Our Beautiful Minds Neurological Alliance of Ireland (NAI) is organising a public information meeting on understanding the brain and the impact of neurological conditions 'Our Beautiful Minds - our brains and how they shape our lives, on Monday, 6th March 2017 in Trinity College Dublin. Speaker...
Published by MS Ireland/NAI on Wednesday February 22 2017 12:10 PM
This week Professor Sabina Brennan from the Neuro-Enhancement for Independent Lives (NEIL) Research Programme in the Institute of Neuroscience at Trinity College Dublin asks us to consider our brain health. We all know people who are really resilient; people who seem to manage to ‘ke...
Published by Professor Sabina Brennan on Thursday November 24 2016 11:00 AM
New MS brain health resource The organisation MS Brain Health have produced a new guide on brain health and MS. This short guide is a resource to help people with MS understand how they can keep their brains as healthy as possible and request the highest possible standard of care from healthcare...
Published by MS Ireland on Tuesday August 02 2016 08:39 AM
Mind Matters: understanding and protecting your Brain Neurological Alliance Ireland (NAI) and the Irish Brain Council have organised a FREE evening lecture on Tuesday, 15th March at 6pm -7pm in Trinity College Dublin entitled "Mind Matters: Understanding and Protecting Your Brain". Th...
Published by Neurological Alliance Ireland/Irish Brain Council on Thursday March 03 2016 08:51 AM
MS Ireland formally endorses recommendations of MS Brain Health report “Brain Health – Time Matters in Multiple Sclerosis” was released in October 2015. This report presents an expert, evidence-based position for policy recommendations aimed at improving outcomes for people wit...
Published by MS Ireland on Wednesday January 27 2016 11:29 AM
Happy Brain Awareness Week! Take a minute to celebrate how hard your 100 billion neurons work to keep your cranium ticking over. To put it in context, you have more neurons in your brain than there are stars in the Milky Way! To mark this annual event, MS Ireland asked me to attend a conference ...
Published by Joan Jordan on Thursday March 12 2015 11:07 AM
Counting the cost The week that’s in it, Emma Rogan takes a brief look at brain research and the importance of researchers and people with MS working together. “Knowing how our brain works is the only way for us to understand ourselves, the world we live in, how we perceive ex...
Published by Emma Rogan on Tuesday March 10 2015 02:39 PM
EFNA launch European survey on the impact of living with a brain disorder **Deadline extended to Friday, 30th January** MS Ireland welcomes the launch of the first European survey on living with a brain disorder by The European Federation of Neurological Associations (EFNA). Aim: ...
Published by EFNA on Monday December 22 2014 10:49 AM
New findings show improvement in balance 27 people with multiple sclerosis underwent a 12 week intervention using a Wii balance board. Researchers used an MRI technique called diffusion tensor imaging (DTI) to study changes in the brain. The MRI scans have shown that use of the balance boa...
Published by MS Ireland on Friday August 29 2014 10:00 AM
There is something about Mary Baker It’s rare to hear somebody frightfully intelligent (Dr., MBE, BA, Hon Dsc) speak so clearly on a complicated subject like the brain. She manages to deliver a powerful message while maintaining a humble and likeable exterior. If she was a rugby play...
Published by Joan Jordan on Tuesday June 17 2014 11:00 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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