articles Source Type: research