On Coming to Terms with Chronic Illness: Keys

Once she knew a boy who collected spare keys and strung them on a cable. 

He never tried to unlock anything–as far as she knew. But he liked the weight

of them. Hundreds. He could hardly lift them. He liked their different shapes.

She liked that each key carried a secret story. She does not, however, like junk 

drawers, stuffed with bent paper clips, leaky batteries, dried pens, plastic forks, 

yellowed recipes. Rotting rubber bands. A single, gummy key. She wants every

thing in its place. Everything found and clean. Once, she had a rabbit–big, white,

bossy, with pink eyes–who lined up her wooden toys, parallel and evenly spaced. 

Now, near her house, people live in tents along the creek. Some sweep their dirt 

stoops. Most have shopping carts full of damp newspapers, broken toys, blenders 

with no cords, take-out containers, art in cracked frames. They adopt stray dogs. 

Her mother was a stray, with no family, forever moving to a new cities, hauling 

her heavy purse, but leaving the rest behind. Friends. Furniture. Photographs. 

Keys. It frightened her how easily her mother forgot the past. She traveled light, 

but her brain was a storage unit of stories and pain. The girl kept scrapbooks, 

proof that she had once belonged to a time and place. Proof she owned a story. 

Now, she has lived a long time in one place. She tries to keep her life spare. She

no longer keeps scrapbooks. She uses an electronic key. She fears she no longer 

has a story. She tries to keep her life spare, but she’s still a tourist of excess: 

She likes seeing intricate cathedrals, graffitied walls, elaborate back tattoos. 

Her dreams are complicated. She is running late. She has lost her bags. Her keys. 

She can’t find her way through the corridors of city streets. Airports. Shopping 

Malls. Hotels. High schools. She is driving too fast. Her steering wheel is loose. 

People’s faces are always changing. She wishes she were a rabbit with toys tidy

and parallel. But now the knots and networks of her body no longer know how 

to speak to each other. They have lost the keys to each other’s houses. They have 

forgotten their shared story. But this is the body she has. She doesn’t have a spare.

Coming to Terms with Chronic Illness: LIES

We are on the edge of the New Age. You 

will no longer be ruled by your losses 

or pain. You will substitute applesauce 

for vegetable oil and the brownies will 

taste just as good. You will be exquisitely 

fashionable. You will be brave in the face 

of death. Your feet will stop growing their 

new wrinkles and veins. Your feelings will

never be hurt again. You will knit your own 

sweaters with wool from the lamb you nursed 

with a baby bottle. You will remember 

what matters: land and animals and love 

and making things with your hands. You 

will write long letters. You will not nest 

with throw pillows, heating pads, and hot 

baths: you will travel with your lean muscles 

and a backpack. You will sleep on rocks under 

stars. The sky will be in your chest. You will be 

boundless and ageless. You will get love-drunk 

and run the streets of far-away cities, whooping 

and hollering–your heart, big and loose. You will

remember everyone’s story. You will embrace 

your bare and mottled face. You will not be afraid. 

You will carve a snow cave and confess your sloppy 

love. You will get better every day. You will teach 

children what is most important. Yoga will fix 

everything. You will see all things clearly.

Coming to Terms with Chronic Illness: Electricity

I visited the exhibit of an artist who had developed an allergy

to electricity and paint and all his dyes. Now, he works 

by candlelight and weaves colorless fabrics large as walls.

Electricity is a mystery to me. It sparks our cars, brights 

our lights, beats our hearts, flashes news along our nerves, 

translates will to action. (All winter, my husband is shocked 

by door handles, shopping cart handles, my nose, my lips. 

His kiss is a star between us.) In the 1800s, doctors believed

mental illness was a disease of the nerves: they prescribed 

the rest cure, rich foods, and dangerous medicines that 

didn’t work. As I child, I thought the song lyric “Here 

comes your 19th nervous breakdown” was about my mother. 

She prescribed herself the rest cure, which looked, to me, 

a lot like depression: so many months lost to dark rooms, 

cold coffee, cigarette butts. Rest wasn’t cure, but symptom. 

Me? I’d outwit, outsprint lethargy with my will. I did. 

Until this illness made the sheaves around my nerves 

feel stripped. I wish I could spread my nerves like a net 

across the bed for a nap, pause leaps across synaptic 

gaps. Has my electricity gone askew? Or are there potholes 

in my paths? Doctors wrote “anxiety” in their notes

(tut-tutted the sensitive imagination, recommended 

meditation) until I finally had a diagnosis; even so, 

they can’t explain why self-electrocution is a symptom. 

Nervous breakdowns are out of fashion. Anxiety 

is trending. Bedrotting as a cure is popular on Tik Tok. 

Doctors prescribed dangerous medications that didn’t work,

Only rest helps. And movement. In some delicately 

textured, ever-changing weave no expert can prescribe. 

I must pay attention to my signals. But not too much 

–or my hissing nerves will drive me frantic. I try to meditate. 

I’m learning a new art. I must feel my way by candlelight.

Coming to Terms with Chronic Illness: Fatigue in December

The moon is a button made of bone 

that closes the great black cloak 

of winter. I move in slow motion. 

I harness myself to an engine 

which drags me where I have to go. 

The elbows of my soul have road rash. 

I am the opposite of a drag queen: 

I remove makeup, tangle my hair, 

and pull on plaid pajama bottoms 

with ragged hems. I want snowfall 

and flannel sheets. I want to curl 

in the pocket of that great black cloak

with its moon-button made of bone. 

I hereby resign from my lifetime 

appointment as lighthouse keeper. 

I am not exhausted by the storms 

–or the saving–but by the watching

and waiting.

Coming to Terms with Chronic Illness: the Junkyard

The things in the junkyard rarely wake 

before noon. Sheet metal, carburetors, 

car seat springs and kerosene tins. The

things in the junkyard have forgotten 

you. Their memories have rusted. They don’t 

apologize for disappointing you or for too 

short lives. The things in the junkyard want

only for hands so they can soothe the rangy 

yard dog, whose voice strains with longing 

and grief. The things in the junkyard have 

no ceiling. They hunker in dirt under stars 

and storms. Their thin and broken bits flap 

in the wind. All their light bulbs are broken. 

But listen: Hear them whisper. They murmur

about that slow, big-eyed cow who, just this 

moment, stares greedily over the junkyard

fence, as if her sweet grass is not enough.

Coming to Terms with Chronic Illness: Little Mice

Just before my marriage ended,

a student asked me to keep 

her pet mouse. I couldn’t say no–

her heart and needs were so big.

We named him Martín Snowplow

after the way he burrowed through 

his white bedding. He was light gray 

with big black eyes and a musk 

so strong, our eyes stung. 

My husband stayed away til late.

I prepared lessons at my desk.

I was always cold and pulled 

an oversized robe over my clothes. 

Martín ran the inside of my sleeves,

tickled my neck, and nudged 

his nose out my collar–until he peed 

and I had to wash my clothes again. 

Martín and I moved to a second floor

studio apartment with a red desk 

and a window that opened on a creek. 

Some nights, I’d lie on my back, 

put Martín on my foot and watch him 

sprint my body length: his serious, 

driven, funny face growing bigger 

and bigger til he reached my chin. 

Mostly though, stunned by grief 

and change, I never did give Martín 

the freedom and attention he deserved.

In Latin, the word for muscles 

is “musculous,” little mice, 

for the animal-way a muscle

moves under the skin. For years, 

I worked my muscles hard. 

They were uncomplaining 

miracles of balance and strength

–even when I didn’t feed them, 

water them, understand they needed 

rest. Then, that year in the studio 

with the red desk that faced the creek, 

those first strange happenings: 

a tightening in the hip, a frozen arm 

and hand, tingles that ran up and down

my limbs, like the prick of Martín’s feet.

I didn’t notice quick enough 

that Martín had fleas in his fur 

and a lump on his side. Two years, 

that’s about as long as a mouse lives,

someone said. You gave him food 

and toys and a little straw house. 

You did what you could. 

Better care may not have saved him;

I wish I’d cared for him better anyway. 

 

Later, I’d learned my muscles were, 

as my physical therapist explained, 

disorganized. They needed to talk

to each other differently. I had to train

them–not with runs, weights, and will

–but through slow motion. 

My husband and I never learned 

how to talk to each other. Not that 

better, slower talk would have made 

a difference. Our needs were so big. 

He never could give me the freedom 

and attention I deserved. Still, I wish

I’d learned to listen and speak earlier. 

Now my muscles, well-intentioned

mice, are lumpy and slow. Some 

are mute. Some are deaf. They scrounge, 

blind, for food they cannot find. 

They’ve forgotten their names. 

Those who can, whisper gently 

to each other with the language

they have left. I massage them, give 

them vitamins, slow walks, water and rest. 

I treat them with the kindness I never did 

when they were beautiful and young.

Coming to Terms with Chronic Illness: Brain Fog

I thrum along the walls, looking for the light switch. 

The tenants aren’t paying the rent. 

The stoplights blink 

wild, senseless patterns. The edges are frizzing;

the center, forgotten. 

Someone is drumming off-rhythm. 

The headstones have no markings. 

It’s like that. 

Or this. I’m trying to double-dutch but miss every jump. 

The gears turn too slowly for the car to start. 

I’m a hutch that holds too much. Or nothing. 

A gully stuffed with old refrigerators. 

Grit on a gusty day. The gurgle of a clogged drain. 

The sludgy bottom of old coffee cups. 

I’m humid and moody. I’ve lost momentum. 

The old gumption has turned grumpy. 

I’ve forgotten my speech in front of the auditorium. 

The amygdala is overwrought and exhausted.

Muggy and pudgy, dumpy and rangy. 

A jiggly flan. A pale pudding. A mangy dog.

The gaudy necklace has lost its gems. 

The buzz-hum drowns the sweet and subtle 

music. A muddy mouse hobbles along 

slowing synapses. Myopic, we squint 

at blurred trees. It's like that.

I want my brain to be a clean afternoon, 

but no one water-skis on this murky pond. 

No one sits on a beach chair

in this gusty cove. I want to second-guess 

everything I’ve ever known 

but can’t hold a thought long enough. 

I’m drowning in dreams. 

Mostly I’m ashamed,

but sometimes relieved to be relieved 

of so much thinking. 

I’ve forgotten to worry. Or I’m only worry. 

I can’t remember which. 

I fear you’re asking for that thing only I can give 

but I can’t hear you through the mumbling.

I’ve forgotten desire. 

I can’t find the doorknob. 

But midday, head on a pillow, I hear—

under the couch, the wooden floor, 

concrete, the rooty-worm layer, 

the clay and the boulders

—that beating heart bedrock, 

homefull and nameless, 

that’s been with us forever. 

It’s like that, too. 

Impossible Things I Remember

As I child, I was confused that I remembered my tail (where would it go in my pants 

and how would I sit?) until I learned we all had one once, 25 million years ago.

I remember the shock of raw air when I was born and my mother’s sadness.

I remember tin toys from the 1940s. 

I think my husband remembers the feel of armor against his shoulder, dough under the heel of his

hand, the joy of thieving. Being a girl.

I wanted my cells to remember the Ireland, land of my ancestors. They did not. Impossible

memories cannot be planned. 

I remember the twitch of my feathered wing tip to change flight speed and direction. 

My nephew, when he was three, remembered his “other mother.” Her name was Lolly, he said, 

and she’d he’d been shot. 

I remember drowning. I remember hunger. I don’t remember breathing under water. 

I no longer remember what I swore I’d never forget: how to macrame, the string patterns

of cat’s cradle, anything from calculus, most sign language, all my French. 

If time and space creases and unfurls like the origami I no longer remember how to fold,

please bury my jukebox full of advertising jingles.

Please release my black cat I had when I was ten. Let me feel her ribs under her thin skin.

Let her nose touch my nose again across these folded dimensions.