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

Progress in MS care through the last decade and into the next: an update to the 2013 consensus of the MS in the 21st Century Steering Group
Alroughani et al., 2025
Read moreMore 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.

Listen to our podcasts
Hear real stories from people with multiple sclerosis (PwMS) and gain a wider understanding of key patient narratives from people living with the condition.

Try MS support tools
Check out MS21’s free tools to improve communication with your patients and their caregivers.

