The Covid-19 pandemic has especially disrupted the lives of people living with chronic illnesses and disabilities and those who care for them. Here, Laura Mauldin examines how the spouses of people living with chronic illnesses and disabilities navigated the care of their loved ones during the pandemic. Through ethnographic research, Mauldin explains how these caregiving spouses took on the brunt of care for their loved ones due to lockdown restrictions and fears of bringing the virus into their homes. The experiences of these patients and their caretakers, Mauldin argues, have been made invisible by both the pandemic and existing policies that do not value caregivers.
What is compassion fatigue? Caregivers explain.
"Suffering from compassion fatigue does not mean you’re bad at helping or caring, it only means the scale between caring for others and caring for...