“Don’t worry. We can fix it.”
How many times have we said this, in how many contexts. We’ve said it as relationships founder. We’ve said it at work when a presentation goes off the rails, when we forward the email straight to the customer, with the full thread intact. Recall, recall, recall. This message has been read. It’s okay. We can fix it.
And we say it to our children. We say it a lot to our children. It’s the pact we make with them when they’re born, tiny and red and already everything. Tiny debutants into the world. No matter what, we’ll always be there. We’ll be there, and we’ll fix it.
When they bring us a construction paper masterpiece torn down the middle, we carefully tape it back together. We are masters of super glue and have even hand stitched the seams of that silly purple Dollar Spot stuffed …hippo? (Horse? For $3, it’s anyone’s guess.) We have half a dozen types of character band-aids. Snoopy. Tinkerbell. Turtles. We try to give them the right words for when they’re frightened, angry, lost. For when friends are cruel, or siblings dismissive. Bring me what’s broken. Bring me what hurts. We can fix it.
Except sometimes we can’t. The relationship ends. The job is lost. Some hurts a band-aid can’t bind. We have to say instead, “I wish I could fix this. I wish I could make this better.”
My youngest daughter has had stomach aches for ages. We’ve taken her to doctors. To allergists. We’ve tried holistic biofeedback and heartburn medication and IBS medication. I’ve emailed her teacher to please look out for medication side effects, and wondered if this is the right path. We’ve tried eliminating fried foods and dairy. She prefers not to actually eat at restaurants, where she’s forever running back and forth from the bathroom – “just to try” – and so we often pack up her whole meal and bring it home while she colors and does the word scramble and circles the hidden objects on her placemat. Her food diary is a puzzle. Sometimes she’ll eat strawberries for breakfast with no issue, but after dinner they’ll make her sick. Cheese is definitely a trigger but yogurt seems to be fine. 50% of the time, she’ll feel better after 30 minutes. 50% of the time, she doesn’t and it can go on for what seems an eternity. She’ll spend the 30 minutes after lunch resting in the school clinic, except for “when it takes two 30-minutes.”
“Tonight went pretty well,” my husband will say, encouragingly. “But she didn’t eat anything,” I’ll say. “Well, that still tells us things,” he’ll reply. What?, I wonder. What does that tell us? That… food … is the issue? And I text my mama friend who knows what it feels like, and doesn’t try to fix it, but says, “I’m so sorry you’re going through this.” And even though I know it’s actually my daughter who’s going through it, I lean into the empathy and let my shoulders sag a little while my fingers fly to pour out the guilt and frustration and exhaustion.
Every time we schedule a new appointment, she’s thrilled because she believes that with this new approach we’re going to fix it. And baby girl, I swear I’m trying. When I held her crying on my lap for bloodwork, her arms and legs windmilling in fear, screaming, “I don’t want to do this!,” me crying, too, and my voice breaking as I tried to sing Hush Little Baby, I told her, “They can look at your blood and see what makes you feel sick. This will be over in a few minutes, and it will be worth it.”
For the blood panel review a few weeks later, she felt nauseous that morning. She held my hand tight in the hospital elevator, in the way that reminds me how little she still is, even as big as she’s getting. She was a little nervous, scared because we’d been there before and it had hurt, but excited. This time. This time we could walk out knowing. But of course we didn’t. Everything was within normal ranges. Just like allergy skin testing had said, too. The doctor called it good news. And I suppose it is. But it’s also frustrating. “Are they going to have to do it again, momma?” she asks, one more little hope extinguished. “No,” I said. “The next doctor can look at these results.” But, quietly, in the back of my heart, I thought, Maybe. Maybe.
And I remind myself it could be so much worse. I remind myself that some parents have spent not just hours but days and weeks and months in hospitals. That some days she feels just fine, and that she’s a sweet, happy child much of the time. But when that red flushed face looks up at me, with splotchy chest and wet eyes, I know I can’t fix it. “You need sleep,” I say, tired myself. “I can’t even do the easiest thing in the world. I can’t even sleep,” she says despairingly. She carries a yellow plastic mixing bowl to bed with her – just in case – though she never actually uses it. But it’s security, along with her worn-to-real, loyal, trusted Sam-I-Am. She gets up, again, and goes to sit outside in the cold night air. “I just feel like I’m allergic to everything inside,” she says. So we open her window, even though it’s snowing. And I lean my forehead against hers. “I wish I could fix this,” I say. And then she’ll turn on her music, pat my cheek and say, “Mama, go get some sleep.”
It breaks my heart to know that she’s already learned what I wanted to protect her against, at least a little while longer: some things you can’t just fix. There is no super glue. No Tinkerbell band-aid. There is simply, I’m so sorry you’re going through this. And if I can’t fix this, I’ll just be here.