Have you ever wondered, “What exactly is my purpose on our little shining blue ball floating around in our vast universe?”
Congratulations, so have I!
It took me the better part of my teenage years – if not very young adult life – to get to the stage where I thought, “Yes! Eureka! Yes, I found out what I am doing here!”
Translated, it sounded more like this, “I know where I am going to live!”
Part of the master plan that had been hiding in my unconscious mind had already been set in motion, albeit drifting rebelliously between my conscious and the harder to access unconscious level, before mischievously appearing again.
Being a perfectionist, of course, it had to be precisely 200 days.
Six months and nineteen days between my first multiple sclerosis symptoms and its very diagnosis.
Little did I know that it would eventually transform my life.
It was September 2004, and I had just dropped off my mother at Dublin Airport for her return to Belgium. On the way home, a strange sensation took hold of the left side of my face, as if it had been injected with thick rubber. Thinking nothing of it, I went back to bed to catch up on lost ZZZs.
While events on the political world stage the last few months weren’t exactly vivacious or dignified, a lot has happened in and outside my own colourful, little Irish bubble also. I didn’t have a foul-mouthed Donald Trump breaking down my every word, but I equally didn’t have an eloquent Obama and Air Force One to drag me away from crime-ridden, questionable places. “Life,” in a way was, just like Einstein once said, “like riding a bicycle. To keep your balance, you must keep moving.”
Even while moving, however, at times I felt the pedals slip from under my feet, resulting in losing balance mid-air. Ungracefully, so. Continue reading “Then & now”→
“Life is 10% what happens to you and 90% how you react to it.” (Charles Swindoll)
If you’re running behind on making a few new year’s resolutions, or perhaps call them ‘new year’s illusions’ by now instead, all is not lost. There are small things you can work on every day of the year.
Given its absurd sense of unpredictability, life with MS is challenging at the best of times. Anything turbulent added to it, and it soon becomes a slalom course with so many twists and turns that each one seems icier than the ones before. Continue reading “Let’s be frank”→
Ten years ago today, and 2.5 years after moving to Ireland, I was diagnosed with MS, an incurable, neurodegenerative illness that would change my life in ways I never imagined. Needless to say, it was an unwelcome event. Little did I know, however, that it would eventually lead to a life well lived.
There was no manual that showed me how to adapt, accept and live with a chronic illness. MS, associated with 50+ different symptoms, impacts each patient differently. There are numerous symptoms I might never have at all, and that in itself gives hope. Continue reading “10 years: a lot to be thankful for”→
While I’m not a religious person, I do respect others who are. Perhaps with the dawn of Pope Francis, I am starting to feel more open to experiencing religion. It was with this in mind that I stumbled onto a nice poem by Pope Francis that I wish to share. So for everyone, religious or not, this poem is for you. Enjoy as I have enjoyed reading it and feel free to share and reblog.
Don’t cry for what you lost, fight for what you have.
Don’t cry for the dead, fight for what was born in you.
Don’t cry for those who abandoned you, fight for who’s with you.
Don’t cry for who hates you, fight for what you want.
Don’t cry for your past, your present struggle.
Don’t cry for your suffering, struggle for your happiness.
With the things that are happening tous, we are learning that nothing is impossible to solve, just move on.
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DISCLAIMER: The information in this site is for educational purposes only. It should not be used as a substitute for personal care by a licensed physician. Please see your doctor for diagnosis and treatment of any concerning symptoms or medical condition.