I’ll begin by acknowledging that despite having had the best of intentions to write at least a post a week throughout January, I’ve instead continued to more or less ignore this blog. I’ve had legitimate reasons for falling short on my WordPress duties, but the guilt nonetheless remains, so I’m just, you know, putting it … Continue reading Check In/Check Up
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.)
We celebrated the official start of summer—and my husband’s birthday, and the solstice, and amazing, lovely people—last weekend with a trip to a cottage on Lake Huron. Friends whom we consider more like extended family have a cottage in the area, and their daughter (who's also like family!) owns the one next door to theirs. … Continue reading Cottage Time
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
This has been a really hard epilepsy week. Last evening marked the third in a row with a tonic-clonic seizure, which I usually have relatively rarely. The result was a restless night due to muscle pain and nausea, and since I was still under the weather this morning, I had to cancel plans, activating my … Continue reading Seizure-Sick
De Morbo Sacro: Life and/with Epilepsy 