This week to mark the occasion of World MS Day, Aoife Kirwan talks to TDs and Senators in Leinster House about the quality of life for people living with MS in Ireland. Read Aoife's inspiring speech! ‘I'm here to talk to you this morning as a person with MS but I am much more than that. I ...
Published by Aoife Kirwan on Thursday June 01 2017 02:18 PM
In the lead up to World MS Day 2017, MS & Me blogger, Trevis L Gleason gets behind this year’s theme Life with MS It could be said that I often quip about my multiple sclerosis as a coping mechanism. “Sure,” I’m oft heard saying when someone bemoans my disease more th...
Published by Trevis L Gleason on Thursday May 25 2017 10:00 AM
To say that 'MS doesn't stop me', I'm lying, or at the very least, exaggerating. To be more accurate, I can say, unequivocally, that I do my very, very best to not let it get in the way. Lucina When the 'MS & Me' blogging team were picking topics to write about earlier this year, I was very ...
Published by Lucina Russell on Thursday May 26 2016 11:04 AM
Access to the UN Convention on the Rights of Persons with Disabilities When people hear news related to the United Nations, they immediately think of countries at war or of those in third world regions that need humanitarian help. But what if I told you that people with disabilities in Ireland ...
Published by Willeke Van Eeckhoutte on Thursday May 28 2015 12:52 PM
'With World MS Day upon us blogger Trevis Gleason believes that he is #strongerthanMS, but not alone' Today, 27th May, is World MS Day 2015. Around the globe people are taking part in awareness events, attending educational programs, talking about the topic of access and hash tagging social medi...
Published by Trevis Gleason on Wednesday May 27 2015 11:58 AM
I took some time to think about my approach to my blog post. “Access” encompasses so many issues it was a little bit daunting to pick one. I wanted to make sure I picked a topic that I fully relate to. One obvious topic is access to treatments or specialists or hospitals... som...
Published by Niamh McCarron on Thursday June 12 2014 11:00 AM
Bite Sized Pieces It was hard to know where to begin with this months topic of 'access', as I don't have any physical access issues. There are, however, other things that get in my way. You could call it restricted access (to my life). I'm thinking particularly of the times when fatigue, nausea ...
Published by Lucina Russell on Thursday June 05 2014 11:00 AM
Does accessibility mean the same thing to you as it does to me? Accessibility, or lack thereof, is really a hobby horse of mine and it really gets my juices flowing, makes my blood boil! Accessibility is not just about ‘getting there’. It should be about what you can do when you get ...
Published by Declan Groeger on Friday May 30 2014 11:00 AM
When I was first diagnosed with MS, I was given information on a number of drugs. At the time I felt that being diagnosed in my early twenties would have to work to my advantage as I would get on treatment faster and have it working in my system for a long time. As my MS was extremely active in t...
Published by Aoife Kirwan on Wednesday May 28 2014 10:00 AM
I’m sure Boris Johnson didn’t have me in mind when he was making London more accessible. More like the 20 million spectator journeys he had to facilitate during the 2012 Olympic Games! Anyhow, I was very happy to reap the benefits of his logistical nightmare when I was planning a trip...
Published by Joan Jordan on Monday May 26 2014 02:21 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
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