• MS,  Multiple Sclerosis

    Healthy eating

    Eating a balanced diet can be a tricky thing sometimes, especially when temptation is everywhere. I often tell myself, ‘Ah but I’m already doing so much for my health by using my own ‘everything-in-moderation’ diet. Since I don’t consume alcohol or other legal and illegal highs, I something think I am allowed at least a tiny dessert… as long as it’s not ice cream. So yes… Busted! Time so to check out the image below and learn what healthy eating should be like.

  • MS,  Multiple Sclerosis,  Trigeminal Neuralgia

    Eyes of sorrow

    "I am utterly afraid of losing my eyesight completely. The pleasure I assign to them is felt every minute of every day. Reading a book, watching the sun set behind the mountains, seeing a flower open during the day, catching those few rays of sunshine in grey clouds… I am often in awe of the images my eyes capture and send to my brain. These images tease and taunt, are overjoyed or full of sorrow, want more or have enough."

  • MS,  Multiple Sclerosis

    #strongerthanms with MS Ireland

    “So, how’s the book,” friends often ask me. “Oh, it’s getting there,” I joke. “I’ve finished one page, the one with the title and my name!” I don’t lack the ambition to keep on writing, but I have an overabundance of low energy levels, so I must ask people to use their patience… patiently when dealing with me. Like all cowards, the illness I write about lurks in the dark within my central nervous system, and it sometimes rises to the surface in unflattering ways. My body does a good job in concealing it for now, but every so often I worry about it rising to the surface and staying there… permanently.

  • MS,  Multiple Sclerosis,  Your career and MS

    World MS Day 2015 Around the World

    For the second year in a row, ‘Access‘ is the main topic of World MS Day.   Access means a lot of things, so do volunteer in if you want to help others achieve everyday issues. Don’t forget to tag your events with #strongerthanMS and @WorldMSDay. Access Our campaign theme for 2015 is access: access to diagnosis, treatment and support; access to buildings, travel and leisure facilities; and access to education, training and employment. What does access mean? When we talk about equality of access for people with MS we mean access to a social, political and economic life. Equality of access doesn’t just mean physical access to buildings, but access to the same tools, services and facilities that people who do not have MS enjoy. Why access? The barriers…

  • MS,  Multiple Sclerosis,  Trigeminal Neuralgia,  World MS Day

    Hope cures old wounds

    “The illness is mine, but the tragedy theirs,” when asked how my family feels about my condition. When I entered the MS academy, I read the small print and knew it wouldn’t be a 365-day holiday. However, I tolerate MS. There’s no resentment or blame, no more heartache, guilt or doubt. I find solace in seeing science produce more and better research results and medication. Clinical trials are moving forward at a pace that will eventually lead to an easier life with an illness that is as fickle as MS."

  • MS,  Multiple Sclerosis,  Trigeminal Neuralgia

    MRI scans, hope or defeat

    A war zone. It seemed like a war zone. Sound effects of an AK47 gun amid MRI vibrations and banging noises usually taking place on construction sites. Tinnitus adding an overlay I can miss like never before. Magnetic resonance imaging is a godsend to ill people. In regards to MS, it gives a clear view of what is physically going wrong inside the brain, spinal cord, and optic nerves. Add some contrast fluid, and you light up like a Christmas tree, just like mine did this morning. Or so I was told. Sudden, loud sounds twitch my head involuntarily. The upstairs part of my body locked in a mask, I now realise how Leo DiCaprio felt when he played The Man in the Iron Mask.