Background: Huntington's disease (HD) is a long-term neurological condition. Owing to its degenerative nature, quality of life (QoL) considerations are important regardless of whether individuals are in the early, middle, or end-of-life stages. Currently there is a shortage of person-centred research looking at non-pharmacological interventions to improve QoL for those with an HD diagnosis. Objective: To assess perceptions of QoL among health-care workers at a specialist HD unit in a UK hospital, as well as their perceptions of how they and others contribute to the QoL of service users. Methodology: Eight participants were recruited using opportunity sampling. They included dietetics, occupational therapy, nursing, physiotherapy, psychology, and speech and language therapy staff. One-to-one, face-to-face, semi-structured interviews were conducted with each participant. The data was analysed using the qualitative methodology grounded theory. Results: Eight main themes arose: QoL; the unit; staff; communication; hopes, fears and behaviour; family involvement; ongoing support; and future directions for enhancement of QoL. Conclusions: It is hoped that the paper will act as a foundation for further exploration of QoL issues and a focus on how individuals with HD and other neurological conditions can be best supported to live with optimal QoL. The paper should raise awareness of HD and be of assistance to health-care workers by highlighting the challenges faced in providing appropriate support, while also making recommendations for future practice.