creative nonfiction

When the Leaves Clap Their Hands

Author: Erin Hutchins

 

“You two may have noticed that we have been going to the doctor’s office a lot lately.”  My father looks at my sister and me.  No I haven’t noticed, I think to myself.  I am only six years old and Erica is eight.  We’re too young to connect the reason why mom had been sleeping so much lately with all the doctor visits.  I look at my parents sitting on our brown sofa holding each other’s hand.  “Your mother has cancer” he states solemnly.  Because we are so young, we just assume that cancer is like having a cold, not life-threatening in the least.  Death seems like an abstract idea at this point in my life, not a real figure that can snatch my mother out of our arms.  We’re kids, our main concern is how fast we get through schoolwork so we can start having fun.  I don’t comprehend the significance of this announcement or how this will change our lives and teach us to rely on God for help.  

       Every day after we do our schoolwork, Mom takes a nap.  But the sleeping becomes more frequent and for longer amounts of time.  This exhaustion leads her to the realization that something is wrong with her health.  Mom visits several doctors to find a cure for her aching back, lack of energy, and the bump in her hairline.  A young physician agrees to remove the seemingly benign swelling, but the lab results come back positive for Hodgkin’s lymphoma.  Neither one of them could know that this minor procedure would serve as a warning that her life is in danger.  After absorbing the shock that her lymphatic system is betraying her by producing mutant cells, Mom and Dad meet with an oncologist to come up with a game plan: chemotherapy, a toxic blend of chemicals designed to kill any cell it comes across, whether it is malignant or not.  She has a port surgically implanted to make it possible to pump the poison directly into her veins.  Ironically, this life-sustaining equipment is designed so that the chemo drugs can virtually destroy her body in order to save it.  She never shows me the medical device marring her shoulder in an attempt to shield me from the full seriousness of this disease.  

Mom and Dad homeschool us because they think that it is the best option for our family.  They view the individualized attention that homeschooling provides as a valuable resource for our education.  Our parents also want to foster friendship between us and believe that having Erica and I learn together will accomplish this goal.  Mom enjoys teaching us and is concerned about the effect her disease would have on our emotional development and education.  If she died, not only would we lose our mother but we would also lose our schoolteacher.  She says that watching a child learn is a miracle and wants to see to our education firsthand.  Because I am only in first grade, the time that was supposed to be devoted to teaching me to read will instead be spent at oncologist appointments and chemotherapy sessions.  The most important time in my education would be sacrificed in the name of survival.

Mom receives her chemotherapy at the University of Alabama at Birmingham’s Kirklin Clinic.  We pass the large fountain spraying water high in the air and walk into the sliding glass doors.  My young eyes take in the well-lit foyer and look at the escalators that I love to ride up and down.  We go up the escalator and to the left, towards the oncology department.  I don’t understand the pitiful appearance our family presents with a clearly sick mother, a father trying to be strong for everyone, and two scared little girls.  I just know that the reality of cancer is starting to sink in and I’m afraid that Mom might die.  Almost every night, I cry myself to sleep while begging God to save Mom’s life.  We sit in a large hallway with high ceilings and a wall made of glass.  In the center of the room, there is tree planted in the floor.  I stare at the tree for what seems like hours wondering how someone grew a tree inside a hospital.  How is life sustained inside a place that my family dreads so much?  Life goes on, even when it seems that it is going to flicker out.  Throughout the long hours waiting for my mom to receive the life-saving treatment she needs, I alternate between looking at the tree and playing with Erica.  

Despite all this, I watch as Mom and Dad cling to their belief that all things work for the good of those who love God.  Because of this faith, she received a promise from the Bible that she would be healed.  While searching the book of Isaiah for hope, she stumbles across a verse in the fifty-fifth chapter that compels her to believe that God will cure her.  She says to us that “when the leaves clap their hands, I will be well.”  I watch her throughout the months of chemo staring out the kitchen window waiting for the wind to blow the leaves in our backyard.  She knew that when summer turned to fall, she would be made well by her Creator.  This powerful faith sustains her throughout the long hours of having poisonous chemicals injected into her port and the nights lying awake wondering what would become of us should she die.  This experience leads my mother to the realization that God is big enough to raise Erica and me and that He can take care of us, even if we did not have a mother.  God uses this revelation to give her peace to accept the outcome He has in mind.

And true to His word, in the fall of that year, my mother went into remission.  We were all ecstatic knowing that God had heard our prayers and had granted us mercy.  In my six-year-old mind, I knew that the disease was gone and would never return.  I am fully confident in this opinion because my parents taught me that God could not lie.  We celebrate during this time because Mom’s thin hair was starting to grow back, she has become stronger, and most importantly, she will live.  Sure, she had to go back several times a year to get a CT scan to monitor her health.  We are always positive that nothing will come of these biannual trips to see her oncologist.  Our pre-cancer daily routine is restored of going downstairs in the morning to do schoolwork, coming upstairs to eat the lunch Mom prepared, and going outside to play with the neighborhood kids.  Mom is grateful that she will be allowed to raise the children that God has given her.

But three years later, the cancer is back.  We make our routine pilgrimage to Kirklin Clinic, fully confident that this visit will be the same as any other.  After going through the rigors of having a full checkup, Mom’s oncologist tells her that she has a hotspot on a main artery in her abdomen and they needed to do a biopsy.  This first time I have ever seen my mom cry was when she told us this news.  I am not sure what to say to make her smile again because everything feels like vain platitudes.  Words are empty, devoid of meaning in the face of another surgery to discover whether or not the cluster of cells the CT scan revealed are malignant.  We still cling to the small bit of hope that the hotspots are not cancerous.  After all, God does not lie.  During her surgery, we sit in a waiting room that I haven’t seen yet.  The walls are a familiar hospital purple.  It seems like every part of the hospital is painted the same shades of purple, green, and brown.  Maybe the uniformity is meant to sooth the patients and their families by providing consistency throughout the clinic.  The hospital designers believe that if the visitors know what to expect behind every door, perhaps they will not be afraid.  We settle into the uncomfortable purple chairs and waited for a nurse to come tell us how the surgery went.  I alternate between nodding off and entertaining myself with games I brought.  I have learned through the years that a hospital visit without a bag full of distractions means for a very long day.  

Eventually, a nurse brings us news that she is in a private room and we could see her.  After going through a maze of corridors and elevators, we arrived at her tricolored room that matches the rest of the hospital.  We watch television on a stiff couch for hours in an attempt to distract ourselves from the reason we are in this building.  This goes on for several days before the lab results are back.  The oncologist meets with our parents in her hospital room while Erica and I sit in the waiting room.  The tense silence between us is maintained as though if one of us speaks, the happiness we’ve had over the past few years will come crashing down.  Finally, Dad comes and takes us to the hospital cafeteria.  We sit at a bistro table in the large room while waiting on Dad to tell us what the doctor said.  He looks at us from across the table and solemnly states “Your mother’s cancer is back.”  I can’t believe this.  I’m only nine years old, and for the second time in my life I am confronted with the possibility of death.  This news means more rounds of chemotherapy, additional doctor’s appointments, and another chance to lose the most important woman in my family’s life.  We hold ourselves together and go to sit with her for another day waiting for the hospital staff to allow her to go home.

Mom sinks to her lowest depths at this time.  I have never felt such despair in my short life knowing that I can do nothing to help her.  Because of the promise God gave her, Mom is plagued with thoughts that He has abandoned and lied to her.  She finds herself asking Him “if You can’t save my body, how then can You save my soul?”   This is a particularly depressing thought when one is confronted with the imminent threat of death.  She never doubts His existence but simply questions if God has lied to her.  Maybe this is a part of faith, the ability to have an intimate conversation with the Creator asking if He knows our pain and cares what happens to us.  No pretense, just an honest discussion of our emotions.  A few days after her surgery, I sit with Mom in the living room with a tense silence separating us.  Mom breaks the quiet by asking if I am angry with God.  I tell her that I’m not angry, just confused and sad.  “Why not?” she says.  “I’m angry with Him.”  This announcement shocks me because I have never heard her say anything similar to this before.  She then tells me that God is big enough to be mad at and can handle our anger.  I’m still not angry at Him, but I do go back to my nighttime routine of crying myself to sleep while praying for her life.  Lying in the dark with tears on my face, I petition Him to once again intervene in our lives.  

During this period, Dad comes home from work and tells Mom that we are not giving into despair.  When Mom wakes up in the middle of the night, they are going to pray and read the Bible until she can sleep again.  Because of this proclamation, we decide to turn to God instead of the grim picture the world gives that life lasts only for a moment and death is nothing but what happens when a heart stops.  In this view, there is no hope of eternity or a God who cares for us.  The rejection of despair allows us to feel hope again that God will work all things out.  Slowly, the melancholy mood in the house slightly lifts and we are able to see that God can carry us through another round with cancer.  We do not have to go through this without hope because God already knows the outcome of our lives, we need only to trust Him.

Later that week, her oncologist calls and asks Mom what she wants to hear.  She says that she wants to know when chemo begins again.  He emphatically states his question again and she replies that she wants to be cancer-free.  The doctor states “you don’t have cancer.”  I hear yelling coming from the other side of the house.  I run to find out what has happened and Mom is shouting God has healed her.  Her physician explains that her healing is a miracle because the cancer that was eating at her abdomen last week is gone now.  She was not put on any medicine to cause this healing nor did she have the tumors removed.  This dramatic turnabout can only be explained that while I slept one night, God answered our prayers.  I feel a profound sense of relief and realize that my mother will live to educate us, watch us walk across the stage at graduation, and send us to college.  My family has mixed emotions about this event.  Mom is ecstatic that she is healed, Erica feels relief, I’m grateful knowing that God hears me, and Dad is extremely humbled that the God who made the world has touched our family.  

 My family is far from perfect, but we belong to the Lord who is total perfection.  We didn’t have to say elaborate prayers to get God’s attention or do anything to deserve this outcome.  I don’t know why my mother was granted more time while others are not.  My only answer is that life is terminal and God is eternal.  Only He can see the ultimate picture, so we must trust that He will bring blessings out of sickness and hope from darkness.

This experience taught me that life and death are in the Lord’s hands and nothing can change that, not even cancer.  I can go through life accepting mortality because I find comfort in the knowledge that God will carry me to the other side.  I know that eventually my mother will die just like the rest of us.  She has not been exempted from the realities of life.  One day she will breathe her last and meet her Savior in person but Hodgkin’s Lymphoma will not be the cause.  When Mom talks about this time in our lives, she often says that “cancer sucks, but walking with Jesus is sweet.”  I find that this is an accurate description for life.  Sometimes it’s really hard and filled with pain, but I know that only He can create beauty in the midst of life’s troubles.    

It's My Flaked-Up Skin, Not Yours

Author: Courtney McCullough

 

I was 12 when they told me the news.

My skin would never be the same, wouldn’t be normal.

“There’s no cure.” The doctor said.

“You’ll have it forever.” Said a nurse.

But what is ‘It’?

 

It is the bane of my existence.

It has caused me to feel so ugly and disgusting.

Like a leper from biblical times.

 

This only got worse my senior year, that last year of high school.

A flare up occurred, triggered by stress of growing up.

Of moving away. 

Of becoming more.

 

I flared up.

Skin turning red and blotchy. 

Scales forming.

From my head to toes.

Even in my ears and on the soles of my feet.

Even on my breasts, my stomach, my ass.

I was covered.

 

My classmates saw. 

They looked at me, disgusted.

They started a saying, thinking they were cute.

“She has Skin Ebola, look out.”

I’d hear it all the time.

Even the teachers who should know better, just stared.

 

I stayed home from school more than ever.

I missed about 10 days. 

The most I’d ever missed.

All because of cruel kids and a cruel skin disorder.

 

Why couldn’t they understand?

I can’t control my skin, it has a mind of its own.

I can try, try to stay calm, meditate and pray,

But it still happens.

 

I tried everything.

EVERYTHING.

Home remedies, lotions, shots, creams,

Even changed my soaps and detergents. 

Nothing worked.

My skin remained ugly.

 

My own mother looked at me with pity.

She always spoke of how it was getting worse.

How awful it looked.

 

They didn’t understand though.

No one understands. 

It doesn’t just look bad.

Looks aren’t everything.

Psoriasis does more than look bad.

It hurts.

Mentally, emotionally, and physically.

 

Those scaly patches?

They peel and bleed.

They get sore.

They get on your joints, making every movement painful.

 

It’s exhausting. 

My skin is literally fighting my body.

It takes energy to create new skin cells, 

Even if they aren’t necessary.

But it happens.

And it wears me out.

Makes me sleepy.

Makes me tired and weak.

 

Then of course,

There’s the hearing issues.

The skin in your ears can turn psoriatic.

I’ve had to get my doctor to clean my ears,

Taking out massive chunks of skin.

No wax, just skin.

Skin that shouldn’t be there.

 

Looking in the mirror to prepare for the day?

It was impossible.

I hated how I looked.

I was ugly.

Scaly and red.

I looked as if I’d been burned.

I was so ugly.

Who could care for me?

No wonder others gave me such dirty looks.

 

I had anxiety attacks.

You would never guess,

But Psoriasis and Mental Illness,

They go hand-in-hand.

With each new scale that appears,

A worried thought occurs.

“What will happen now?”

“What will be said?”

“When will this be over?”

“When… When will I die?”

 

Then a miracle happened.

I was able to try a new medicine.

One that worked.

A pill. 

My skin was cleared.

Not overnight,

But within weeks.

I looked normal.

Normal.

 

I’d forgotten:

How beautiful I am when I smile, 

How lovely my skin looks in the light,

How healthy I look.

Because of a few flakes,

And a few dirty looks.

 

What would I say if I could see them again?

The ones who looked at me as if I was a monster?

 

It’s my skin.

Sometimes it misbehaves. 

Like a child.

It thinks it’s protecting me

From some unknown enemy.

So it raises my defense, creates more skin.

It tries to keep me safe.

 

It doesn’t realize how it looks.

How ugly it makes me feel.

How painful it is.

All it thinks of

Is that there is an enemy.

An enemy that needs to be stopped,

And stopped quickly.

 

Psoriasis.

It’s an autoimmune disorder.

I can’t control it.

I can try to treat it,

Can try to calm myself down,

Avoid triggers,

But it can still flare up.

 

Psoriasis is not:

Curable.

Contagious.

Or easy to deal with.

 

It’s a burden for life.

Something I’ll always have to 

Treat and hope stays ‘in remission.’

 

It’s hard to live with,

Knowing the stigma.

Knowing how the dirty looks hurt.

How the words cut deep.

How the media and people expect

‘Beautiful’ people to look.

It hurts and it’s harsh.

 

People say they feel bad.

They pity.

They try to give advice.

 

Want to do something that is actually useful?

Stop acting repulsed.

Stop acting like it’s contagious.

End the stigma.

 

Millions of Americans deal with Psoriasis.

Some deal with it better than others.

Help make it easier.

Don’t stare.

Don’t point.

Ask questions.

Spread awareness.

 

End the stigma.

Stop the shame.

Help us to help ourselves

Realize that we are beautiful too.

 

And if you feel you must be nasty.

If you feel that you must give say something like

“Why don’t you take better care of yourself?” or

“My cousin’s friend uses this, it was cleared overnight.”

 

Remember this:

It’s my flaked-up skin, not yours.

Feels, xo

Author: Mira Nugent

This year I am a full time college student who hasn't missed a single class and I've been trying from the very start to make better grades. I may not have studied as much as I should but at least I got out of bed togo and take the test and when I finished, the biggest smile spread across my face as I waited for my friends to finish theirs. Am I hundred percent sure that I passed with flying colors? No. But I can guarantee that I didn't fail.

Not only am I a full time college student, I also work full time. When I was in high school I made a comment to Aaron that I will never work in fast food and I will never apply to Piggly Wiggly. Now that I've been there for a year and a half, I don't know what I was thinking. I started at the bottom and it was hard because I got crappy hours. I've been with this store for a year and a half and I couldn't be any happier. I love my coworkers and I love the customers, even the ones who think that I am part of the machinery. It's all a learning experience and what I learn there, I apply to my everyday life. Many people ask me what I plan on doing after school because who would want to work at the pig forever. I don't plan on being there forever but I don’t plan on leaving any time soon. The Pig has done so much for me and I can honestly say that.

I am not writing this to make stabs at Aaron or to make people feel sorry for me. I'm writing this because I want to inspire people. I don't want to be your hope but I want you to understand that it gets better. I am honest and I take chances. I make mistakes and I try to fix them. I still want to just stay in bed and avoid the world but I tell myself to get up because there are bigger plans at play here. I know it is harder than that but if you can at least say that you're trying then I would call that a victory.

We're all human, we all make mistakes. 

We're all humans, we are all beautiful.

We're all humans, we all have someone who admires us.

Please take this for what it is. It's not a cry for help but a victory scream. This past year I have experienced so much and I'm glad that I had the chance to feel all of it. Please know that you aren't experiencing anything alone, there is always someone there. Always

 

Miranda, xo

Candy Corn

Author: Ryann Taylor

There is no candy more disgusting than candy corn. Not only does it not actually resemble corn, it also has a sandy texture that makes it crumble in my mouth like a piece of dirt. Yes, I have put dirt into my mouth before like any normal almost-five-year-old would, and in case you are wondering, no, it isn’t good.

    So today on this most horrible of days, the principal of my preschool has decided to bribe me to risk my life with none other than, you guessed it, candy corn.

    “Ryann, if you flush the toilet I’ll let you have a piece of candy corn.”

    She sounds nonthreatening if you don’t look at her pursed lips and her beady, black eyes, but I do. She stays perched in her big, cushy blue chair behind her desk. Her hands are folded on top near scattered papers I couldn’t read, even if I could see the tops of them, and near one solitary picture frame. The most hideous thing of all is the clear jar on the corner of her desk that contains the candy corn; it’s still only half-way filled like it was the past two months I’ve used the bathroom in her office.

    “Ryann…?”

    My fingers reach for my left pigtail, and they give it a slight tug. I let my fingers slide through the hair my mom brushed out this morning and put into two separate ponytails—pigtails.

    “No thank you;” I smile like my mom tells me to when I say no to something I don’t want to do. The principal’s lips are still in a tight line. Maybe she didn’t see me smile since her desk is so tall.

    I’ve used the bathroom. I said “no thank you.” That’s all there is to do. My new Velcro shoes flash as I take a few steps to the door, but a blue-jean clad thigh blocks me. Farther up from that thigh is a plaid shirt and the sympathetic face of my pre-school teacher.

    “Excuse me.”

    She doesn’t budge. I don’t get it. I said “excuse me.” 

    “Now, Ryann, you can either flush the toilet or I’ll have to call your mom.”

This is coming from behind me—from behind a tall desk.

“We’ll still give you candy corn,” my teacher croaks, smiling at me like candy corn is going to convince me to risk my life. I swivel and my shoes flash again to look at the principal.

Principal beady-eyes makes a “cheese” face at me. Her fingers are still tapping on her desk. The door to her bathroom is cracked how I left it a minute ago, and the neon, skittle-yellow light pierces my eyes. 

“Will one of you go in with me?” I beg, feeling my fingers reach again for my pigtail.

Beady-eyes shakes her head. Her “cheese” face is gone. The line is back on her face.

“What if something happens to me?” My feet begin to shake as they think about what they’re going to have to do.

“Nothing is going to happen to you,” beady-eyes sighs and stops tapping her fingers to motion towards the bathroom door.

“I’ll wait here,” my teacher promises behind me. Like she cares. She’s the one who wouldn’t let me out of this stinking room.

If they were to call my mom would she defend my precious life? Who would do the dusting for her if I didn’t survive? Who would take my toys? Then again, my mom makes me flush at home. The toilet at our house isn’t as—

“Ryann? Do we need to call your mom?”

I shake my head and take the wobbly, flashing steps it takes to get into the blindingly bright bathroom. I push the door further open just in case I get sucked in; one of them will see me and pull me out. I hope.

The stool I had just used a minute ago sits beside the toilet, waiting for the toilet to take its next victim. Maybe I’m being dramatic. That’s what my mom always says. I would think I was being dramatic too if I hadn’t witnessed the toilet’s loud roar and how it spits water while eating my pee and toilet paper.

Why does it like toilet paper anyway? I’ve tried it before. It’s not so great. It just tastes like dusty paper.

    My hands press against the chilly, brick wall as I place one foot on the stool carefully. I don’t want to wobble and fall in. Then I’ll definitely be a goner. 

    Inside the toilet there’s still pee with a now soggy string of toilet paper sitting on top. I’m going to have to set my hand on the seat to reach the lever. 

    “Can you see me?!” I yell outside before I take the risk.

    “Yes.”

    That’s all? They’re not concerned?!

    I set my hand on top of the shiny, silver lever and push down.

    I jump back as it roars and swirls and spits at me. 

    I land on the tile floor with my body in a bridge; hands on the floor, feet on the floor, tummy in the air.

    I walk out of the bathroom, not looking at the principal.

    My teacher smiles down at me. She places her hands on her thighs so she can bend down; “good job! Now you get candy corn!”

    Before I can even protest, the principal has left her desk and is by my side with the clear jar half-way filled with old candy corn.

    “You can take three pieces,” the principal shoves the jar in my face, and I don’t know what to do—other than take three pieces of candy corn. I count them out. One, two, three. They sit in my hand, cool and hard. 

    I look over at my teacher and her face is beaming. She nods at me. 

    I’ll let her have the satisfaction. I place all three pieces in my mouth and take a cautious bite down. It’s just as sandy as I remember.

Those We Never Remember

Author: Audrey Bearss

Were we special? No, oh no. We were forgotten, in the backwoods of the South doomed to community colleges and thrift store jeans. Yet we were perfect to each other. We drew on our eyeliner way too thick in dirty mirrors with an image of Joan Jett pulled up on somebody's cracked iPod in the corner to compare; as we crowded the tiny church bathroom well past maximum capacity. Pictures of some summer romance tucked in CD cases hidden in our book bags to trade. Dollar Tree lunches shoved down before the football smacks someone in the face. Amoung the dead of the cemetery we sit. Telling them our stories and imaging who they were. Homecoming queens, nerds, and rockers. Sprawled out on hot hoods as The Rolling Stones invade the parking lot and three chicks pound the diesel truck's hood in rhythm cause we're too young to drive and too bored to go inside. Ripped away by the month of May, only to be remember when a leg from a wreck goes numb, an Algebra I formula appears, or a tattered old guitar magazine is found in the depths of a closet.

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