MS Ireland research programme is now open The Multiple Sclerosis Society of Ireland encourages and promotes MS research as a way to improve understanding of the disease, leading to better treatments, interventions, strategies to manage the impact of the disease on a day to day basis, ...
Published by MS Ireland on Wednesday November 06 2013 01:29 PM
Volunteers from D&B Information Solutions tranform the garden at Ireland's only respite and therapy centre for people with MS Recently the staff at our MS Care Centre had cause to be extra cheerful as 22 helping hands arrived at the Centre ready to work! The team of 11 volunteers ...
Published by MS Ireland on Thursday June 27 2013 11:00 AM
The MS Ireland blog is your space to talk about the things that matter to you. It's an opportunity to come together with a community of like-minded people and share your stories, advice and tips. Of course, it's also a great place to ask questions, meet new ...
Published by MS Ireland on Thursday June 28 2012 03:35 PM
UK Recommends MS Treatment Gilenya, Medicine Remains Currently Unavailable To Patients in Ireland • NICE – National Institute of Clinical Excellence (UK) recommends that Gilenya is made available to patients in England and Wales • The once a day oral the...
Published by MS Ireland/Novartis on Tuesday March 20 2012 03:16 PM
Dublin Brain Bank launches new website The aim of the Dublin Brain Bank is to facilitate an archive of brain tissue, which will help clinical and neuroscience researchers uncover potential cures for neurologically devastating diseases. Visit Dublin Brain Bank
Published by MS Ireland/Dublin Brain Bank on Friday March 02 2012 04:46 PM
Nominations sought for Carers of the Year and Young Carer of the Year Awards 2012. The closing date for nominating a Carer for Carers of the Year and Young Carer of the Year is fast approaching and people who wish to nominate a Carer for these awards are being urged to do so before...
Published by MS Ireland/Carers Association Ireland on Thursday March 01 2012 04:56 PM
MS Ireland become a partner in National Carers Week. Ava Battles, Chief Executive of MS Ireland discusses MS Ireland's decision to become partners in National Carers Weeks. “We are delighted to be involved with Carers Week 2012. As a progressive, neurological condition...
Published by MS Ireland on Wednesday February 29 2012 05:00 PM
Local flower arrangers raise funds for Charity Reverend William McMillan, MBE presenting cheque to Olivia Kirwan, MS Ireland. Photo courtesy of Joe Curtis A group of flower arrangers, from both North & South, decided to raise funds for charity and to celebrate the life of 80...
Published by MS Ireland on Monday February 13 2012 05:12 PM
Tuesday 6th March 2012, Radisson Hotel, Golden Lane, Dublin 8 The theme this year is 'Securing and Protecting Investment in Neurological Care and Rehabilitation in a Recession'. The event will provide key updates from the clinicians leading each of the national clinical programmes in n...
Published by Neurological Alliance of Ireland on Monday February 06 2012 05:14 PM
The Disability Federation of Ireland is looking for feedback on a new policy they are helping to create. Many people with MS use personal assistants to help with aspects of daily life. The Disability Federation of Ireland is looking for feedback on a new policy they are helping to create. ...
Published by MS Ireland/DFI on Wednesday February 01 2012 09:53 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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