Autumn’s Lesson

I’m three chemotherapy appointments in. Halfway until I get scanned again to see how effective the drugs and healing work have been. I still dread the days following treatment. My care team is helping me to manage as best I can. They help me balance drugs to reduce nausea and other side effects. However, chemotherapy is still a cell killer, so it’s just doing what it’s gotta do. I continue to take care of myself. I sleep when I need to sleep. I eat high-protein foods that don’t make me nauseous. I keep clean to ward off infection. I meditate to centre my soul. The usual routine.

My moods have changed over the last month. It seems appropriate that I’ve been watching the gentle shifting of the leaves outside my living room window through this time. The cotoneaster hedge is particularly companionable to my shifting emotions. It’s gone from deep green through an array of oranges to crimson red and now, sparse fiery dots on dark fractaling branches. My moods, too, have passed in vibrant autumn colours: crimson frustration and heaviness the shade of brick. I’m more an even-toned umber today, resting on the stability of my branches. Perhaps tomorrow will be more saffron orange or slate blue… it remains to be seen. Nonetheless, I’m weathering the seasons of emotions as best I can; It’s stormy, to say the least.

Through the storms, I’m learning to be gentle with the expectations of myself. Tasks take twice as long, and I need more time to rest in between. In addition to that, over the last month, I have struggled to find motivation. It’s a constant hue of foggy blue pervading every attempt at action. I usually set a few tasks I want to finish. Simple things: do laundry, water plants, connect with a friend… I’m learning—with great difficulty—to accept that I can’t do everything. It’s a difficult lesson that I’ve never fully ‘got’ in my thirty-five years. I’ve consistently wanted more of myself than is humanly possible and always fallen short; It’s a tough mindset to unlearn.

Another habit that battles the high expectations is my tendency to be overly defensive of everything I choose to do, especially the pleasurable things. It’s like an internal war with a yellow army screaming, “You’re not living up to your potential” and the blue team saying, “NO, I am enough and deserve joys.” I’ve had some help finding activities that nourish me, though. The kinds of things that connect with my purpose and ignite me with meaning. For instance, I’ve started brainstorming activities that combine nature and technology, which I hope to turn into story-based activity guides. I’m reading books that nourish my creativity (Wild Mind by Bill Plotkin). And, I’m making felted mushrooms that remind me of our ecological interdependence, which will hopefully turn into gifts one day. Even though I’m not working as quickly as the yellow army might like, I find just a bit more peace when I’m pursuing something meaningful.

Perhaps it seems trite to speak of finding purpose or meaning; it certainly cozies up with such adages as “think positive” and “life is a journey.” Indeed, in the days of battling nausea and slipping between fatigue fuelled naps, it’s another red-hot army on my heels. I look at my companions, the leaves, and I wonder what they are telling me. They cling so desperately to their dark branches. Then one day, in a burst of fiery orange, they let go and allow the wind to take them. They will provide shelter for critters and eventually release their nutrients back to the soil for the next generation of plants. Each stage comes as it does. And luckily for me, the scenes come in an array of colours as vast as the rainbow! So, trite be damned, it’s just another colour of the rainbow.

Showing off my first felted mushroom

Loss

“These lovely people whose orbits have collided with mine…”

I was afraid I’d lose myself—become rewritten. I worried that therapy would erase me, my passions, my life.

A month into chemo, I find I am not lost. I am not erased. But this isn’t easy.

A month in, strong, strong emotions. I hate chemotherapy. There’s nothing to like about it—nothing to even fool myself into liking about it. It sucks. It makes me feel like shit. I barely have the energy to lift my head. My legs ache. If I’m not proactive with preventing nausea, I’m up at 2 AM puking. It sucks.

I’m losing my hair: “Thinning” (I’m unlikely to lose all my hair with the particular chemo I’m on). I’m caught by an unexpected sadness seeing my hands and fingers coated in the dark thin threads snaking every which way. I was warned, but tears wash away in the spray of the shower anyway. I wouldn’t mind being bald, honestly. The worst part is the numerous strands jumping out against my bathroom’s shiny white tile floor and threatening to clog the shower drain. I’m going to have to clean all this up. Barf. It’s yet another signal of how real this is and how powerful the chemotherapy drugs are. Even on this good day where I plan to eat a fancy dinner and take a long walk, my hair is falling out. I’m going to shave my head, I’m sure of it.


Unfortunately, my upcoming chemotherapy is delayed. A high fever, antibiotics, and borderline white blood cell counts indicate my body needs more time to recover from this cycle—a mixed blessing. As usual, I make sure to eat well and walk daily. I throw in some dancing for good measure. I still meditate every day—five hundred consecutive days of meditation this week! Add that to a couple of 250-day streaks broken by a missed morning, and that’s over a thousand days! I suppose all of this is healing. But, my heart is unsettled.

I feel myself on the rocky terrain of discovery, uncovering what each day and week are. I’m gentle with myself even as fears and passions lurch from my heart in a coded language I’m not sure I understand. I want to write and draw and change [eco-social systems of oppression]. Alas, I find myself boxed into my couch watching another season of British Bake-Off. It is what it is.

My birthday approaches. The love my friends and family have shown me over the last two months has been nothing short of the best birthday present I could ever want. The food, the company, the cards, the rides, warm blankets, and books. The list goes on, but there’s no way to fashion these words into a worthy monument of what they are: love.

It pains me that I can’t find the words to express how powerful this is. These lovely people whose orbits have collided with mine, who have shared in the joy of life, who have co-created places where we live fully and ready to take on a brutal world together. And at this moment, as I take on the lot this chaotic universe has landed me in, I find myself not too small or insignificant to receive care. Even as it feels the entire world is burning, I matter enough for people to show up at my door with baskets and blessings. There is so much space in love like this, the way it multiplies between us. And I find I am not lost.

I spent some time getting hugged by Shaker at Whispering Equine #horsetherapy

Magpie’s Menagerie

The following story is an experiment in a “rough-verse storytelling. I want to get more of my meandering stories onto the site alongside my personal updates. Most—like this one—will be first drafts as I move more value onto practice than perfection. This is a start.

“Magpie with Cape v1” by Kat Dornian

Magpie’s Menagerie
by Kat Dornian

Magpie collects her things.
A beautiful array of knick and knacks:
Buttons and foil, beetles and fluff.

Magpie arranges them, day in and out.
Adding to her hoard, lovingly displaying
the ribbons and caps, rocks and cones.

Magpie searches for more.
Flitting about for the debris left out
on steps, on stones and hidden in coves.

Magpie is never satisfied.

Magpie re-arranges, again, everyday.
Button here, ribbon there, fluff below, rock above.
Her newest foil scrap lacks a spot.

Magpie places and re-organizes.
Worrying about the collection —
trying the foil here, the foil there.

The lovely foil

Wind blows a mighty gust.
Catches foil, carries it away:
Flitting and floating, falling and falling.

Magpie sails after foil.
But she’s too late.
Lovely shiny sparkly foil, caught by River.

River takes foil far
while Magpie screams down stream—
desperate cackles and mournful titters.

Wind and River pass by.
Watch Magpie as she woefully sorts
buttons… beetles… fluff.

Magpie spies on River.
She pleas with Wind at every sunset,
expecting her foil to be returned.

“Foil is long gone, far past,”
River and Wind whisper to Magpie.
Still, Magpie clears the perfect spot.

River turns to ice, Wind turns cold.
Magpie nestles deep in her nest:
Beetles and rocks, buttons and ribbons.

An old scrap tickles her.
A treasure long neglected
across the months of spring to autumn.

Magpie remembers now —
the way the tarnished thing shone before it was forgotten
and coaxes it from hiding to its spot.

The lovely foil.

Wind may one day play though
and take old foil to the River.
But now, it cradles under Magpie’s breast.

Treasure for this moment.

First Cycle

My first chemo cycle is coming to an end. Each cycle starts with a dose of drugs that halt quick-regenerating cells from regenerating. If all goes well, the cancer cells—mutant human cells—can’t figure out what to do and die off. Healthy cells get their act together and spring back.

Following the in-hospital bit of chemo, they gave me a bottle with more drugs inside. These drugs drip into my body for 48 hours. They put me on steroids to help as well. As a result, I feel kind of buzzed all the time. By day three, my body’s not doing so well. It’s starting to crash. Nausea and fatigue. My body’s healthy cells not doing what they usually do—not regenerating like normal. It’s exhausting, and I’m coming off the steroid buzz at the same time. I try to stay healthy. I wash often. I go on little walks. I eat protein-rich foods and try to stomach vegetables. Bread is digestible, so I eat that most. I remind myself that I’m safe and healing. I’m tired. I am so tired, but I try to get up every hour and sip some water.

Food is a struggle on these low days following chemotherapy. I stay away from soft yolks and soft cheese and raw nuts. I can’t eat and drink things at room temperature—a chemo side effect. It was just “weird” at first, but after every liquid spawns an explosion of soft-headed pins in my throat, I give up on anything below tepid. The warm drinks start to taste tiring, so I experiment with herbal teas. I long for a cool glass of water.

I begin understanding hope differently. In August, when I described hope to my journal, it was “a field of sunflower stretched to infinity” with sights set on images decades and years away. Slowly over the last month, hope has become much more active. Hope shows up in the acts of every moment. I think the best way to describe it is in the story of planting a seed (and I do mean this very literally, but it works metaphorically as well). Hope is planting a seed. I cannot control the seed’s reproduction, nor the sun and rain. But I can plant that seed in the best spot I know for it. I nourish it, and that act of nourishment is hope. I can’t protect it from every ravenous sparrow or insect or mouse, but I can give it protector plants nearby and build shelters. The seed may grow, or it may not. It may not make a stunning flower or a substantial fruit. That’s what gardening is. But hope is planting the seeds. And like this seed, I’ve been nourishing my own body as a practice of hope without expectation. My journal now reads, “hope is helping wounds to heal.” I’m finding so many actions that are hope. The actions are not reactionary nor transactionary; From eating my proteins and washing my feet to riding my bike for the planet and writing politicians for equity. I’m finding releasing hope from expectation makes it, well, much more hopeful to engage*!

A week after chemotherapy starts, I feel myself bouncing back. I can go on long walks; I soak up the sun and smells of late summer. By day nine, I actually want to do things. I want to read, write, and dance again. It feels like there’s more sun coming through the windows. A couple days on, and I’m cleaning the house readying for the next cycle to start. Dusting, vacuuming, and washing. I trim my nails and take a bath. This cleaning will be a pre-chemo ritual. It feels good to clean, to prepare the nest for my body when it’s low. To put things in their place.

I enjoy a glass of cold water. Cold water has never tasted so good. I appreciate how much I have savoured the moments in my life like this. One day the memories will be broken apart into hundreds of trillions of atoms and dispersed across the cosmos; Right now, those moments fill my being.


* I must give credit to the sower of this understanding of hope: Frank Ostaseski in The Five Invitations. A number of years ago that book helped me to reframe forgiveness. My understanding of forgiveness moved away from forgetting and towards healing my own wounds. The book also speaks about not confusing love with attachment, which also resonates with me so much.

Month One

One month with a cancer diagnosis. It’s moved quickly and yet so slowly as well.

August began in a whirlwind. I had a DJ gig, a teaching appointment, and hopes of finishing my thesis. I had a colonoscopy, MRIs, CT scans, bloodwork, and bone scans. I had appointments with gastroenterologists, surgeons, and oncologists. I had to tell loved ones and confront the sense of dread weighing on me.

It wasn’t long before my work and school commitments fell away. The only thing left was to wait, to focus on healing, and to endure the waves of nausea and cramps from the cancer in my colon and liver. Waiting is difficult for me. I’m impatient. I want the cancer out like a house guest who’s overstayed their welcome. Sleep helped to pass the time. Even with the fatigue, one can only sleep so much.

I told my friends and family about my diagnosis. I received help and several messages (many still unreplied to). I think about them everyday, like I should organize something, but a general discomfort pervades even simple things like that.

I’m trying to find a comfortable space to do things. I’ve set up inviting plants friends everywhere. I’ve decorated with the puff of wool, dried grasses, and simple beeswax candles I’m told to love so much. And yet, I’m restless and uncomfortable. I don’t know where the days go when I tally up the minutes: I meditate, stretch, line up rides, lie down, feel sorry for myself, wish things were different, meditate, try to read, try to watch tv, try to clean, try to be helpful, hate myself, hate this situation, meditate as though it’s the only cure, pace, compose thank you notes and stories in my mind, sleep.

I’ve received relief from work and school. All I have to do is heal now; I remind myself of this everyday. All I have to do is heal. I feel the force of a transition in this healing. The way the cancer is building in gooey, mutated masses within me. That house guest who’s still here even though I’ve asked them to leave three times. The house guest who’s clumsy and loud. I wrap this cancer, this overstayed guest, in a large leaf and I swaddle it. I don’t know why yet. I’m not even sure I should. There’s little direction here.

I’m just doing my best. I’ve always done my best.

I enter the new month greeted by chemotherapy. It is unknown and scary. Questions prevail but only time will tell how my body reacts. There are predictions, but everyone is different. Chemotherapy will help stop the cancer from replicating and spreading. It is the fortification of a boundary between “me” and “it”. I will heal, the unwelcome guest will tire and shrink.


Near the beginning of the month, I wrote a poem about my uninvited guest. Later, I came across Rumi’s poem titled The Guest House. The latter prescribes a practice of inviting and being grateful for all the emotions that come. I was struck by the contrast of my own moods towards cancer and Rumi’s wisdom towards emotions.

A Welcoming Home
by Kat Dornian

A welcoming home

might have loose bounds
allowing in all sorts.

A flustered flurry
of a party inside.

Warmth, bounty, comfort
for anyone who comes.

A home of love
torn apart e’ry night
by everyone needing
a warm hearth.

A home of love
flaking away with each guest.
Carried in pockets, upon shoes,
replaced with trash, dirt.

A home of love
devoid of boundaries means
all move in… until
I no longer remain;
A stranger in my home
no traces to be found.
Eaten from the inside out.


The Guest House
by Mewlana Jalaluddin Rumi, translated by Coleman Barks [Source]

This being human is a guest house.
Every morning a new arrival.

A joy, a depression, a meanness,
some momentary awareness comes
As an unexpected visitor.

Welcome and entertain them all!
Even if they’re a crowd of sorrows,
who violently sweep your house
empty of its furniture,
still treat each guest honorably.
He may be clearing you out
for some new delight.

The dark thought, the shame, the malice,
meet them at the door laughing,
and invite them in.

Be grateful for whoever comes,
because each has been sent
as a guide from beyond.

Here’s a drawing of me after receiving my “Power Port” (for delivering chemotherapy drugs). The photograph is a bit bloody, but I think you can get the gist from my quick sketch… I was pretty high on sedatives at the time, haha.

Welcome to Kat’s Story

I’ve been diagnosed with cancer. While my body works to quell the growths, words tumble out. Words of pain, words of healing, words trapped inside for too long.

Welcome to my blog. I’ve created this site to share my writings as I embark on my cancer journey. The stories you’ll find here aren’t about cancer necessarily. But much like the cancer cells, they have multiplied inside me over time. Unlike the cancer cells, they have far more purpose.

I was diagnosed in August 2021 with colon cancer. I’m young in the cancer community (it seems whenever I think I have moved beyond being a so-called young adult, I find myself in another situation where the term applies). I’m 34, about to turn 35 soon. I’ve taken good care of myself with daily meditation, regular exercise, a blossoming healthy relationship with food, meaningful pursuits, and a strong network of friends/community. I’m hopeful this otherwise healthy body will see me through the treatments… but it will be a tough slog.

You’ll find some stories here, mixed with poetry and meditations. I’ve been most fascinated with science fiction since being introduced in University. My boyfriend at the time lent me his copy of Callahan’s Crosstime Saloon by Spider Robinson and my stereotype of science fiction was transformed. While I’d grown up in a household that loved Star Trek and fantasy, I’d long poo-poo’d science fiction novels as mere pulp. Now, I love the imagination and metaphors in the stories.

I’ve had stories brewing in my head for years, but other pursuits and a fear of a not being good enough left me with few words on the page. While my main priority now is healing, I’m taking the opportunity to write when I need to, releasing it into the world, and maybe even letting the writing be a source of healing.

Kat living the best life on a St. Patrick’s Island bike ride (2018)