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.
Katie brings the sparkle in her blog, ‘J is for Joy,’ for our A to Z of MS series — from stage lights to friendship, she shares how burlesque helped her find joy beyond MS.
MS Ireland is excited to launch a new fundraising initiative — the MS Ireland Lotto — to help support our regional services across the country.
Our third guest on the Living with MS Podcast is Suzanne Ryder. Suzanne is a new member of the MS & Me Blog team. Listen to the episode here or on your favourite podcast platform.
Chloe Mitchell shares her inspiring MS blog, ‘I for Inspiring,’ as part of our A to Z of MS series — a story of purpose, resilience, and hope.
The Dean Medal Travel Bursary is to encourage the understanding of MS among young researchers, in memory of Geoffrey Dean, MD (1918 – 2009)
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