Why I Put my Drug-Affected Daughter Back on Drugs

Why I Put my Drug-Affected Daughter Back on Drugs

8-year-oldgoesviralwithhard-rocktune

By Melissa Hart

“Stupid Mommy! I hate you! You’re an idiot!”

It’s 2:45, the end of the school day. I cower in a corridor like a kicked mutt surrounded by serene hemp-clad parents and their eight-year-olds. Patchouli oil emanates from their golden arms and legs. They bend their sunny open faces toward one another—faces that cloud and pinch at the sight of my second-grader.

She’s flushed and furious, sweaty curls standing on end. She smells of spilled tempura paint and noodle soup from her overturned Thermos on the floor. Her green dinosaur boots stamp a frenzied tarantella around me as she screams.

“You never do what I want. You’re the worst mother ever!”

Shame flames my cheeks. The other mamas in the hallway, the bearded longhaired papas, probably believe her. I’m Snow White’s Evil Queen, Rapunzel’s Mother Gothel. In short, I most surely suck.

I don’t meet the eyes around me, I don’t say a word. I turn, chin ratcheted at an ignoble angle, and walk out the door praying my child will follow. She does, still shrieking insults. Then, she kicks me.

My transgression? I’ve left the Honda in the garage on this sunny day and asked her to walk a half mile home with me.

*     *     *

“She needs medication if she’s going to stay at this school.”

My daughter’s principal, boyish and skinny as a weasel, sits in the counselor’s office across from the tranquil second-grade teacher and me, and delivers his verdict. “In the classroom,” he tells me, “she screams over math and reading assignments. She does cartwheels behind the teacher when she’s delivering a lesson. A boy called her ‘weirdo’ and she slugged him. She refuses to sit at her desk for anything academic and wants to spend all her time at the Peace Table.”

The Peace Table. Most schools have detention. My kid’s classroom has a hand-carved wooden table where a troubled student can go to chill out. My child has, I discover, taken up permanent residency there. We’re gathered together in the principal’s office today because two hours earlier, he bent low to her ear to suggest she return to her desk, and she shoved him.

“She threw my back out.” He reaches behind him to massage his injured lumbar. I bow my head, but he isn’t finished. “I saw a documentary on kids adopted from Romania. They had reactive attachment disorder—all the same issues as your daughter. The only thing that helps these kids is medication . . . mood stabilizers.”

Gently, the teacher’s mouth falls open. Marijuana’s about to be legalized in Oregon and the smell of it competes with patchouli in the afternoon corridor. My fellow parents may rock the ganja, but our school’s a hotbed of anti-vaccination activists. They carpool up to the Capitol to protest mandatory inoculation, hold chicken pox parties and embrace each other in celebration when their kids present with the itchy red spots. Once, I mentioned to a father in the corridor that I’d taken my child for a flu shot, and he got up in my face.

“Why,” he snarled, “Would you poison your daughter?”

Me, I’m a fan of modern medicine. My child is vaccinated, and when she falls ill, she takes Tylenol. But mood-altering drugs? For a second-grader?

I want to remind the principal that my husband and I adopted our daughter at 19 months old from a skilled foster mother in Oregon—not from Romania where kids once languished, cribbed in their own excrement, for a decade. Instead, I spread my palms out on the table in supplication. I’m beaten, pummeled by years of similar meetings in preschool, in kindergarten, in first grade. I think of a summer camp counselor who summed up my child’s temperament in one sentence:

“She’s not one who earns a lot of stickers.”

At last, I address the principal. “We’ll do,” I say, “whatever you think is best.”

The second-grade teacher stands up, long hair swinging. At six-foot-four, she’s quiet royalty in the shabby room. “I’ll meditate on her,” she says, by which she means she’ll actually stay up an extra half hour that night to sit in lotus position and ruminate upon my child and her issues. “I think there are alternatives,” she concludes mildly, “to drugging your daughter.”

I’d love to believe her. But I think we’ve run out of options.

*     *     *

Research abounds on the effects of constant loving touch and eye-contact with babies. In parks and grocery stores, infants dangle from frontal packs like Sigourney Weaver’s alien baby. My husband and I wore our own daughter in a soft cloth backpack until her feet nearly touched the ground; we gazed into her eyes and hand-fed her long after she could feed herself. But even those ministrations weren’t enough to soothe prenatal exposure to god-knows-what substances, coupled with early emotional neglect.

At birth, relinquished by parents who—in social worker speak—”had priorities other than child-rearing,” she moved in with a career foster mother—a woman who devoted her life to giving bereft babies a decent start in life in exchange for financial stipend from the state. The foster mom—a stoic big-hipped brunette with a passion for dragon decor–drove her charges to medical appointments and arranged for occupational and physical therapists to visit her home. With four children roughly the same age howling the same basic needs, she found little time to coo and cuddle. My husband once walked into her kitchen to find four toddlers arranged in a high chair assembly line, opening their mouths in turn to receive spoons of canned pears.

“She’s a feisty one,” the foster mother told us on the day we met our new daughter. She chuckled, a toddler under each arm, their chubby hands clutching hand-knit stuffed dragons. “Falls asleep squalling in the middle of the living room floor. I just step over her.”

I gazed at the strange little girl tottering across the sunny summer porch. She was dressed in a peach pantsuit with her curls gelled backward. Somewhere, she’d picked up a pointy lawn ornament, which she brandished it in my direction. With her face wrinkled into a scowl, she looked like an aggrieved elderly bingo player who’d been dealt a crappy card.

I didn’t know then about the trauma that foster babies experience—hadn’t considered what it felt like for her to be ripped from the only body, the only sounds and smells she’d known for nine months and embraced by an incubator for a week, and then a car seat and a high chair and a crib, but not by much else.

Perhaps, when no one responds to her pleas for assistance with a wet diaper or with a favorite ball that has rolled under the couch, she learns to holler like hell. She learns to kick and yell and scream because it earns her attention—even if it’s attention in the form of exasperated assistance. Lacking that, she shuts her eyes and withdraws into herself. Alone behind her closed lids, she ignores the fuzzy dragon-slippers that step over her. She searches for peace.

*     *     *

It’s Parent-Teacher Night. My husband and I walk into the second-grade classroom with its walls plastered in colorful drawings and watercolors around rows of two-seater tables. We weave through a crowd of parents embracing and planning play dates and roller-skating parties to which our child is never invited. We stop at a desk in front of the teacher’s podium. “Here’s her name tag,” I tell my husband. “Front and center.”

“She’ll always sit where I can put a hand on her shoulder if I need to.” The teacher looks down at me from her awesome height. “A soft touch helps to focus her.”

As other parents exclaim over their children’s hand-knitted flute cases and beeswax candles molded into the shape of Mozart or Lao Tzu, we look at the curious one-legged stool that stands in place of a chair at our daughter’s seat. “It gives her sensory information,” the teacher tells us, “and helps her to be aware of her body in space.”

We look at her, blankly. She smiles. “It calms her down.”

We heft the weighted blue blanket under our child’s desk—another calming device—and note the noise-canceling headphones. There’s a necklace on her desk—a black string with a blue and white rubber triangle. It’s for chewing; otherwise, she gnaws her pencil in half.

We move toward the Peace Table at the back of the room. “She spends a lot of time here looking at books,” the teacher tells us, “particularly if she’s having a rough day.”

My husband and I sink into the little chairs at the scrubbed wooden table. We grip each other’s hands, no words for our humiliation.

“Breeze is racing through the Little House series,” I hear one mama tell another. “She wants to be Laura Ingalls Wilder. She sewed her own sunbonnet and apron.”
“I wish Moss would read,” a father says. “It’s all about lacrosse at our house.”

My daughter refuses to read. We’ve blown through soccer lessons, basketball, ballet, gymnastics, horseback riding, aerial silks. Each coach and teacher says the same thing. “She doesn’t like to listen,” by which they mean, “She’s giving us a boatload of grief, and we’re sinking. Please, please bail.”

“We’re sorry,” we tell them and slink away from the field or gymnasium or dance studio in the wake of our failure.

At home, presented with requests to feed the cats or set the table or finish lessons sent home from school, our eight-year old howls. If we persist, the insults begin. “I hate you! You’re stupid!” And—wait for it—”You’re not my real parents.” She calls it the “Everything Feeling,” those emotions that collide within her and explode in all directions, causing her hands and feet and words to lash out and hurt someone else as much as she’s hurting.

I look around at the life we’ve created for her—the bedroom full of books and dress-up clothes and musical instruments, the photos on the wall of our family vacations to tropical beaches and wildflower mountains and national parks. I fight an urge to shake her little shoulders and stare into her big brown hostile eyes and yell, “Why can’t you just be happy?”

            But I don’t . . . because I know better. The Everything Feeling’s got me in its grip as well, and has since I was her age.

*     *     *

            I’m eight years old. My mother—my confidante and playmate and Brownie leader–buckles my siblings and me into our station wagon and flees from our chic Los Angeles suburb. She deposits us in a scrappy duplex half an hour north in a scrappier beachside community. A makeup less woman–Budweiser in one hand and Marlboro in another–embraces her. She’s my mother’s new lover. “We’re leaving your father,” Mom tells me.

And, I add silently, my friends and my school and my Brownie troop, our cats and never-ending rabbits and the cute neighbor boy who’s taught me to shoot the bird and pass gas like the Fourth of July.

I don’t say a word; I don’t cry. I’ve heard the midnight screaming and the shattered glass. I’ve seen the black eyes, her bruised nose. I’ve felt her fear and mine, and I’m old enough to grasp the necessity of loss.

To a point, and then, not.

Something in me begins to hate my mother for not protecting me from trauma. I despise her new girlfriend—her rasping voice and her habit of striking a match on the zipper of her Levi’s. I flee our duplex every chance I get and run wild on the beach with a pack of stray dogs. I go feral. I growl at the nicotine stink of the living room as we eat dinner on tired carpet in front of the cold empty fireplace. I fall asleep to the wail of the foghorn on the jetty with my teeth and fists and stomach clenched tight.

It takes my father three weeks to find us. He appears at the front door with a patrol car’s lights whirling behind him and demands that my mother meet him outside. She and her girlfriend stand in the doorway, arms folded across their Superman t-shirts, sans bras. They shake their heads. “No way,” they say.

An officer steps from the car. Red and blue beams flash across the sandy volleyball court between duplexes. He walks up the steps and presents a piece of paper. My mother’s face crumples. We follow our father—me first, then my younger sister and brother, down the stairs and into his Buick. It’s 1978. The DSM IV has recently deigned to remove homosexuality from its list of mental illnesses. Still, a psychologist declares my mother unfit to raise children.

I never live with her again.

As a concession, the judge allows us to see her two weekends a month; apparently, she can’t turn us gay in 48 hours’ time. Every other Friday, she drives down in her VW bus to pick us up from our father’s house. I murmur tearful goodbyes to the stepmother we’re learning to love and shed more tears on Sundays when I’m ripped from my mother. I can’t feel her arms around me, smell her, or see her for ten days at a time. I forget how to draw a deep breath; I walk on tiptoe and read a novel a day between school and bedtime, four on the weekends I’m not with Mom.

“Why can’t you just be happy?”

Each of my parents demands this throughout my adolescence. Every other Sunday night, I sit in my bedroom on the ice-blue carpet, head pillowed on the rosy bedspread, and replay my weekend at the beach. Saltwater and sand still cling to my calves as I sit there for hours, eyes shut tight, hands shaking. No one comes into comfort me.

Therapy? No one has time. Mood stabilizers—out of the question. The Reagans are in the White House; red ribbons tied on the fence around my school remind me to just say no to the hooded stoner kids lounging in my classroom’s back rows. Drugs are for weak people, my father and stepmother tell me, mixing a third gin and tonic. “We’re fine. We’ve got this.”

My insomnia begins that year. My mother’s first girlfriend leaves her. I lay rigid in the darkness, worrying about her until the wee hours. Is she lonely? Is she suicidal? What if she dies? In my father’s bedroom, the battles begin anew—the slamming doors, the screams, the shattering glass. My brain waves twist and warp, training themselves into terror.

But I know nothing of neuropsychology. All I know is a longing to run the safety razor across my wrists as I stand in the shower at six AM. A crushing depression follows me to school, trailing me onto the high school track and the drama club stage.

I don’t do drugs—I do musical theater. I try unconsciously to restructure my neuropathways, boosting serotonin with exercise and music and laughter with friends. Some days, I almost achieve a retraining. But fear triggered by years of Sunday-night separations, by domestic disturbance and an officer at the door suggesting my stepmother take us to a friend’s house until my father stops losing his shit—these incidents reinforce my faulty neuropathways until I stand sobbing in the shower at dawn

*   *   *

I make it through college eschewing all other meds save Benadryl—two of the pink pills at night when chamomile tea and melatonin tablets fail. When diphenhydramine stops knocking me out, I add acetaminophen to the mix. Tylenol PM enables graduate school, marriage, and the adoption of my daughter.

In the daylight, I’m functional. My child is in preschool each morning with a teacher who loves her. But then, she hits kindergarten. Our world becomes afterschool meetings with principals, IEP circuses. The rooms of our house echo with screaming and slammed doors. At night, I lay in my husband’s arms and curse the anxiety that robs me of sleep.

He finds me a psychologist, a mellow and intelligent young man who tells me how much my husband loves me, how much I need help. He tells me a story of his husband—a man my age plagued by insomnia until he went on a low dose of Ambien. “It’s okay to take sleep aids,” the therapist concludes, but I shake my head.

Beholden to a prescription, I explain, means more than just a half hour wait at Rite Aid once a month. It means inadequacy, a failure to function like everyone else, to get a grip.

“Lots of people take prescription meds,” he argues.

I think of Nancy Reagan’s red ribbons and shake my head. “I’m fine,” I tell him. “I’ve got this.”

I take up long-distance running; now I’m thin and muscular and exhausted. Periodically, I break out in hives. An allergy, I tell myself, to sports gel or Gatorade or the flax seeds I spoon into kale smoothies. But when my lips bulge and my eyes swell shut and my husband drives me to the emergency room looking like the Elephant Man and with his same wheeze, the doctor refers me to another who diagnoses Hashimoto’s Disease. Three and a half decades of anxiety and sleeplessness have caused my immune system to attack my thyroid.

“Take this pill every morning.” The pharmacist at Rite Aid shows me the little blue oval of Levothyroxine.

“For how long?” I ask him.

He blinks surprise behind his spectacles. “For the rest of your life.”

*     *     *

Shortly after Parent-Teacher Night, I attend a regional adoption conference. Adoptive parents, foster parents, and social workers share watery coffee and stale maple-glazed donuts in a chilly borrowed office suite, listening to a sociologist talk about the effects of early trauma on a child’s neurological development. Brain scans appear on her PowerPoint like a couple of cauliflowers. “This is the brain of a normally-developing child at three years old,” she tells us. “And this is the brain of a three-year old foster child who’s experienced trauma and neglect.”

We study the runt cauliflower, significantly smaller, and listen to the list of potential stressors affecting our kids. They start in the womb with little pre-natal care and periodic baths in drugs and alcohol. They extend to the shock of delivery and removal from the birth mother, then placement in a sterile neo-natal unit and a transfer to foster parents who may or may not offer physical affection and a tranquil, structured environment.

Some foster parents—mostly retired and courting sainthood—have the luxury of accepting one drug-affected infant at a time. They carry the child everywhere, cuddling, crooning, and feeding them pudding while gazing into their eyes–the works. Others juggle several needy kiddos at once. Money and time, in short supply, don’t permit a whole lot of baby wearing and eye contact.

“Foster kids’ brains have a different structure,” the sociologist tells our goose bumped group of conference participants. “They have a low volume of calming chemicals and a high volume of excitatory chemicals. Our kids view conflict—any conflict—as a threat to their survival. Adoptive parents, no matter how noble their intentions, represent one more trauma.”

Someone raises a hand. “What about medication? Anti-anxiety drugs, anti-depressants?”

The presenter taps the poor little wrinkled cauliflower on the screen with her pencil. “Meds can help,” she says. “A lot.”

She clicks off her laptop and invites questions from the group. I flee to the restroom. In a sterile stall I sit and stare at the door. Right there on the cold toilet seat, I have an epiphany that changes my life.

My brain needs help.

I slink toward my little white anti-anxiety pill at 44 years old, resolute but convinced that I’ve failed at the basic human tasks of sleep and moderate optimism. Within two days of swallowing it, I sleep an eight-hour night. “Everyone’s getting medication for Christmas!” I joke with my husband.

Everyone that is, except our daughter.

            *   *     *

Our eight-year old, I continue to insist, needs affection and attention and hip hop lessons—not mood stabilizers. Never mind that she screams over her plate of spaghetti because it’s got the wrong sauce, screams over the loss of her favorite TV show, chases the cats, fists me in the stomach, and falls into bed squalling. “We’ll find her a good therapist,” I tell my husband. “That’ll help.”

We agree on a kind Polish counselor who does sand play therapy with innumerable plastic Disney figures and teaches our child to lie on her back in a warmly carpeted office and blow soap bubbles, breathing deeply to combat stress. The woman teaches her “rabbit breaths” —short bursts of inhale and a long exhale designed to replace hyperventilating over second-grade math assignments and requests to set the dinner table.

None of it helps. My daughter shoves the principal, who begins sending her home from school mid-morning. “We’re a charter school,” he says. “We’re not set up for behavioral disorders. Think about moving her to a special education class at the public school.”

I grit my teeth. I’ve been a special ed teacher, know first-hand the challenges of wrangling a class full of kids—each with specific needs and none getting optimum attention. I’ve stepped over plenty of squalling children myself to attend to the one toppling computers from desks and punching holes in the walls. “She is not,” I tell the principal, “switching schools.”

In the dank patchouli corridor, when my daughter actually does manage to make it to 2:45, I meet no parent’s eyes. The other second-graders line up in the doorway and shake the teacher’s hand and grasp their hand-woven lunch baskets, heading off in pairs for afternoon play dates and Friday night slumber parties. My child’s the last to leave. She huddles at the Peace Table while the teacher gently reprimands her for the latest shrieking/hitting/spitting incident. At home, she shuts herself up in her room and slumps on the bed.

“I feel like a broken light bulb,” she tells me, surrounded by piles of schoolwork she hasn’t completed.

“What do you mean?” I ask her.

“I’m different from everyone,” she mutters. “I shouldn’t be here.” And then, “I want to be dead.”

I stare at her—my suicidal eight-year old in her blue Frozen t-shirt. The words under a smirking blond Elsa read “My castle, my rules.”

For the second time in a month, I experience an epiphany. What other choice did Elsa have, I think, after 18 years of loss and neglect? Her parents were dead. A propensity for frigid temper tantrums kept her locked in her room. Why wouldn’t she retreat to the top of a mountain, build a fortress of solitude, and take charge of her environment?

Maybe if she’d just swallowed a little mood stabilizer once a day, she wouldn’t have iced an entire kingdom.

I call my husband. He phones a developmental pediatrician and makes an appointment for diagnosis and a prescription. I call the principal and withdraw our daughter from her second-grade classroom. “We’re going to homeschool her,” I say, the sentence absolving me of IEP meetings and outrage and shame. Elsa’s words ring through my head, full of triumph.

My castle, my rules.

*     *     *

It’s 2:45, the end of the school day. My child, a third-grader now, runs to meet a bus full of friends outside the building that houses their afternoon program. They race into a classroom full of art supplies and sewing machines and games and books and beanbags. She has time for a quick hug, a swift, “I love you, Mama,” before melting into a group of giggling girls.

At home, I open my laptop beside her colorful math and literature textbooks, the flash cards, the globe, the Borax crystals and the paper-and-string robotic finger she’s created. We’ve been homeschooling for six months now. We laugh a lot. Sometimes, we argue. On our worst days, when I resent having to wake up too early and stay up too late to attend to my own work, or my daughter fumes at having to study when she wants to lounge on the couch reading Garfield comics, we cry. But mostly, we relish small daily revelations and the one big one—she’s finally happy.

She takes mood stabilizers for six months. They chill her out, but give her a Winnie the Pooh physique and a slowness not conducive to gymnastics and hip-hop classes. With the pediatrician’s permission, we cut the dosage in half and wait for the return of our demon child.

She doesn’t resurface.

Instead, she wakes up smiling, singing, even—excited about her day.

We quarter the pills, then abandon them altogether for a low dose of Ritalin which allows her to learn multiplication and fractions and spelling without chewing her pencil in half.

Several mornings a week, we walk up the hill to a forested park, on a quests for newts in the stream and Cooper’s hawks in the Doug firs. We discuss planets and poetry and how baby chickens can breathe inside the egg.

One day, on a sunny morning on which we’ve discovered four types of lichen on a fallen branch and spent 20 minutes identifying a colossal mound of gleaming black opossum dung, she slips her hand into mine.

“Remember when I was so bad at school?” she asks me.

“You weren’t bad,” I respond automatically. “You were scared and angry.”

We walk past a patch of sunny daffodils. I point out a deer path winding through the tall grass, but she persists.

“I was mad at you for leaving,” she says. “Every day, I missed you.”

I squeeze her little shoulders and stare into her big brown affectionate eyes, remembering what it felt like to be torn from my own mother 10 days at a time.

“I know,” I tell her, and we walk hand in hand toward home.

Author’s Note: It’s been almost a year since I completed the final draft of Rabbit Breaths–a year of homeschooling, of meetings with developmental pediatricians and counselors who diagnosed my daughter with severe ADHD. We’re still looking for the right medication that allows her to function calmly and happily in the world. Not medicating isn’t an option, but my husband and I have greatly stepped up our attention to nutrition and sleep and exercise and outdoor exploration and the arts. As well, we discovered Russell Barkley’s excellent Taking Charge of ADHD and a local parent/child support group. We take each day an hour at a time, practicing (and sometimes failing) our patience and creativity. Most days, we remember to laugh.  

Melissa Hart is the author of the YA novel Avenging the Owl (SkyPony, 2016) and the memoirs Wild Within: How Rescuing Owls Inspired a Family (Lyons, 2015) and Gringa (2009). She’s a contributing editor at The Writer Magazine.

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Commencement Speech for My Special Needs Second-Grader

Commencement Speech for My Special Needs Second-Grader

Conceptual shot of child education. Brown teddy bear in graduation cap leaning on books

By Melissa Hart

Members of the second grade class: two years ago, you scampered down these hallowed halls to play with the unpainted wooden dollhouse and the felted gender-neutral puppets and the classroom newt in a kindergarten done in womb-pink. Among you moved a little boy named Oliver.

Oliver wasn’t like other children. He forged his own way, eschewing circle-time and songs and hand-clapping games, and sprinting for the nearest exit at recess. His voice rang out above all others, commanding attention. He was, in short, a trail-blazer—a child so original that the teacher’s aide devoted her days to him.

As you struggled to form letters and numbers on your soft ecru paper, the aide bent over him, fingers gripping his around the hand-carved pencil, sometimes for half an hour while you soldiered on alone. You wonder now: What did Oliver have that I didn’t have? I’ll tell you:

A learning disability.

Like yours, dear children, Oliver’s parents visited a vast array of educational institutions. They pored over commentary at GreatSchools.org and debated into the wee hours self-directed curriculum versus whole-child learning and how each might ensure happiness.

Oliver–like the 22 of you now sipping chamomile tea while covering your soft ecru paper with watercolors–learned to finger-knit yarn spun from the alpacas you fed on your field trip, becoming so attached to his string that he wound it around his fingers until they turned purple, and screamed and bit the aide. Inspired by his teachers and principal and his tearful disbelieving mother, he forged a new path to a behavioral classroom across town.

He didn’t try to be special, dear hearts; he simply was.

I tell you this because today–as the morning glories stretch and beam from the garden boxes you lovingly decorated—there’s another child in your midst who shows the same spirit that you may recall from Oliver’s days.

Unlike that boy with his feet planted firmly on the spectrum, however, this little girl came into the world drug-affected and placed in foster care. As a toddler, she enjoyed the perks of regular feedings and diaper changes, unhampered by distractions such as caregiver eye-contact and physical embrace. Thus, she learned to sound her barbaric yawp so that she, like Whitman rolling naked in his leaves of grass, might make herself known.

You know her as the child in the front row, directly in front of the teacher’s podium, with all the privileges that weighed blankets and noise-cancelling headphones confer. The letters ADHD mean nothing to you—but you marvel at her ability to turn cartwheels behind the teacher. She’s memorized the words to over 100 songs and locks herself into the bathroom daily to belt them out. She isn’t like you, dear hearts. She marches to the beat of her own drum and refuses to learn with the rest of you how to play the pentatonic flute.

Like Oliver, she doesn’t try to be special; she simply is.

Education is a community-driven endeavor, and you exhibit this daily. For years, the little girl in question watched you arrange playdates and sleepovers in the hallways. She heard thrilling tales of birthday parties to which she wasn’t invited. Just this morning, two of your fathers dialogued in the classroom about a class camping expedition—a trip apparently open to a select few. How inspiring to know that you gather so lovingly to support one another at a school that prides itself on inclusiveness.

A mystery to you, the little girl’s mother who shows up each morning with a smile plastered across her face as you gather outside to jump rope while her child screams because she’s forgotten her homework. What pride the woman exudes as your parents remark on the artful display of her daughter’s uneaten lunch on the floor among her shoes and jackets where they lie below your own neatly-hung Columbia windbreakers and precise rows of Bogs.

How unfriendly that mother appears with dark circles under her eyes as your parents pair up to arrange warm-hearted diversions after school and on weekends. It’s impossible to picture her, dear ones, weeping at night for all she’s been given, not the least of which is a flexible schedule that allows her to work early in the morning and late at night, the better to homeschool.

So you see, dear ones, this story does have a happy ending. Next year, the little girl in question will turn cartwheels each Monday morning in gymnastics class and take professional singing lessons at the music studio downtown. She’ll study on her living room couch, travel weekly to wetlands and science museums and animal shelters. Hell, her mommy may even adopt an alpaca.

For a moment, as you pause on the threshold between your second and third grade classrooms, you may glimpse the future—six more years in these same hallways fragrant with patchouli and the bliss that only true oblivion can provide.

It’s your future, dear ones. Keep in touch.
Melissa Hart is the author of the YA novel, Avenging the Owl (Sky Pony, 2016) and the memoirs Wild Within and Gringa. Web: www.melissahart.com.

 

Sitting with the Loss of My Daughter’s Sisters

Sitting with the Loss of My Daughter’s Sisters

By Melissa Hart

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My mother lost custody of me in the homophobic 1970s when she left my father for a woman. My daughter lost her mother to addiction at birth.

 

At nine, I read a novel in which a boy’s beloved hound dog got mauled by a cougar—ripped open from breastbone to pelvis so that her entrails spilled out and festooned a nearby bush like Christmas tinsel as she attempted to follow her master home. That’s how I felt when my mother and her girlfriend left me on my father’s front porch Sunday nights, and I watched their VW bus disappear down the street for 10 days—like my entrails were cascading from my gashed abdomen, pooling in a pile around my white Keds.

And that’s how I felt 35 years later, watching my nine-year-old daughter say goodbye to her older sisters on our front porch after 24 hours of let’s pretend and coloring books and hiking trails while I wished their adoptive mother a safe journey two and a half hours back down the highway.

My mother lost custody of me in the homophobic 1970s when she left my father for a woman. My daughter lost her mother to addiction at birth. She didn’t miss the parent she’d hardly met. But her sisters with their identical timbre and diction, their shared love for dollhouses and hip hop, their shared trauma—these girls, she missed.

My husband and I adopted her from Oregon’s foster care system. Another family had adopted her sisters—one of them developmentally delayed—and couldn’t parent a third infant with significant medical needs. We agreed to an open adoption, to visits with them when time and schedules permitted. For several years, our meetings consisted of tentative hours at shopping mall playgrounds and children’s museums as we got to know each other, gradually lengthening into daylong playdates and this season, a sleepover.

They tell you that as a parent, you’ll experience all the ages and stages of childhood again vicariously through your kid. I never found this to be true until the moment my daughter stood out on our winter porch with the kitchen vent emanating smells of her favorite macaroni and cheese, and she told her sisters goodbye.

All at once, memory walloped me. The girls clung to each other with goosebumps raised on their skinny arms, called “I love you, Sissy!” with their breath creating smoke flowers in the crisp air. Then, two of them walked to their car and one of them stayed behind, and my insides spilled out.

 *   *   *

Every other Sunday in the eighties, when I stepped through my father’s door, I paused for a moment to take the temperature of the house. Almost always, he sat in his bedroom upstairs paying bills and listening to Vin Scully recap Dodger games on the radio. My stepmother stood in the kitchen describing for my younger siblings the new dessert she’d concocted from crushed Oreos and vanilla pudding or fresh Meyer lemons and cream cheese or bottles of stout poured into chocolate cake batter.

Alone, I sat on the carpet in my room and pillowed my head on the bed. No one came in. If I missed dinner those Sunday nights, if I shook my head at my stepmother, mute with sorrow, she returned to the dining room explaining my absence as “hormones.” I listened to my father’s overloud laughter and pressed my hands against my sternum, wondering how on earth to hold myself together for ten days before I could see my mother again.

Losing a family member over and over becomes a Sisyphean series of cruel small deaths. It would have been easier not to visit my mother every other weekend all the years of my adolescence. It would be easier not to see my daughter’s sisters, to let the girls get on with their lives 100 miles apart. But easy isn’t always optimal.

*   *   *

This winter on our porch, I left my daughter waving goodbye to her sisters in the car disappearing down the road. I went into the house and sat at one end of our big green couch, legs splayed inelegantly across the cushions, and reached for the warmest, softest blanket I could find. Then, I waited.

How do you help a child through grief and loss? The first few years, I met the moment of the sisters’ parting with a barrage of what I believed to be comforting distractions.

“Let’s go see a movie!” I told my daughter. “Let’s go to the trampoline park! Get ice cream! Go roller skating!”

She took my suggestions, mute, eyes wide and glittering as an animal’s when it’s in pain, and I congratulated myself for avoiding the chilly disregard of my father and stepmother. But last summer, after a playground visit with the sisters ended much too quickly, she hurled these words in my face: “Mommy, I don’t want to do anything!”

I heard her, and thought with a spinning head, what now?

The Buddhists tell us to sit with our pain, to make friends with it. Three decades ago, I sat with the loss of my mother surrounding me until I fell into bed exhausted. I think about what I wanted from the two parents with whom I lived—not space to process the transition as some obtuse child psychologist had counseled my father. Not even the whimsical desserts that my stepmother presented on her silver cake tray and I failed to recognize as reparation. I would have said no to a trip at the cinema or a game of Monopoly. I longed only for someone to say, “You hurt,” so that I could nod and push my insides back in and soldier on.

So this winter, I sat on the couch with a soft plaid blanket on my lap, and I waited. My daughter walked into the living room without looking at me. She closed the door against the 34-degree wind rattling our front yard cedar and wandered into her room.

I’ve failed, I thought. But she returned. Eyes downcast, she walked over to me and sat on the couch, straddling one of my outstretched legs. Then she crawled between them and lay against my chest. I covered her with the blanket and put my arms around her.

I couldn’t tell her it would be okay. Because it isn’t okay.

But if we can acknowledge that, not okay becomes more bearable.

My daughter and I sat there together on the couch for an hour and just breathed. She dozed a little in the warmth from the baseboard heater. I closed my eyes, as well.

For once, maybe I got it right. I didn’t do anything. I didn’t say anything. I just sat there with her, the slippery tangle of our entrails surrounding us, and held on.

Sky Pony Press will publish Melissa Hart’s debut middle-grade novel, Avenging the Owl, in April. She teaches for Whidbey Island’s MFA program in Creative Writing.

Photo: Andrew Pons/unsplash.com

Why We Still Need Annie, 91 Years Later

Why We Still Need Annie, 91 Years Later

By Melissa Hart

annie

The golden lights of the Shubert Theater, circa 1978, dimmed over a packed house. Onstage, seven orphans in ragged brownish pinafores appeared on scrawny cots. One stood up. “Annie,” the other girls called her. In the midst of pain and grief over her lost parents, she cuddled a smaller girl and sang to her about the mother surely sewing her “a closet of clothes,” the father paying bills just before they came to get their baby . . . maybe.

I clutched the program in my eight-year old hands and blinked, hard. My younger siblings perched on the red velvet seats beside me, my mother on the other side. She’d recently lost custody of us for coming out as a lesbian—in the homophobic 70s, a judge had ruled that we were to live with our wealthy volatile father except for two weekends a month.

In her VW bus on the 90-minute drive between her home and his, every other Friday and Sunday evening, my mother pushed in the eight-track to Annie and we belted the songs to mixed delight and horror from other open-window drivers on Pacific Coast Highway. Late at night in my father’s house, I lay awake with the lyrics to “Maybe” swirling through my head. I felt orphaned.

What is it about this little musical that perseveres? Born of a 1924 comic strip about a millionaire who—in a bizarre p.r. move—hosts an orphan over Christmas and decides to adopt her, it’s endured various incarnations over almost a century.

The version I saw as a child starred Patricia Ann Patts in a red dress and a wig of orange curls, cuddling a dog (it’s real, Mom!) on stage. Since then, Annie‘s been the subject of countless stage productions and at least three films—one made for TV, two feature—proving that in the midst of dystopian thrillers and fantasy blockbusters, we still gravitate toward simple rags-to-riches redemption tales.

As I grew into a savvy urban adolescent, however, I hardened my heart against the musical’s saccharine sentiment. What kind of a world did I live in that would separate a mother from her small children because she lived in a romantic relationship with another woman? Why—in the midst of my father’s raging—would I want to immerse myself in the fictional world of mistreated orphans, most with no hope of ever finding a benevolent Daddy Warbucks?

My seven-year old brother became obsessed with the 1982 film version. This one starred Carol Burnett as the pathetically-ferocious orphanage owner, Miss Hannigan, with Tim Curry as her sadistic brother. Magnificent when they hit the screen, the film struck me as entirely forgettable, otherwise. And yet my brother watched it over and over on the VCR for weeks.

“I like the dancing,” he said when I suggested another movie, but I suspected he felt his own connection with the orphans and longed for our mother’s gentle home.

My brother has Down syndrome. Seventeen years later, he moved in with my mother and her partner after my father moved across the country and permanently relinquished him. That year, the made-for-TV version of Annie came out.

This one attempts to incorporate an interracial cast, with Audra MacDonald as Oliver Warbucks’s African American secretary. Perhaps this inspired director Will Gluck to cast an Anglo secretary to Jamie Foxx’s Daddy and Quvenzhané Wallis’ Annie in the 2014 feature film.

Having read scathing reviews, my husband and I reluctantly took our eight-year-old daughter to see it this past Christmas. She didn’t care about sloppy choreography or a stupid subplot involving some incomprehensible commentary on cell phones; she sat with her big brown eyes fixed on the screen as Wallis sang “Maybe” to another little girl, and reached for my hand.

The hard shell around my heart cracked open, and tears welled up in my eyes. In this new version of the story, Annie is a foster child just like my daughter had been before we adopted her… just like the 130,000 kids across the U.S. relinquished by their parents and in need of a permanent family. Wallis plays a girl in a home with several other girls who—because they’re older than four—have little chance of ever finding a permanent home. The revised lyrics to “It’s a Hard-Knock Life” reflect the reality of adoptive parents who mostly want babies and toddlers.

“No one cares for you a bit

When you’re a foster kid.”

“Why did Annie’s parents leave her?”

After the film, our daughter’s questions flew thick and fast. “Why did she have to live in a foster home?” “Was my foster mom mean like Miss Hannigan?” And most troubling, “Why didn’t Daddy Warbucks adopt all the foster kids?”

We bought her the soundtrack, and she listened to it over and over on her red plastic karaoke machine, belting out the songs into a little yellow microphone. It’s “Tomorrow” that’s her favorite—not “Maybe.” She knows where her birth mother is, and why she can’t take care of her. She’s had us as adoptive parents for seven years now, paying the bills and sewing her closets of clothes, calling her “baby” with adoration in our eyes.

“The part that gets me the most,” my husband tells me, “is the Tomorrow song when I think of our daughter. I want so much for her to have that attitude towards life. Makes me teary just thinking about it. The rest of it just gets to me. Again, and again, and again, and again . . .”

Still, I remind him, at least we’re no longer hearing “Let it Go” from Frozen 20 times a day.

This newest version of Annie isn’t going to win many awards, but maybe that doesn’t matter. The story speaks to so many of us, whether we’ve been orphaned in the strictest sense of the word, or by varying nebulous degrees. Lots of us have lost our parents—literally or figuratively—and there’s something about the cheery pre-teen orphan that offers comfort . . . if we can just hang on ’til tomorrow.

It’s this song that my daughter chose to sing at her school’s talent show last week. All of four feet, with Wallis’ same big hair and wide smile, she crooned into the microphone surrounded by K-8 classmates who rewarded her a capella solo with applause and cheering.

Some of the older kids and parents and teachers know that for the first 19 months of her life, my daughter had a pretty hard-knock life. They see the photos of adoptable foster children in the grocery store; they may even donate toys and coats to them around the holidays. For two minutes on stage, she became a symbol of those young people who, for one reason or another need a little extra love. With a poise I’d never seen before in public, she sang:

“When I’m stuck with a day that’s gray and lonely,

I just stick up my chin and grin and say,

The sun’ll come out tomorrow . . .”

That evening, she reminded us all in that crowded, hot auditorium to muster up a little more optimism, a little more compassion for everyone, Annie-style.

Melissa Hart is the author of the memoirs Wild Within: How Rescuing Owls Inspired a Family (Lyons, 2014) and Gringa: A Contradictory Girlhood (Seal, 2009). She teaches for the School of Journalism and Communication, University of Oregon. www.melissahart.com

 

Illustration: canstock.com