News

We are delighted to announce the winners of this year's awards

Our Annual Awards are the Society’s way of recognising the contribution many of our members make within their families, local communities and MS Ireland.

Nobody enjoys going back to the place where it all began, the room where you were told you had multiple sclerosis.

Your follow-up appointments don’t have to be an emotionally overwhelming time. If you go in prepared, you’ve won half the battle. Whether you’re a list-person, a cheat-note person or prefer to go in gung-ho with nothing, seeing your neurologist is the most important part of your treatment plan, so it deserves some work beforehand. Take it from someone born with a very practical minded streak who loves making plans, love schedules and lists!

The MS Readathon is back!

• One of Ireland’s oldest fundraisers, the famous MS Readathon is back for its 34th year.     
• MS Ireland is hoping to replicate last year’s successful virtual campaign where almost 10,000 readers and over 300 schools took part.
• The fundraiser provides vital services and supports to the 9,000 people in Ireland living with MS, he most common debilitating neurological condition affecting young adults in Ireland.

visit www.msreadathon.ie to sign up and support the MS Community

In the summer of 2020, MS Ireland received an email from the production company of Netflix's smash hit comedy series 'Sex Education' starring Asa Butterfield and Gillian Anderson. The production team were looking for someone to play the role of Roland Matthews, a father , living with MS who is warm, cheeky, sharp and witty.

MS Ireland put out the call on our social and email channels, which caught the eye of David Layde. David is and actor from Dublin and is living with MS the past 11 years, he applied for the role and the rest is history! Recently we caught up with David about his experience staring in one of Netflix's biggest series.

It is safe to say this year has been the year of the ‘staycation’ and exploring our own back garden. This time last year we had all hoped that by now the pandemic would be a bizarre distant memory. Perhaps, you had dreamed of plane hopping to some exotic, sunny location during the summer. Finding some perfect getaway to relax and reflect on the absurdity of the last year while sipping a cocktail and looking out across a crystal-clear sea with waves breaking over ivory sand. But alas, it seems that the way we travel is not set to change anytime soon.

I know that the 12 months just ended, when the pandemic has continued throughout, has been very challenging for many of the community of people living with and affected by MS that MS Ireland serves.

The innocence and compassion of childhood are qualities that I often wish we carried through to adulthood. If they had, I believe they would make us more empathetic and understanding human beings.

MS Ireland and Novartis launch first podcast series to support people living with multiple sclerosis in Ireland.

• MS Explored – The Podcast, created by MS Ireland in partnership with Novartis Ireland, provides valuable information on living with and managing MS
• The podcast series has been developed in response to the urgent need for easily accessible information resources for the MS community
• Topics explored include navigating the patient journey following diagnosis, the impact living with MS can have on family life, and tips and useful advice for resources to support
• Hosted by MS Ireland’s Aoife Kirwan, the series features top healthcare experts including as well as people with lived experience of MS

You can listen to Episode number 1 here

An anonymous survey is being co-ordinated by Prof Ronan Killeen, Consultant Radiologist, St Vincent's University Hospital and Dr Brendan Kelly, PhD candidate UCD and Radiology SpR and designed with input from MS Ireland. 

MS Ireland launches dedicated resource ‘Understanding MS@Work’ for people living with MS and their employers to become more informed on the daily impact of MS. 9 out of 10 people with MS say the pandemic has helped steer conversations with their employers about the benefits of working from home long-term.

• New research among MS Ireland members reveals impact of COVID-19 on employment, and how working life with MS can be better understood by employers
• 80% of people with MS say the way they work has changed as a result of the pandemic
• Although 85% say their employer knows they are living with MS, more than one-fifth (21%) of respondents cited ‘lack of understanding / empathy’ as the issue that most impacts their working life