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This literature review asked what the experiences of people living with motor neurone disease was before and during the COVID-19 pandemic and during the COVID-19 pandemic, especially in terms of their condition and the support they received from health and social care services. A key theme identified was lack of knowledge among professionals when they cared for people living with motor neurone disease and their families. This lack of knowledge often resulted in delayed diagnosis and poor standards of care. COVID-19 impacted on the care of people living with motor neurone disease and their families, and there is a paucity of evidence on how services were perceived by these groups during the COVID-19 pandemic. The experiences of people living with motor neurone disease and their families are currently missing in the literature. In conclusion, further studies are required to include care of people living with motor neurone disease and their families. <\/jats:p>","DOI":"10.12968\/bjcn.2022.27.4.188","type":"journal-article","created":{"date-parts":[[2022,3,30]],"date-time":"2022-03-30T16:40:48Z","timestamp":1648658448000},"page":"188-198","source":"Crossref","is-referenced-by-count":9,"title":["Perceptions of people with motor neurone disease, families and HSCPs: a literature review"],"prefix":"10.12968","volume":"27","author":[{"given":"Helen","family":"Brewah","sequence":"first","affiliation":[{"name":"Queen's Nurse, Florence Nightingale Scholar and PhD student, University of Portsmouth"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kevin","family":"Borrett","sequence":"additional","affiliation":[{"name":"Mental Health Governance Lead, Solent NHS Trust, and PhD Supervisor, University of 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