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Summary of Research: Caregiver Involvement in MS: Duty or Disruption?

Jϋrg KesselringAlexey BoykoAlice LaroniTrishna BharadiaPieter van GalenNektaria Alexandri
Published in: Neurology and therapy (2023)
This Summary of Research summarizes a previously published discussion between people with multiple sclerosis (PwMS) and their caregivers and healthcare professionals (HCPs) about how to include caregivers in consultations and decisions about multiple sclerosis (MS) care. The aim of the discussion was to help HCPs to understand differences in these relationships so they can adapt the style of consultations to support everyone.
Keyphrases
  • multiple sclerosis
  • palliative care
  • general practice
  • white matter
  • healthcare
  • pain management
  • quality improvement
  • primary care
  • affordable care act