It’s me! It’s been (practically) forever! Don’t get too excited: I’m just dropping in to wish you a happy end to 2018 and beginning to 2019. Since I keep meaning to compose a long catch-up/excuse post and then collapsing under the pressure of having so much to catch up on and not knowing how much … Continue reading It’s Almost 2019! Time for a Disjointed Post.
You might (rightfully) wonder why I decided to write about a lost object and a newfound friend at the City of Toronto's Solid Waste Management Services in a blog that's ostensibly about living with chronic illness(es). I asked myself the same, or at least a related, question. OK, questions—plural—since my brain isn't good at stopping … Continue reading Lost Engagement Ring, New Hero at Waste Management: A Happily Ever After
Though I'm a little late to the party (sorry, that was a groaner), I wanted to weigh in on an unlikely controversy that has many members of the epilepsy community angry. I'm angry, too. In August, Netflix released the film The After Party. I haven't watched it—I'll admit that I'm a little curious, but I know … Continue reading Representation Matters: Netflix, “The After Party,” and How to Hurt One Group in Order to Entertain Another
For complicated reasons that aren't the topic of this post—sorry—I've been trying to stay in bed, sedentary, for much of the day (and night, but that goes without saying) since last Wednesday, when I got some not-great news at a medical appointment. Mandatory bed rest when you're physically very unwell is pretty easy; turns out … Continue reading Compulsively Knitting for Fun, Entertainment, and Distraction
Due to excuses mostly unrelated to epilepsy, I haven't been posting on this blog as frequently as I once did—I'll try to be better, but no promises. I had an appointment with my epilepsy specialist on Thursday, though, so I figured that I'd make the effort to write a shortish entry with a (kind of … Continue reading Boring Update
In my last entry, dedicated to gloating about a major reduction in my tonic-clonic seizures, I indicated that I'd give an update about my complex partials "in a future post." Believe it or not, I'm following through, and in a relatively timely manner, no less. This is that future post. The future is now. I … Continue reading Best Month Ever! (Well, in the Past Year.)
After reviewing his records of such things, my husband informed me a few days ago that my tonic-clonic seizures have almost disappeared. In fact, over the past two months, I’ve only experienced one. One. I knew, or at least suspected, that I wasn't having very many of them, but it hadn't occurred to me to check … Continue reading Bye(?), Convulsive Seizures
I’m writing this for my dad on Father’s Day, but it might be a while before he sees it. It’s the weekend, and he manages to confine his usage of the internet (including checking his e-mail) mostly to working hours. Although the fact that he’s a M–F, 9–5 technology guy can be inconvenient from time … Continue reading Pops
I was discharged from the neuro ward last Monday evening (appropriately, I guess, the date of my release coincided with Purple Day [for epilepsy awareness]). Except for an appointment a few days ago and a ten-minute walk yesterday afternoon, I've been more or less chilling ever since. I hate chilling. Although I'm super happy to … Continue reading I’m Home, Getting Better, and Really Cranky
As of last Thursday, and after two rounds of treatment, I'm officially finished my neuro day-hospital program. It feels super good. Time to reflect! Given my tendency to worry that I've plateaued or am plateauing in my recovery, I've found it important, especially over the past month or so, to keep reminding myself that I've made … Continue reading Graduation!
De Morbo Sacro: Life and/with Epilepsy 