Six Months, and All I Have to Show for Them Is Significant Progress and a Cheesy Paint by Numbers

While eating the second avocado of my breakfast this morning, I realized that today is the six-month mark of this hospitalization. Six months. That's ... a significant amount of time. Seriously. So much has changed outside these walls since I got here: seasons have passed, a pandemic has begun, major change is taking place in … Continue reading Six Months, and All I Have to Show for Them Is Significant Progress and a Cheesy Paint by Numbers →

It’s Nice Out, and I Hate It

Looking out my window and at the weather app on my phone tells me that it's no longer winter, which is a little hard for me to process since this hospital stay began in early December and the last time I was outside was in February. Lemme tell you: I'm not a fan of everyone … Continue reading It’s Nice Out, and I Hate It →

A Post about Dolls

First, an update on this hospital stay: I’m still here. I’m still tired of being here. I’m now tired of writing about being here. And that, my friends, is all the justification I need to shift gears and blog about dolls. This isn’t going to be a controversial post about whether or not parents should … Continue reading A Post about Dolls →

Cooperative Ketoing

I've now entered a new stage of my ketogenic-diet-for-seizure-control experiment. More accurately, since this is a joint effort in which he cooks the food and I eat it, my husband and I have made the transition to a stricter and, with any luck, more effective phase of (my) ketoing for (my) medical purposes. It was … Continue reading Cooperative Ketoing →

A Glimmer of Hope for “a Challenging Case of Very Intractable Epileptic Seizures”

It's a pretty normal Saturday in hospital land. I've eaten many things and drunk many Ketocals. I've socialized a little (something I wasn't doing much of when my postictal psychosis was at its worst) and considered building a new LEGO set. I've had a seizure. My seizure frequency means that I wake up knowing that … Continue reading A Glimmer of Hope for “a Challenging Case of Very Intractable Epileptic Seizures” →

Another Update

Hey! 👋 It’s me with another of my incredibly sporadic updates. There’s been a lot going on in my brain over the past few weeks, so naturally I'm choosing now, when I’m most likely to commit egregious spelling and grammar errors and to produce a longwinded and disjointed post, to break my blog silence. If … Continue reading Another Update →

Eight Weeks, and All I Have to Show for Them Is a Mostly Unedited Blog Post (and lots of empty Ensure Plus bottles and many seizures and significant progress)

For several weeks, I kept going back to the same now-musty post in my drafts folder, making minor changes, staring at what I’d written, and then inevitably becoming overwhelmed and distracted by other tasks, 9.5 times out of 10 a meal or a bottle of Ensure Plus. It was time to acknowledge that the longer, … Continue reading Eight Weeks, and All I Have to Show for Them Is a Mostly Unedited Blog Post (and lots of empty Ensure Plus bottles and many seizures and significant progress) →

Some Positive VNS News in the News

Yes, I mean news news, not news of the personal-and-complainy variety. Yesterday I ran across this article about five-year-old Emma, who's the first patient in Canada to have the most recently released VNS model implanted. When she was seven months old, Emma was diagnosed with the seizure disorder infantile spasms (IS); her parents are hosting an … Continue reading Some Positive VNS News in the News →

Another Year Wiser(ish), Very Thankful

It was my birthday last Saturday. I'm another year older! (Yay?) Yes, I've acquired some additional signs of my impending old age over these past twelve months. I've also, however, gained some real wisdom. (Yay for real this time.) It's been quite the year. I won't claim not to be the person I was in … Continue reading Another Year Wiser(ish), Very Thankful →

Epilepsy in the News: GO Transit, Questions of (in)Accessibility, and an Angry Blogger

This video and article about a young girl (Pepper) with epilepsy whose parents were told that she couldn't ride an accessible GO Transit car popped up in my social media feeds a few days ago. As you might imagine, it made me so, so angry. In the interests of encouraging you to click this link so … Continue reading Epilepsy in the News: GO Transit, Questions of (in)Accessibility, and an Angry Blogger →