2018

Homecoming. 325 days from home.

I was taking the bus downtown. I left the neighbourhood I’m currently staying at, which I do like (though it’s kind of hipster-ville which admittedly creeps me out at times:), scooted aboard a bus and headed towards one of our SallyAnn shelters.
As the bus passed the very touristy Yonge Street and headed into the downtown Eastside of Toronto, we headed into ‘the hood’.

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Hospital Beds and Beeping Machines (a guest piece from my daughter as to how she views life with MS)

By Cate Oxford
I woke to the sound of a knock on my bedroom door. I had been in that strange realm between asleep and awake, when the world is a foggy kind of grey. I looked at the clock, it was early, too early. Too early for everything to be okay. I look to see my mom standing at the door. She opens her mouth.
“Hey, sweetie. So, dad couldn’t get out of bed this morning. We had to call the hospital. I just wanted you to know before the paramedics show up.”

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No swimming at the lake this year; 230 days away from home

For at least the past 10 years we as a family have been going to a camp to spend a week together. It has become a part of my annual rhythm of life to go there with other family friends, leave behind the day-to-day grind, enjoy being in nature, and relax. One of my favourite things to do there was to swim every afternoon in the lake. Something about floating around in lake water really does it for me (especially being able to pee guilt free in the water…) I think partially because it evens the playing field. When I’m in the water I don’t need to walk and I seem to be able to swim just fine. Like everyone else, I’m simply swimming around without the need of a mobility device.

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