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Services Questionnaire: COVID-19 has changed the way we normally deliver group programmes. The purpose of this short, anonymous questionnaire is to find out what your preferences are for classes, groups and information services into the future. This will help us to plan how groups and services will be delivered. As always, our ability to provide group programmes and classes varies from county to county as this depends on funds and resources available in each area. There are 12 short questions and it will take you approximately 5 minutes to complete. Please click the link below.

Thank you.

You can complete the survey in the link below

I was diagnosed with MS twenty-five years ago last January.

Twenty-five years! A full quarter of a century!

So, what’s the difference between now compared to the day of my diagnosis? That day in 1996 I was pretty normal, with a very slight numbing sensation in my right shoulder and down my right arm. Today, MS has taken a significant toll on me, leaving me with fatigue, brain fog, a bad (*very* noticeable) limp in my right leg and very frequent bouts of extreme facial pains.

MS Ireland would like to congratulate Prof. Alan Thompson on winning the 2021 Charcot Award. The Charcot Award recognises a lifetime achievement in outstanding research into understanding and treating MS.  Prof. Thompson who is the Dean of the Faculty of Brain Sciences at UCL in the UK, is a long-time supporter of MS Ireland who has focused his 40-year career on the care and treatment of people living with MS.

The paints dance across the page, running into each other in ways you hadn’t planned but looking all the more beautiful for it.

It’s like an analogy for life really. No matter what way you plan, life will do its own thing but that doesn’t mean it’ll be any less beautiful and worthwhile

This year Father’s Day for me is bittersweet. Last May, I lost my father suddenly aged 60. His departure from this world was shocking and just like MS, it came in the blink of an eye and my whole life changed.

When I was asked to write this piece on access my head immediately spun. There are so many topics to choose from such as access to parking, buildings, medications, services …the list is endless!
 

ln the end I chose how we were accessing the services we need in the new world we are going to be living in. This virus came from nowhere and ripped through our communities.   Our lives have been turned upside down and we’ve had to find new ways of living. The question we need to ask is will some of these changes stay with us even after the pandemic has passed?

Applications are now open for the Multiple Sclerosis Society of Ireland's annual awards. Nominate someone special today.

“Good morning everyone I need to speak to you about the coronavirus and Covid-19," When the Taoiseach spoke these words live from Washington there was urgency in his words, but I wasn’t listening to them. Well I was, but none of them registered. I was sitting in the ER department of the Galway Clinic and a young doctor had just given me the results of an MRI I had in the previous hour.

“We need to admit you Mr. Walsh, something has shown up in your scan and we need to do more tests” he said. “Is there any history of Multiple Sclerosis in your family?” he asked.

MSIF have updated their COVID-19 information to include: 

World MS Day 2021 took place on Sunday May 30th and the theme of this year's campaign was 'Connections'. In the days leading up to World MS Day and on the day itself MS Ireland was featured in national and regional media on television, radio and print. 

We had some brilliant ambassadors sharing their stories on what life is like living with Multiple Sclerosis all of which you can now read and watch back below.