Climbing

 

Charlotte Doyle
The title page for the book The True Confessions of Charlotte Doyle by Avi with a black and white illustration of the bow of a sailing ship

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There is a passage in the children’s book The True Confessions of Charlotte Doyle by Avi that I’ve been thinking about a lot throughout the pandemic and shutdown. The premise of the book is that our protagonist, Charlotte Doyle, was put on a ship from England by herself in 1832 to join her family in the United States. She wasn’t supposed to be the only passenger, but she ends up being the only passenger, the only child, the only girl or woman on the voyage. The captain promises to look out for her-they are from the same class after all and he can’t have her falling in with the uncouth sailors-until it becomes clear that the men are going to stage a mutiny and she eventually realizes that they had just cause because the captain is cruel. She decides to join the crew, who have justified suspicions about her initial closeness to the captain, and so is presented with an initiation rite to solidify her place and her protection with them. She has to climb the tallest mast up to the crow’s nest and back down again.

It’s a terrifying task. The heights alone are bad enough to frighten anyone her age, much less the rough and unstable rigging. The swaying of the ship becomes more and more pronounced the higher she climbs. At some point she realizes that her reward for braving this seemingly insurmountable obstacle is that she will have to do this same impossible thing multiple times a day as part of her work for the crew for the rest of the voyage. It truly seems unthinkable until it is done. Then it becomes just part of her life.

We keep being presented with terrifying or incredibly difficult tasks where the reward for facing them is that we get to keep facing them over and over, but with now some new measure of familiarity and experience.

About a month ago I took my first COVID test because I was symptomatic. With all my chronic illnesses, with all my pain and fatigue and prickly skin and fog throughout the years-even when I went to the ER with chest pains and had to rule out a heart attack and even when I’ve had walking pneumonia- I have never had shortness of breath. I have never felt like I was gulping for air, that every few breaths I had to concentrate to consciously expand and fill my lungs against the constriction of my ribcage. I asked my doctor if taking a COVID test was appropriate and she sent me to their respiratory clinic-a converted immediate care center where I was to wait in the car when I arrived so that the whole staff could get into multiple layers of PPE. When I was allowed in, I was the only patient, and was given a second mask to go over my cloth one. Plastic sheeting narrowed the lobby into a ribbon of a hallway so that all the soft surfaces of the waiting room had a barrier between me and them. I told the doctor all of my symptoms, as much of my backstory with chronic illness as I could. We did a chest x-ray in another thoroughly sterilized room. It was explained to me that this particular COVID test doesn’t have false positives but there is a ten percent incidence of a false negative, so even with a negative I would need to quarantine for ten days after being symptomatic. At the end of the appointment I would take the test by driving to the back of the building and sitting in my parked car, head leaning against the headrest as the nasal swab went further up than I expected. I went home, had my husband get my brand-new prescription inhaler from the pharmacy. I limited my movement inside my own house so that I had less contact with my kids, wiped down everything I touched and waited two tense days for the negative result.

I was terrified. From years of doctors not taking me seriously I was terrified to speak to a new one. From years of chronic illness I knew that if I had contracted COVID that it might be horribly difficult to fight off. I might not be able to. From years of my children covertly worrying about my health I knew that this could wreck any emotional well-being we had carved out of isolation and disruption. The building I went into for care looked like the set of a horror movie where I was not meant to make it past the first act. The idea that I might have been around other people who didn’t have fifteen layers of protection between us felt like the worst mortal sin I could have carried. Not knowing what was causing my shortness of breath sent me into a purgatory not knowing how long I might have to live in not knowing-it might have been forever.

Now? The memory of feeling so terrified that day that I couldn’t silence alarm bells pounding through my brain has faded just a few weeks past my quarantine ending. I don’t know and can’t say whether it becoming a normal “something-I-did” is psychologically healthy in the long run, but it is protective now. I have data in my mind of what would need to happen if I was sick again, or if one of the kids was, or if someone else in my family was. I would not need to contemplate every foothold and rough rope as I climbed a second time, experience would have given me ease with something I would rather have absolutely no familiarity with at all. But that choice wasn’t up to me. My reward for doing something terrifying is that I would know how to deal with it myself again, or be able to carefully shepherd someone else I love through the process.

So quickly, so rapidly, the circumstances of our lives have changed. Our understanding of the world has changed. In some ways, irrevocably. Some things that have needed to change have finally broken open. Just like the mutiny on Charlotte’s ship, building wealth on the broken backs of people you couldn’t care less about has inevitable consequences. Some things that should never have come to pass are terrifyingly present and a clean cold light is shining on them. For example, a country’s leader who barely looked up from a Tweet or a golf club as 160,000 of his people died. I marvel pretty much every day at some new understanding or revolution or horror that in ordinary times would have been years in the making (or undoing) but now happen and become a new reality in the blink of an eye. Because it’s all so fast it’s exhausting and hard and it’s difficult to give each moment the depth and detail of exploration it deserves. But it all changing so rapidly gives room for new ways of thinking about ourselves, our world, how we have always operated within it and whether that is at all acceptable to our souls.

We keep climbing to the top of the main mast, gritting our teeth against fear, keeping as intense a focus as we can on splintering wood or fraying knots or the wide gap between footholds big enough to swallow us up if we slip. And when we get to the top and realize we are proved capable of doing what seemed impossible just a little while before, there is some exhilaration and freedom to look out from those dizzying heights to see ourselves and the world differently. When we come back down to the deck there are crew members who have become friends waiting to do this hard work every day. We now belong to each other in ways we hadn’t before. Our reward for facing down the impossible fear is to keep showing up, to keep facing it for as long as it takes with other people who are showing up with us to do the same.

Before and After

 

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Enamel Pins
Part of my enamel pin collection in small boxes. You can see a Princess Leia, a rainbow brain, a hedgehog, a goldfish, and a record player among other pins

On the last day we got to hang out, the kindergartner I work with came in from recess bouncing. I watch out for him on the playground, making sure he has lots of time to be goofy but that he doesn’t start a revolution of five-year-olds refusing to come in when the whistle blows. On Fridays my job is (was? I don’t want to think about this in the past tense) easier because it’s hot lunch day, but then he books it inside while I struggle to keep my speed-walking from becoming a full-on sprint, quietly calling after him “No parkour-walking feet, walking feet!” By the time I catch up with him and have folded myself into the tiny chair next to his desk, he’s bopping his head chomping on his first bite, declaring through a mouthful of chicken fingers, “I did good today!”

“Oh absolutely, dude. That’s going in the report.” I’ll circle a big smiley face on the daily form.

“It’s supposed to be filled in, not circled.”

“You’re right, my man, I forgot.”

On Mondays, without the lure of once-a-week fast food, the way I got him to cheerfully come inside from the playground was by switching up the enamel pin I would put on the lanyard for my employee ID, covering it up with my hand and asking if he had noticed which one I was wearing. He would giggle and shake his head “no”. The rules of our game meant I wouldn’t reveal which pin I was wearing until we got all the way to the classroom. On Mondays, and Mondays only, we would walk in together at a leisurely pace, his eyes squinting in a smile locked onto me until I removed my hand for the big reveal right inside the classroom doorway.

The last Monday I worked he was absent, home sick with super-ordinary-for-small-kids-in-the-spring croup. I was home with the same ordinary virus the next few days and then? Then school was over for the year.

I miss the routine of changing my pin once a week. I miss taking thirty seconds each Monday morning to let him know that we are a team bound together by games and silliness and affection. I miss picking out which one would seem like a good-enough surprise, a good-enough reward for coming in from outside. That last Monday the pin I had put on was Dory, the blue tang, swimming in her coffee pot. It’s my favorite, and his favorite, too, and the first pin he noticed that set off our game.

I’m not changing it until I see him again.

This was a piece I wrote this week as an assignment from the Steppenwolf Education Department-for Maker May they had a two part webinar with essayist Samantha Irby and Ian Belknap of Write Club discussing and developing Live Lit-pieces that are meant to be performed. Maybe I’ll eventually figure out how to post a video here as well, to adhere better to the spirit of the assignment! These were written and revised with a two minute limit in mind, about something from before lockdown that you miss terribly. I want to thank them so much for everything. It was a welcome change of pace, and some of the only new writing I’ve been able to get myself to do. Incidentally, my eleven-year-old had an almost identical writing assignment for his online classes this week. Although his video conference was, like, his twentieth, and mine was my first.  

Shared Trouble

I wrote this flash non-fiction a while ago about a blizzard that happened in Chicago in 2011. I’ve been thinking about it a great deal as the whole world prepares to shut down to stem a pandemic and stares down what it is like to be locked away from other people for extended periods of time. My chronically ill friends already know what it is to be isolated at home when no one healthy seems to realize that this is how we’ve already been living. 

Shared Trouble
At least two inches of snow packed against the side of a picket fence, giving the impression of soldiers in formation facing a formidable foe together.

I had enough bottled water and milk, Goldfish crackers and juice boxes, diapers and wipes for at least a week, if not two. I had enough packages of chicken and ground beef and pork chops and hot dogs in the freezer to make dinners for seven nights. Cans of soups and beans and bags of rice in the pantry. If the power went out I had industrial size jars of peanut butter and jelly and several loafs of bread, individual cups of applesauce, mandarin oranges.

In the house I had an extensive first aid kit, wraps and splints, thermometers and burn cream. I had backup ibuprofen for children and adults. All the flashlights had batteries. Extra batteries. Chargers.

We had our DVD collection if the cable went out but the electricity didn’t, board games, the blue cube cloth bin of Hot Wheels cars and the entire cabinet full of Hot Wheels tracks, the bookcase full of stories to read aloud. If the wind howled too violently, we had the old couch cushions we used to pad the tile floor of the laundry room during tornado warnings. We had a thick pile of blankets and footsie pajamas.

Everyone called the day before the blizzard asking if I was ready. If we had fuel for the snowblower (always), a full tank of gas in the car (yes), water and food and emergency supplies (I do). In every conversation my parents, my in-laws, my brother, my brother-in-law warned me that the crowds were hectic at the grocery store or the lines were long at the gas station and I verbally shrugged that I didn’t need anything. They got confused. I was confused at their confusion until it crystallized-they didn’t know this was how I always had to live.

At this point it had been four years that my husband had been traveling for work almost every week. It had been two years of being a mom to two small boys, and the only caregiver 24 hours a day for three or four day stretches. It had been one year since the pain started that wouldn’t go away and didn’t then have a name. I was always prepared for multiple days of isolation with a four-year-old and a toddler. We weren’t always trapped, but we were too often trapped by my sudden, changeable and unpredictable limitations. The week of this blizzard, my husband had left before the forecast showed what was coming, and flights weren’t returning through white out conditions. It was just the three of us, as it often was.

My family misunderstood what sort of help I might need because I’d adjusted to my new reality when they weren’t looking. Cold had started to make my muscles crack under the strain, light dazzling off snow might send me into migraines. The room could spin or my limbs would get heavy or my hands would cramp too hard for me to hold a potato I was supposed to peel for dinner. Our home was well-stocked and prepared because I needed to care for two little people when my body would sporadically make it nearly impossible to leave.

I spent the night of the storm awake and alone, bolt upright in bed feeling the air in the room vibrate with energy as the windows shook in the wind, and watching the lights flicker out but eventually hold. Lightning began, but instead of brilliant and shining, the light was gauzy and diffused through the snow. Thunder rumbled loudly enough to keep me vigilant and alert, but quietly enough that the boys stayed asleep in their beds. I could have used my babies snuggled up against me, light snores giving me white noise and the weight of their arms draped on mine, keeping me from clutching a phone in one hand and a flashlight in the other. I could have used the solidness of their needs to keep me from worrying what if, what if, what if. But they weren’t and this night passed like so many others by myself-watchful waiting to see if a problem cascaded into an emergency that meant I needed to call for help. How many nights had I spent alone waiting to see if a pain became unbearable, if a blinding crack of a violent headache meant I needed to call 911, if a weight pressed on my chest was my heart failing? How many mornings had I woken up worse for a horrible night but still alive, tasked with making our little life at home happy? How many times had I quietly panicked and never told anyone?

By the time the streets were halfway plowed, family came to dig us out. I happily made hot cocoa for our guests. It was nice to have company.

Something a blizzard can do, because it’s large and dramatic and a shared trouble, is bring people who might understand how to help to your doorstep.

My illnesses, small against the scale of the world, invisible because I could almost cope, and almost untranslatably personal, often didn’t.