As I sit here, staring at a blank page, I realize I haven’t been around as often as I would like to and also that there were a number of issues I talked about here that I didn’t update. So here’s a summary: Continue reading
Or maybe not?
This is a great idea from Australia to raise awareness for multiple sclerosis.
Visit the website and support the campaign: http://thisbikehasms.com/
Read more: http://www.adweek.com/news/advertising-branding/ad-day-grey-just-designed-bicycle-has-symptoms-ms-168767
One of these days I was scrolling down my Facebook news feed and I saw this video someone I met through dance classes had posted.
I already knew movement was of the utmost importance when it came to neurological disorders, but I found this video so compelling and heartwarming that I immediately googled where I could learn more about dance and movement therapy. Et voilà, there will be a workshop in February – and me, of course, I already enrolled.
So if you read me complaining about how tired I am and how I always keep myself too busy for my own sake – like I did back in October – then you’ll know why. I’m hoping I can do things a little differently this time though, like taking a day off from work or skipping some assignment for college so it won’t take such a toll.
But you know me, my love for dance and my love for the mysteries of neurosciences. My wanting to heal. And my need to actually do something I’m passionate about. To fall in love.
I never have a Christmas wish list. There’s not really anything I want. I already have everything. All of the meaningful things in life. Two beautiful kids, a loving man, and the best sister. Parents that love me, friends, and a roof over my head. That’s all I need.
Gifts have never been on my priority list. Material things are just things. So when asked what I want for Christmas I usually say nothing or I don’t know. What could I possibly want?
A new leg, a new eye, not to walk like a drunk. Just kidding!
A couple nights ago and like most nights I was unable to sleep. Thanks again MS…lol. I don’t want to keep anyone up with lights or the TV so just like every other night I have nothing better to do but entertain myself with thought. A traffic jam in my brain. Yes I…
View original post 420 more words
Click to enlarge.
So this was the day, four years ago, when I heard the words that changed my life.
I’m not going to write a huge post about how these past four years have been for me (kind of hard). I’m just going to say I finally realized my MS is not Voldemort and I actually started saying out loud that I have it. Of course I don’t go around introducing myself “Hi, I’m Sónia and I have MS” – and of course work is also a different story – but in specific contexts, like when I met a physical therapist and asked for her number (because I have MS and who knows if one day I may need you), or when I tried to explain the lady at the drug store I can’t just take anything for insomnia and/or depression (because I have MS and it might interfere), it makes sense that I stop hiding and being ashamed. It’s just a fact, not a judgment. I have MS.
I’m also glad that even though I changed in many aspects, I haven’t lost sight of who I am. It’s inevitable to change when you’re faced with a condition like MS. Some changes you make consciously, some changes the disease makes for you and you only realize later on, but you’re bound to change. Still, I’ve managed to keep the core of what makes me who I am mostly untouched, through all the damage, the angry words, the sorrow in my heart and the scar tissue in my brain that just won’t heal itself no matter how much I pray. In this way, MS can’t tame me. I will be fiercely holding on to what I feel makes me human – to my essence. That’s what I’ll be celebrating tonight. And who knows, in the end, even Voldemort was defeated.