MS Research Ezine Issue 8 Out Now!
We are delighted to announce the release of MS Ireland's Annual Research Ezine, featuring a range of insightful articles on MS.
We are delighted to announce the release of MS Ireland's Annual Research Ezine, featuring a range of insightful articles on MS.
MS Ireland is seeking expressions of interest from young people living with MS to attend the European Multiple Sclerosis Platform (EMSP) Young People's Meet-Up held in collaboration with MS Ireland in Dublin. Accommodation for Friday night and reimbursement for travel costs will be provided. If you’re interested in attending, please send your expression of interest with the subject line ‘EMSP Young Persons Network’ to aoifek@ms-society.ie.
Call for participants with and without MS, who are aged 18-60 years.
Three writers* will be awarded with a residency at the beautiful Kylemore Abbey in Connemara.
We are thrilled to announce that Dr. Brendan Kelly has been awarded the prestigious Dean Medal.
As the festive season unfolds, we want to express our sincere gratitude for your continued support. Your generosity has been a source of hope for those navigating the challenges of Multiple Sclerosis (MS).
“Dearly Beloved, we are gathered today to bid farewell to a dear friend of mine.
Please join me as I say goodbye to my companion of almost ten years. We’ve been through the ups and downs that life has thrown at us this past decade, but our relationship has soured in recent weeks. Today I say farewell to Copaxone, my first and (formerly) dependable disease modifying therapy (DMT).”
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
As I enter my 12th year of living with Primary Progressive Multiple Sclerosis even thinking and writing the word Disabled is uncomfortable for me. One of the hardest aspects is accepting the slow progression of disability that MS is bringing, all the while feeling I don’t belong in this category. It’s like I am some kind of interloper.
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