Low quality of life and psychological wellbeing contrast with moderate perceived burden in carers of people with severe multiple sclerosis

J Neurol Sci. 2016 Jul 15:366:139-145. doi: 10.1016/j.jns.2016.05.016. Epub 2016 May 12.
No abstract available

Keywords: Caregivers; Illness burden; Outcome measure; Palliative care; Primary progressive multiple sclerosis; Quality of life; Secondary progressive multiple sclerosis.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Caregivers / psychology*
  • Cost of Illness
  • Cross-Sectional Studies
  • Employment / psychology
  • Female
  • Humans
  • Linear Models
  • Male
  • Middle Aged
  • Multiple Sclerosis / therapy*
  • Multivariate Analysis
  • Palliative Care / methods
  • Perception
  • Psychiatric Status Rating Scales
  • Quality of Life / psychology*
  • Severity of Illness Index
  • Socioeconomic Factors
  • Surveys and Questionnaires
  • Young Adult