young widowhood


Roadside Memorial Day

It had to happen. Roadside memorials being a bitch to set up and maintain and what with friends and relatives forever asking to see pictures of the latest anniversary or holiday grave decorating, a cemetery app was inevitable. It’s handy – literally – and Facebook update ready (I’m assuming because if one can’t update the graveside status for the FB peeps – what good is it really?)

And it’s creepy wrong on levels of levels. There’s so much that’s sick on both sides of this app – seller and buyer – that it’s hard to know where to begin.

It reminds me of prayer cards.

My Catholic experience with death and funerals includes holy “baseball cards” with pictures of the deceased, born on and expiry dates, a prayer of some kind and a cool religious icon on the front.

Which, I guess, is creepy too except that you didn’t carry them around and whip them out like the latest baby photos.


Photo of Terry Fox, Canadian cancer fund-raise...

Image via Wikipedia

Terry Fox Day is a Canadian thing. During the month of September, communities all across the country organize run/walk events to raise money for cancer research in Terry’s name. This year marks the 30th anniversary and celebrates the $500 million that has been raised in his name since his attempt to run the length of Canada thirty years ago.

What made Terry’s run special and inspiring to Canadians was the fact that he’d lost part of his leg to a cancer that would go on to claim his life at the age of 21. His cancer returned after a three-year remission during his trek and he never saw the finish line, but his family was determined that the run become an annual event and it has.

I first heard of Terry as a high school student. We read about him in our Catholic high school back in Iowa. It was one of those grisly teachable moments that the nuns and priests were so fond of when I was a child. “See how lucky you are that you aren’t one-legged and being eaten away by cancer?” was the gist of the lesson.

As an American though, I didn’t know the run went on to become a yearly event.

Until I emigrated to Canada three years ago.

Terry Fox came back into my life via Dee, who discovered Terry in kindergarten and developed a morbid fixation that plagued us for months.

At the school assembly, where footage of Terry’s original run was shown and the children received morbid Terry tattoos, Dee met up with death too young – again.

She created a tiny little shrine for the tattoo in our dining room and all manner of death, cancer and why questions haunted Rob and I more than our own dead spouses do when they are feeling feisty.

Last year, Dee asked if she could skip school on Terry Fox Day. She didn’t want to see any more pictures of him. They made her feel sick.

“So you don’t want to take a toonie or go on the walk?” I asked.

The kids bring “toonies for Terry” and go on a 3km walk in the afternoon. She loves donating coin. We can’t walk past a street musician without tossing change, and she adores group walks, which is ironic because “walking” her father is the eye-rolling height of boring in her opinion.

“No, I want to bring a toonie and walk, ” she said. “I just don’t want to hear about him or see him anymore. He makes me sick.”

A quick flurry of emails between her teacher and I resulted in Dee being excused from the assembly after which she happily strolled hand in hand with her teacher.

This year? Same thing. Pictures of Terry give her “a sick feeling in my tummy” and she would rather stay home from school (she adores school so much that she can make weekends unbearable for Rob and I) than endure the sight of Terry.

More emails. A new, and fortunately equally sympathetic, teacher will handle distraction duty.

My own feelings about the cancer run/walks is predicated on the fact that my late husband died of something rare and unglamorous and, therefore, not worthy of fund-raising. The boobie bracelets for breast cancer and the fun-runs for cancer research in general distract from the fact that most people die of something other than cancer.

Rob’s heart attack is a stark reminder that cardio-vascular ends await more of us than cancer does and, between it and accidents, that’s how most of us who don’t die old and asleep in our beds will shuffle off this mortal coil.

Despite losing my father to lung cancer and Rob losing Shelley to melanoma, I feel removed from the whole cancer thing most of the time.  I have read too much to believe that there is a cure anywhere or ever, and I am a bit hesitant to cheer for treatments that mostly seem aimed at allowing death to whittle away at you at the expense of life’s quality and at the greater expense of the physical, spiritual and mental well-being of your loved ones.

Dee took a toonie. The school’s gym isn’t finished and so there will be no assembly, but her teacher will shield her from any reading material the class goes through. And she will walk. She does love to go on those walks, which I am grateful she is healthy and able to do.


Animated sagittal MRI slice of my beating heart

Image via Wikipedia

The Canadian health saga continues with Rob’s first cardiac rehab meeting yesterday. His cardiologist – the one I’ve yet to even lay eyes on and who he saw just once during his procedure (which the doctor didn’t perform but merely supervised in any case) – referred Rob to a five week program designed to assess his fitness to return to work and get him back on the healthy heart road via an exercise program and fun little classes on weight control or sexual function.

Oh, that last wasn’t an either/or, but examples.

The cardiac rehab is located in Edmonton. Per usual the parking options were limited. So hard to come by in fact that a portion of the orientation is devoted to parking issues.

Rob was probably one of the youngest participants. Certainly no one else showed up with an eight year-old in tow. There was perhaps one gentleman in his late 30’s or early 40’s, everyone else was qualified for the discount menu at Humpty’s.

As we walked in, each patient receives a personal packet of info containing his/her appointment schedules and a menu of rehab class options in addition to the ones pre-selected to match his/her “event”.

No one has heart attacks. There are “cardiac events” only. It’s a pc thing.

The nurse who conducted the session tried hard to be brief and witty and was neither, but she told a little story at the onset which neatly sums up the health experience here from my perspective.

The operator at the hospital received a call one afternoon from an elderly woman wanting to inquire about the status of a patient.

“Who is the patient?” asked the operator.

“Helen Finley,” the old woman replied.

“Well,” the operator said, “I’ll be happy to get an update for you. Let me put you on hold and I will contact the nurse on the ward for information.”

A few minutes go by and the operator returns with good news.

“The nurse tells me that Helen is doing quite well. Her blood work came back normal and her blood pressure and other vital signs are good. In fact, she’s doing so well, that her doctor is planning to release her this evening.”

“Oh,” the old woman’s voice shook, “that is good to hear.”

“I’m glad I could help, ” the operator said. “Is Helen your daughter?”

“Oh no,” the old woman said, “I’m Helen and no one tells me nothing.”

Of course no one laughed. I suspect that any of the other people in the room could tell stories that mirror our experience. But the nurse didn’t mean to highlight one of the chief problems with the system here; she was trying to make a point about asking questions. The assumption being that patients are in the dark because they don’t ask questions rather than the fact that often there is no one to ask questions of.

After the presentation, which could have been mailed to Rob and lost nothing by way of information, we hung around until the auditorium cleared. Rob’s goal for the afternoon being to arm wrestle someone into giving him return to work clearance.

“After your stress test tomorrow and a couple of monitored exercise sessions,” the nurse explained, “you will meet with the occupational therapist, who will give you her recommendations to take to your family doctor. He will give you clearance.”

“Um, that’s not what I’ve been told, ” Rob said and went on to inform her of the buck-passing he’s encountered ever since he first asked “when can I go back to work.”

He had hopes of heading off to work on Monday when Dee returns to school. I kinda had hopes in that direction myself, but it could be another week or so.

Provided nothing goes wrong at the stress test.

That thought just won’t completely go away, and it’s silly because Rob hiked six miles not two weeks after he got home from the hospital. He’s installed air conditioners, and this last weekend, we were up and down the stairs at the Shaw Conference Centre from the river to Jasper Avenue more times than my legs care to recall. If he was going to drop, he’d have done it by now.

And his job is, frankly, physically more restful than any of his hobbies are.