News

I have been diagnosed with Relapsing Remitting Multiple Sclerosis for 10 years now. That’s one MRI per year- plus the clinical trial related ones. Let’s say that I have been in a giant, buzzing magnet over 20 times.

Interim progress report

Applications Now CLOSED

A travel bursary to encourage the understanding of MS among young researchers, in memory of Geoffrey Dean, MD (1918 – 2009)

MS Ireland were delighted to launch our submission for Budget 2024 in the AV room on World MS Day.

European Multiple Sclerosis Platform (EMSP) alongside 25 national MS Societies and with the support and leadership of MS experts across Europe, will be leading on this research project titled Impact of Multiple Sclerosis Symptoms (IMSS) survey to shed light on the symptoms of MS, their prevalence and severity and how they are being managed across Europe. 

Applications are now open for MS Ireland's annual awards. Nominate someone special today.

To be environmentally conscientious and to reduce unnecessary costs, MS Ireland is now able to send AGM notices to our members by email since the passing of our Constitution in 2016. However, we need our members consent to the furnishing of the accompanying AGM financial documentation via our website instead of by post. To allow us to do this please complete the approval form here and return to Alice McKeon, MS Ireland, National Office, 80 Northumberland Road, Dublin 4.

How common are communication problems in progressive motor conditions and what impact do they have on people's lives.

We know that MS impacts those living with it in different ways and there are over 9,000 people living in Ireland living different lives- NO TWO PEOPLE LIVES ARE THE SAME. This project aimed to highlight this and challenge some of the misconceptions about MS and what people living with MS look like.