This week from the MS & Me archives series - Helen Farrell looks at her smartphone use... I have a confession to make; quite often my smartphone gets more of my attention than my husband does, and it is a mutual situation with both of us tapping away in the evening as we read what has happen...
Published by Helen Farrell on Thursday August 03 2017 10:30 AM
This week from the MS & Me archives series - Lucina Russell discusses how words people use to speak about people with MS has an impact on our identity. There’s also mention of dating and road frontage! I’ve always hated labels. As a child, it was the itchy, scratchy ones on ...
Published by Lucina Russell on Thursday July 20 2017 11:00 AM
This week Niamh McCarron lets us in on challenges she confronts, the bridges she has crossed and the fears that sometimes haunt all our nights. “We’ll cross that bridge when we come to it”. That's my normal approach to dealing with uncertainty and fear. The truth is, I wi...
Published by Niamh McCarron on Thursday June 08 2017 05:51 PM
This week Declan Groeger is not a ‘Muscle Mary‘ but believes exercise has helped him maintain a positive attitude and helped to preserve his mental health. I am passionate about exercise now but that wasn’t always the case. I am a convert and an advocate for the cause. I am not...
Published by Declan Groeger on Thursday May 18 2017 10:45 AM
This week Aoife Kirwan articulates her many MS related fears and why she thinks MS is a bit like Ramsey Bolton! When I first thought about a blog dedicated to fears, I was a bit reluctant to start it. I do have many MS related fears but I don’t often give myself time to really think a...
Published by Aoife Kirwan on Thursday May 11 2017 12:01 PM
'This weeks blog is from Lucinda Russell. She takes us on a journey of clinics, friendship and what ifs? Read on for a fresh take on the day.' In the early days of my diagnosis with Multiple Sclerosis in 2011, everything about my neurology appointments in Beaumont Hospital caused me a...
Published by Lucina Russell on Thursday April 13 2017 10:45 AM
This week we have a guest blogger, Michelle Henley from Cork. She has kindly shared her story with us. We’re calling it 'Love, Family and Grand Plans'. Share your comments and the story with others. This time two years ago life was great, I had returned to education. I had my life to...
Published by Michelle Hanley on Thursday March 23 2017 11:04 AM
This week Aoife Kirwan has gone back in time, to the day she was first diagnosed with MS; standing face to face with her newly diagnosed self, she shares with us what she would say to herself on that day. Recently I took a trip with some of my fellow bloggers to Lisbon. During a chat over coffee...
Published by Aoife Kirwan on Thursday February 02 2017 11:00 AM
This week Lucina Russell reflects on her recent good health and wonders if stress has affected her MS progression. I feel like a bit of a fraud writing for ‘MS & Me’ these days. Truth is, Dear Reader, that I have been in such good health, that I haven’t been spending much t...
Published by Lucina Russell on Thursday January 26 2017 11:00 AM
This week Declan Groeger shares his MS journey. Have you ever embarked on a journey only to find that the starting point was not where you thought it was or started a mystery trip where the route and length of the journey are unknown? My MS journey officially started in 1988 but I believe...
Published by Declan Groeger on Thursday January 12 2017 11:25 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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01 November 2017: Group led Yoga class for people with MS
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