I pull into the driveway and glance up to my porch. In front of the door sits a big brown non-descript package. There could be ANYTHING in there. A surprise! Each month I indulge my fancy and play the part of someone who does not already know what she will find when she tears the packing tape off and unfolds the flaps. I try my best to conjure the limitless expectations of Darren McGavin’s character, Ralphie’s dad, in A Christmas Story as his “major award” is delivered. It’s here, it’s here! Some days I even tap my fingertips across an invisible word on the cardboard and slowly, profoundly emulate his wishful interpretation of the letters, “fra GEE lay.” The irony is that though the box doesn’t actually bear such a stamp, my forehead could easily read “fragile” at such moments.
Upon my first kick-shove of the box into the front door, the game ends. For I know what it is. It came last month and the month before. It’ll come next month.
It is nothing so fantastic, light and burden-free as a leg-shaped lamp.
Sometimes I let it sit just inside the front door where I won’t often pass it. I pretend that it’s too bulky for my short self to carry downstairs and dispatch into its storage space with what’s left from the last box. Rare are the times it doesn’t send me to such willful denial of its existence that I’m rendered unable to spirit it away in the name of tidy, objective detail management.
Today I let it sit.
This box changes nothing, adds nothing, promises nothing. It’s not a surprise for my girls; it’s nothing for me or for my husband, our house or our cars. It’s not full of gifts I’ve carefully picked out for others. In fact, we have no choice at all in this. It’s delivered for the cognitive and communicative differences, low muscle tone, sensory issues and motor processing problems that conspire to make this box a requirement on a monthly basis.
Inside are purple-wrapped cubicle stacks from the medical supply company for my 8 year old with Rubinstein-Taybi Syndrome. The customer “care” reps at the company are sticklers about calling them incontinence products. The generic looking logo on the package demurely refers to them as pull ups. But I call them what they are: diapers.
Diapers have been in our lives for more than 12 years, with a brief respite of about 18 months in there before my younger daughter was born. I have only 2 kids. Sure, my mom had 10 kids and used cloth diapers, so she has me way beat in quantity, duration and effort. But from the very beginning she had a general idea of when it would end.
It’s the fact that there is no clear path to the end that makes it daunting. I have long ceased finding the act of doing the changing particularly inconvenient when we are at home. It’s just part of everything now. But the ways we have to consider her dignity, her privacy - who knows, who doesn’t know, who might mention it around whom – that is what’s exhausting now. Energy further evaporates when I inevitably wonder if we’ll still be managing these things a decade from now, 2 decades, 4…
We grapple with the few scant invitations and social engagements she gets, wondering how we can figure the logistics if she needs to be freshened. When we visit other homes, I measure how long we’ll stay by whether the host is likely to be able to discreetly handle my request for a plastic bag and to know where the outdoor garbage receptacle is without asking too many questions. We size up public restrooms, worrying about space, germs and location of waste bins.
Low rider pants are a bane when you have a child who employs a sensory satisfying stance of a tripod - hands and feet near each other on the ground and her derriere airborne. The slippage of her Levi’s partners with the impossibly high waist of the papery Medicaid-funded pull-up knock-offs to leave no shred of mystery.
You can’t chat about this with your family and friends. Even my friends within the disability world, we guard our child’s dignity and our own fragile case we keep some things in, and we keep quiet. I can’t bear to hear the earnest suggestions of others, thinking I’d never considered the techniques used with my older daughter, thinking perhaps the problem is that I have given up. I haven’t. I believe in my heart of hearts that it will happen one day. Whether that day is weeks, years or decades from now is the question. The blithe statement mothers of preschoolers offer mothers of toddlers sends me to a place I don’t like to spend too much time in. “Well, don’t worry, it’s not like she’ll go off to college in diapers.” It’s possible. A kid could go off to college in diapers. If that kid would be accommodated in college, that is.
There are worse things, yes. But it adds a daily layer of complication and general hope-suck that compound the energy-devouring effort already put into every single detail of this disability life.
This is just so incongruous with who she is, how clever she is, what a social, complex, witty, inquisitive, powerful young lady she is. Whether we want to admit it or not, knowing someone wears diapers whether as a result of being very young, very old or very different, it simplifies that person in most people’s eyes. It reduces them. Her dad, her sister and I are in constant combat with this reduction of our limitless girl every single day.
There it all is, laid out. I cross my fingers for her dignity, that you who know her and read this will protect it as you would her physical being. I cross my fingers that the combination lock requiring so many developmental mysteries to align just so, clicks and pops open one day.
I cross my fingers for a porch void of anti-surprise packages.
Yeah. I know about this. In fact, I've been watching the door all day, wishing the UPS truck would show up because I have nothing to put on my 9 year old son tonight. So far, nothing, which means a trip to Walgreen's.ReplyDelete
And I don't know. I just don't know. It mostly doesn't bother him. Or doesn't seem to, but occasionally he cries and I wonder, does it bother him always and he just hides it? And there's the caution and the carefulness and the privacy issues and washing the sheets (because really, what kind of diaper could keep up with a kid who uses a water bottle as a sensory something-or-other all day long?) and the cost (oye, the cost!) and I see no end in sight.
And mostly it's OK, except when it's not.
"And mostly it's OK, except when it's not." Precisely, Adrienne. SO with you.ReplyDelete
Thanks so much for sharing this. It's important to be able to share everything.ReplyDelete
We ran a recent post about a mom whose child became toilet-trained (hate that wording!) at 11. I'm not promoting the technique they used -- it's just nice to know that things can change sometimes over time.
We have to work against that stigma of a person using diapers being simple or reduced in some way. There are all kinds of people who are incontinent for different reasons.
Thanks for sharing your story. Louise
wow what a powerful postReplyDelete
Oh, I feel your pain. My daughter does not suffer from the same illness, but has so many special needs issues. We too want to maintain her dignity. Every day is a battle. There seems to be no end in sight. You are pushed and pulled so many ways as a parent. One day you completely understand how the school district wants to help you, on other days you know they are just going through the motions. Friends come and go - mostly go. Play dates nearly non-existent. I try to stay away from writing about my daughter on my blog. I want to make people laugh, and think about other things. But sometimes I cannot help it. Every now and then, I write about our struggles. I did last night. Please check out my post called "Damaged Goods - a 2011 Retrospective." I think you may be able to relate.ReplyDelete