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

Boring Update

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

Two Weeks to Two Months: A Tangible Sign of Progress (Yay!)

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!)

I’m Home, Getting Better, and Really Cranky

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