Tag Archives: Multiple Sclerosis



Imagine if your physical body could heal itself every time you’re ill.

Our mind has the power to heal heartache and/or to show strength in times of need, yet our bodies lack that magnificent paradox. The answer lies in how we look at our emotions; are they your friend, or foe? And how do you view your physical body?

After some feeble attempts trying to write a few paragraphs the past few weeks, I was sent back to the drawing board after each occasion. Not good enough. Already done this. Needs more research. Too tired. Continue reading



You’ve probably been there before.

You say to yourself… “I will absolutely, unequivocally, no-doubt-about-it stay under the duvet to get rid of a bad ear infection, facial pain, unrelentless fatigue and a bout of the flu.”

Sometimes you also think, “I suppose everyone has a point when they say I have to listen to my body a little bit more.” Continue reading

Positive 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. Continue reading



Thirteen years ago today I moved to Ireland. A teenage dream turned reality.

Little did I know that 2,5 years later, my life would be transformed in a way I had never imagined. Still, there are no regrets, and where anger could have resided, none is left for two chronic illnesses that could easily have been my downfall.

Not one to dwell on issues past, I never allowed myself to live in Oscar Wilde’s famous gutter for a long period. When he said, “We are all in the gutter, but some of us are looking at the stars,” I realise I still am that stargazer, that dreamer, that person who loves Irish history and sociology, nature and literature, photography and psychology.

I am also still that believer in historical and moral justice, a dreamer who wants to see eight centuries of domination over Ireland undone, but knowing all too well that from a political and royal viewpoint, this is dream one dream too many. Continue reading

Positive MS News: September 2015



  1. Less vitamin D and melatonin bad for multiple sclerosis
  2. Multiple sclerosis relapse risk influenced by melatonin levels
  3. Melatonin could help treat multiple sclerosis
  4. Melatonin Linked to Seasonal Relapses of Multiple Sclerosis

Continue reading

Are you Cinderella yet?

Almog albalach_Clock Flares_YEJqQwSome days I feel like a half-baked Cinderella. There’s some promise at 8am, but by 10am my fairy tale book is closed until further notice. In the background, that all-important Cinderella clock keeps ticking forward. My body is in a rut: sleeping, eating, exercising, resting, eating, sleeping and back again.

And that Cinderella shoe?

Taken by someone else altogether.

In other words, and very much like  a psychological broken record, I keep finding out that I am 100% present, but physically I am a goner. Continue reading

I don’t miss myself


Rugby world cup.

At last.

England in a fashion faux-pas. Coin toss aside, they resembled players of Wales, China, Japan or Kyrgyzstan (Fijian, red is Fijian).

Mum’s nine day visit to Ireland now over.

Visited Dublin Zoo once again. New camera making me rather shutter-slow, hence prevalent photographic bonding with rear ends of several animals.

Otherwise, hardly left the house.


Thank you, MS. Living with a chronic illness is not all it’s cracked up to be. Chronic means chronic. I don’t get to choose the days, the hours, the moments.

Hence, a triad of medical events in the space of twelve days, now extended into a three-week period.

Flu. Impatient, it could not wait landing on my doorstep before that all important flu jab. Must remember that viruses follow idiotic timetables and adapt accordingly.

Seriously. Continue reading

PLEASE VOTE! MS Ireland company blog shortlisted!

MS & Me, the group blog of MS Ireland for which I also write, has been shortlisted

for the Blog Awards 2015 edition in the company Best Health and Wellbeing category!

We need YOUR vote though to become a finalist.

*** The PUBLIC VOTE is now open for the 2015 Blog Awards Ireland! ***

Voting will be open for TWO weeks from Monday, 7th September!

The PUBLIC VOTE will be worth 30% of the overall mark.

The other 70% will be decided by a panel of judges.

Please cast your vote below by clicking here,
or on the colourful Blog Awards image below!

Thank you!

Ava, Diana, Trevis, Joan, Declan, Aoife, Lucina, Helen, Niamh, Emma & Willeke

Please share…



About Willeke

Neurologically challenged by MS and personally by her will to succeed, Willeke is a disability awareness advocate seeking to improve neurological services in Ireland. By highlighting difficult issues that come with a MS diagnosis, she hopes her words and tenacity can bring justice to people most in need of a modern, inclusive healthcare system that looks after every aspect of life.

©Willeke Van Eeckhoutte and Ireland, Multiple Sclerosis & Me, 2011-2015. Unauthorized 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.

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