I've been going to see my epileptologist every two weeks or so to have my VNS adjusted—and for other epilepsy stuff—since, um, December? (Maybe since sometime in November. Please excuse my imprecision; I'm going to go ahead and use the "bad memory for neurological reasons" line, but really I'm just too lazy to scan through … Continue reading Two Weeks to Two Months: A Tangible Sign of Progress (Yay!)
A few weeks ago, I lost approximately a third of a tooth. I want it back. I'm still figuring out what to do about it. Over the past year, I've chipped or broken seven or eight teeth during tonic-clonic seizures, but this was by far the largest chunk to fall victim to my epilepsy's hijinks. … Continue reading A Shortish Post about Difficult Dental Stuff
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
Note: I wrote this blog entry yesterday and only got around to posting it today. Some of the content is slightly outdated. This will be short, for a reason that will soon become evident. It might also be sloppy, but not as bad as the garbled text messages that I was sending a few … Continue reading Crushed Dream: An Unexpected and Unwanted (Obviously) Hospital Stay
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!
If I'm not mistaken, my last post, about travelling with my VNS, ended with something about how I was starting to get anxious about the trip back to Toronto. At the time I wrote it, I was mostly joking. It turned out, however, that those simple words were enough to jinx the homeward voyage. Not … Continue reading A Delayed Update about Delayed Travel
I've never consistently tracked my seizures. Here's where, before continuing with this blog post, I make excuses for my shortcomings as a seizure diarist. First, there's the memory thing. If I have a partial seizure before bed, when they usually occur, I sometimes have to be told the next morning that it happened since I'm … Continue reading Above Average
Remember the post—I think it's this one—in which I scoffed at how my epileptologist had warned me that I'd feel a "big jolt" when he programmed my VNS and then the sensation ended up being more of a big ’ol nothing, to the point that I was concerned that there was something wrong with my … Continue reading And Behold, a Jolt!
I realize that since I live in Ontario, I have no business being surprised by super-cold temps in January. The last week or thereabouts, though, has been cold-weather-warning cold, let's-not-leave-the-house cold, three-layers-and-still-not-comfortable cold. So yeah, it's been incredibly cold, in case that wasn't clear from the previous paragraph. This quasi-arctic weather—and I say this as … Continue reading It’s Really, Really Cold, and Seizure Me Doesn’t Seem to Know or Care
Since the last time I blogged, I've made steady progress in the direction of adjusting to life with a VNS device implanted, cyborg-style, in my chest: I went to my family doctor and found a better solution for my nausea. I've almost completely eliminated ongoing pain by managing it with a combination of ibuprofen and … Continue reading Vanessa
De Morbo Sacro: Life and/with Epilepsy 