Of the approximately 1 million people living with multiple sclerosis (MS) in the United States, more than half receive informal, unpaid care or support from family or friends (caregivers). Caregivers are the invisible backbone of the health care system and are now even more vital in the ongoing pandemic response as they support telehealth services and replace curtailed health care. Caregivers are often caring for people with MS who are at higher risk for severe COVID-19 illness. As a result, caregivers are under immense pressure to protect themselves from infection and prevent transmission, often without clear guidance or personal protective equipment. This presents very stressful situations for caregivers, which can result in depression, anxiety, and worse health outcomes for them and their care recipients. Few researchers have conducted psychoeducational interventions for these caregivers.
