ECTRIMS Patient Community Day: why researchers need people with MS to get involved episode artwork

EPISODE · Oct 28, 2025 · 1H 9M

ECTRIMS Patient Community Day: why researchers need people with MS to get involved

from The MS Trust podcast · host MS Trust

Send us a message about the podcast. For questions about MS please contact our helpline 0800 032 38 39In this episode we explore the biggest breakthroughs from ECTRIMS 2025, the world’s largest MS research conference. We look into new treatment insights, the push for inclusive research, and how people with MS can shape the future of care.Featuring Brett Drummond from MS translate, Natalie Busari from The Nerve of My MS, Dr. Claire Winchester research and engagement, at MS Trust , and Lucy Taylor our MS Trust CEOEpisode notesECTRIMS 2025 news round-up - news from the MS TrustCriteria used to diagnose MS updated  - news from the MS TrustECTRIMS patient Community - video recordings from the dayMS and Cognition - info from MS TrustDiet and MS - info from MS TrustLeave a gift in your will -  info from MS TrustMS Trust new strategy - info from MS TrustThe Nerve of My Multiples Sclerosis - Natalie Busari Instagram  

Episode metadata supplied by the publisher feed · Published Oct 28, 2025

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Send us a message about the podcast. For questions about MS please contact our helpline 0800 032 38 39 In this episode we explore the biggest breakthroughs from ECTRIMS 2025, the world’s largest MS research conference. We look into new treatment insights, the push for inclusive research, and how people with MS can shape the future of care. Featuring Brett Drummond from MS translate, Natalie Busari from The Nerve of My MS, Dr. Claire Winchester research and engagement, at MS Trust , and Lucy ...

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ECTRIMS Patient Community Day: why researchers need people with MS to get involved

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