Category Archives: Terminal Cancer, Day by Day

Grieving in Public

Sometimes when I talk to friends/family/strangers about the cancer I confuse them, because I’m not wailing and crying on them. Some people are uncomfortable around crying people (maybe most of us are) and so perhaps this is a relief, that they don’t have to deal with me sobbing, but I often sense that they’re confused: why aren’t I crying? How can I smile and make cancer jokes and get my grocery shopping done?

It’s a funny thing, to feel pressured to grieve in public. Sometimes I let the crying come, depending on the person. There are wonderful, sympathetic huggers in my life. But most of the time I suck it in, focus instead on relaying the updates that Brock would be comfortable sharing: I don’t mention the diarrhea, but headaches are okay.

I’m careful not to be too specific about our treatment plan (pills), because we are surrounded by well-meaning hippies and if I open that door then there will an onslaught of homeopathic advice. I know people have loving intentions, and they want to be helpful, but those suggestions enrage me, and suddenly I’m holding back mean words instead of tears.

(Brief pause here to watch a favourite Mitchell and Webb clip …)

Ha.

From a practical perspective (and we’re very practical people), if I cried on every single person I ran into who asked about the cancer or Brock, then I’d be crying quite a lot and wouldn’t get many of my daily tasks accomplished. I like it that our community cares about us, and I like it when people ask how Brock’s doing. I am trying to figure out a response that doesn’t confuse the nice people who check in with us.

How to Spend the Rest of Our Lives

I expect that different people respond to a terminal diagnosis in different ways. No doubt depression, anger and fear are natural reactions.

We haven’t experienced many of these feelings. Instead, we seem to have found a way of living, both me and Brock, that is working beautifully for us. In fact, I’m happier these days than I have been for years.

One of my hospice books says that dying people tend to become a more concentrated version of who they were before: spiritual people become more spiritual, angry people become angrier. My man and I are even-keeled, loving, pragmatic individuals with a sense of humour. And this approach to life just happens to be wonderfully suitable for living with terminal cancer.

When we go out these days, we order alcoholic drinks if we feel inclined, regardless of the time of day, plus the most interesting item on the menu, and always dessert. We make cancer jokes all the time. Our conversations include tidbits of final wishes and the funeral and palliative care preferences and how Isaac should be raised and educated.

We just returned from our friend-sponsored holiday and Brock did things he’s never done before: joined us in the huge soaker tub for a family bath, initiated a family bike ride on the beach. First-time activities after 9 years together. I’m happy to see him being more spontaneous and open to experiences. He seems to be enjoying “family time” more these days.

I hope we can keep this up for a long time. This approach and attitude to life is saving us.