november 2, 2023
The day I had my first seizure was the scariest day of my life. I don’t even remember it. I remember waking up in a hospital bed in Greenwich, Connecticut. The sheets were scratchy and I had an IV, heart monitor, and leftover wires stuck to my head from the EEG they performed while I was in a mini-coma.
I slept for two days, I was in the hospital for five. They didn’t let me shower, I forgot how to read. I made a nurse cry when I threw a copy of a book I could not read at the wall of my hospital room and begged for her to let me take a shower. I could feel her empathy radiate towards me when she picked up the book I had just thrown and set it at the end of my bed. She was crying for me when she had to deny my fifth request for a shower -
I was so desperate to be clean of this event, I even told her I would shower with the door open and she could pop in to make sure I didn’t suffer any more mysterious convulsions. Her name was Sarah, and I could tell she felt for me when she had to tell me no, I could not wash myself clean of this. I never could.
I did not remember the battle, the seizure itself, but I had the scars - most of them on my chest, a result derived from the moment I stopped breathing altogether and the EMTs had to do that thing where they rub two shock-ya-back-to-life-thingies together and yell “CLEAR!”
That’s the scariest part of it, not remembering. Not remembering the migraine I had for two days leading up to my seizure, not remembering grabbing lunch with a friend the week before, not remembering saying goodbye to my family when they moved to Texas a month earlier. A month of memories, ash. I lost a lot, mostly memories and people. My partner at the time, who found me asphyxiating on my own vomit mid-event, broke up with me a few weeks later.
“I just… didn’t sign up to date someone who has all of this going on.”
Okay, fair. I did have a lot going on, but I am a person, and people typically have a lot going on. Especially people who had recently flatlined twice in Greenwich Fucking Connecticut. All I had to hold onto when I was in the hospital was him, and hold onto him I did. Probably a little too tightly.
While I was in my mini-coma, he was responsible for filling out my intake forms. He knew I was bipolar, yet when the form required him to check yes or no as to whether or not the patient suffers from a mental-illness, he chose to check no. I guess the town was too small and the stigma too large.
I didn’t find out that seizures and bipolar disorder were related until I had dinner with my ex-almost-girlfriend (don’t ask, that’s for another day) about a month later.
“Okay but how do you know it had to do with my bipolar disorder?”
“Quincy, I work for the state psych-ward. When we admit patients with bipolar disorder, we don’t ask them if they’ve ever had a seizure, we ask them when their last seizure was.”
Yes, chef.
I spent months thinking that my body could betray me at any moment, that I could just fall over and seize and die with no rhyme or reason. All of this because someone checked no on an intake form when they should have checked yes.
Thanks, asshole.
It knocked the breath out of me to feel someone’s shame surrounding my mood disorder, so in that moment, I promised I would never deny it myself.
So here it is; 2020 I had a life-threatening seizure that was triggered by a manic-high. As a result, I will be on anticonvulsants for the rest of my life. I have a whole lot of this going on, but it’s who I am. To deny my illness is to deny myself, and I will not move through life in denial, but in radical acceptance of who I am.
My pill container is full. Two blue pills a day, one yellow, one white, one orange and two chewy adult-vitamins; I like tasting fruit-medley in the morning when I sit with a cocktail of medications in one hand and a cup of coffee in the other. It’s been three and a half years since my last seizure, my meds are working, and I have a partner who will not hesitate to check yes on an intake form if and when I have another epileptic event (it’s inevitable). I am sitting here with a thankful heart, hoping that both Sarah The Nurse and my ex-almost-girlfriend are doing well.
I haven’t had a seizure since my first, but it was bad enough to warrant my being mediated for epilepsy for the rest of my life. Every few years, I have to up my dosage and make sure they keep working the way they are supposed to. Every time I up the dosage, I experience a pretty dramatic shift in my mood. I become paranoid, irritable, and reactive. This is the first time I have upped my anticonvulsants since I sought out a separate prescription to help with my mania, and it sucks. Sometimes, I just have to admit - this shit sucks.
I started this blog to document my success story with Abilify, but I feel like as soon as I started to adjust to that, I was diagnosed with ADHD. Then, when I was just starting to get used to my ADHD meds, I was asked to readjust to a new anticonvulsant dosage. I feel like the entire time I have been blogging, I have simultaneously been adjusting - but maybe that’s just life, having a whole lot of this going on, but adjusting anyways. Maybe this isn’t a blog about med-changes after all,
maybe it’s just a blog about me.














