The MS Trust podcast
Our podcast brings together a range of voices from the MS community to cover all aspects of life with multiple sclerosis. We know that living with MS can be life changing and can feel overwhelming at times. That’s why we’re here with you at each stage of the journey.
Look, we know that we don’t have all the answers. But our podcast’s aim is to bring you the most up to date, trusted information from experts across the MS space including neurologists, therapists and researchers.
Plus, hosts Helena and Nick hear real-life experiences from the MS community and find out your tips, tricks and the things that make you tick. We pose your burning questions to our experts and find out the information that you really want to know.
Listen now for helpful information on symptoms, treatments, updates and a whole lot more.
The MS Trust podcast
ECTRIMS Patient Community Day: why researchers need people with MS to get involved
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 Taylor our MS Trust CEO
Episode notes
- ECTRIMS 2025 news round-up - news from the MS Trust
- Criteria used to diagnose MS updated - news from the MS Trust
- ECTRIMS patient Community - video recordings from the day
- MS and Cognition - info from MS Trust
- Diet and MS - info from MS Trust
- Leave a gift in your will - info from MS Trust
- MS Trust new strategy - info from MS Trust
- The Nerve of My Multiples Sclerosis - Natalie Busari Instagram