Bartlett, Chelsea, Hughes, Julie L, Miller, Laura · The British journal of occupational therapy · 2022 · DOI
This Australian study interviewed five people with ME/CFS about how the illness affected their ability to work and participate in daily activities. Participants described losing the ability to do the things that mattered to them—first hobbies and leisure activities, then work, and eventually basic self-care tasks. They also faced challenges from lack of understanding about ME/CFS, financial difficulties, and limited healthcare support.
This study addresses a significant gap in understanding ME/CFS from an occupational perspective in Australia, highlighting how the disease creates cascading losses in daily functioning that directly impact quality of life and mental health. It provides evidence supporting early occupational therapy intervention to prevent further deterioration and preserve meaningful activities.
This qualitative study with five participants cannot establish the prevalence or magnitude of occupational disruption across the ME/CFS population, nor can it prove causation between specific environmental factors and occupational loss. The findings are not generalizable beyond the Australian context or to ME/CFS populations in other healthcare systems. Correlation between disease progression and occupational loss is described but not quantified.
About the PEM badge: “PEM required” means post-exertional malaise was an explicit required diagnostic criterion for participant inclusion in this study — not that PEM was studied, observed, or discussed. Studies using criteria that do not require PEM (e.g. Fukuda, Oxford) are tagged “PEM not required”. How the atlas works →
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