Christmas… rescheduled!
Sometimes life just throws tantrums and curveballs because of your illness – missing out on Christmas with my nieces and uncle at the very last minute is just one of those moments. But then you realise that your family’s love, acceptance and support will keep you going long after the Christmas holidays, no matter what. Instead of Father Christmas giving you presents, they want him to take away your sorrow. They know that Christmas can’t be bought in a store, but instead is given in invisible mountains of love. They feel your anguish and wished they could take your physical pain from you. They root for you, uplift you and guide you. You feel empowered by them being there, even when divided by country borders. You know they believe you,…
MS News: November 2015
Highlight! Multiple sclerosis health news roundup 2015: MS prevention and treatment breakthroughs Study To Test Impact Of Chocolate On Multiple Sclerosis Fatigue Oxford Brookes to Study if Chocolate Could Actually Help Cure Multiple Sclerosis Chocolate could ease multiple sclerosis symptoms
Giving Tuesday!
We're busy planning something fun for #GivingTuesday! Keep an eye out to see what we're up to on 1st December! pic.twitter.com/32eSGCl7ne — MS Ireland (@MSIRELAND) November 26, 2015 Multiple Sclerosis Ireland – Please donate to support the outstanding services the only MS Care Centre in Ireland offers to people with MS, and keep its much-needed respite care going! Happy giving! ©Willeke Van Eeckhoutte and Ireland, Multiple Sclerosis & Me, 2011-2015. Unauthorised use and/or duplication of this material without express and written permission from this blog’s author and/or owner is strictly prohibited. Excerpts and links may be used, provided that full and clear credit is given to Willeke Van Eeckhoutte and Ireland, Multiple Sclerosis & Me with appropriate and specific direction to the original content.
Balancing life and a chronic illness
Reality. It’s what’s for breakfast. After some feeble attempts trying to write a few paragraphs the past few weeks, it was back to the drawing board each time. Not good enough. Already done this. Needs more research. Too tired. Not fit enough. You know moments like these, you sit down, determination almost physically squeezing ink out of your pen. Cup of coffee at the ready, you start and a few minutes later you have to hold on, waiting for energy to kick your bum to open up your half-closed eyes. Reality. Seamus Heaney once said “writing is a snapshot of consciousness”. I was lucky being semi-conscious this week. I could hardly make sense of myself during those few moments I tried to put pen to paper.
How (not to) be sick!
That's me. I forget how to be sick. The fact that physically I am crumbling under a lot of neuropathic pain, can’t frown my forehead into cute wrinkles, have no feeling on the top of my scalp, have constant bees in my ears of tinnitus, stabbing facial pain and intense fatigue, is something I refuse to show anyone carrying a medical degree. It’s a survival instinct of sorts.
MS News: October 2015
It was a busy month. ECTRIMS (European Committee for Treatment and Research in Multiple Sclerosis Congress; October 7 – 10, 2015 in Barcelona) came and went, with insight and data offered on existing and new therapies.
]MS News: September 2015
Highlight! Less vitamin D and melatonin bad for multiple sclerosis Multiple sclerosis relapse risk influenced by melatonin levels Melatonin could help treat multiple sclerosis Melatonin Linked to Seasonal Relapses of Multiple Sclerosis