Impact of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) on the quality of life of people with ME/CFS and their partners and family members: an online cross-sectional survey.
Vyas, Jui, Muirhead, Nina, Singh, Ravinder et al.·BMJ open·2022
This large international study surveyed 1,418 people with ME/CFS and their family members to understand how the illness affects quality of life for both patients and loved ones. People with ME/CFS reported very low health status (averaging 34 out of 100) with major difficulties in daily activities, pain, and movement, while their family members experienced significant emotional distress including worry, frustration, and sadness, plus practical impacts on family life and finances. The study found that the worse a patient's quality of life is, the worse their family member's quality of life tends to be as well.