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Summary of Research: Caregiver Involvement in MS: Duty or Disruption?
Jürg Kesselring1, Alexey Boyko2, Alice Laroni3,4
1Department of Neurology and Neurorehabilitation, Kliniken Valens Rehazentrum, Valens, Switzerland. Juerg.Kesselring@kliniken-valens.ch.
Abstract:
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.
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