The ECTRIMS Podcast

MS nurses are at the heart of MS care, but as treatments become more complex and demands grow, what support do they need to keep going?
 
In this special MSToronto2026 episode, host Brett Drummond is joined by Colleen Harris, Nurse Practitioner at the University of Calgary MS Program, and Jenny Slough, Lead MS Specialist Nurse at UCLH, Queen Square.
 
Together, they reflect on MSToronto2026's Nurses' Sessions, the opportunities and challenges facing MS nurses today, and the value of a global nursing network.
 
How are complex new therapies changing the nurse's role? How do nurses make the most of short appointment times? And why do nurses themselves so urgently need support?
 
Whether you're an MS nurse, work alongside one, or simply want to understand the vital role they play, this is a conversation worth hearing.
 
This ECTRIMS podcast episode is supported by an educational grant from Alexion, AstraZeneca Rare Diseases. Bristol Myers Squibb, Novartis, Roche, Sanofi, and UCB. Educational grant providers have no input into the podcast series content.

🎙️ What does the future hold for people living with NMOSD and MOGAD? With new treatments emerging and research advancing, there are important reasons for hope.
As part of Patient Community Day 2026, we're pleased to share the second episode in our two-part ECTRIMS Podcast series, exploring the latest research and the perspectives of people living with MS and related neurological conditions.
Host Brett Drummond sits down with Taylor Ann Macey, Director of Patient Engagement at the Sumaira Foundation who lives with NMOSD, and Dr Eoin Flanagan, Professor of Neurology at Mayo Clinic, for a conversation about scientific progress and lived experience.
What are the challenges of living with a rare neuroimmune condition?
How are new treatments changing the outlook for NMOSD and MOGAD?
And why are the involvement of people with lived experienceand so important in shaping future research?
From the isolation that can come with a rare diagnosis to the growing optimism around treatment and research, this conversation highlights both the challenges and the possibilities ahead.
 
This ECTRIMS podcast episode is supported by an educational grant from Alexion, AstraZeneca Rare Diseases. Bristol Myers Squibb, Novartis, Roche, Sanofi, and UCB. Educational grant providers have no input into the podcast series content.

What does the MS community need from research – and how can we make sure the voices of people living with MS help shape what comes next?
As part of Patient Community Day 2026, we're sharing a special collaborative episode from RealTalk MS and the ECTRIMS Podcast, hosted by Jon Strum.
Jon is joined by Karen Jacoby, MS advocate and person living with MS, and Peter Feys, Professor of Rehabilitation Sciences and Neurorehabilitation at Hasselt University – for a conversation that puts the patient perspective at the centre – exploring the relationship between research, lived experience and the priorities that matter to people affected by MS.
Recorded at Patient Community Day in Toronto, the episode forms part of the wider conversations taking place during the 10th Joint ACTRIMS-ECTRIMS Meeting – but this one is specifically for, and about, the MS community.
This episode was produced and hosted by RealTalk MS – a Supporting Partner of Patient Community Day – and is being shared across ECTRIMS channels with permission from Jon Strum to help the conversation reach as many people as possible.
 
This ECTRIMS podcast episode is supported by an educational grant from Alexion, AstraZeneca Rare Diseases. Bristol Myers Squibb, Novartis, Roche, Sanofi, and UCB. Educational grant providers have no input into the podcast series content.

Three days of science, debate and discovery.
For the final episode in our special MSToronto2026 podcast series, ECTRIMS Executive Committee member Jaume Sastre-Garriga joins host Brett Drummond direct from Toronto.
Together, they unpack the key insights from Day Three, including the Late Breaking Abstract session, before stepping back to reflect on the Joint Meeting as a whole.
What stood out across the week? Which developments and conversations could have lasting significance? And as thousands of researchers and clinicians prepare to leave Toronto, what comes next for the MS field?
Recorded at the 10th Joint ACTRIMS-ECTRIMS Meeting, this is our final dispatch from Toronto – bringing together the science, conversations and ideas that shaped an extraordinary week.
This ECTRIMS podcast episode is supported by an educational grant from Alexion, AstraZeneca Rare Diseases. Bristol Myers Squibb, Novartis, Roche, Sanofi, and UCB. Educational grant providers have no input into the podcast series content.

Today, our special podcast series brings together two major voices from the North American MS community:
Tim Coetzee, National Multiple Sclerosis Society
Pamela Valentine, MS Canada
Scientific progress in MS is accelerating. But is that progress reaching the people who need it?
Alongside their reflections on the key takeaways and conversations from Day Two of MSToronto2026, Tim and Pamela join host Brett Drummond to look beyond individual studies and ask some bigger questions about where the MS field goes next.
Where does the MS community need progress most urgently? How can researchers, clinicians, patient organisations and people affected by MS work together more effectively? And how do we make sure scientific advances ultimately translate into meaningful change in people's lives?
This ECTRIMS podcast episode is supported by an educational grant from Alexion, AstraZeneca Rare Diseases. Bristol Myers Squibb, Novartis, Roche, Sanofi, and UCB. Educational grant providers have no input into the podcast series content.