'The world was going through what we go through everyday': The experiences of women with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) living with their partners during the COVID-19 lockdown in the United Kingdom.
Sehmbi, Tarnjit, Wearden, Alison, Peters, Sarah et al.·British journal of health psychology·2024
This study asked 21 women with ME/CFS in the UK about their experiences during the COVID-19 lockdown, particularly how living with their partners affected them. The researchers found that while lockdown disrupted the routines these women had carefully built to manage their illness, having their partners at home more often was actually helpful. Interestingly, the lockdown made them feel less different from the rest of society, though they worried greatly about catching COVID-19 and making their ME/CFS worse.