MS Ireland is inviting the community to visit its National Centre on Tuesday, 23 September 2025, from 11am to 2pm at 65–67 Bushy Park Road, Dublin 6.
For full details and to register, visit: Renew – A New Vision: Visit MS Ireland’s National Centre
Our latest Living with MS Podcast guest is Hannah Morris-Bankole, who is a new member of the MS Ireland MS & Me Blog team. Hannah is a mum of 6 children living in Galway and currently doing her PhD in psychology. Listen to the episode here or on your favourite podcast platform.
In our A to Z of MS series, Shirley Keane O’Brien takes us to L for Life Coaching: “Me, myself, and MS — how it helped me reclaim my spark.”
Dear Member,
Please see below the Notice of the Multiple Sclerosis Society of Ireland’s Annual General Meeting (“AGM”).
All documentation, including the Notice and the AGM Information Pack, is now available on our website.
Votes for the AGM may be registered in person, virtually at the AGM, or by proxy.
MS Ireland warmly welcomes the recent decision by the Health Service Executive (HSE) to reimburse the subcutaneous (SC) form of Ocrevus® (ocrelizumab).
The special visit to our new MS Ireland Resource Centre in Limerick is now over. Thank you for your support—we look forward to sharing more opportunities to connect as the centre opens its doors to the community.
As part of our A to Z of MS series, Nadia takes us to the letter L. For her, L is for List — especially when facing the dreaded big shop.
We are asking our community to take part in a very short, anonymous survey to help identify the words that best reflect MS Ireland’s values.
Your feedback will ensure our values reflect what matters most to people living with MS, their families and supporters.
ECTRIMS Patient Community Day – an online and onsite event hosted by the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) and supported by MS Ireland – is your opportunity to join a global gathering of education and support, and learn about the latest advancements directly impacting your ongoing care and treatment options.
In ‘K is for Keep Going’ for our A to Z of MS series, Paul shares his journey of resilience — from martial arts training to flare-ups, he reflects on pain, perseverance, and finding strength in the small wins.
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