Last week, I went half-blind.
I was sitting at home, minding my owns, watching a little television and eating some ice cream. All of a sudden, the bottom of my left eye started getting grey and spotty, like I had been staring at a solar eclipse for too long. The greyness spread into most of my eye, to the point where I couldn’t see anything. Eventually, the problem subsided after about 10 minutes, and I assumed that it was a weird mix of not getting enough sleep plus watching too much YouTube that day, so I didn’t think anything more of it.
Then, on Wednesday, the same thing happened, but for about 30 minutes.
And on Thursday, 2 hours.
And then on Saturday, all day. On Saturday, the problem had morphed from a minor annoyance into a “hey, there is probably something wrong here.” I actually couldn’t see at all out of my left eye, and that was about the point when I decided to make a trip to the eye hospital. Nearly falling down the stairs and walking right past my students who were on the left side of my peripheral vision was starting to seem a bit excessive. Unfortunately, the eye hospitals had all closed for the weekend and I had to wait until Monday, but that gave me a nice excuse to laze around on Sunday and attempt to “recuperate.”
Sadly, I chose a bad day to go to an eye hospital wearing a summer dress. A typhoon had hit Tokyo that morning, and the resulting winds and torrential downpours left me, my beautiful dress, and my loafers soaked and chilled to the bone. I got to the hospital at around 7:45am, fumbled through my sorely-lacking Japanese language arsenal to ask for an appointment, and sat down getting ready to have the doctor tell me that everything was okay (just like every other doctor usually says to me).
The doctor hummed and hawed and asked me to look left and right and up and down and top right and top left and I was worried that I was doing it wrong because he hummed and hawed some more and then asked to see my left eye again and again, and by this time I was starting to get a little worried. Sigh. And then the doctor said, “you have an inflamed optic nerve.”
And then he said, “This is typically associated with brain tumors or multiple sclerosis. We will need you to get an MRI immediately.”
The problem with being a mild hypochondriac (well, an overly anxious Ukrainian is a better label, I suppose) is that after all of those benign symptoms that you interpret as being horrible signs of doom, one of them will eventually creep in and be an actual horrible sign of doom. So, as the doctor said those words in his broken English, I translated it into, “You’ve got terminal brain cancer, start saying your goodbyes.”
And then I asked him for a Kleenex. And then I sent a panicked email to my manager with my good eye, upset and wondering how the heck I would pay for an MRI on my English teacher’s salary. I had no idea how much it would cost, but images of Michael Moore’s “Sicko” flooded my memory. I wondered, would I have to choose which part of my brain to get scanned if I couldn’t afford the whole thing — kind of like a “Magnetic Russian Roulette Imaging”?
After a few more kleenexes and more panicked emails, I boarded the train to get to the next station, where I had to walk 10 minutes in the typhoon-esque rain and ridiculous winds to get to the neurological hospital. As I was tromping along in my already-soaked shoes, I wondered, “how could this day possibly get any worse?”, and no lie, at that moment, my umbrella did that awesome thing where it turns inside-out and upside-down, leaving me wet and looking more foolish than a man who had just slipped on a banana peel. I suppose I should’ve known that would happen.
As I burst into the neurological hospital looking like an escaped and dangerous patient from the psychiatric ward, the weight of the situation really hit me. Is this really happening? Why couldn’t it have just been migraines like I thought it had been? I had always wanted an MRI, but not to check for brain tumors or multiple sclerosis. Sheesh.
I sat in the hospital waiting room, shivering and waiting for my name to be called. At around 1:40, they called me in. Very few people in the hospital spoke English, and so the MRI techs had a detailed list written by somebody who spoke “Japanglish” (as I like to call a really poor hybrid version of Japanese and English). First, the tech asked me to please remove my jewelry.
Check.
“Please take off shoes.”
Check.
“Sound will be very loud. Earplugs for you.”
Okay.
“Uhhh… (giggle, looking at other tech) please remove… Brassiere… (embarrassed look, red face, more giggling)
Fine. I laughed, too, because the word “brassiere” is funny.
I hopped into the MRI machine, and believe it or not, it was the best part of my day. After getting over my whole fear of brain cancer thing, I realized that I was actually quite excited to have an MRI done. After looking at hundreds of MRI scans in university, I always wanted to see what the inside of my noggin looked like. I told that to my neurologist (this sounds strange to me… having a neurologist…) and he actually got a little bit excited about my nerdiness. He told me that after the scan, he would walk me through my brain to show me all of the cool stuff happening in there.
Inside of the MRI room, next to the daunting machine, the tech told me to lay still for 40 minutes, gave me a blanket, asked if I was okay, and gave me an emergency button to squeeze in case something horrible happened. Because Japanese signs tend to be a little melodramatic (one of the signs next to the machine said, “NO O^2!!!!” with a skull and crossbones, meaning… “If you forget to breathe, you will turn into a ghost,” I presume), I was a little bit worried as they imported my body into the giant white, presumably oxygen-deficient chamber. After I took a few deep breaths, however, I found the clicks and whirs of the machine a bit reminiscent of a hip hop riff. I started making up music in my mind and thinking about happy memories, hoping that the MRI would be able to see them. I imagined the doctor would commend me on my beautifully active frontal lobe, and be thrilled with my amygdala (it’s so… almond-shaped!).
The time went by extremely quickly and I even caught myself drifting off a few times, but I quickly stopped myself when I realized that I tend to move a lot when I sleep and that movement would make for a blurry scan. All in all, however, my first MRI experience was a load of fun. Like a 40-minute trip to the spa, with more magnetic resonance.
The MRI finished, and I went to the changing room to put on my “brassiere,” only to hear the techs giggling with embarrassment once again. Oh well. I walked out of the chamber and found my manager sitting in the waiting room, waiting for me. I was so happy. She had wet feet and the look of “if you die, lots of students will be upset. Please don’t die. I need you.” This is precisely why I like my manager so much. She needs me.
So we sat in the waiting room, talking about work and chimps who have pet dogs and exercise together when the neurologist called me into his room. We took a deep breath and headed in together. The doctor, determined to impress me with his MRI skillz, walked me through all of the different cross-sections of my brain.
“See, this is your pituitary gland! But you know that already….”
“But, can you see? You have a big hippocampus! Just like a normal Caucasian!”
Part of me was reveling in the sight of my grey matter, but another part of me was scouring the scan for anything that looked abnormal. After 10 minutes of 3-dimensional rotations, the doctor finally told me that I was cancer-free. I high-fived my manager, paid for the MRI (which was roughly the same price as my typical haircut… I really should find a cheaper hairdresser) and headed back to the eye hospital for one more round of, “cancer = no; please fix me?”
The ophthalmologist gave me a prescription for anti-inflammatory medication that has a side effect of causing ulcers, and anti-ulcer medication that has a side effect of….. I don’t know. It’ll be a surprise. All I know is that I am looking forward to being able to see with both eyes again. It could take up to 8 weeks, and I choose to ignore the fact that I am at an increased risk for developing MS now that I have this stupid disease. I figure it’s a bit futile worrying about whether or not I will get it in the next 10-15 years, considering there are a plethora of other diseases that I can worry about contracting in the interim.
Happily, my brain isn’t broken. Somewhat unfortunately, however, I now have to blame my lack of organizational skills, my laziness, my incapacity for learning new languages, and my bad memory on something else. That’s okay, though. I think my non-brain-abnormality-related laziness is pretty darn cool.
Sorry for the extended blog, mum and dad. I hope you found it more amusing than worrying.
Goodnight.
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