Lassa fever, a viral disease, was first isolated in the late 1960s and affects 300,000 to 500.000 people, causing 5000, to 10,000 fatalities annually across West Africa. Although there are studies on the causes and prevalence of Lassa fever, there is a paucity of studies regarding the Quality of Life (QoL) and lived experiences of survivors, limiting the ability of governments to adequately meet their needs. The purpose of this study was to describe the Quality of Life (QoL) and lived experiences of Lassa fever survivors in the Southsouth region of Nigeria. Fifteen survivors of Lassa disease were interviewed. Findings revealed seven areas of concerns: culture care and therapeutic communication, emotional support, physical symptoms, social activities, and work productivity. Findings are useful for health care providers