Newsletter

Patient Community Newsletter

Receive the Latest Updates on MS Research, Care, and Community Resources

Each edition of the ECTRIMS Patient Community Newsletter highlights accessible research insights, educational resources, and initiatives from our network of 40+ Supporting Partners, helping people living with MS stay connected to the latest developments in care, advocacy, and community support.

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Read the latest edition and explore the resources shared by our global MS community.

In this issue, ECTRIMS explores how patient registries help shape real-world MS research, highlighting how people living with MS contribute valuable data that helps researchers better understand the disease beyond clinical trials. The newsletter also features initiatives and resources from our Supporting Partners, including:

Raising awareness for World NMOSD Awareness Day (27 March) with NMO Brasil
New research on patient-reported outcomes shaping MS treatments from the European Charcot Foundation
A podcast exploring invisible neurological experiences in MS from BeeWellWithMS
New research on hormones and reproductive health in MS from MS Together
A free online course on MS symptoms and diagnosis from the MS International Federation
The PROMISE Project improving mental health support for people with MS in Ireland
The CLAIMS initiative, exploring how artificial intelligence could support MS treatment decisions

Newsletter

Receive the Latest Updates on MS Research, Care, and Community Resources

March 2026 Newsletter

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