Caregiver Involvement in MS: Duty or Disruption?
Author:
Funder
Merck KGaA
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Link
https://link.springer.com/content/pdf/10.1007/s40120-021-00299-4.pdf
Reference49 articles.
1. Scolding N, Barnes D, Cader S, et al. Association of British Neurologists: revised (2015) guidelines for prescribing disease-modifying treatments in multiple sclerosis. Pract Neurol. 2015;15:273–9.
2. Dennison L, McCloy Smith E, Bradbury K, Galea I. How do people with multiple sclerosis experience prognostic uncertainty and prognosis communication? A qualitative study. PLoS ONE. 2016;11:e0158982.
3. Kidd T, Carey N, Mold F, et al. A systematic review of the effectiveness of self-management interventions in people with multiple sclerosis at improving depression, anxiety and quality of life. PLoS ONE. 2017;12:e0185931.
4. Boström K, Nilsagård Y. A family matter—when a parent is diagnosed with multiple sclerosis. A qualitative study. J Clin Nurs. 2016;25:1053–61.
5. Parker G. Disability, caring and marriage: the experience of younger couples when a partner is disabled after marriage. Br J Soc Work. 1993;23:565–80.
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1. Insights for Healthcare Providers on Shared Decision-Making in Multiple Sclerosis: A Narrative Review;Neurology and Therapy;2024-01-05
2. Psychological factors and brain magnetic resonance imaging metrics associated with fatigue in persons with multiple sclerosis;Journal of the Neurological Sciences;2023-11
3. Summary of Research: Caregiver Involvement in MS: Duty or Disruption?;Neurology and Therapy;2023-06-21
4. Shared decision making in the treatment of multiple sclerosis: A consensus based on Delphi methodology;Multiple Sclerosis and Related Disorders;2023-02
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