At every stage of the MS journey, nurses are the steady link between patients, families, and the healthcare team.

In this episode, host Brett Drummond speaks with Amy Perrin Ross, MS Specialist Nurse and Program Coordinator at Loyola University Chicago (USA), and Miguel Ángel Cortés-Vicente, Multiple Sclerosis Consultant Nurse at CEMCAT – Centre d'Esclerosi Múltiple de Catalunya (Spain), about the evolving role of MS nurses — from care coordination and patient engagement to leadership in research and innovation.

They share insights from the 2025 ECTRIMS Congress Nurse Sessions, exploring how nurses are advancing health literacy, supporting shared decision-making, and integrating AI to improve patient care.

While much of MS care focuses on physical symptoms, mental health challenges—like depression, anxiety, loneliness, and stigma—often go under-recognised.

In this episode, host Brett Drummond speaks with Dr. Rebecca MaGuire, psychologist and MS researcher at Maynooth University, who also lives with MS herself. Together they discuss why mental health must become a core part of MS care, what the latest research reveals, and how clinicians and communities can better support emotional wellbeing throughout the MS journey.

Patient Community Day 2025 set a new attendance record, highlighting the growing desire among people living with MS to connect with experts leading the charge in understanding the disease and advancing effective treatments.

After the event wrapped up in Barcelona, host Brett Drummond caught up with Julie Petrin, Director of Impact and Evaluation at MS Canada and a person living with MS, and Non Helena Smit, CEO of MS South Africa, to reflect on key takeaways and share what they're looking forward to at next year's event in Toronto.