Article Category Archives: Creative Nonfiction

Nana

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When I knew her, Nana smelled like roses and powder. She smoked pack after pack of Craven A cigarettes and laughed with the sound of those years of ashes in her throat. She sat in an armchair in the corner of the apartment that she shared with my grandfather, her cigarettes on a small, round table beside her with a lighter—those were the days of lighters—and an ashtray with a beanbag bottom. And a glass of Tang lemonade (yes, Tang made lemonade too). And the TV guide.

The apartment’s balcony was trimmed with Nana’s geraniums, ugly, red, scraggly but lasting year after year. There were clumps of dirt in their pots and my little brother, my big sister and I would throw them over the balcony—the clumps, not the pots—and watch them shower onto the windshields of the innocent cars in the parking lot below.

Nana was funny and gentle and soft. And strong as steel. She ran interference for us kids, over and over again, growing in stature each time she did. Every Sunday, all four of her boys and their families would crowd into that tiny overheated, under-ventilated apartment and she would make tea and we would sit for hours and hours. The boys—always “boys” no matter how old—were loud; they’d laugh and argue with my stubborn and handsome grandfather. My Nana and her four daughters-in-law, all of whom remember her with great fondness (unusual for daughters-in-law, I know), sat on the edges, talking and serving. Everyone smoked the air blue, so we kids hung like puppies out the window onto the balcony, looking for something to breathe.

betweenthehouses

Between the Houses by Tessa May

Nana would often bake for us, too, layering the icing sugar on thick in one corner of the cake for my brother who ate so much she wondered where he put it all and, I think, secretly admired him for his unstoppable appetite. Or she would make chicken salad sandwiches—heaven on white bread with the crusts carved off and the sandwiches cut into four triangles—with sweet pickles on the side. On dreary days, she taught us how to play gin rummy and for my sister, who was older and had a head inclined to games of strategy, she played cribbage.

I loved Nana’s smooth, crepe skin, pink and soft as petals. I loved the wobble of her arms and her apron that covered her from shoulder to the hem of her dress. I loved her fuzzy blue eyes that swam behind her wire-framed cat glasses. I loved her feet—always sore although I didn’t know it then—and the small, embroidered slippers she wore in the house. They seemed to be from China and were very exotic in my child’s mind.

I loved the high spool bed I shared with her when I was a young child. I would pretend to sleep while beside me her huge shadow kept me awake with its gentle snoring. I would stare at the painting of the Sacred Heart of Jesus hanging on the wall at the foot of the bed and hold my breath so I wouldn’t wake her.

I loved that on those long ago Friday nights, when we arrived at their place after driving from Moncton, Nana and Grandad were eating dinner off folding tables in the darkened living room, watching wrestling on the small TV. Nana loved wrestling. I loved that too.

Centre Stage

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Drama was a way of life in our house; everyday events blown out of proportion, life lived around my mother.

“I gave up my career for you,” my brother and I were told as children. We felt her frustration at a performing dream abandoned in the shape of the wooden spoon, the burnt meals and the hurled pots. It was not until we were adults that we did the math and realized she had not trod the boards for nine years before I was born, longer before my brother.

My mother was, once upon a time, the star of a small touring company, based in a tiny theatre in the not overly large city of Dublin, Ireland. She dreamed of a career in movies but met my father instead. After they married, they moved a good deal, following his career in documentary film. A sojourn in England, where we were born, led to a move to Toronto where all thoughts of acting took a back seat to raising small children in the absence of a frequently on-location husband.

It was a move back to Ireland in the sixties that raised the spectre of acting careers past. Great was her disgust when my mother discovered that several latter-day “talentless” co-stars were still starring in current productions. Trips into town were punctuated by elderly gents clasping my mother to their chests, claiming they had seen her in The Cherry Orchard, Lady Windermere’s Fan or Romeo and Juliet and would she accept their undying love. Fellow thespians were equally effusive with air kisses and “dahlings,” followed by endless recitations of who was “resting,” who had died and who was sleeping with which director. My mother simpered and gushed with the best of them while my brother and I waited, rolling our eyes. Enquiries as to when she would be returning to the stage were invariably met with, “Oh I couldn’t possibly…” and a gesture in our direction.

Over the years, she was offered, and always turned down, “too-small” parts in some production or other. She was particularly incensed when asked to join the local dramatic society.

“Amateurs!” she spat. “I couldn’t possibly. I was a star.”

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Red Sky at Night by Monica Lacey

It wasn’t until the local church asked if she would direct a production of Everyman that she hit closer to her stride. A certain amount of demurring and trotting out of stock phrase followed. She relented, after a couple of weeks spent surreptitiously casing the congregation during Sunday service. Auditions were held and those whom my mother had earmarked for a certain part were flattered, cajoled and bullied into attending.

In no time she whipped that motley crew into a semblance of a cast; lines were learned, costumes fitted, music selected, props rounded up and the press invited. The church was packed for the single performance, which went off with only one hitch. God, played by the Vicar lying on his stomach in the belfry and represented by a single flashlight beam, was caught by a fit of coughing and missed the cue for his final line. My mother, drunk on applause and the adulation she knew was her due, graciously overlooked this faux pas but her enthusiasm for church-going dropped off noticeably after that.

For her next foray into the realms of directing, my mother proposed that my all-girls school put on a production of A Midsummer Night’s Dream. As a member of the board of directors, she felt our education lacked drama and who better to fill that void than herself. Our hall, shoe-horned into the narrow garden of one of the two Edwardian houses that comprised the school, boasted a tiny raised stage, which was deemed unsuitable for any play production. My mother barreled on regardless.

Auditions caused her some consternation as we were, by and large, devoid of talent. In desperation, my mother cut the play down to just the fairy/players scenes, with lines kept to a minimum and comedy racked up to the max. The production went off with many a hitch. Lines were forgotten, girls ducked out of rehearsals, costumes didn’t fit, props were lost, scenery fell over, and the fairies got the giggles. As the curtain descended on the chaotic production, my mother vowed never to produce another school play as long as she lived.

The following year, the head-mistress made an unusual announcement. It was felt that the annual prizes for academic and sporting prowess were not inclusive enough, and now prizes would be given for creative projects such as knitting, sewing and writing so that every student had a chance to shine. I was a top-notch underachiever in the academic and sports areas but I was certain I could knock their socks off in the play-writing department. I knew plays, I read plays, I attended plays. And so I wrote a play. And my play, a frivolous period piece, won first prize: no one else entered.

One of the major short comings of an all-girls school is the lack of boys. We were at the age when we spent more time studying that subject than any other. A plot was hatched to produce my play, with boys from our brother school rounding out the male characters. We approached the head-mistress for permission to use the school hall and, no doubt in light of my mother’s recent efforts, were turned down flat. Boy deprivation reaching epic proportions, we approached the headmaster of the brother school with our scheme. He agreed to consider the idea and consult with the English master; please could we send over the play. Several days later, assent was given; would we come to the school, meet the hapless boys who had been selected by the English master, check out the much larger stage and okay the set designs that the boarders would build over the coming weeks.

Rehearsals began a week later at our house, with me directing. Us girls developed serious crushes on several of the boys and they all fell in love with the girl playing the lead. A lot of fun, flirting and not much rehearsing ensued. As the performance date edged closer, my mother decided to look in on a rehearsal. To say she was horrified by the lack of progress would be an understatement. She gave us all a tongue-lashing and announced that she would take over the direction of my play.

After that, things moved at a more professional speed. Once again, lines were learned, moves were plotted, measurements were taken, and a week before the dress rehearsal, a trip to my mother’s old costumier was planned. We spent hours digging through velvet waistcoats and frothy crinolines before coming up with the perfect look.

The dress rehearsal was predictably awful but the set and costumes looked stunning and the lighting and incidental music provided by the boys fit the mood perfectly. The day of the performance dawned and classes were given scant attention. By seven, the cast was mustered, costumed and grease-painted, nerves running riot as the curtain rose.

The performance was a great success. I stood in the wings with my unneeded prompt book, shocked by the realization that something I had written was being enjoyed by a hall full of people. As the final curtain fell, my mother strode to centre stage to claim her directorial applause. Linking hands with her leads, she bowed over and over, acknowledging the crowd with a dignified inclination of her head. It wasn’t until the cast trickled off the stage that she saw me in the wings and beckoned me forward. By then the performance had passed to the audience. Chairs squeaked, arms were thrust into coats, programs were dropped and jokes were traded as they headed homeward. Standing alone on the empty stage, nursing my bruised, upstaged teenage ego, I vowed to leave future theatrical efforts to the family prima donna.

My mother never acted or directed again, although a spell as a costumed interpreter at a historical site filled her later years. Eighteen months after her death, I had the opportunity to play a background performer on the set of a local movie. As I sat in full glare of lights, camera and action, I imagined her somewhere above my head, grinding her teeth in frustration that I had made it into the movies before she did. Has the torch passed? No, not likely.

*

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Supper Helper

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“Who wants to be supper helper?” I call out, beckoning one of my three teenage kids from behind their closed bedroom doors. I am sitting in my wheelchair and aiming my voice down an empty hallway. It’s time for them to choose between setting the table and preparing supper, or cleaning up afterwards.

I admit the phrase “supper helper” is now a misnomer. I coined it years ago, when the kids were young. Back then, I cooked our evening meal and it was their job to set the table. Eventually though, as I’d started to prepare supper, I’d realize I was too tired to finish. I would chop the onions, sauté with garlic and halfway through cooking, call in one of my kids as supper helper. Soon, they were also putting on rice to boil and creating salad. And when I could no longer handle cutting a round onion with a sharp knife, being supper helper meant learning to cook.

Tonight we’re having the turkey soup my daughter made yesterday. She sets out four bowls — one for herself, the second for her brother, another for her sister, and one for me.

“Let’s put some vegetables on the table, too,” I call out.

At that moment, I’m transported to the dinner tables of my childhood. For the first eight years of my life, my grandmother prepared supper, allowing my mother to work outside the home. My father and grandfather seated themselves at the table just before my mother served the evening meal. We began by bowing our heads as we made the sign of the cross and shared a short prayer. What followed was praise for my grandmother’s cooking — mixed with giggles between siblings. Supper ended with a nod to the authority of my parents, who dismissed us from the table. Afterwards, the four children cleared off and washed the dishes, and the dog ate the leftovers. Those childhood suppers were structured events and there were expectations: the rest of the world was put aside for the duration of the meal and children had good manners.

Authority is not a hallmark of my parenting, yet I still find myself wanting to re-create those meals of my past. Tonight, as I say, “Let’s put vegetables on the table,” I am reminded of a priest standing behind an alter, raising the Communion Host for the Blessing: “Let us pray.” Let us put vegetables on the table. Supper can be a ritual, one which I still enjoy. At this point in my journey with multiple sclerosis, however, I have to remind myself that my physical inability to cook and serve food does not take away from the mental capacity needed to ensure everything comes together.

“Yeah, well, what do you want?”

My daughter stands at the fridge, the door open for an annoyingly long time, hand on hip, face cocked to the side. Vegetables suddenly sound superfluous and she sounds rude. But I’m not fooled: she’s super smart, better at math than I am, and with a competitive streak, she manages to be one of the top students in her class. For now I’ll ignore my mother’s “shoulds” and will not be bothered by the tone of my daughter’s voice.

Besides, the soup she made last night was delicious and I enjoyed watching her cook. She moved around the kitchen efficiently, chopping an onion, sautéing the garlic. She added potatoes for their starch and carrots because they are sweet. She pulled the meat off the turkey carcass in a way that would make her great-grandmother proud.

“I want,” I respond, “to serve you a salad.”

I point out that we have cherry tomatoes and the washed lettuce is stored in Tupperware. (Sometimes I can do such things myself; other times I make sure the vegetables are washed, chopped, and stored by the students I hire for extra help.) But I still have to get my daughter to put the salad on the table and tonight she’s a teenager who just doesn’t want to. I’m a tired mother who is grateful for anything done, but it has become too difficult for me to prepare a bowl of soup and salad and then to eat it. Asking my kids to help with chores is okay. Asking them to take care of me doesn’t feel okay at all. They’re too young to be concerned with my welfare. I want to be concerned with theirs.

How can I look after them? I can be creative. I can adapt. I can call in help. I can teach my kids the skills they will use later in life: the importance of family meals, how to make turkey soup from scratch. But little by little, this chronic illness is taking away my physical abilities. It is a sadness that seems to hold our family quietly.

At the supper table, my son serves me the soup, while his sister chastises him for spilling it on the table. I cannot really know what sadness or frustration may have touched these mysterious, beautiful teenagers today. So I will ask if they want to hear the funny story I heard on the radio and they will respond, “Sure, just don’t ruin the story by laughing halfway through it.” I will protest because it is a good story. Listening for my grandmother’s voice reminding me to be thankful, I can share the company of these kids over our meal.

Wooden Spoons by Jennifer Raven

Wooden Spoons by Jennifer Raven

Baby Steps

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Zoe had burnt her French toast and flung it in the garbage. She’d made a wrap, too, but the eggs had not set. She’d slammed the wrap on the counter and disgusting blobs of egg white now clung to the sides of the toaster. Finally, she had settled for half a piece of toast and peanut butter. Susan knew Zoe hated toast.

“We could make biscuits together,” Susan said, purposely keeping her voice soft and steady.

Breakfast had been disastrous, but baking was the only activity that soothed Zoe and gave her some sense of accomplishment. Susan pulled out the cookbook and copied the directions onto a piece of paper, outlining the steps in a way that would be easy to follow.

Find baking tray.

Put all ingredients on kitchen table.

Get measuring cups….

“Okay honey, take this three-quarter-cup measure. Pour in the buttermilk. Good. Now add that to the dry ingredients.”

Susan watched as Zoe poured the buttermilk, then quickly repeated the step twice.

“Okay… so why did you add three?”

“You said three cups.”

“No, honey, you misunderstood. I said fill the three-quarter cup.”

Zoe sprang up, fired the cup across the room, and strode out of the kitchen, shoving and overturning a chair in her path. Susan stood still and silent. Down the hall a door banged.

Susan dropped her shoulders and took three slow, deep breaths. In for three. Hold for six. Out for six.

Zoe was thirty-five, no longer a baby, yet she’d lost so much in the last sixteen years: the ability to think things through, to follow directions, to control emotions. She grew frustrated by her difficulty figuring anything out. But the more Zoe overreacted the quieter her mother would become. Susan had long ago learned that explaining, negotiating, or arguing didn’t work with someone whose brain struggled so hard.

One more long, slow deep breath then Susan scooped some of the buttermilk out of the bowl and finished making the biscuits, all the while listening for the sound of things being thrown or broken. Nothing. That was progress. With one ear still open, she continued to clear up the mess. Susan knew Zoe needed time and space, things the hospital had never offered. The staff had always seemed too quick to call security, man-handle, inject, lock up.

All was quiet. Susan walked softly down the hall to the living room. Zoe was on the couch, feet tucked under her, a pad of paper on her lap, and a tube of bright blue acrylic paint clutched in her fist. A dozen books, more tubes of paint, papers, crystals, bottles of essential oils, and bits of craft materials littered the coffee table in front of her. A plastic pill container with the day’s ration of anti-psychotics and anti-depressants sat beside a glass of water.

Zoe aimed the blue tube at the paper and squeezed hard trying to dislodge the dried paint that had sealed the opening after the cap disappeared. The tube split and the paint shot onto the floor, her hands, her clothes, her new pillow. Zoe sat frozen, bright blue streaming down her wrist and dripping onto her lap. Susan reached for the roll of paper towel under the coffee table, then gently took the tube from Zoe and wiped her daughter’s hand.

“I’ll just get some wet cloths,” Susan said.

She wiped up the globs of paint as best she could. Zoe said nothing. She lay curled up on the couch, a throw over her head. It was a huge improvement over last year when Zoe had overturned the coffee table and thrown water glasses. The year before that the glasses had been aimed at Susan.

“Good for you, Zoe, for staying cool. I know it’s frustrating.”

No response.

“The biscuits are almost done. Would you like some milk?”

Silence.

Susan arranged the biscuits and jelly and thought about the last few days. Weeks. Exhausting, yes, but nothing like it had been. Despite the mess in the kitchen and living room, the last hour could be counted a success for both of them. Susan had not raised her voice. She had not chattered endlessly, and Zoe had settled in spite of the paint and failed kitchen experiments.

“Hey, I think we both did pretty good getting through the last few minutes.” Susan moved a few things from the coffee table to the floor to make room for the biscuits.

“Why are you so nice to me?” Zoe was now sitting up, the throw slung over her feet.

“Well, I know you’re frustrated. And I do think you did a good job settling down. I have no reason to not be nice. And … I love you. No matter what.”

Susan sat down on the couch. Zoe leaned into her mother. They sat quietly, unaware of the passing of time. It was the moment that mattered. And later, if Zoe wanted to talk she would listen and say little. It would be a few more hours before Susan would allow herself to cry in the shower. And then, sitting on the bathroom floor, she’d pull herself together, one slow deep breath at a time. Baby steps.

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Dancing with the Universe by Melissa Sue Labrador

Made This Way

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cecile

I am awakened by the sound of my phone. I glance at the time before I answer: 4:00 a.m.

“Hi Mom. What’s up?” I try to sound awake.

“Cecile,” she gasped, “you have to help me … call my doctors. Tell them I need to go back to work. If you call them, they will listen to you, but they won’t listen to me….” She continued talking. It didn’t matter if it was day or night. It didn’t matter if I answered or not.

*

On July 28, 2008, my mom was on a field trip with a group of students and child/youth workers. What should have been a fun, exciting day turned tragic. She stepped off the bus and into the path of a vehicle. She sustained many injuries — broken bones and lacerations. But it was the injury we could not see, the traumatic brain injury, that has brought the most challenges to her and our family.

Until my mom’s injury, I had no idea what the term “traumatic brain injury” even meant. Yet in Canada, fifty thousand people a year sustain brain injuries and over a million live daily with these struggles. Depending on the area of the brain affected, repercussions vary. For my mom, the injury affected her frontal lobe. Doctors said she’d never return to work and would require twenty-four-hour supervision.

My mom is a strong, independent woman. Trying to convince her of these changes while living fifteen hundred kilometers apart has been far from easy. My father was her main caregiver after the accident, but he did not weather the storm very well. Phone calls were difficult: “I don’t know what to do, dear. I just don’t know what else to do.” I could hear the weariness in his voice.

When my mother’s emotions ran high, she ran too. One night about three months after the accident, she slipped out of the house and four hours later, at three in the morning, someone brought her home. They had found her sleeping on a bench down by the bay. The more upset and angry she would get, the more her other deficits, such as facial recognition, would emerge. In a fit of rage she once tried to kick my father out of the house because she thought he was an impostor.

Although some days were without major incident, none were easy. The doctors told my father that almost ninety percent of marriages fail after traumatic brain injury presents in their lives. He was determined to be in the ten percent and I admire him for that.

But as calls from home became more scattered and hard to follow, I began to feel uneasy. I made the decision to fly home for a few days, to try to sort things out, and to get my mom back on track with her medical appointments. It was January 2009, five months after the accident. I expected to be confronted with challenges, but what I walked into was utter chaos: dishes piled everywhere, unopened mail strewn about the living room, and my mom clearly overwhelmed, devastated.

In need of insight into the emotional and behavioural changes in my mother — and ways to help both parents — I requested and was granted access to her medical assessments. I found them fascinating. I learned the functions of the brain, that the left frontal lobe deals with language and positive emotions while the right controls non-verbal aspects of communication and negative emotions. In my mom’s case, the entire right frontal lobe was damaged as well as part of the left. I poured over her medical results looking for a new picture and a new way to navigate her recovery.

Getting my mom to her medical appointments was very challenging. “I hate them!” she would scream. “They make me so angry! There are so many doctors, so many appointments. They make me feel stupid!”

My father and I agreed that she was especially distraught following her rehab and therapy appointments. I watched her closely when she returned from the next two sessions. She was right. Clearly, they were not bringing the results we needed; each appointment only seemed to increase her anxiety and frustration.

One afternoon, a few days before I was scheduled to fly home, my eyes landed on a large canvas in the hallway. I  hadn’t really noticed it before but now something captured my interest. It was a sketch of a sad girl with writing at the bottom. I recognized my mom’s handwriting. She never “did” art before the accident. I was intrigued and the words stirred a deep emotion. I had an idea.

cecile2_cropped“Mom, did you do this?” I asked.

“Yes! That’s how I feel! I give up!” she screamed. There seemed to be a lot of screaming. “I have more but you won’t like them,” she added with the disdain of an angry teenage girl. “Your father says they are too scary to put up on our wall.”

“Show me, Mom,” I said.

She stomped to the bedroom and started pulling out canvasses from under the bed and behind the closet doors. I was amazed.

“They make me feel better,” she said in a voice still filled with defiance. “I do them when I get home because I hate those doctors. They don’t listen to me and they don’t understand.”

I made a list — and went off to the art store. I filled my shopping cart with brushes, canvasses, and paints. I practiced what I was going to say a hundred times but in the end, it was simple: “Mom, you need to keep painting.”

Tears flowed. She hugged me as I left to board the plane. “We’re going to get through this aren’t we Cecile?”

“Yep, we are going to get through it, Mom. We are just made this way.”

*

It has been six years since my mother’s accident. In that time, she has attended painting seminars that have helped her gain technique and confidence in her art. The negative and dark feelings in her work are not as prominent as they once were. Although she still turns to her painting as a therapeutic process, it is almost as though, over time, the canvas has absorbed the anguish. At the Brain Injury of Canada conference in Halifax this year, my mom’s art was displayed along with work by thirty-one other brain injury survivors.

Art by Wendy Proctor.