The ECTRIMS Podcast Podcast By The European Committee for Treatment and Research in Multiple Sclerosis cover art

The ECTRIMS Podcast

The ECTRIMS Podcast

By: The European Committee for Treatment and Research in Multiple Sclerosis
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The ECTRIMS Podcast is a sounding board for MS experts & advocates to discuss innovative work in MS research, treatment and care with the greater MS research community, while offering a collaborative platform for MS and healthcare experts to promote & nurture the advancement of research.2022 Hygiene & Healthy Living Physical Illness & Disease Science
Episodes
  • Fenebrutinib in Relapsing MS: FENhance Trial Results Explained
    Apr 22 2026

    New Phase 3 data presented at the AAN conference 2026 provide compelling evidence that fenebrutinib may represent a high-efficacy oral treatment option for people living with relapsing multiple sclerosis.

    In this exclusive episode, leading experts Prof. Ludwig Kappos from University of Basel and Dr. Jiwon Oh from Barlo MS Centre join host Brett Drummond to unpack the full FENhance 1 & 2 trial results.

    Together, they explore:

    • How fenebrutinib performed against teriflunomide in relapsing MS
    • Why BTK inhibition continues to generate strong interest across the MS treatment landscape
    • What the results reveal about relapse reduction, MRI outcomes, and disability progression
    • What the safety profile of fenebrutinib looked like in this cohort of patients

    Listen for a deep dive into the science, clinical context, and future implications for MS care.

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    26 mins
  • How MRI and OCT are Changing Multiple Sclerosis Diagnosis, Prognosis, and Treatment
    Apr 8 2026

    Imaging techniques in multiple sclerosis are evolving rapidly, with MRI and emerging biomarkers playing a central role in diagnosis, prognosis and disease monitoring.

    In this episode of the ECTRIMS Podcast, neurologist Gabriel Bsteh and host Brett Drummond explore how MRI, optical coherence tomography (OCT), and imaging biomarkers are reshaping the way clinicians diagnose and manage MS.

    They discuss the 2024 updates to the McDonald diagnostic criteria, including the introduction of the central vein sign (CVS), paramagnetic rim lesions (PRL), and the inclusion of the optic nerve.

    The episode also examines how imaging biomarkers may be used to:

    • Predict disease progression
    • Provide prognostic information at diagnosis
    • Monitor neuro-axonal damage over time
    • Support treatment decisions and personalised medicine

    This episode is essential listening for anyone interested in multiple sclerosis, MRI, OCT, biomarkers, and advances in MS research and care.

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    25 mins
  • Does the Label Given to My MS Disease Course Matter?
    Mar 19 2026

    How much do the labels used to describe multiple sclerosis actually reflect the lived experience of people affected by the disease?

    In this first episode of the new ECTRIMS–MS Journal collaboration series, host Dr. Anneke van der Walt, Controversies Editor at the Multiple Sclerosis Journal, speaks with Jon Strum, MS caregiver and host of the RealTalk MS podcast, and Kathryn Smith, patient advocate and volunteer with the National MS Society, and person living with MS.

    Together they explore a deceptively simple question: does the label given to an MS disease course actually matter?

    Jon argues that disease labels shape perception, communication and expectations for people living with MS and their families. Kathryn explains why those same labels increasingly fail to capture the day-to-day reality of living with the disease.

    They discuss:

    • Why traditional MS disease course labels can feel disconnected from lived experience
    • The emotional and practical impact of terms such as relapsing-remitting and secondary progressive
    • The concept of PIRA (progression independent of relapse activity) and what it reveals about MS progression
    • Why functional outcomes and patient experience should play a greater role in how MS is described
    • The importance of patient voice in research, clinical conversations and scientific publishing

    Although they begin from opposing viewpoints, Jon and Kathryn ultimately arrive at a shared conclusion: the MS community may need a new language — one that better reflects biology, individual experience and the realities of living with the disease.

    Note: This episode is part of the MS Journal Controversies in MS series, specifically its new Controversies: Patient Voice section – a dedicated space highlighting the lived experiences of people affected by MS. Please see the following articles for more information:

    • "Yes" – The label does matter
    • "No" – The label does not matter
    • Commentary
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    24 mins
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