Patient power revolution in multiple sclerosis: Navigating the new frontier
Neurol Ther. Nov 2018
This article, published in November 2018, summarises a debate between patient and HCP members of the MS21 advisory group held at the European Charcot Foundation Conference in November 2017. During the debate, our panel discussed the risks and benefits of patient engagement and shared decision-making in MS care. This publication is MS21’s first manuscript with a patient lead author.
Related MS21 data
Disease progression in multiple sclerosis: A literature review exploring patient perspectives
Patient Prefer Adherence. Jan 2021Read more
More support from MS21
Expand your knowledge
Read the latest peer-reviewed manuscripts, congress posters and patient lay summaries from the MS21 team, demonstrating our commitment to evidence-based approaches for improving MS care.
Be part of the data
Tell us about your experience in treating people with MS in one of our quick surveys – you could help to shape future MS21 resources.
Try MS support tools
Check out MS21’s free tools to improve communication with your patients and their caregivers.