An editor once told me that an essay I’d written was just too sad to be inspirational.
I hadn’t really been aiming to inspire, but simply tell the truth as I knew it. And sometimes the truth is, undeniably, sad.
The truth hit me full in the face today when I got an email from my son’s group home director. I knew a message like it would come eventually, but still was not prepared for it.
It’s been three months since Daniel moved to his new home in Wisconsin, after aging out of the residential school he attended for six years. It wasn’t easy to find this new home, for a variety of reasons, foremost being Daniel’s behavioral history, which includes aggression and biting. Finding qualified facilities for people like my son is challenging, to say the least.
Most of the time Daniel is easy going, engaged, blowing his bubbles or working a sticker book, enjoying the DVDs he knows by heart. He laughs often, loves music and riding in the car. He has adjusted well to his new home, and is usually compliant and easily occupied.
But he can also turn inexplicably aggressive, and sometimes violent. While infrequent, his outbursts are sudden, rage-full, threatening. He’ll lash out, actively seeking to hurt the people caring for him or getting in the way of what he wants. He is capable of becoming a person almost unrecognizable from the bright and beautiful young man I love so deeply.
It is incredibly sad to type these words about my son, and know that they are true.
Two weeks ago Daniel began attending a day program for disabled adults four mornings a week. We knew instituting this new regimen wouldn’t be simple, as, like many autistic persons, Daniel does not typically embrace changes in routine. Nevertheless, we were anxious for him to begin structured, purposeful activity, however modest, rather than spend day after day within the walls of his group home.
The email I received today detailed two incidents which occurred at the new program in the last few days. In the first, Daniel grabbed a pot of coffee and splashed the hot liquid across his legs while trying to gulp some down before it was taken from him. The next day he became agitated, without apparent cause, and lunged at his caregiver, then bit the peer who tried to intervene, breaking the skin and necessitating an obligatory trip to the hospital.
Caregiver, peer and Daniel are fine, I’m told, and the group home manager remains confident that Daniel will adjust to the day program with time.
But it is incredibly sad that after 20 years I still don’t understand why my son behaves the way he does, and I am still so powerless to help him.
For three months friends have asked me how Daniel is doing, how the move has worked out. I want so much to tell them that it’s great, it’s beautiful, a perfect fit after such a long and difficult search. I feel almost obligated to provide a positive report to these caring people: that after all the turmoil they’ve borne witness to, our efforts finally paid off, and I can offer a happy ending in repayment for their support. Perhaps, too, by saying it to them I can convince myself that it’s true. But I know by now that the truth is more complicated than that.
How could I tell my friends that it’s working well, that everything is fine, when I knew the day would come when it wouldn’t be fine, that the honeymoon would be over; and the next time they ask I’ll sense their letdown, their confusion at my dispirited, uncertain answer, which may be the only true answer I can give? Because Daniel’s insidious, baffling behaviors moved to his new home with him.
I don’t want to tell my friends that I’ve been waiting for the other shoe to drop, dreading the call or email detailing a set-back, further limiting his options, his chance to lead a productive, meaningful life. I can’t admit my fear that perhaps we made a mistake, that maybe we didn’t pick the right place after all, even as I know our options were so limited as to make “picking” the right place practically moot. I don’t want to confess how scared I am that he’ll never come around, never grow out of these behaviors which so restrict his potential, his future, his relationship to us and the rest of the world.
I don’t know how to tell them how unbearably sad it is to know that he is miserable when he lashes out, and I live too far away to comfort him; that this can’t possibly be what God intended for my son, and yet it is happening, it happens again and again and we don’t know why or how to stop it.
When I visit him now our outings are dictated by his unpredictability, the bleak certainty that I can no longer control this six-foot man-child, if he becomes without warning a person frightening even to me. We are confined to drives in the safety of my Jeep, roaming the streets of a town I don’t know, a world away from all I once dreamed for him.
And how can I express, in the wake of his abhorrent behavior, that I share moments with my son that make up for it all, that remind me of who he really is, that there is more to him than the aggression, which in its enormity eclipses the loving and sensitive young man I know him to be?
Will it mean anything to those who have witnessed his rage if I recount the moments when he is joyful and laughing, rocking back and forth in his seat as we drive, windows down and air blowing clean across our faces, listening to a Red Hot Chili Peppers song again and again, volume cranked high? Would anyone believe that he understands me when I tell him, “Here it comes, Daniel!”, that he laughs then, as the bass solo pulses through our bodies, washing away for a few blessed moments the anguish that autism, in its awful duplicity, has inflicted, and I have Daniel again, my real Daniel, my true and beautiful son?
Because that is the truth, as well. And I hold that truth against my heart, when it is breaking.
My heart breaks for Daniel and you as well. He is such a beautiful boy who is locked inside a body that can’t express his frustrations. I can only imagine how I would lash out too if I didn’t know how to let someone know what I felt or needed. You are in my heart and thoughts today as you try to make the terrible situation just that much more better. Your love and support of Daniel has given him the best care available and it is so devastating that sometimes that doesn’t feel like it will ever be enough to prevent him from lashing out. I just have to believe that the doctors will find a way to help him march again without tripping so often.
Thank you, Marla, dear friend. I know you truly understand (doubly) what I’m trying to express. You have walked this journey for years as well, and know the anguish and unique joy that only comes from this special parental relationship. Thanks for always, always being there for me.
Once again you brought tears to my eyes and my heart just aches for you all. All you can do is keep marching on. You will stay in our prayers.
Thank you, Lori. You’ve been helping me through the journey for many years.