Background
The UK and Ireland’s restrictions to contain the spread of COVID-19 undoubtedly impacted on the lives of vulnerable populations. The arrival of a vaccine, while providing hope to caregivers, does not alter the detrimental impact of the pandemic on their lives. Research is urgently needed to provide future support to family carers who were already experiencing heightened stress and daily challenges as they cared for an individual with profound and multiple learning disabilities (PMLD).
During COVID-19, family carers were placed under further stress due to increased care demands, additional anxieties, practical difficulties created by the pandemic, and diminished support. Whilst caregiver stress is often lessened through social support, the reduction of social support during lockdown may have been particularly severe for family carers of people with PMLD because their access to professional support and services such as respite care will be significantly diminished.
Findings from a number of online surveys are now available which demonstrate higher levels of mental health problems, including severe anxiety, stress symptoms and depression among carers of people with learning disabilities. However, these studies do not give a complete picture of the lives of family carers which mean that we now need to explore their experiences of COVID-19 to suggest how they may be supported after the pandemic. All people with PMLD have high support needs and require 24-hour-a-day care. During the restrictions, families would have been under increased pressures to continue caring for their family member with PMLD with limited support. It is critical to recognise the impact of COVID-19 on family carers and document their lived experiences to determine how they could be better supported in the future. This work will allow for recommendations on the reconfiguration of services or other supports to enable the provision of more targeted and effective care.