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Showing posts with label sons. Show all posts
Showing posts with label sons. Show all posts

Friday, June 8, 2018

Sequence

by Sarah Belliston

Ever since my son Jack could walk, he’d head to my bookcases and pull the books from the shelves into a pile. Sitting there like a hen hatching chicks, he’d pick a thick volume and set it on his outstretched legs. He’d turn it sideways so the weight of the book rested on his feet and the cover opened into his lap. Then his dexterous middle fingers would run along each side of the book, catching just one page, and flip it down. One by one. Over and over. When the book was finished, he’d turn it around and repeat the process. My family joked that he was reading; I joked that he loved books as much as I did.
At eighteen months old, a team of doctors diagnosed Jack with autism spectrum disorder.

A hybrid is something born from two different species, or a composite built from two different things. Hybrid cars are supposed to be good for the environment. We would not have the purposeful inventions of the liger, the tangelo, or the blood lime without hybridity. (Lions and tigers do not live in the same areas so the crossbreed of the liger has only been documented in captivity.) Because of their genetics, these hybrid animals are often, though not always, infertile.
At conception, the DNA of each parent is put into a blender and cut into pieces, so the child gets a unique mix of the parents’ chromosomes. When those chromosomes merge to make sequenced pairs, they can only match with the same structure. Different species have different structures, but related species like zebra and horse or citrus fruits have enough in common to make a hybrid. In plants especially, the seeds sometimes carry the genes for multiple colors or varieties. Depending on how the plant is pollenated, a recessive color could become more common despite being he recessive trait. When the seed grows up to have the same desired trait as the parent plant, gardeners call this being “true to the parent.” Many genetic probabilities work the same in plants as in humans. These probabilities can sometimes be determined by a Punnett square.
For example, my husband, Scott, has a genetic blood disorder called hemochromatosis. Two of his five siblings also have the condition, which is relatively mild as long as you know you have it. Those with the disorder absorb too much iron, which can cause liver failure if left unmanaged for too long. Another relative had hemochromatosis and developed cirrhosis of the liver late in life, never once having drunk alcohol. My husband has to get his iron levels tested every few months. When his iron becomes too elevated, he donates a pint of blood, which makes the body produce new blood, which in turn uses up the high iron levels and returns his system to normalcy.
Before we married I took a blood test and found out I carry the recessive gene for hemochromatosis. One study estimates that ten percent of Caucasian people are a carrier, and one in 200-500 develop the disorder. Our Punnett square looks something like this:

Sarah h

Sarah H
Scott h
hh
hH
Scott h
hh
hH








Each of our future children would have a fifty percent chance of having hemochromatosis and a one hundred percent chance of being a carrier.
My mother asked me if I was okay with these odds. I said yes. I married my husband. His genes mixed with mine and the sequence of our combined DNA made a hybrid, what we thought was a good hybrid with smiles and laughs and ten fingers and toes.
I considered the known problems, but I didn’t think of the unknown. When autism appeared, I wondered what our Punnett square would have looked like. And what my decision would have been.

Some autistics have symptoms from birth, while others go through a type of regression, usually before the age of five. This regression involves a breakdown of neural pathways in the brain that can affect communication and sensory perception. Some regressions happen overnight; parents wake to find an autistic child in their neurotypical child’s bed. This kind of regression produces the common metaphor of autism as a kidnapper that has stolen the child.
Other autistics, like my son, regress slowly, so slowly I couldn’t tell you exactly when it started. All I remember is that after his first birthday I noticed more and more signs. By his fifteenth-month well-child visit I had to admit he hadn’t met any of his communication milestones. At the hearing screen a month later, I watched him lick the hinges on the door as the specialist said, “Have you considered autism?”

Science doesn’t know why people develop autism. A Punnett square is impossible. There may be a genetic component, but if so, scientists have identified over 200 possible genes that could mutate in multiple ways and result in a spectrum disorder. My most recent talk with a geneticist said they can identify a genetic cause in less than ten percent of cases. The identification success rate gets even lower when the autistic does not have intellectual delays. I think of Jack and how he did first grade math at four years old. Testing him wouldn’t give me any more answers. My husband’s sister was diagnosed with Asperger’s after we were married. Her son, who is a few years older than Jack, is also autistic. It was in the sequence all along.

There is no cure for autism. Instead there is what I like to think of as “symptom management,” which usually consists of behavior modification therapy. This therapy focuses on substituting wanted behaviors for the isolating repetitive actions autism is known for, like replaying the same five second portion of a video 200 times or flipping pages in a book for hours.
Jack started behavior modification soon after diagnosis. When he was almost three, we decided to stop. Behavior modification works amazingly for many, but it didn’t work for Jack. The therapy had made his behaviors worse and caused a larger regression. Before using behavior modification, he mainly ignored my attempts to interact with him. After the intervention he would lie down and will himself to sleep in order to escape unwanted stimulus, i.e., me.

Six months later after we stopped behavior modification, Jack was more interactive with me but we weren’t making any progress on his communication. I travelled across the country for a weeklong training on a different kind of therapy based on relationships and social communication instead of deterring behavior.
The program is called Son-Rise and has a reputation in the autism community for the claim it can cure autism. I was more interested in the therapy because it focused on attempting to understand the purposes behind the autistic’s actions. The program also has the central idea that the reward for social interaction should be the joy of the other person, not a treat or motivator (as in behavior modification). So, instead of a cue to look someone in the eye, the parent/facilitator acts in a way that makes them interesting to the autistic and then rewards any glance with an overexcited response. In essence, they teach the autistic how interaction with another human being can be fun.
By the end of the week, there were many things about the program I knew would not work for my family or my child. To complete the program with fidelity, you need a dedicated playroom where the autistic stays for eight hours a day while different volunteers rotate through, ensuring that every moment is maximized for therapy and the environment is controlled to decrease the likelihood of surprises for the autistic. I could do the gluten-free and casein-free diet they suggested because Jack only ate a few items anyway. But when they told me to take away screens, I balked. Since then, I have come to see the wisdom in their words. Some autistics, and some neurotypical children, have delicate nervous systems that cannot handle the input from a personal, interactive screen. They become isolated, irritable, and have frequent meltdowns. However, Jack is not one of those kids, at least not yet.
So when I came home, I adapted the new therapy to our family and my son. We used our whole house as his playroom and tried to be observant and ready to interact with him all the time, instead of just for set hours. I saw an immediate increase in Jack’s eye contact and verbal communication. When I slowed down and focused on his reactions, he gave me more of them. When I flipped pages next to him, he stopped flipping and came over to take my book, which would turn into a game of passing books from one pile to another. Our “game” was a baby step to interaction, but leaps ahead of where we were before. Our future suddenly looked brighter, and the trip we’d planned to visit my brother across the country looked brighter too.

At the Son-Rise training, one female facilitator told a story of helping a child to say their first word. When she tried to celebrate with the parent afterward, the parent denied hearing their child speak. The session had been videotaped, and the trainer said she had to play back the tape three or four times before the parent could hear what their child had said. When I heard this story, I wondered how it was possible for a parent to ignore auditory evidence, but on that trip to visit my brother, I found out exactly how it could happen.
Sometimes Jack connects with people right away. When we got to my brother’s apartment, Jack connected with his then twelve-year-old cousin, Tyson. A good big brother to three younger siblings, Tyson happily sat with Jack in front of the television. They watched the credits of a show scroll by, and Jack supplied a steady stream of what I thought was gibberish. Tyson said, “I think he’s reading the names. I can almost understand what he’s saying.” I brushed off the idea immediately. I had heard this gibberish plenty of times when Jack stood in front of our television at home or flipped pages in his books.
Later that night I sat on the floor next to Jack as his three-year-old hands and eyes concentrated on an iPad. He had gotten into an ebook app and was flipping the digital pages as fast as he could. A steady stream of gibberish accompanied the motion. I thought about what Tyson had said. I scooted closer. Jack’s gaze was fixed to one spot on the screen, the top left corner of each page. Staring with him, I listened again and it was as if a translator had been slipped into my ear. All of his gibberish suddenly made sense. I heard “the,” “and,” “this,” and “can.”
Jack was speaking.
Jack was reading.
His sequence was wrong. He read the first word of each page instead of left to right and top to bottom. He read heavy volumes instead of picture books. But there was no denying it anymore. I wondered how long he’d been reading, how long I had been unable to hear.
I felt for those other parents, the ones who didn’t understand their child’s first word. Maybe their child was like Jack who, I realized, often dropped consonant sounds, so “pig” was a short i sound and “horse” was “ohss.” Maybe the parents were like me and couldn’t believe their child spoke because the action was tied to something unimaginable, like a child who could read before he could speak, or like understanding that autism doesn’t break someone’s brain, it only makes them process information in a different sequence.

In critical disability studies, there is an “affirmation model” of disability. The idea is that society and culture have trained people to view and portray disease and disorder as negative and pejorative. This model analyzes literature that highlights the good events or actions that wouldn’t otherwise happen if disability didn’t exist. Words in the Dust is a novel that tells the fictional story of an Afghan girl with a cleft palate. The deformity allows her to pursue an education, whereas fixing her cleft palate would result in marriage and little opportunity for learning. In John Elder Robison’s memoir, he writes how his undiagnosed Asperger’s allowed him to understand machinery in a way that led him to create pyrotechnics for KISS after he dropped out of high school. Naoki Higashida, a nonverbal autistic, writes in his book that taking away his autism would fundamentally change who he is as a person.
After reading these stories, I wonder if autism will turn out to be a positive or a negative for Jack. I’m not sure what about Jack is his autism and what isn’t. I don’t know if his ability to match his voice to any melody or sound would still exist without autism, or if his laugh would still bubble up from his center and spill over into everyone within hearing distance. Would his unusually blue eyes still twinkle? Would his gaze still make people stop and pay attention if it was more frequent?

In truth, I don’t know if my husband’s gene pool caused my son’s condition, gifting him the particular sequence that resulted in his autism. There are more members of Scott’s family with autistic qualities, but it could be something in my genes that is hidden in me but manifested in Jack’s hybrid sequence. A theory called the female protection effect thinks that genetic mutations must be more severe to cause autism in women, which means that I could have passed on faulty autism genes to my son without having any symptoms myself. Another study found that copy number variations (where sections of DNA are repeated and the number of repeats varies between people in the population) are more commonly passed on from the mother’s egg than the father’s sperm. At least for one specific area called the 16p11.2 region, found in about one percent of people with autism. However, the study points out that simply having a mutation in this area does not mean the individual will always develop autism.
At this point in the research, it feels to me like it’s just as likely that everyone has a gene that could result in autism. Autism affects almost every family I know. Some more than others. One in fifty-nine children are diagnosed on the spectrum in the United States. The statistic just changed in 2018. The rise is attributed to the growing number of mild forms of autism getting an official diagnosis. An article I recently read talked about the detrimental part of having a genetic profile. Two individuals with the same sequential defect can have very different outcomes. Genetics do not determine prognosis, and yet if parents know of a serious mutation, they may think their child is not capable of progress.
After diagnosis, the thing I most wanted was for someone to tell me that my son was capable of learning, that spending hours and years trying to teach him would result in success. I didn’t want to put him or myself through the hardship of therapy without a guarantee. If he lacked ability, maybe the kind thing would be to leave him happily sitting on the floor alone with his books.
Maybe he was happy there by himself, but I also know that he was happy when a few months ago he wrapped his little arm around my neck and gave me a kiss for the first time.
Even so, I am going forward with more genetic testing. If there is an answer in the sequence, I still want to know.

I used to think that autism appeared one day and changed my son. When I began this essay I wanted it to be about how my son was a hybrid of himself and autism. But really, autism was part of him all along. I am the one who has become the hybrid.
I spent my life before Jack unconnected with autism. Now, it is my life: in my life, my house, my writing, my brain, and my heart. I begin each day thinking of autism. I’ve become the autism lady, always ready to regale people with my laundry list of facts and opinions. Now those opinions include the possibility that perhaps my son has benefited in some way because of his hybridity, his sequence.
Moments are more important to me now than milestones. I judge my success as a parent, and Jack’s success as a child, not on achieving the goals we set, but on attempting them. I have hope and am more willing to entertain the impossible. If I had never thought my son was capable of reading, I would not have been listening, and I never would have heard his words.

Sarah Belliston lives in Utah with her family while she attends BYU for her MFA in Creative Writing. She loves a good book, a good movie, and a good musical but hasn't figured out how to do all three at once. 

Wednesday, February 14, 2018

Those Boys

by Susan Moldaw

          Despite my skepticism, about a year ago I went to see a medium at a mindfulness spa in Arizona. The medium met me in the hotel lobby and led me to a small, windowless room with two straight-backed chairs and a desk between them. We sat and faced one another across the wood divide. She had full cheeks, a snub nose, and a blond bouffant that fell blowzily past her shoulders.
           “You’re here because your father wants you to understand he’s with you all the time,” she said. Her clear voice conveyed authority. She tapped her high-heeled sandals against the concrete floor.
          I reached for the box of Kleenex on the desk, my rational mind already a muddle. My father died five years ago.
          “Is there a Bill in your life?” the medium continued, looking dreamily off to the side with a slight upward curve of her lips.
          “That’s one of my sons.” I drew in my breath.
          “He talks to your father. Out loud. So do you.” She smiled kindly. “Your father wants me to tell you that he hears you.” She cocked her head and looked away. “Bill is doing well. Your father says he’s proud of him.” She frowned. “Wait. There’s another son. You have others?”
          I nodded. “Triplets,” I said. “They’re twenty-four.” Bill, Jack, and Stuart.
          “He’s telling you not to worry about them. They’re going to be okay.”
          I dabbed my eyes with the Kleenex. My father hadn’t liked my sons’ father—my ex. We’d suffered years of family drama, divorce, and the aftermath, and all along my father reassured himself—and me—that his grandsons would be okay.
          The medium smiled. “He’s a funny man, your father,” she said. “Good looking too. Wait! He’s putting his hand over his heart.” She laughed softly and said, “He loves those boys.”
          I wiped my eyes and mumbled that I knew.
          I stumbled out of there towards my room, clutching Kleenex, but by the time I slid the electronic key card into its slot and had flung myself face down onto the quilted bedspread, I was furious at the medium’s presumption. I didn’t need her meddling. I’d felt my father’s presence many times since his death. Except, I wished I could tell him that, despite everything, the boys and I were doing fine.

Mauna Kea Beach Hotel, Hawaii, 1992

          From the patio adjoining our beachfront rooms, I saw my four-year-old sons curled up on their grandfather’s—my father’s—lounge chair, stationed by itself in the middle of a vast lawn that stretched from our rooms to the beach. He was leaning back, smoking a fat cigar, and the four of them were laughing. A breeze ruffled palm trees that lined the grass along the long, curving, fine white sandy beach. The pungent, noxious odor of the cigar wafted to my room. This was our family’s third Christmas vacation with my parents at the Mauna Kea.
          What the hell is he doing smoking in front of them? I thought.
          Inside the room, I took smoked salmon and a bagel from the minibar. Breakfast was included in the hotel’s costly charge and—following my father’s example— we’d order extra from room service, stashing salmon, kippers, cottage cheese, bagels, muffins, papaya, berries, shrimp, and tomatoes in the bulging minibar.
          “At least we’ll save on lunch!” my father would say.
          My mother, deferring to his humor and what she deemed his superior judgment about money, life and family, went along too, as she mostly did, though since his death she runs her own show.
          Back on the patio, I ate while watching the lawn scene. My father sat up and the boys jumped off the chair, sprawling at his feet. He leaned over and traced something in the air just above the lawn, using the cigar as pointer. His navy T-shirt hung loosely over red bathing trunks, his straw hat lay on a towel. He always brought the hat Hawaii-bound, stowing it in the airplane’s overhead bin on top of his neatly folded navy blazer, finally plopping it on when we disembarked.
          I stopped eating and walked over.
          “Dad, can I talk with you for a minute?” I said.
          We walked slightly away from my sons. My father smiled and familiar grooves appeared along his eyes and cheeks. His brown eyes were serious.
          “Yes?” he said.
          “I don’t want you to smoke in front of them,” I said. “It sets a bad example.”
          He held the cigar behind his back. “Is your mother around?” She hated his occasional cigars and for years he hid the evidence, until he finally stopped smoking.
          “She’s at the hair salon,” I said.
          He took another puff. “They know I’m not really a smoker,” he said, just loud enough so the boys might hear. “Besides—I’m telling them about the facts of life!”
          I looked at my sons. Jack and Stuart were giggling and rolling on the lawn, silly together, as they often were. Bill was sitting quietly, with his head turned, trying it seemed, to catch the conversation.
          “The facts of life?” I said.
          “Not that.” He spoke more loudly, so there was no mistaking they could hear. “Hard work and discipline! Good values! All the things that matter.” He gave me a kiss on the cheek. “They’re good boys,” he said. “They’re going to be okay.”

San Francisco, California 1997

          My husband, nine-year old sons, and my parents were eating dinner at the Matterhorn, a cozy, wood-paneled restaurant that reminded my husband and me of our vacations spent hiking in Switzerland, both alone and with our sons. Cheese fondue bubbled in a brass pot on the white linen tablecloth. Everyone’s plates were stacked with sourdough bread. One of our sons stood in front of my husband, his face white, his eyes wide and terrified, while my husband berated him for spilling water. The other two stared at their plates, knowing any one of them might next become the object of their father’s anger. My father watched briefly with a set expression, then looked away—unable to stomach the humiliation of anyone, least of all his grandsons.
          A few days later, my father told me, “I can’t keep watching him tear those boys to shreds. Have dinners without us. We’ll visit when he’s not around.”
          We sat in our family room on a deep, red corduroy couch. My husband was out of town and my parents had dropped by. My mother was upstairs with my sons. I was struggling—privately— with my own decisions—leave the marriage, stay? What would do the boys the least harm? No options were good. My eyes fell to the white wool carpet. “I need you, Dad,” I said. “Please come with us, sometimes.”
          Wind rattled the old paned windows behind our heads. Bare tree branches tapped their code on the wavy, rippled glass. My father leaned into the softly textured pillows. Then he patted my hand.
          “I’ll be there,” he said. His voice was kind, his eyes, sad.
                    
          Five years later, I finally got out, in a contentious divorce that went to court, where a judge ordered my sons to attend Connecticut boarding schools for their first year of high school. They’d only applied to boarding schools to satisfy their father. My attorney asked for a stay, and a week later I brought the boys to testify. One by one they took the stand. They wore button down white shirts, khaki pants, and white athletic socks bulging out of their brown loafers. They looked impossibly young.
          Jack and Stuart said, no, they wanted to stay in San Francisco and didn’t want to go to boarding school. Bill said his father told him he’d bring him home on weekends, and if so, boarding school would be okay. Bill trusted his father’s promise; Stuart and Jack doubted.
          I rolled my eyes. Home to San Francisco from Connecticut on weekends. The judge and I locked glances. I felt certain she read my hollow-eyed plea for her not to send my sons away.
          A week later, determined to get them out of the marital fray, she upheld her prior order and sent them to three different high schools in Connecticut.

          I visited my sons midway through the first term in October for conferences and vacations. I walked into Stuart’s dorm room at dusk and found him ensconced on a bottom bunk, leaning against the Indian bedspread that covered the wall behind him.
“Well?” he said, looking at me from the darkness. Stuart had had enough of boarding school; they’d all had enough. My sons were counting on me to bring them home.
“I’ve changed my mind. Boarding school is the best option.” My voice cracked. “There’d be no peace in San Francisco.” Their father and I agreed on nothing.
Shadows darkened, obscuring Stuart’s expression. A door slammed, somebody turned up the volume on a stereo and Metallica blasted. Stuart got up and picked a gray hooded sweatshirt off the floor.
“Whatever,” he shrugged, pretending he didn’t care, though I knew he was angry. He pulled on the sweatshirt and we left for dinner.
Bill understood boarding school was for the best, when I told him; Jack was resigned. No one had come home on a weekend.
“You’re doing the right thing,” my father said later, in San Francisco. His encouragement loomed large for me. He was determined to step into the void left by my sons’ father. He and my mother were already making plans to fly East to visit each school in February on Grandparents’ Day.

          The four years of boarding school melded into one long visit East for me and my parents, punctuated by the boys’ school breaks and summers in San Francisco. My parents would meet the boys and me in Connecticut or New York; sometimes they met the boys without me, usually one son at a time because their school calendars differed. In New York, we always stayed at the Regency Hotel. I had stayed there years before with my parents during college, and later, on business. The Regency had morphed in style since those days, from Louis Quatorze to business sleek. Dinners were at Gino’s, one block over from the hotel. The Maître d’ greeted me and my mother and shook my father’s hand, calling him by name and bringing him a Grey Goose vodka, and the boys each a Roy Rogers. Breakfasts, my father and the boys ate around the corner at the Viand Coffee Shop, my father always having scorned the Regency breakfast as overpriced, though my mother and I ate there. My sons told me how they perched at the counter with its view of Greek cooks yelling orders, frying eggs, and making to-go bags at the register. On one of their trips they coined an expression, “LBTJ” (let’s blow this joint), a phrase they employ to this day in honor of their grandfather. Always, at the end of a visit, my father smiled and shook his head.
          “Those boys,” he’d say to me, “they’re going to be okay.”
          We were lucky that their high school graduations fell on separate days, during two consecutive weekends at the end of May. In April, my father and I took all three boys shopping for graduation suits at Paul Stuart in Manhattan, where years before my dad had shopped with my now ex-husband. The manager fitted their jackets and pinned their trousers. Afterward, we went to the shoe department, where my father insisted on buying the boys expensive dress shoes.
“They’ll last a lifetime,” he said, well pleased, as if a good pair of shoes could protect his grandsons from the vagaries of life.

 The summer after the boys’ graduations, my father called to tell me in a cheerful, matter-of-fact voice that he had cancer. “It’s a question of attitude,” he asserted. “I’m going to beat it.”
I wasn’t worried. He was invincible. A few days later, my mother phoned, using the voice she reserved for emphatically stating her husband’s needs. “Your father must hear from his daughters every day,” she said. My sister, in Santa Fe, said she had called to tell her the same thing. I felt slightly more concerned about his health then, but thought this was just my mother’s usual overzealous protection.
Nonetheless, I began daily calls and weekly visits to their home in Atherton. One Sunday my father and I drove to a small strip center a few miles from his home for non-fat frozen yogurt. He wore his favorite navy-blue sweats and a baseball cap. Now that he was retired from a lifetime in the retail business, he had time to kibbutz, and he quizzed the manager about sales figures.
“Terrific!” he said, learning that business was outshining last year’s. We ate the yogurt in the car and rushed home to watch the start of his beloved Washington Week in Review. In his library office, he settled into the leather recliner, and after a few minutes, I looked over. He was snoring under his mohair blanket.
That winter, he announced he was cancer-free, and I was elated. My parents spent a joyous two weeks with my sister and her family in Hawaii. But soon after they got home, the cancer popped up in a new spot.
I asked the cancer surgeon why. We stood in a long hallway at Stanford Hospital. My father was getting radiation treatment.
“It’s an invasive cancer,” he said. “You knock off a few tumors and new ones take their place.”
It flashed through my mind that maybe he wasn’t going to beat this disease, but what I mostly thought was how discouraged my usually optimistic father would be—good news followed by bad, on and on. I must have looked dejected because the surgeon touched my arm and said, “It’s tough.” He had invented a cyberknife and had used it to remove tumors from my father just months before. “I’m going to invest!” my father had said, after the operation. He loved all things entrepreneurial.
In May, after their first year of college—Bill in LA, Stuart in Massachusetts, and Jack in Florida—my sons flew home. My father was spending most of his time in bed by then, worn out from his radiation treatments. I picked the boys up from the airport and drove to my parents’ home. I was worried about how my sons would react to seeing their gaunt and ailing grandfather, but they went straight to his bed and got under the covers with him. Later, after they left, I walked into my father’s room. He patted the bed. I sat down and leaned close. His expression was earnest, the way it always was when he spoke from the heart.
“Those boys,” he said. “They’re going to be okay.”
After a week of sleeping at my parents’, one night I went home to take a breather. The next morning, I returned to take my father for his radiation treatment, but when I got there I saw that he was sleeping heavily and knew I’d never get him up for the appointment. I went to find my mother. We stood uncertainly by the side of the bed. My father’s chest rose and fell. I grabbed the phone and called his doctor, and then a hospital transport service. I phoned my sister. “Come now,” I said.
A few hours later, three men with a gurney came into my parents’ bedroom. They went to the bed and lifted him. My father cried from the pain in his back. They put him in the ambulance and my mother went with him. I followed behind. Midway to the hospital, sirens started. Someone stuck a hand out the ambulance window and waved at me to follow. We sped to the hospital and they whisked my father into the emergency room. By now, my sister had arrived.
In the emergency room, my father perked up when the doctor asked him who the president was.
“George Bush, the bastard!” he said.
He spent three days in the hospital, hooked up to machines. My sister, mother, and I took turns staying overnight. My sons came and went. My father mostly slept, breathing through a plastic mask. One afternoon, I was standing in the hallway with my sons. A nurse rushed out. “He opened his eyes!” she said.
We filed into the room. One by one we went to his bedside to say good-bye.
“I love you, Dad,” I said. Tears streamed, though I knew he didn’t want to see me cry.
His eyes were warm and kind. “I love you,” he said, through the plastic mask.

The day of my father’s funeral, the sun shone and the air was cool. The boys wore their graduation suits and shoes. My mother, sister, sons and I each put a rose into my father’s grave and a shovelful of dirt. At the end of the service, as everyone was leaving, I looked at my sons. They stood in a group hug, their arms around each other, their heads and hearts close. They’d grown into loving young men—straight shooters, too— like their grandfather.

A few years before he died, my father walked into my home office in San Francisco. The bookshelves were filled with photos of my sons.
“There’s no photo of us!” he said, referring to himself and my mother.
He was wrong. There was one photo hidden behind my sons’ photos. How little I understood, then, that someday I’d long to see my father’s smile, his eyes, his face. There are many more photos of him now. There’s a picture I particularly like from Stuart’s high school graduation. He and my mother flank Stuart, who has a big unlit cigar stuck in his mouth. My mother’s pearl earrings and gold and ivory carnation pin sparkle. My father and Stuart are both wearing silk twill ties, my father’s an all-over pattern of yellow and white ovals on a red background, Stuart’s a red and white stripe. They’d bought them together at Paul Stuart. My father looks pale behind his oversize sunglasses. It was a broiling Connecticut day. He’d had cancer then, but we didn’t know it.

I woke in the middle of the night in tears two months after my father died. I had the start of a eulogy for his memorial service. On the small notepad by the side of my bed, I wrote, ‘When my heart broke, his heart broke.’

          I sometimes stay at the Regency on visits to New York. One time, I took Jack, who transferred to a college there, to see the musical, The Book of Mormon. Afterward at the hotel, Jack did homework sprawled on the enormous bed. He talked about his friends and life in the city. Listening to him, I realized he was only a few years older than I’d been on my first stay at the Regency with my parents. If my father were with Jack and me, he would shake his head and complain about my breakfast bill, then scrounge around the mini-bar for shelled peanuts. He would quiz Jack about his homework, and want to know what exactly did he plan to do when he finally got that college degree, knowing that—whatever Jack decided—he, and his brothers, were going to be okay.
          I’d like to tell him he was right—not that I ever doubted. Each of my sons inherited their grandfather’s entrepreneurial spirit and desire to live a purposeful life. He’d be proud.

          At the end of my visit with the medium she told me to watch for hawks—they were messengers from my father, a sign that he was around.
          A simple Internet search reveals that hawks are believed to be messengers from the divine, with powers of awareness and enlightenment. Any medium worth her salt could have said it, to anyone.
          And yet—a few years ago I noticed hawks flying at the place north of San Francisco where my husband—I’m happily remarried now—and I spend summers. I like to sit outside and watch them soar.
          “How do they do that?” I asked my husband. He’s a pilot; he knows these things.
          “They’re carried by rising air currents,” he said.
 I watched the hawks, thought of my father, and knew our boys would be just fine.


Susan Moldaw works as a chaplain in San Francisco. Her writing has appeared or is forthcoming in Brain, Child Magazine, Broad Street, Lilith, Literary Mama, Narrative, Ruminate, and others. 

Thursday, November 9, 2017

The Shoulder of Orion

by K.C. Frederick

        I saw two planes collide over Detroit when I was a kid. I was in our back yard, where my father had covered a patch of dirt with concrete and installed a swing set. It was next to a lilac bush and, in my memory, the lilacs were in bloom. In most of my memories of the back yard, the lilacs are in bloom. I once buried my coin collection near the lilacs: there were Indian-head pennies, flying eagle pennies, even a large cent, bigger than a silver dollar, from 1818. I started collecting coins from the piles of change that showed up each night on our kitchen table, my father’s leavings of the day’s play in the numbers.
        The coins were in a tin box that may have held tobacco once. Some of the coins I bought from dealers, and I think the hoard may have been worth a bit of money after a while, but all my later efforts to dig it up proved fruitless. Did the stuff just disappear?
        I was near that lilac bush and it must have been spring with the fragrant purple flowers in bloom around me. The only other flowers I remember from that yard are the peonies that were always covered with ants. Maybe I was on the swing. To my right was a cyclone fence that looked into the alley, its concrete surface covered with broken glass that never deterred us from playing softball in its narrow confines, playing balls off roofs of what we called barns. The alley was also the place where the black rag-picker came with his horse-drawn cart. We called him the sheeney-man. He had a white beard and he was missing a hand, as I remember, but there’s no way of verifying this.
        If I looked in the other direction, I could see the church towering over the roof of our house—the brick wall of the church was what you saw when you looked out our front window. With the adjoining brick rectory and the large brick-walled yard where I’d go at night with my flashlight to get night crawlers, the church took up the entire block. On the other side of the block were the grade school, the high school, and the nuns’ residence. The nuns, as I remember them, were always prophesying doom, God’s wrath inflicted on a faithless people. Maybe I was the only one, but I believed them. I was a lonely kid, so what God thought of me was important. I tried not to incur His wrath, but in case others did, I generally kept from looking at the night sky, since the nuns had made me aware that the stars could begin to slide out of place, the prelude to a cataclysmic demonstration of God’s disfavor.
        I have no way of knowing what I was up to on the day I saw the mid-air collision, but my memory is that I just happened to look up at the sky above Sam the barber’s and I saw two silver planes crossing each others’ paths, then something bright and glistening tumbling earthward. In my memory all this happens in complete silence. The day is warm, the sky is cloudless, there’s the flash of silver, smooth motion followed by a fluttering fall, like the strip of cellophane you used to have to tear off of a pack of cigarettes. Silent, weightless, the world turned into a snow globe with only a single shining flake making its way slowly downward through the transparent medium.
        The details elude me but I know I’m not making this up. My father took us later in the day to see the place where one of the planes crashed into a house. My father was a big man in the numbers then. A sharp dresser, he held himself a bit stiffly and was known for the big parties he threw at his place on Harsens Island, parties  even the mayor might attend. This was before the cops raided our house, before the trial in which my father’s lawyer persuaded him to separate his case from that of his associates, some of whom went to prison; it was before my father started drinking heavily, a behavior that would result in his losing the numbers and losing most of the properties he owned. He was in and out of rehab after that. Sometimes he saw bears in the house. When he was sober, he worked at low-paying jobs like being a night watchman for the city. He’d gone from the top to the bottom, driving to Hamtramck in his beat-up Ford (he left it unlocked in our street hoping someone would steal it, but nobody took him up on it) looking for a bargain on kielbasa or Silvercup bread. Having lost his high station, though, he didn’t blow his brains out but soldiered on, a Polish peasant to the end. His capacity for survival was a remarkable lesson to me.
        Though he was gregarious with his friends, he wasn’t warm with his children. He used a strap on us, but he was less physical than his own father. Later he was too distracted to inflict severe discipline. When he was dying of lung cancer many years later, I wheeled him out to the back of the house that looked toward the alley, where every now and then a sound would come from the scrap yard near the railroad tracks, the protracted, unsettling shriek of metal scraping against metal. Di I was leaving soon for Boston, where I worked. It was likely we weren’t going to see each other again. “I’m going to miss you,” he said.

I’ve done a little Googling and I’ve discovered that there were two collisions of planes over Detroit in the spring of 1948, both on the east side, which would have beenconsistent with my memory. I would have been thirteen. The earlier collision seems the one I likely saw. The student pilot, I learned, was thrown from his plane, fell through a roof and a porch, and his body was driven into the ground. I didn’t know any of this as a kid. I suppose our car dragged along with others past the scene, we may have glimpsed a part of the wreckage, certainly we’d seen the damage to the house, but all that’s blurred, and I must reconstruct it. What I do remember is looking up to see a silent encounter in the sky, a piece of silver fluttering down toward the houses of Detroit, a distant, wondrous sight.
My family left the city long ago, but not before the neighborhood deteriorated precipitously. Today weeds come up from the sidewalks, there are lots of vacant lots, and many of the houses that remain are ruins. In the right mood, you could convince yourself that wolves roam there at night. The huge church has been empty for some time. Shorn of its statues, it was sold to some Baptists who couldn’t afford to heat the vast spaces and sold it for peanuts to a developer. I wonder if the lilac bush is still in our back yard. Is it possible that a lucky kid will dig up my coins some day?
In Ridley Scott’s’ Blade Runner the replicant Batty, facing extinction, feels compelled to tell Deckard, his pursuer, “I've seen things you people wouldn't believe. Attack ships on fire off the shoulder of Orion. I watched C-beams glitter in the dark near the Tannhäuser Gate. All those moments will be lost in time, like tears in rain.”
Indeed.


K.C. Frederick grew up in Detroit and lives near Boston, where he continues to be a lifelong Tiger fan in the heart of Red Sox Nation. He’s published six novels and many stories, winning awards in both genres.

Friday, July 22, 2016

Tough Guy

by Darryl Graff

The sign-in book at The Hamilton Arms nursing home in Lancaster, Pennsylvania was filled with my signature: “Darryl Graff … Visitor … Jules Graff … Resident.” Sometimes, I would look through the pages of the sign- in book at the names of the other residents. They had so many visitors. My father only had me and my wife, Regina. It broke my heart, and my father… well, I couldn’t imagine how he felt. My brother, his first- born son, was too busy being a yuppie to see his own father dying in diapers, in a nursing home. Regina and I came every Sunday. An eight-hour round-trip train ride from Manhattan.

As had become my habit, I kissed my father on his head; it was soft, bald, and wrinkled.

“How you doing, tough guy?” I asked.

I started calling him “tough guy” when he first went into the nursing home. It was my way of making him feel stronger. I know a lot of things, about a lot of things; I know that once you hit that nursing home bed, if you don’t get out of that bed and walk around the room, the bed is going to get you. After a month, I could see the bed was going to win, but if anyone could get out of the bed and walk this thing off, it would be my father. I only remember him being sick one day in my entire life. He went to work every day to provide for his family, and he drank heavily every night for seventy years. I called him tough guy because, well, he was a tough eighty-nine-year-old guy.

“How’s your job?” he asked in a faint whisper.

The man who taught me how to cook was lying there with a feeding tube pumping liquid into his stomach.

I started to tell him details of the job, but that’s what I do six days a week. Details, everything is details. Everything has to be exact. I stopped talking about work. It was pretty clear to me he had no idea what I was saying anyway. So I decided to save the details for the job. Instead, he wished out loud for an adult scooter. So he could just get on the road and start driving, and not stop until he was far away from this place. Before he could get on the highway, he wanted to buy Regina and me lunch at the nursing home restaurant that didn’t exist.

When I was a kid, sometimes my father would have Chinese food delivered from the place on First Avenue. We’d shut off the lights and eat Chinese food by candlelight. Now, I was sitting under hot fluorescent lights next to my father’s bed. I held his hand; the feeding tube made a gurgling noise. This was my only day off. Some day off.

Thank God for Q’s Duke Bar on Liberty Street, a sad little bar. Mostly biker wannabes and long-ago burnt-out townie factory workers.

Regina and I went there every Sunday before catching the train back to New York City. How did my Jewish New York City father wind up in Pennsylvania Dutch Country? Well, it had to do with a woman. It usually does. If the Q’s Duke Bar had a sign-in book, I would have signed it every Sunday.

We got to Penn Station at 8:30 a.m. for the 9:15 to Lancaster. It was Christmas day. My father would be dead in a few weeks. We got in line at the Zabar’s in Penn Station and waited, in a slow, jerky line of tourists and junkies. I got some beer and Regina took care of the sandwiches for the trip. At the cash register, there was one lonely looking box of Christmas cookies. I threw them in the bag with the beer and the sandwiches—a little something for the women who worked at the nursing home.

After chain-smoking a few cigarettes on Eighth Avenue, Regina and I ran down the escalator and onto the 9:15 train to Pennsylvania. A half hour outside of Philadelphia, it started snowing, and kept snowing, and snowing. When we got to Lancaster, the city was shut down by the biggest blizzard in years.

“We’re never going to get a cab. How are we going to see your father?” Regina asked.

“I’ll flag down a car and explain, it’s Christmas day. My father’s dying in a nursing home. Somebody’s got to give us a ride.”

Regina waited in the train station. I stood on the street corner in knee-deep snow for an hour and never did see a car. We walked into the Q’s Duke Bar, wet, cold, and defeated. Dark, crowded, loud, Led Zeppelin, NASCAR racing, whores, tattoos, a pool table, and next to the pool table, a small buffet table. It was Christmas dinner at the bar. Ham in a crockpot, hot dog buns, potato salad, and paper plates.

“Merry Christmas!” some biker babe yelled as we sat down in front of a large-screen TV.

“Have some ham.” And we did.

We wound up sharing the Christmas cookies for the nurses with the whores and speed-freak bikers. “Merry Christmas!” they yelled as we left to catch the last train back to New York City.


The Biltmore Theater restoration project I was working on lasted nine months. My father’s nursing home project lasted five months. On February 14, 2004, at the Hamilton Arms Nursing home, I didn’t have to sign in. Instead, I had to fill out a personal items form. It wasn’t much, just a gold wrist watch. Forty years of dedicated service.

The Groff Funeral Home on Main Street in Lancaster, Pennsylvania, was only six blocks from the Q’s Duke Bar. It was a very professional place. The “grief counselor,” or cashier, seemed nervous that we didn’t have a car in the parking lot.

“I’m from New York City,” I explained to her. “I don’t drive. I don’t have a car.”

She couldn’t give me my cremated father’s remains fast enough. I handed her a check. She gave me a small box in a paper bag. We walked to the Q’s Duke Bar and sat at a table. I went up to the bar and got two drinks.

“Get an extra glass. We’ll have a toast,” Regina said.

I poured some beer into Jules’ glass. Regina and I clinked glasses.

“To Jules!”

Back in New York City, it was freezing cold in Central Park.  We kept walking until we came to the right spot, a big oak tree overlooking the Conservatory Pond.

I could sit for hours and watch those remote control ships go around and around the pond. One guy even had a remote-controlled submarine.

It was the 1960’s. Anything was possible. I wanted a remote-controlled boat badly. At the Gramercy Pharmacy on First Avenue and Twentieth Street, in the back was a single spinning rack of toys. One day, I saw a little plastic boat; it was orange and white. My mother bought it for me, and my father took me up to Central Park. He had rigged up the boat with a string wrapped around a stick, and told me it was a remote-controlled boat. I set my boat in the pond and let the string out. It was my maiden voyage. I passed the Mayflower, the Santa Maria, and the submarine. There I was, finally a sea captain. After about four minutes my ship took on water. It listed to the left and sank straight to the bottom. The string was tangled; I pulled and pulled, then gave up.

We spread Jules’ ashes on the hill overlooking the pond, under a big old oak tree.

“Rest in peace, tough guy,” were my last words.

I finished the Biltmore Theater. My boss, Josh Gray, gave me a $5,000 bonus.
“Thank you, Darryl.  You did a great job,” he said. “I know it was especially hard for you, with your dad dying and all.”

Two months later, he laid me off.



Darryl Graff is a New York City construction worker and writer. His essays written about life in the city, have been published in Akashic Books, Heart & Mind Zine, Fat City Review, The Flexible Persona, Hippocampus, and Gravel. “Tough Guy” is an excerpt from his nonfiction narrative The Local, about a union construction worker who inadvertently lands in the middle of hostile Union takeover.