How do you make your decisions? We all know how being better informed means better decision-making but we don't always get the information we need. This week from the MS & Me archive series Joan Jordan talks about the importance of being well informed about MS drug treatments and medications....
Published by Joan Jordan on Thursday August 24 2017 10:35 AM
‘This week Helen Farrell examines how the years of living with MS have made an impact on her hopes for the future’ This week a brand new MS medication, Ocrevus (ocrelizumab), was approved by the Federal Drugs Authority (FDA)in the United States for both primary progressive (PPMS) and...
Published by Helen Farrell on Thursday April 06 2017 11:00 AM
This week Niamh McCarron shares with us her pre-holiday preparation plan. Whether it is a room with a fridge, a great day trip or making it through security with medication intact, she has the tips on how to get your great escape in a calm, prepared way. Seven tips for holiday heaven. Since disc...
Published by Niamh McCarron on Thursday July 14 2016 11:16 AM
In the second of our year-long series of debate blogs, Trevis talks about NOT taking an MS disease modifying therapy'. Firstly, let me state unequivocally that I believe that multiple sclerosis disease modifying therapies (DMT) work. They work for different people to differing levels of success ...
Published by Trevis Gleason on Thursday March 10 2016 11:15 AM
In this week’s MS & Me blog, Niamh takes a look at why she decided to go on medication to manage her MS. In reality, it wasn’t a deeply-considered decision that I made. The option to not take any medication wasn’t really presented to me. I was under the impression fro...
Published by Niamh McCarron on Thursday March 03 2016 11:08 AM
*The dawn of 2016 brings a break between literal and figurative storms. We look forward to a new year, a better year and another year of the MS & Me Blog * As 2015 wound itself up the MS & Me Blog team was able – for the first time in its entirety – to gather in Dublin to cel...
Published by Trevis Gleason on Thursday January 07 2016 10:15 AM
I was on my way to pick up the kids from soccer practice the other day when I realised I had forgotten my phone! It was too late to make it back home to retrieve it and as it turned out, I had to wait a while for the final whistle. With my only other option being the car manual, I decided to re-r...
Published by Joan Jordan on Thursday November 19 2015 10:30 AM
Have I imagined it? Could there be a social aspect to medication? Having an incurable and unpredictable illness is never going to be a bundle of fun and the thought of taking medication for the rest of one’s life doesn’t do anything to alleviate the situation. Therefore we must take ...
Published by Declan Groeger on Thursday May 07 2015 11:05 AM
From Willeke's own experience her medical team has been pivotal to her care and have been outstanding so far! With an illness like multiple sclerosis, a diagnosis doesn’t come alone. Depending on the type and severity of your MS, you are immediately served by several people from different ...
Published by Willeke Van Eeckhoutte on Thursday October 02 2014 11:00 AM
Whenever I meet a fellow MS-er, I ask them their name, where they are from and what meds they are on. It doesn’t take long to move on to the benefits of their prescribed drug and if they outweigh the side effects brought into their everyday lives. Some side effects and limitations of a drug...
Published by Joan Jordan on Thursday May 15 2014 11:30 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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