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Telling; whether to tell or not to tell, when to tell, who to tell… it’s not just a newly diagnosed thing

The Patient Reported Outcomes for MS Initiative (PROMS) - Global Survey. You are invited to participate in a survey created for people with MS, by people with MS.

MS Ireland are delighted to share a new development on our website titled ‘MS and Finances’. 

Today, Tuesday November 28th we celebrate and express heartfelt gratitude to the incredible backbone of MS Ireland – our dedicated volunteers, passionate fundraisers, committed board members, and tireless branch workers. Your unwavering support and efforts make our mission possible and deeply impact the lives of those in the MS community across Ireland. 

Minister of State with Special Responsibility for Disabilities, Anne Rabbitte, has this week announced that twenty projects will receive funding under the Disability and Participation Awareness Fund including MS Ireland for the Move Smart MS programme.

MS Ireland conducted a comprehensive survey aimed at understanding the experiences and needs of young people living with Multiple Sclerosis (MS), aged 18 to 35. The primary objectives of this survey were to assess how young people engage with MS Ireland, their awareness of the organisation, and to identify the barriers they face. The data collected included both qualitative and quantitative responses. 

24th Reconvened National Annual General Meeting (“AGM”) (since incorporation – the Society was founded in 1961) of the Multiple Sclerosis Society of Ireland Limited was held on Thursday, 30th November 2023 at 8.00 p.m. in the MS Care Centre, 65 Bushy Park Road, Ranelagh, Dublin 6 and via Zoom

The MS community is a strong vibrant gathering of different people affected by or interested in MS. Whether you want to be an active member or just receive information and updates, we welcome anyone to become a member of MS Ireland.