Minister launches National Disability Inclusion Strategy On Friday 14 July, the National Disability Inclusion Strategy 2017-2021 was launched by the Department of Justice and Equality. In launching the Strategy, Finian McGrath, Minister for Disabilities, said that: “This is an all of...
Published by MS Ireland on Monday July 17 2017 11:11 AM
MS Ireland shares the disappointment of the Disability Federation of Ireland and other charities that Budget 2017 failed to address key issues for people with MS and other long term illnesses and disabilities. Whilst there were some welcome developments in the Budget, such as the increase in hea...
Published by MS Ireland on Wednesday October 12 2016 04:42 PM
Do you or someone you know use Assistive Technology to support them in their daily lives? The Disability Federation of Ireland in collaboration with Enable Ireland are doing some research on Assistive Technology provision for people with disabilities in Ireland. We are interested in hearing the ...
Published by Disability Federation IrelandI/Enable Ireland on Monday September 05 2016 08:44 AM
Campaign on hidden disabilities MS Ireland is supporting the I See Beyond campaign which is being run by Headway and Epilepsy Ireland. The campaign aims to raise awareness of the fact that whilst many disabilities may not be visible at a glance, they are real and can make life for people very di...
Published by MS Ireland on Monday February 08 2016 10:47 AM
MS Ireland's Statement ref: Autologous Haematopoietic Stem Cell Transplantation (AHSCT) 'Multiple Sclerosis Ireland welcomes progress in stem cell treatment for people with MS, as news of success in the UK with Autologous Haematopoietic Stem Cell Transplantation (AHSCT) (sometimes referre...
Published by MS Ireland on Tuesday January 19 2016 11:30 AM
Summary of Key Measures Health Just €280m in new money goes forward to next year’s health budget, a mere 2% raise on 2015. €8 million for expansion of therapeutic services for children, particularly speech and language Funding for the National Maternity Str...
Published by Disability Federation of Ireland (DFI) on Friday October 16 2015 04:31 PM
Nationwide during January 2015 What is the Disability Access Route to Education (DARE)? The Disability Access Route to Education (DARE) is a college and university admissions scheme which offers places on reduced points to school leavers with disabilities. DARE has been set up by a number of c...
Published by MS Ireland on Saturday January 03 2015 10:27 AM
Cooking pot with siphon attachment for people with a disability Andrew Fahy, is on the International Entrepreneurship Masters programme in the University of Limerick (UL). He is currently completing a Strategic Commercialisation Project to complete the final stage of a Business Masters. Andrew i...
Published by MS Ireland/Andrew Fahy University of Limerick on Thursday August 07 2014 09:46 AM
Fresh cuts met with shock Following the surprise cuts to housing supports this week MS Ireland joins other representative groups for people with disabilities and the elderly across the country in criticising the move. The cuts affect people with disabilities in two areas: the housing adaptation...
Published by MS Ireland on Thursday January 09 2014 11:07 AM
Service for people with disabilities The National Advocacy Service (NAS) was set up to provide an independent, representative advocacy service for people with disabilities. It is organised and managed by the Boards of five Citizen Information Services and is supported by the Citizens Information...
Published by MS Ireland on Monday November 25 2013 10:29 AM
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
Global experts publish recommendations for overcoming challenges to improve clinical trials in progressive MS A special issue of Multiple Sclerosis Journal, sponsored by the International Progressive MS Alliance, has been published, containing papers that review the challenges and the potential solutions to improving clinical trials and their outcomes so that new treatments become available for people living with progressive MS. All of the papers are available to view and share Topics covered include: The evolving role of people with MS in clinical research - Some progress but more is needed Progressive MS trials: Lessons learned Targets of therapy in progressive MS Fluid biomarker and electrophysiological outcome measures for progressive MS trials
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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31 October 2017: Ongoing Group physiotherapist led exercise classes for people with MS
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