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Registration is open to join Multiple Sclerosis International Federation (MSIF) for the webcast on mobility challenges in progressive MS on Thursday, 20 June 2024 at 11:00 am EDT, 4:00 pm BST, 5:00 pm CEST
This is an open invitation to all members of your Society to attend our public discussion on ‘Sex Differences in the Immune System’ in the Trinity Business School, Trinity College Dublin, on June 12th (6pm-9pm).
MS Ireland launched the results of the comprehensive “My MS My Needs” survey on World MS Day at a briefing in the AV Room of Leinster House to Oireachtas members, all eager to deepen their understanding of the challenges faced by the over 10,000 individuals living with MS in Ireland.
In early 2023, MS Ireland undertook a comprehensive survey aimed at delving into the experiences and needs of young adults aged 18 to 35 living with Multiple Sclerosis (MS). The survey, which 126 people responded to, sought to gauge awareness of and engagement with MS Ireland, experiences at the time of diagnosis, challenges faced, and suggestions for improvement.
We are thrilled to share the wonderful news that, thanks to your participation and support, MS Ireland's Readathon 2023 raised an incredible €248,993!
This blog title gives me anxiety. What does a “better me” mean? Should I be writing an article like the many I’ve seen where people tell stories about how better their life is since MS diagnosis and how much they have achieved? People climbing mountains or running marathons? I have read a lot where people seem grateful for MS. I’m happy for them but let's get one thing straight from the start - I am not grateful for my diagnosis. MS has in no way improved my life. It sucks and any of the positive things that have come from it, like my learning mindfulness and becoming a calmer person, I like to think I would have discovered in time anyway.
My MS My Needs survey highlights the needs and experiences of people living with Multiple Sclerosis (MS) in Ireland.
MS Ireland invites researchers to contribute to the MS Research Ezine.
Listen to Alison Cotter, MS Ireland Advocacy and Research Officer on Newstalk Breakfast Briefing being interviewed with Shane Beatty on the findings from “My MS My Needs” Survey.
We understand that recent media reports may have caused concern with our community. We would like to remind you that our Information Line and Community Worker Service are here to support you.
MS Ireland advises all individuals using any medication, to remain informed about potential side effects. It is important to discuss any concerns or unusual symptoms with your healthcare provider. They can provide guidance tailored to your specific medical needs and help you make informed decisions about your treatment.
MS Ireland is committed to providing support, information, and resources to help you manage your condition safely and effectively.
Our Information Line is open Monday – Friday, from 9:30am – 5:00pm. We are here to help.