Worth It

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My husband enjoys pointing out that I look more like my Uncle Bill every day, especially when I’m smiling.  Which wouldn’t be so bad, except Uncle Bill is 90.  Having my picture taken has become an exercise in self-consciousness.

My likeness to my uncle doesn’t bother my son, however.  I’m told by his caregivers that he asks for me every day, wanting to know when I’m coming to visit.  He’ll fetch a photo of me from his bedroom and tap my image to make sure he is understood.

“Mah?” he asks earnestly. “Mah?”

If only my visits these days even remotely resembled the outings I once hoped to provide him.  Instead, the obsessions governing his behavior make it almost impossible to bring Daniel safely into the community when I am alone to manage him.  His impulsivity, bolting, and tendency to grab what he wants, from anywhere or anyone, severely limit our participation in most public experiences.  Autism has dictated the whole course of his life, and now dictates our time together, as well.

We stick to the McDonald’s drive-through, eating in my car in the parking lot, safety locks engaged.  I drive through the rural hills outside town to spend time alone with him, and ask about his life away from me: his activities, his housemates, the meals he most enjoys.  I don’t really know if he’s listening.  He answers with an occasional “Yeah!” or alarmed “No!” if I suggest a new route, a different fast food outlet, a departure from our established routine.

Before long he’s itching to head back, anxious to stop at the gas station for the highlight our visit: selecting a soda from the cooler, which he’s allowed to drink once we’re back at his group home.  He’s ready for me to leave then, sometimes hastening my departure by waving his arm and instructing, “Bye!”

He seems content with this routine.  It appears enough for him just to see me, to receive my kisses and occasionally stroke my hand, reassured that I’ve come back again, his touchstone, his connection to the life we used to share.

I wish it were enough for me, that I could accept these rigidly defined encounters as what he needs from me right now, that his idea of happiness differs from my own.  I try to convince myself that if a soda from a gas station is enough for him, providing that small pleasure should be enough for me.

There are times I can hardly bear it.

I expressed this to his caregivers during my visit a few weeks ago.  I’d brought a pizza for lunch that day to escape the monotony of another meal in the car, and we talked while Daniel and his two housemates ate at the dining table.

“It’s disheartening,” I told the two women on duty at his group home, who I’ve gotten to know during the seven months since Daniel’s move there.  “I feel sick that this is all we share together, that I can’t do more for him, you know?”

They did know.  They face the same challenges when bringing Daniel into the community.  They’ve seen how tightly he clings to ritual, to my visits unfolding precisely the same way each week, perhaps giving him a sense of control when so much of his life is determined for him.

They don’t know the Daniel I remember, who once enjoyed a fuller, more varied experience.  They don’t know that we used to go to parks, and playgrounds, read books together or eat at Perkins without incident; that we’d found a small beach near his former school where he tossed sticks and pebbles across the water as he did when he was a boy.  They couldn’t imagine us strolling through Target, where Daniel chose snacks and sticker books and magazines, unburdened by the compulsions which now drive his waking hours.  They couldn’t fully understand my despair, the loss I feel at his shrinking experience, how week after week I dread confronting anew the reality of his limited, shallow world.

“Do you want us to go with you?” one of his caregivers, Danielle, suddenly offered.  “I mean, we could take the guys and get ice cream or something.  We’ll help you keep an eye on him.”

I considered Dan’s reaction to a break in our prescribed routine, the agitation it may cause, but decided it was worth a try.

We followed them to Frostie Freez, picking up cones in the drive-through, then met at a nearby park.  Disconcerted, Daniel asked repeatedly for “store,” but accepted my assurances that we’d hit the gas station after we had our cones.

We chose a picnic table near the jungle gym, keeping a watchful eye as Daniel spotted the large fountain drink sitting unattended while a father pushed his toddler on the swings.

“Don’t worry, Daniel,” I told him, stroking his arm and squeezing his hand.  “We’ll get a pop when we’re done with our ice cream.”

He plowed through his cone, and I entertained him with photos on my phone while the rest of the group finished their ice cream. After just 10 minutes he’d had enough, anxious for his gas station stop, the activity he’d been counting on.

Walking back toward our cars, though, I was elated.  We’d broken from routine, if only briefly.  Impulsively, I held my phone out to Danielle.  “Will you take our picture?”

I hugged my son around his waist, self-consciousness forgotten, smiling as Danielle snapped a picture, Dan grimacing slightly at the delay but trying to return my affection.

“C’mon, Dan!” the women called, as Daniel produced the cheesy grin he always supplies when told to smile.  “Give us a real smile!”  Danielle kept snapping, trying for a good shot of both of us, as Daniel shuffled his feet, bored with this sentimental journey and ready to move on.

Danielle fiddled with the preview function of my iPhone’s camera.  I let go of Dan and reached forward to examine the phone.

That was all it took.  Daniel was suddenly bolting full speed toward a picnic table 30 yards away, McDonald’s bags and cups spread across its surface.

The scene is scorched on my memory: three middle-aged women running in wild pursuit, knowing we’d be too late, me in flip flops, bulky canvas purse banging against my hip, all of us shouting with desperate futility, “Stop! Daniel! Daniel, stop!”

Danielle cried out in warning to the woman and young girl who watched our approach like deer in the headlights, frozen in puzzled horror as Daniel barreled straight for them: “Grab your food!”

It was over in seconds, frothy milkshake upended, landing with a splat at Daniel’s feet, most of the sticky liquid missing his mouth completely in his haste to consume it, the forbidden beverage, the temptation he may have withstood had I not wanted a photo to commemorate our successful divergence from routine.

I uploaded the pictures to my laptop when I got home.  Daniel looked anxious, torn, trying to roll with the experience but worried by the threat to his ritual.

All week I agonized.  Was forcing an experience I wanted for my son worth a near-catastrophe, another public humiliation?  If Daniel is happy with a trip to the gas station, why isn’t that enough for me?

The following week we stopped for his soda at the onset of our drive rather than on the way home.  He was more relaxed that way, laughing and rocking in his seat, cradling the coveted bottle on his lap, secure, able to more fully enjoy the ride.  It was a positive visit, a happy one.

I looked again at those photos yesterday, at my own image, glowing and smiling freely, joyous to be with my son, in whatever small moment we were allowed, however far it fell from what I dream for him.  The scene that followed does not negate the joy of that moment, the hope sown by reaching for something more.

I don’t know yet how to find the right experiences for my son, those which may bring greater fullness, and curiosity, and joy to his life now, as a young man.  But continuing to seek them is worth it to me.

It will always be worth it.

The Garbage Ditch

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My friend David Royko, whose blog, The Chronicles of Ben, relates his family’s experience with severe autism, recently posted a story on Facebook about a man who had confronted his young son’s bully.

The story has drawn nearly 12,000 comments on the Yahoo!News site from which David pulled the story.

Not surprising, as the headline blazed, “This man pummeled an 11-year-old kid for bullying his 9-year-old autistic son.”

According to the article, the father boarded the school bus his son rode, and targeted the child his son pointed out as his persecutor.

“The father grabbed the 11-year old by the hair, pulled hard and raised the child out of his seat, then shoved him on the side of the bus where the window meets the wall,” Richmond Police Lt. Mark Gagan told CBS San Francisco.

Charged with child abuse and bodily injury to a child, Burnis Hurd remains jailed pending $50,000 bond.

While many of those commenting on this story disapproved of his tactics, most seemed to at least understand the father’s fury at his son’s tormentor.

I fall into that camp of thinking.

Of course I don’t condone adults abusing children, under any circumstances.  Few of us do.

But I understand how chronic worry, stress and fear for our children could lead to behavior we’d never deem ourselves capable of, until we’ve experienced these emotions on a daily, relentless basis.

****

Yesterday I received another email from my son’s group home director, detailing several recent escapes, or “elopements” as they are called in the adult family home business.

Apparently seeking the soda over which he’s become so obsessed, Daniel ran outside while staff’s backs were turned, entered the house next door, and helped himself to soft drinks sitting on the kitchen counter.  Close on his heels, staff shepherded Daniel quickly back home and smoothed things over with the neighboring family.

He bolted again the next day, and while staff intercepted him on the sidewalk, the neighbors this time called the police when they saw him coming.

Officers responded, conferred with the group home staff who explained Daniel’s situation, and, according to the email, “all was fine.”

The email continued, outlining another confrontation my son had that very morning with a peer at his day program, another scuffle over a cup of coffee resulting in Daniel being struck with the coffee mug.

Distressing news in itself.  But my mind was still frozen on the image of my non-verbal, autistic son, unable to explain his actions (assuming he understands them himself) when confronted by armed police and a home owner justifiably furious at a 22-year-old breaking into his home.

Consumed by a panicked restlessness, I wanted to take action, any action, to relieve my mounting hysteria at one more piece of unnerving news: fury at the neighbors who called police; at the group home staff; at my son’s insistence on behaving this way; at the ghastly twist of fate that burdened him with autism.

My first impulse was to call my son’s group home director or shoot off an enraged email demanding to know what the hell was going on, why they weren’t safeguarding my son.  But I believe they are doing the best they can with Daniel, a difficult client whose obsessions are matched only by his cunning at fulfilling them.  I needed to calm down before I responded.

“I’m going over to the police station,” I abruptly told my husband, fueled by a sudden urge to speak to the communications officer I’ve known for some years, who heads up our police department’s efforts to protect its disabled citizens through awareness and tracking programs.

“Is she expecting you?” the receptionist asked when I arrived at the station.

“No,” I replied, giving my name.

“What is this regarding?”

“Project Lifesaver,” I answered, referring the program wherein disabled residents may be equipped with a microchip, fastened to clothing or shoelaces, which can trace their whereabouts should they wander from home.  By now I’d formulated a vague plan to get some literature on the program to share with my son’s group home director, or the police department in the town in which he lives.

After making a call, the receptionist told me the officer I sought was in a meeting.  “Your best bet is to leave her a voice mail.”

“Is there anyone else I can talk to about Project Lifesaver?” I asked.

“No, I’m sorry, you’d really have to talk to her.”

“Do you have any literature on the program?” I persisted.

She shook her head with seeming regret.  “You’d really need to talk to her.”

Disappointed, I turned to go, then asked, “Can you let her know I stopped by?”

“I can’t guarantee she’d get that message,” she replied.  “It’s best to reach her by phone.”

Emotional and irrationally irked by her blithe response, I plunged recklessly forward.  “So, you don’t have, like, a message system, little cubby holes or something, where you could leave a note for her?”

She’d gotten up from her desk by this time, and came toward the bulletproof glass separating us.  “I could leave it on her desk,” she replied, as if speaking to a child.  “But I have no way of telling when she may get the message.”

Accepting I was beaten, and recognizing that it was perhaps unwise to create a scene inside a police station, I left, fighting tears of rage and helplessness as I hurried back to my car.

My husband bore the brunt of my emotional overload when I got home.

“She didn’t want to be bothered taking a message!  I mean, I completely get that she was in a meeting!  I didn’t expect her to come running out!  But the receptionist did nothing to help me when I was in obvious distress!  Aren’t they supposed to respond to citizens of the community?  What if I’d been in real trouble?  What if I was teetering on suicide?  What if I was, say, a teenager who had just given birth in her car, and wanted to talk to the one cop she knew before abandoning her baby?  Instead of leaving her baby at a Safe Haven zone, she could have ended up doing anything!  She could have left her baby in a garbage ditch!”

My husband remained calm throughout my tirade, waiting patiently until I came to a breathless halt.

“‘Garbage ditch’?”  He squinted his eyes.  “What’s a ‘garbage ditch’?”

****

Years of incidents with my son have yet to desensitize me to the often irrational fears for his welfare that haunt me every day.  With recent concerns over his new living situation, my anxiety seems to be heightening even as I tell myself I should be used to it by now, that I should live through these events with greater equanimity.

That’s not how it works, though, maybe for any parent, but certainly not for those whose children have disabilities that make them particularly vulnerable in our society.

I’m fortunate that the consequences of my tantrum yesterday were not as grave as those of the father whose rage at his son’s mistreatment landed him in jail, and a morass of legal trouble he’ll be mired in for years.

My only consequence was making a fool of myself to my husband.  And he’s seen that many times before.

The communications officer I went to see called me back that afternoon, listened to my fears and offered suggestions for talking to the police department in my son’s new town.  She’s sending me information on several monitoring programs for disabled residents that may help Daniel’s situation.

She apologized for the indifference the receptionist had shown me, which already seemed trivial in light of more pertinent concerns.  I feel silly that I reacted as I did, even as I recognize that my behavior was born of years of worry for my son.

At least it didn’t land me in a garbage ditch.

This time, anyway.

Laugh at Your Own Risk

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People say I tell a good story.  I don’t know whether that’s true or not, but raising a child with autism certainly provides a lot of material.

The story lately concerns Daniel’s obsession with beverages: his, mine, yours — anyone’s.  Even the old lady’s at McDonald’s.

It began over a year ago with him snatching staff members’ sodas, at school and in his group home, and gulping them down as fast as possible.

Now any drink is fair game.  His beverage swiping has increased so dramatically that we can no longer take him to restaurants or even Starbucks, where, along with his lemon cake, Daniel will help himself to the coffee, latte or Frappuccino of any hapless patron in his path.

The last time I took him inside a McDonald’s was nine months ago, during a Sunday lunchtime.

We finished eating, and Daniel took our trays to the trash as usual, then suddenly bolted toward a family seated a few yards away.  Targeting the youngest child, a boy about six or seven, Daniel grabbed the cup from the kid’s hand and raised the straw to his mouth.

Horrified, I heard the boy’s father’s startled protest — “Hey, hey!” — as I struggled to retrieve the cup, which six-foot Daniel held high out of reach.  He polished the drink off in seconds.  Mission accomplished, he relinquished the cup as I grabbed him by the arm.

“I’m so sorry,” I said, turning to the stunned family behind me.  “My son is autistic, and doesn’t always behave the way I’d like him to.  I’ll get you another drink.”

The father, grasping the situation, told me not to worry, it was fine, no problem — all the kind, understanding words most people use when encountering the unusual behavior of a disabled person.

His compassion did little to soothe my own upset, though.  Dragging Daniel by the arm, I returned to the counter.  “I need another drink this size,” I told the clerk, holding up the boy’s cup and pulling two dollars from my wallet, keeping a grip on Daniel with the crook of my arm.

The clerk looked at me blankly, as though a soda had never before been ordered in the history of her McDonald’s employment.

“I need a drink this size,” I repeated urgently, holding the money across the counter.  She just stared at me with her mouth open, finally pulling a fresh cup from the stack behind her, then shaking her head when I tried to pay.  “I can’t take that,” she whispered, like I was offering her a bribe.

“Well, all right,” I replied, beyond caring whether I paid or not.  I grabbed the cup and pulled Daniel back to the victimized family.  The father tried to refuse the cup, but acquiesced when he saw my distress.  Apologizing profusely, I hustled Daniel toward the door.

But the party wasn’t over quite yet.

Nearing the exit, Daniel abruptly wrenched free, darting to a table occupied by a tiny, white-haired woman in her nineties, and what appeared to be her daughter, herself at least 75.  In a flash, he grabbed the older lady’s soda and bolted toward the bathrooms, guzzling the drink as he ran.

“He cannot be allowed to do that!” the daughter called stridently across the restaurant, over my own admonishments in Daniel’s direction.  “He cannot be allowed to do that!”

Desperate now, I called to the woman as I rushed past, “I’m sorry, he has autism — ”

“Yes, I realize that,” she called after me.  “But he cannot be allowed to get away with that!”

Neighboring customers cast wary glances our way as I snatched the now-empty cup from Daniel’s hand and turned back to his latest casualties.

“I’ll get you another drink,” I told the woman, “after I get him in the car.”  Before she could respond I dragged Daniel out the door and into the backseat of my Jeep, rebuking him incoherently across the parking lot.  “You stay right here, do you understand me?”  I hit the lock on my key fob and ran back inside.

Still clutching the original two dollars, I approached the women’s table, where the daughter had, apparently, undergone a change of heart.

“It’s ok,” she said indulgently, waving off the money I offered.  “It’s ok.  It’s ok.”

But I’d passed my stress threshold by then.

“It’s not ok!” I cried, verging on hysteria.  I tossed the money on the table in front of her.  “It’s not ok!  It’s never going to be ok, so please, stop saying that word!”

*****

Telling the story in the weeks to come, I was able to laugh along with my audience at the whole preposterous scenario.  It was a relief to laugh about it, after the fact.

But that incident underscored how parenting this child, how living for years through these events, has shaped my attitude and behavior, just as autism shapes Daniel’s.

I was telling a family member about my ordeal a few days after it happened, still shaken, mourning my son’s ever-shrinking world, and the disability that had robbed us of sharing even a meal together at McDonald’s.

She was already chuckling as I reached the epilogue: driving from the restaurant, disgraced; me sobbing in hopeless futility while Daniel, already focused on his next request, asked repeatedly for Starbucks.  I’m ashamed to admit how I screamed at him, again and again, as we drove back to his group home, another visit ruined by this hideous, inscrutable disorder, and my dismal collapse under its strain.

“It’s actually not that funny,” I said, annoyed by her failure to see the larger, more devastating picture.  “This is a pretty big problem for us right now.”

“Well, I’m sorry, Kristen,” she told me, giggling.  “But I just have to laugh at that one.”

I said nothing more.  But that family member topped my shit list for months to come.

And that is my problem.

All my friends in the special-needs community have experienced these episodes, multiple times, surviving them only by recognizing and rolling with their absurdity.  Better to laugh than to cry, right?

There are times when I can’t laugh, though, when the ramifications of Daniel’s behaviors outweigh their hilarity, when idiosyncrasies we once found quaint now impinge so dramatically on his chance to live even the semblance of a normal life.

But is it reasonable to expect those who aren’t living this to truly understand, to intuit the difference between a “funny” ordeal, and that one, final episode that breaks me?  Do I have the right to dictate their reactions, when they are patient enough to listen at all, to commiserate with the difficult parts of my life that have no real bearing on their own?

This is my worry to struggle through, as best I can, while the rest of the world struggles through their own.  Months of resentment later, I recognize that it is my problem, my failing, to ask those around me to view my experience through a lens that is mine alone.

I suppose it is better just to laugh.

But only when I say so.