Conference in Dublin a success! We’re delighted to day that the EMSP Spring Conference was a complete success! It was an honour to host the European MS community here in Dublin last week. For those of you who were unable to attend don’t worry, we will be publishing full reports from ...
Published by MS Ireland on Wednesday May 14 2014 11:00 AM
Isn’t this MS and Me blog an exciting feature? I am really enjoying reading the experiences of others and the shared understanding. Please make sure you comment on what you read. It has been a while since I spoke with you all. Much has happened in the winter months that have lead me down d...
Published by Emma Rogan on Thursday February 13 2014 02:06 PM
“Last year Emma won the World of Difference competition run by the Vodafone Ireland Foundation. Her chosen charity was MS Ireland and she spent 2013 working on advocacy, informing the public and learning all about Irish health and social policy.” Selecting MS Ireland for the World of...
Published by Emma Rogan on Thursday November 21 2013 10:20 AM
New international report says we’re poor on number of neurologists but good on equality The Multiple Sclerosis International Federation (MSIF) launched their 2013 Atlas of MS which provides an overview of Multiple Sclerosis across the world. Ireland again fared poorly in the provisi...
Published by MS Ireland on Friday October 04 2013 10:02 AM
Emma Rogan to compete in Brussels Half-Marathon, 6th October 2013 There are more than 2.3 million people in the world living with Multiple Sclerosis. On Sunday 6th October, to raise awareness of the 600,000 people with MS in Europe, Emma Rogan is taking part in the Brussels Half-Marathon. ...
Published by MS Ireland on Thursday October 03 2013 02:45 PM
Link in with other Young People with MS If you are 18 - 40 years and would like to link in with other young people with MS you're invited to the Menlo Park Hotel, Headford Road, Galway on Saturday, 20th July from 2.30pm - 4pm to get together with other people from the West and Mid West ...
Published by MS Ireland on Wednesday July 10 2013 02:36 PM
Emma Rogan speaks about the Importance of Living Differently My name is Emma Rogan. In September 2012 I entered the Vodafone Foundation Ireland World of Difference competition. This is a programme that gives people the opportunity to work for the charity of their choice for one year. The V...
Published by Emma Rogan, MS Ireland on Wednesday June 26 2013 10:25 AM
Emphasis on Young People at World MS Day event in Warsaw, Poland The Polish MS Society marked World MS Day 2013 by organising an event - at the headquarters of the Polish Ombudsman - on matters concerning people with Multiple Sclerosis, particularly young people with MS. The special gu...
Published by MS Ireland on Tuesday June 11 2013 11:17 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
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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