Eight years after we met studying abroad in Germany, six and a half after he moved to Canada, my American husband is now officially my American-Canadian husband. (As of not last Monday but the Monday before, but life's been a little weird as of late, so it's taken me forever to get around to documenting … Continue reading We Are (Now Both) Canadians!
Well, this is it: my fourth, and final, weekend in the epilepsy monitoring unit. One of the best parts about being here has been having a medication holiday. If you're a regular reader of my blog, you know that I'm really not a fan of Topamax, one of the anticonvulsants that I take. Since … Continue reading Oh Hey There, Old Friend
Just a quick note to inform you that on Saturday night, after over two weeks of waiting/lounging around the hospital eating bad food and attempting to work, I had a tonic-clonic seizure. Since I’m in the EMU for, you know, epilepsy monitoring, and since my epileptologist needs to capture a certain number of seizures in … Continue reading The Most Welcome Tonic-Clonic Seizure in the World
One of the EMU techs came into my room a few afternoons ago and told me about a new policy: for ten minutes of every hour, I'm supposed to sit quietly, eyes closed, and "chill out." "I'm asking all my patients to do this," she said. "It's so that we get some clean EEG readings." … Continue reading Forced Meditation
Well, it finally happened: I had a seizure last night! Just a complex partial, but I'll take it. I've ever been this happy following an experience that should be semi-traumatic, except for maybe after a seizure the last time I was in the EMU. I had my electrodes changed yesterday, too, so it's basically like … Continue reading At Long Last, a Seizure!
Being in an epilepsy monitoring unit is, it seems, the best anticonvulsant I've tried yet. At home, I have at least a few seizures a month, and that’s while on my medications. Here, I just finished tapering off Vimpat and still haven’t had a single “event.” Gotta get the seizure train rollin’ if I want … Continue reading Best Anticonvulsant Ever
There was a new epileptologist doctor on duty today, and she suggested that I try sleep deprivation to get the seizure train rolling. This means staying up until four in the morning, sleeping until nine, then making it through the day without naps—which, to be honest, is an only slightly shifted and shortened version of … Continue reading Sleep Deprivation for a Cause
Some of the young adults that I've been collaborating with since the epilepsy summit that I attended in DC in July 2014 met in Toronto this past weekend to discuss our progress, plan upcoming projects, and work on our current one. It was an engaging, intense, fulfilling few days, and for the first time in … Continue reading Epilepsy and the Importance of Community
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This morning my husband and I woke up early (well, early for a Sunday) and went downtown to the starting point for the inaugural Purple Walk for Epilepsy, which took place in conjunction with BuskerFest in support of Epilepsy Toronto. Before continuing, I'll say that Tristan Thompson, a famous NBA player, was there, and I was … Continue reading Purple Tears (of Gratitude)
De Morbo Sacro: Life and/with Epilepsy 