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The MS Ireland National Conference — Living with MS: Conversations on Care, Connection and Mental Health — takes place on Saturday, 15 November 2025 at the Cork International Hotel.
If you can’t attend in person, you can still be part of the day. The conference will be livestreamed from 10am on our YouTube channel:
Watch live here: https://www.youtube.com/watch?v=X7DixAHSZhg
Full livestream schedule coming soon — keep an eye on our website, social media, and eNews for updates.
MS Ireland are partnering with the University of Limerick Physical Activity for Health research centre on a study of physical activity. This online survey is part of a large, multinational survey coordinated by a group of MS researchers (including our own Prof Susan Coote) in the Rehabilitation in MS Special Interest Group for Mobility. The survey will be completed by people with MS in 17 countries.
Get together for People Living with MS in the Macroom area. A chance to meet others living in the region with tea, coffee, scones and chat! All welcome.
Monday 1st December 11am
For more details, contact the Southern Regional Office 021 4300001 southern@ms-society.ie
Explore our Living with MS Publications and Resources section, where you will find information to support your journey with MS. This collection includes guides on treatment decisions, quality of life, and various aspects of living with MS. Click on the titles below to download these helpful resources.
As part of our A to Z of MS series, Nadia brings us to the letter N. For her, N is for Nostalgia — an attic full of old memories sparks a warm reflection on her past and her MS journey.
Do you have Multiple Sclerosis (MS), or do you care for someone who has MS? Can you help make a difference for yourself and others who have MS? We want you to join our Public and Patient Involvement (PPI) Advisory Board and help shape a clinical trial on the impact of MS on people’s cognition.
MS Ireland welcomed Taoiseach Michéal Martin to their National Conference today, where he met with people living with Multiple Sclerosis, listened to their experiences, and discussed the need for strengthened neurological and mental health supports across the country.