{Originally published on Chicken and Cheese.}

Not too long ago, we bathed The Poo while chatting about all the people who love her.

We listed off all her grandparents, and then spent time explaining how we, her parents, were also children.

“Your grandma and grandpa are my mommy and daddy,” Mr. Chicken told her, as he sluiced shampoo from her hair using a small container of water. “And meema is Mommy’s mommy.”

Suddenly, without warning, The Poo realized a new truth about our extended family.

“Mommy!” she exclaimed, the gears in her head grinding away. “You don’t have a daddy!”

I winced, her words hitting me as hard as any blow. My father’s been on my mind of late.

This is, you see, my season of loss.

*****

Even as we welcome a new soul to our household, my mind wanders – dreadfully – to this date on the calendar. Four years ago today, at 3:30 in the afternoon, my father drew his last breath.

Each year I think the hours will come and go like any other, just a pair of numbers and nothing more. I believe I will keep house and tend children, spending my time as I would on an ordinary day.

But this day, this terrible day, will never be ordinary again.

The immediacy of my grief has faded; that much is true. No longer do I wake in the heart of the night, veins pounding with dreams the color of blood. No longer do I wake each Aug. 26 precisely at 4 a.m., the time my telephone rang with the news that an ambulance was ferrying my father to the emergency room.

But when August begins to wane, a bruise rises to the surface, tender and easily irritated. The warm weather and the slant of the sun prompt recollections I’d rather forget – walking my parents’ dog in the late afternoon the week before my dad died, while they were away at The Mayo Clinic; the hope I felt when the doctors reported that the cancer was dead; the terrible tremor in my dad’s voice the last time I spoke to him on the phone.

I called to tell my mother I wanted to come out to Minnesota. I was on vacation, and something inside urged me to get on a plane and be with them.

{Originally posted on Schmutzie.com}

Over one year later, I am still discovering the shape of my grief over the loss of my uterus.

I miss a thing I could never see. I have no documentation of its existence. It does not show up in family photo albums. My clothing fits as it did before the surgery. I never touched it with my hands. I cannot trace its outlines in pictures or where it is no longer on my body.

The only evidence that it was ever here is a pregnancy test that I keep pushing to the back of the bathroom cupboard behind the cleaning supplies.

I do not like that it was cut up into tiny pieces and vacuumed out of me. I do not like that it became medical waste. No part of any body should be made into medical waste. Our bodies hold far too much power, far too much meaning, to be so degraded.

I am angry that I could not take it with me, that I could not find my own place to put to it to rest. I hate not knowing where its pieces are. I imagine it having its own sapling beneath which it could rest and feed its growth. I need to imagine it being less alone.

The shape of this grief is little more than a chronological line between two points, from there to here. It has yet find its flesh.

{Originally published on “Et tu?“}

For whatever reason, I keep stumbling across blogs by mothers who are battling cancer lately.

One of the things that’s most striking about every one of them is how much looking through their posts highlights how fragile life is, and how little control we really have over our destinies. The post at the bottom of the page, from last Wednesday, might be titled something like “Feeling great!” and recount high hopes and improving health. And then the latest post, from today, might be titled “Bad news” and tell of dire test results and the choking realization that the author will probably not live to see her children grow up.

Just now I was doing my usual blog reading during the
kids’ naptime, and I came across yet another blogger who just received
a grave cancer diagnosis. She’s a mother, she’s not even 30 yet, and
there’s a good chance that she doesn’t have a lot more time.

Oddly, I was able to keep a stiff upper lip through most of the post, until she got to the part about all the plans she had: how she had her life neatly in place, her plans for the next few years all settled, and this diagnosis completely derailed everything. Nothing seems within her control any longer, and that’s one of the things she’s struggling with the most.