How to get involved We will join with individuals and organisations across the world to mark World MS Day on Wednesday, 31st of May. This is one of the highlights of our year when we come together to celebrate and empower the 9,000 people living with Multiple Sclerosis in Ireland. The them...
Published by MS Ireland on Friday May 05 2017 09:24 AM
Irish actress Aoibhinn McGinnity, Sara-Jane Tracy and her brother James Tracy, Irish rugby player launch campaign MS Ireland is calling on supporters to Kiss Goodbye to MS from January 17th until February 14th 2017 and to help raise funds for MS research and essential services for more than 9,00...
Published by MS Ireland on Tuesday January 17 2017 12:18 PM
Fiona O’Reilly (48) has been living with Multiple Sclerosis (MS) for the last 3 years. Some days are worse than others. Some days she can barely move at all. On others, the loss of feeling in her feet and her lack of balance put her at constant risk. The MS Care Centre on Bushy Park Road i...
Published by MS Ireland on Thursday December 22 2016 10:55 AM
Vote for our video entry From now until the 7th December and we are inviting the public to vote for our 'Better Together' video entry. We really need your help on this as only the top 10 most-voted-for videos in each category will be shortlisted for the final round. The winners will be ann...
Published by MS Ireland on Thursday November 10 2016 10:13 AM
Join MS Ireland's CEO, Ava Battles on Sunday, 23rd October 2016 Deirdre Eustace is an inspirational person with Multiple Sclerosis and a resident of the MS Care Centre for 20 years. Deirdre won a 'Skydive' at a recent fundraising event and dared Ava do it for her and raise funds for the MS Care ...
Published by MS Ireland on Tuesday September 27 2016 10:37 AM
Deirdre O’Kane and David Rawle launch the 29th MS Readathon The 29th MS Readathon launched on Tuesday, 20th September in the National Library of Ireland with Deirdre O’Kane and Moone Boy actor David Rawle, joining MS ambassador family Gerard Murphy, who is living with MS, and h...
Published by MS Readathon Team on Wednesday September 21 2016 09:28 AM
Save the Date! MS Ireland will join with other societies around the world to raise awareness of multiple sclerosis (MS) and mobilise the public around issues affecting people with MS and their families. The theme will be ‘Independence’. This includes employment, but ...
Published by MS Ireland on Wednesday March 09 2016 12:26 PM
Rosanna asks MS Ireland supporters to pucker up and ‘Kiss Goodbye to MS’ Best-selling author Rosanna Davison announced today Thursday, 4th February details for MS Ireland’s new fundraising campaign, Kiss Goodbye to MS. Rosanna is joined by Aoife Kirwan, who lives with MS, as t...
Published by MS Ireland on Thursday February 04 2016 10:00 AM
Prize draw winners announced Following the prize draw on RTÉ's fab News2Day we are delighted to announce the winners of the MS Read-a-thon School and Readers Prize Draw! School Prizes €2,500 worth of books, kindly sponsored by The O’Brien Press: Kilfenora National Scho...
Published by MS Read-a-thon Team on Wednesday January 20 2016 04:30 PM
Is going global! Kiss Goodbye to MS is a global fundraising campaign that raises funds and awareness for multiple sclerosis. Kiss Goodbye to MS asks people with multiple sclerosis (MS), their friends, family and colleagues to raise funds and awareness for people living with MS all over Ir...
Published by MS Ireland on Thursday January 14 2016 05:00 PM
Fund for students with disabilities to be extended to part-time students The operation of a €10m fund for college students with disabilities is to be reformed to ensure more people benefit and with fewer delays. The fund for students with disabilities exists to financially assist students with disabilities while they are in education. Students apply to the fund via the Disability Support Service in their college. The fund can be used for: Assistive technology equipment and support Personal and Academic Support Transport To date, this fund has only been available to full-time students, however one of the reforms recommended by a recent review was that it be extended to part-time students also. You can read more about financial supports available to students on page 9 of the latest issue of MS News
This week Emma Rogan feels a little bit… awkward. No one who walked into the room left without having some of their ideas changed to a more sex-positive way. It was after lunch, it wasn’t in the dark and they didn’t whisper when they spoke about positions, difficulties climaxing, drugs that help or toys that work about lubrication, orgasmic spinal centres not getting enough stimulation and vacuum device to help with erectile dysfunction in loud voices and in public! They were talking about sex and people with MS. “For most people, sexuality and its expression are a natural and important component of self-concept, emotional wellbeing and overall quality of life” World Association of Sexology Sex is a core part of being a human yet in this society it’s a topic so weighed down by disgust and shame that having a sex-positive discussion is almost impossible. Add to this living with a nerve-signal, body-altering condition and we’re all silent. I have scars in/on my brain and spine and damage to my nerves causing loss of feeling. I’ve not always been able to feel the touch of a lover and I’ve faked so many orgasms I can’t count. I’ve had great sex, fall-asleep sex and everything in-between. Sex only got better when I was honest about whom and what turned me on. There are thousands of women with MS and their sex-partners having unfulfilling sex lives for all sorts of reasons. Maybe it’s because of the dreaded T word- talking. Maybe being diagnosed with MS has severely impacted how we feel about our body and our personhood has been seriously harmed. Maybe it’s a traumatic experience in the past that has damaged our bodily integrity. Maybe when we’re in front of our neurologist our sex life not on the priority list. If we value your sex life, we must talk about it. Otherwise, we leave the clinic without a referral to a therapist or having a conversation with the MS nurse or a getting prescription for something useful or tips on what would work for us. We’re complicated creatures and if having MS is having an impact on how we feel about ourselves, we need to deal with it. If there are issues with our relationships, we need to talk with our partner and consider seeing a couple counsellor. If it’s something physical (loss of erogenous/clitoral sensation) speak to your neurologist or an urologist. Ask someone and learn to talk about it so when you do talk with your girlfriend or boyfriend, wife or husband or with someone you trust, you start getting sexual healing. MS Ireland has a trained psychosexual therapist on their staff, Mary Leonard (maryl@ms-society.ie) and she’s available if you need her help. Get in contact with an accredited therapist. Imagine living in an Irish society free of repressive attitudes, where people are decent to one another, disagree and still get on and where there’s a celebration of what it means to be a living, breathing human being. Imagine sex being a routine, part of daily life without competition and not about performance. Being with someone who really turns you on, you can talk to and who makes you happy is worth talking about. Sex doesn’t need to be mind-blowingly amazing every time but pleasurable, yes. The people from earlier were Charalampos Konstantinidis and Moira Tzitzika at the EMSP Spring Conference in Athens, 2017. I’m not a Greek goddess no matter how amazing I think I am. I’m an ordinary woman with needs and desires and I know what and who makes me feel good. Learning about and understanding the issues I have is a step towards me learning how to ‘overcome obstacles effectively’ (Moira Tzitzika). Having MS has not diminished my desire to have a healthy, sex-positive life and if talking about it helps, being awkward is something I know I can overcome. I’m on Twitter @emmadragon a lot and am eager to chat about this and other MS topics. Moira Tzitzika MSc, BTEC, EFT, ΕCPS, MSMC Charalampos Konstantinidis, MD, FEBU, FECSM MS Trust Sexuality and MS: A Guide for Women
Over the coming months the MS Ireland Western Regional Office are hoping to run a 'Mindfulness Course' for people with MS. However, we would like to gauge the level of interest in such a course before we book a qualified facilitator. If you are interested please click on the email below and let the team know what day/time/location that would suit you best and send it back to us here in the Western Regional Office western@ms-society.ie at your convenience.
Thursday, 26th October @ 6pm (Irish Time) Dr. Nonnie McNicholas, St Vincent’s University Hospital, will provide an update for people with MS and their healthcare professionals on the hot topics from ECTRIMS covering the main updates and research themes from the conference. Tune in on Thursday, 26th October at 6pm Irish Time. Click the link below and use the following password ThinkMS to login. http://esc.eventresult.com/default.asp?EventCode=Novartis&RoomCode=Novartis
Briefing Document and Position Paper on the need for an MS registry in Ireland MS Ireland has produced a Briefing Document and Position Paper on the need to establish an MS Patient Registry in Ireland. The paper outlines: What patient registries are Why registries are important Current patient registries in Ireland MS registries internationally MS Ireland’s position and recommendations The paper can be accessed here This document has been prepared by Harriet Doig, Information, Advocacy & Research Officer, MS Ireland. Questions and comments can be directed to harrietd@ms-society.ie
Have you got something to say about what your life is like living with MS in Ireland? Will you share it with the world? Find out how to get involved with our community blog MS & Me...
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