First ever patient survey of outpatient neurology services now calling for responses The Neurological Alliance of Ireland (NAI), the umbrella representing over 30 patient organisations, in partnership with the National Clinical Programme in Neurology, has launched the first ever patient experien...
Published by Neurological Alliance Ireland on Tuesday October 17 2017 10:36 AM
Findings from the first national audit of neurology services highlight widespread deficits A report on the findings from the first national audit of neurology services, launching today, points to widespread deficits accross neurology services nationwide. The audit, based on reports from ea...
Published by Neurology Alliance of Ireland/MS Ireland on Wednesday February 17 2016 01:19 PM
Neurological Alliance of Ireland Election Campaign Over 800,000 Irish people are living with neurological conditions like multiple sclerosis, stroke, acquired brain injury, Parkinson's disease, epilepsy, migraine and dementia as well as a multitude of rare and genetic conditions. Ireland'...
Published by MS Ireland/Neurological Alliance of Ireland on Monday January 11 2016 09:27 AM
We are happy to announce that registration for the Neurological Alliance of Ireland (NAI) Keynote Conference is open. The event takes place during Brain Awareness Week, details below, and is free of charge but early registration is advisable. Closing date for registration is 20th February. Title...
Published by MS Ireland on Wednesday January 21 2015 03:02 PM
Raising awareness of living with a neurological condition in Ireland 10th - 15th March 2014 Brain Awareness Week is an international awareness campaign, highlighting the work of neurological organisations (like us) and the experiences and issues of the people it represents (like you). The ...
Published by MS Ireland on Friday January 24 2014 11:00 AM
'Help us to tell the Government what it's like to live with a neurological condition in Ireland' The Neurological Alliance of Ireland (NAI) have launched an online survey to find out the impact of the recession and cuts in the health services on people with neurological conditions and their fami...
Published by NAI on Thursday January 09 2014 09:45 AM
...For World MS Day Whether you’re strapped for time and money or not, there are plenty of things you can do to raise awareness, raise the issues and raise funds this World MS Day. What’s Your Motto? Mottos can lift our spirits and motivate us to make the most of every day. Y...
Published by MS Ireland on Tuesday May 14 2013 01:45 AM
Celebrate the brain this May Across Europe in May people and organisation will focus on the power and mystery of the brain. The initiative is being led by the European Commission and aims to focus attention on neuroscience and the importance of greater collaboration, advocacy and research. &ldq...
Published by MS Ireland on Monday April 08 2013 09:33 AM
Neuro Groups Demand Action MS Ireland joined The Neurological Alliance of Ireland (NAI) for their Lobby Day in Leinster House to present a grim picture of neurological services to gathered TDs and Senators. Person with MS, Emma Rogan spoke of her personal experience of living with a neurological...
Published by MS Ireland on Thursday February 28 2013 10:01 AM
Play Your Part, Protect Neurological Care in 2013 As Ireland prepares to host European Month of the Brain in May 2013, as part of its EU presidency, we still lag far behind the rest of Europe when it comes to neurological care. A recent report by the HSE showed that over 5,000 people were waitin...
Published by MS Ireland/NAI on Wednesday October 10 2012 10:45 AM
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
Global experts publish recommendations for overcoming challenges to improve clinical trials in progressive MS A special issue of Multiple Sclerosis Journal, sponsored by the International Progressive MS Alliance, has been published, containing papers that review the challenges and the potential solutions to improving clinical trials and their outcomes so that new treatments become available for people living with progressive MS. All of the papers are available to view and share Topics covered include: The evolving role of people with MS in clinical research - Some progress but more is needed Progressive MS trials: Lessons learned Targets of therapy in progressive MS Fluid biomarker and electrophysiological outcome measures for progressive MS trials
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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31 October 2017: Ongoing Group physiotherapist led exercise classes for people with MS
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