Page 112 of Touch and Torque


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The weight loss strikes me first. It’s not the gaunt, skeletal look of end-stage disease, but it’s enough to show weeks of nausea and her body rerouting every bit of energy it has left. Her face is sharper now, cheekbones more prominent, skin carrying that fragile, almost translucent quality I see at work and absolutely hate seeing on my own mother. Her silver hair is still tidy, but it’s grown out at the ends and noticeably thinner from the chemo. She’s wrapped in a dark green cashmere cardigan despite the warmth of the room, like even the softest fabric is barely enough these days.

Her hands rest elegantly in her lap as I cross the room. Her eyes, at least, are exactly the same—sharp and unflinching.

“You’re doing the assessment,” she remarks.

“I’m saying hello,” I reply. I lean down, take her hand, and kiss her cheek. She holds on a second longer than usual, and I feel how fragile she is.

I lower myself into the chair opposite hers. The room holds its breath between us.

“How are you, Mom?”

She smiles, softening the usual seriousness in her face, warmer than I’ve seen in a long time despite everything. “I’m good. Cynthia, my day nurse, keeps my medication schedule perfectly on track.”

“Cynthia’s right to be strict,” I say, glancing toward the hallway. “Did Marcus set all this up? The staff and equipment?”

“Most of it. Patrice still runs the house like a general. There’s another nurse, Rosa, who does overnights three nights a week, andthe physiotherapist comes on Tuesdays.” She lists it all out like she’s giving a corporate briefing instead of talking about her own cancer. “Your brother’s been here every Sunday since September. I didn’t ask him to come, and I haven’t discouraged it.”

“He didn’t mention that to me.”

“No,” she says simply. “He wouldn’t.”

Of course he wouldn’t. Marcus has clearly been holding this whole family together while I was off in San Diego pretending distance was the same thing as independence.

We talk for a while about her treatment, the latest tweaks to her chemo regimen, and all the clinical details that give us something safe and solid to hold onto.

I pour her a cup of tea from the pot on the side table and hand it over. She then decides to dive straight into the heavy stuff.

“Lance,” she begins, chin slightly up, her eyes on me. “I’m sorry you felt the need to leave home.”

I pause. My mother rarely apologizes, and she almost never catches me off guard. Today she’s doing both.

“Mom, that was a long time ago,” I say, aiming for casual.

“I’m not making excuses for how things went,” she continues, setting her tea down. “I may not have realized how hard I was being on you for so long. When you left and started building a life without us, I thought it was better to let it be. That doesn’t mean I missed you any less.”

I shift forward on the edge of my seat, staring at the floor. “I should’ve been around more, not just for a few days at Christmas.”

“For me, that’s probably more than we deserve.”

“I kept my visits short and left before anything real could get said.” I meet her eyes. “I’m sorry.”

“No,” she replies fast. “I didn’t make it easy for you to come back. I understand that now.” She smooths an invisible wrinkle on the arm of her chair. “I’ve rehearsed this conversation for years.Now that you’re actually here, I realize I’m less prepared than I thought.”

“That’s new.” I crack a small smile. “You, not being prepared.”

“It is,” she agrees, with that dry edge that’s all hers, the one I’ve been stealing for my own sarcasm.

My mind goes back to how all of this began. “Remember the last time I saw Aunt Matilda?”

She nods, probably recalling her sister’s final days and the little time she got to spend with her before she died. Life had been too busy, even with family facing a terminal illness.

Aunt Matilda was my mother’s older sister and only sibling, a lawyer specializing in healthcare law who eventually founded Hearthside Home, a palliative care hospice in the Eastside suburbs outside Seattle. The family thought it was deeply eccentric, which, in Bradford language, translates roughly to ‘We don’t understand it, therefore it concerns us.’ She was always my favorite aunt.

She never married, never had kids, and always said she already had more than enough family in her staff and patients. She said it like she meant it, and it never sounded sad coming from her.

She was one of the few adults in my life who actually laughed at my jokes like they were funny. She’d call just to see how things were going at home and at school. She listened to me like I was a real person, not just a rough draft of whatever my parents had already decided I should become.

When she got seriously ill, she was admitted to her own hospice and cared for by the team she had built. She spent her final months in the place she had spent her life trying to make bearable for other people. I’ve thought about the irony of that for years and still haven’t decided if it was cruel or kind.