Heart problems after the first dose prompt a review The European Medicines Agency (EMA) has begun a review on Gilenya (Fingolimod) after reports of heart problems after the first dose. One patient in the US also died within 24 hours of the first dose, although the cause of death has no...
Published by MS Ireland on Tuesday January 24 2012 09:58 AM
MS Ireland is delighted to announce that Michael D. Higgins, President of Ireland, has accepted our invitation to become our patron. The President will be the sole patron of MS Ireland, succeeding Mary McAleese as the previous patron of the Society. Michael D. Higgins, President of I...
Published by MS Ireland on Tuesday January 17 2012 10:01 AM
It is with great sadness that we announce our charity shop in Bray, Co. Wicklow will close its doors for the last time on FRIDAY 23rd of December. For over 20 years the Bray Shop has been an active part of the local community and played an important part in MS Ireland’s fundraisi...
Published by MS Ireland on Monday December 19 2011 10:04 AM
Researchers say a variant gene which reduces vitamin D levels could be directly linked to MS. News article from BBC News Health A rare genetic variant which causes reduced levels of vitamin D appears to be directly linked to multiple sclerosis, says an Oxford University study. ...
Published by BBC News on Tuesday December 13 2011 10:08 AM
Mark Mitchell wins national volunteering award in Dublin Castle. MS Ireland is delighted to announce that MS Person of the year 2011 Mark Mitchell scooped one of ten national volunteering awards in a glittering ceremony attended by The President of Ireland, Micheal D Higgins. Mark is the curre...
Published by MS Ireland on Tuesday December 06 2011 10:12 AM
Charity 25's €2WILLDO campaign raises €5975 this quarter for 25 Irish Charities Charity 25 raised €239 for MS Ireland. MS Ireland is delighted to be part of Charity 25. To support MS Ireland and other charities all you need to do is text: Text 2WILLDO and ...
Published by MS Ireland/Charity 25 on Thursday November 17 2011 10:21 AM
Corporate Social Responsibility (CSR) is a practise that is as beneficial to a company as it is to a charity or local community... The MS Ireland Midwest Regional Office recently played host to some very enthusiastic and hard-working volunteers from Dell Limerick as part of their CSR proje...
Published by MS Ireland on Monday November 14 2011 10:30 AM
NAI and DFI launch new website Multiple Sclerosis Ireland is delighted to be part of the new Neuronetwork.ie website launched by the Neurological Alliance of Ireland (NAI) and the Disability Federation of Ireland (DFI). Neuronetwork is a unique online tool that aims to provide users ...
Published by MS Ireland/DFI/NAI on Friday October 28 2011 10:39 AM
Call on people with MS to make a submission... Minister of State for Disability, Equality and Mental Health, Kathleen Lynch T.D. released a report on the future policy of disability in this country drawn up by an Expert Reference Group at the request of the Department. The ...
Published by MS Ireland on Tuesday October 18 2011 10:45 AM
Report details the social and living conditions of people with disabilities. Joan Burton TD, Minister for Social Protection, (Wednesday, 21st September 2011) launched a new ESRI report on the social and living conditions of people with disabilities. The report was commissioned by m...
Published by ERSI/UCD on Thursday October 06 2011 11:08 AM
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
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