Write it out…

Not long ago I listened to a radio interview. This was one of those entertainment pieces, the kind of thing you listen to because it isn’t about politics, murder, or other such real-life nastiness. Asked to make sense of a recent experience, the guest offered the simplest of replies:

“It’s hard to say…I haven’t even written about it yet.”

This little gem caught my attention so much I didn’t really hear the rest of the interview. The details didn’t matter; what stood out was this tiny, piquant glimpse into how meaning gets made – the process of coming to terms with an experience. It also likely grabbed me because here’s someone else suggesting they have to write about something in order to make sense of themselves.

Admittedly it lands a little close to home because I’ve found myself trying to make sense of several things lately but lack the words to describe it. This blog has been the place where I write “randomly”, letting words fall out in order to see what’s rattling around in my head. But with recent events, that hasn’t happened. The words don’t seem to land on the page and continue floating around in space, morphing into other shapes or sometimes disappearing altogether.

This is your brain…if your brain were an egg talking to itself

I’ve guessed it’s because the events are happening too fast, too quick for my brain to fully pull together. Or maybe it’s not a brain thing – maybe the issue is that these things are all too visceral, too emotional, for the brain to catch them. There are feelings and motion, but sometimes the event demands a reaction and the brain just has to respond to what is there without having the luxury of making sense.

Curiously the events I’ve been thrust into lately are brain related in other ways – a relative expressing a high degree of neurocognitive disorder (that’s dementia to everyone else) and my own battle with migraines. The brains have gone on strike, it seems.

Attempting to reign mine in, we tried medication that resulted in me having a great deal of difficulty completing sentences. Try writing a book in that condition. Anomia (inability to remember the names of everyday objects) makes it kinda hard to complete a paragraph, or at least construct one who anyone other than the author can understand. I couldn’t even remember the word “anomia,” which meant when I tried explaining this to my employer, I sounded something like this:

“It’s sort of like you are coming up to what you know is supposed to be there but you can’t quite find it so you skip over it hoping you can come back around to it and it’ll slip into place, but it doesn’t really happen so you’re just left looking at this empty hole knowing something is supposed to be there but you’re the only person who knows what it is.”

And then your employer tells you to go home because they think you’re drunk. My brain had a great laugh at me that day. It also gave me a migraine.

The fact that I can write this suggests a change occurred; deciding the cure was worse than the problem, we discontinued that particular medicine. But this is a continued experiment – and gets into that euphamistic “lifestyle change” thing. I’d have loved it if taking a pill were the only thing one needed to do to conquer something like migraines. But as with most chronic health problems, the treatment isn’t a 45 second commercial promising bliss and small-print debilitating side-effects. It’s a long process of discovering what could work along with what doesn’t – which means learning a lot of what you thought was okay about how you live your life falls in the “doesn’t” category.

For the short time my brain was on holiday, I took a brief walk into my relative’s dementia land. I am not in any way claiming I had the experience of someone who is falling into a cognitive decline. What I am claiming is that as the medicine’s side-effects starting taking away my ability to think, react quickly, solve problems, and use words, I realized that the me I thought I knew was disappearing like a ghost. It was terrifying and I had no idea what was supposed to be in its place. An athlete who loses their leg, a painter who loses a hand – it is an experience of being confronted with our primal fear that without what we can do, we become no one.

I’d like to say that I plowed forward and found myself, but the truth is I called the doctor and said “I can’t handle this.” A 3-day migraine attack was better than disintegrating, and at least I know how to survive the migraine. So I don’t have a pithy answer for how to deal with that harsh look in the existential mirror. But I also don’t think there is a pithy answer – it is something that takes time to figure out, presuming it can be figured out.

When I sit with my relative, we have conversations that follow no chronological, or any-logical, order. The bedroom we sit in morphs into a type of Tardis as we travel across space and time:

“Are you here to help me pack?”
Where are you going?
When do you leave?
“Any moment now. We have to get on the plane.”
How long have you been here?
“I just got here.”
Why  are you going to Ohio?
“For work. Shouldn’t you be in school?”
I don’t have school right now.
“Did you pass all your classes?”

And on it goes…in the same sentence I am a working adult, a grade-schooler, a parent, a teenager. Dead relatives are resurrected, and last night’s baseball game is recalled play by play. My children’s names are forgotten.

I’m living in the sandwich of my generation, but I can’t tell you anything about how it tastes. No one really asks for this, but resentment seems pointless. How do you hold a grudge if the mistakes of the past no longer exist? The way you knew yourself in response to this person must also become someone else, because the person before you floats trans-dimensionally and you’re just trying to not get lost. There are many people living in this, and information exists to explain it. And yet, if you ask me to make sense of it all…

I haven’t even written about it yet.