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Issue #26, May 2002

 

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MY PARENTS ARE DYING

No this is not going to be a therapy column… or even a downer…  I hope not.  Hope has taken on a strange quality to me lately…  I actually need it.

Sure I’ve “needed” it in the past.  Kind of like you need ice cream once in a while.

“Oh please, God, I hope I get that job, gig, girl, comic book” whatever.

But these days there isn’t even the opener of “Oh God.”

It’s gotten way past that point.  It’s just

“I hope they’re okay.”

Let’s give you some background:

My parents live on the East Coast, and I live out here in sunny, too goddamn liberal for its own good, slacker, northern California.  My parents have been out here once in the 4 years I’ve lived here.  They trained across America on Amtrak for their 30th wedding anniversary and stayed in a big hotel on Union Square in San Francisco.  They set foot in my apartment, in the Mission District in San Francisco, once.  My mother isn’t too fond of my living situations, namely that they are cheap, and I don’t take all that good care of them.  And, granted, when they came out (2 years after graduating college), I was not taking care of my apartment, in Albany, especially well.

And now both of them suffer from cancer.  A lot of my family has had this disease… so many in fact that I consider myself an armchair oncologist.  So much so that when someone else’s family get afflicted with it I feel totally fine giving advice, dispensing moral thoughts on what can be expected of the death and grieving process, and fucking prescribing MRIs and what kind and what level of toxicity of the chemo that that person’s loved one should be receiving.

This is my mother’s third bout with breast cancer (second mastectomy, second full reconstruction surgery both scheduled the same day).

My father’s story is one of raging disease combating modern science.

One day my father wakes up and has some numbness in his legs.  Batteries of tests ensue in which nothing, nada, zipola is found.  Then just because one of the wacky tests needs it they take some spinal fluid.  And there they are floating in his spinal fluid, cancer cells.

Traditional chemo starts, fails.  Direct injection chemo to his fucking spine starts, fails.  And then the juggernaught of modern science steps in.

No more of this standard pussy shit.

They drain his spinal fluid—that’s drain, as in take it all fucking out—irradiate it separately while they bombard the rest of his body with gamma rays (why isn’t he the Incredible Hulk?), so that his bone marrow will create super T cells which they harvest (I love this oncologist language).  Then they pump his “clean” fluid back into his spine after adding these harvested super T cells to it and make him wear a mask in public because his immune system is that of a newborn, and declare him in remission.

Two months later, at Christmas, he can’t feel his legs again.

And just like that modern science bites the big one, my mother’s breast cancer returns (or her sympathy cancer as I like to call it) and the score board reads:

CANCER:  2 (or 3 or 5 or 778,897,000 depending how you look at it)

MORRISONS:  0

So they put my father back on injected chemo (that’s right into his fucking spine) just to keep his nephrology at bay (that’s a fancy oncologist word for not being able to feel your legs) twice a month and give my dad 15 months.

Are you ready for the fucking kicker?

So my mother’s sympathy cancer shows up, and all of a sudden my dad’s spinal fluid is clear.  No more cancer cells.  Clean.  And he’s been clean for the last three injections.  So they move him down to one injection a month… but have not declared him in remission.

So I hope.  I hope like I’ve never hoped before.  I hope it stays away.  I hope by removing two pounds of my mother’s flesh, it stays away from her too.  I hope like a man with a gun to his head hopes that the fucking barrel won’t spin, breaking the firing pin and jamming the gun.  I hope so much that I sweat.  I hope so much that I think I am shitting hope.  I hope so much that it is hard to stop thinking about hope when I start.

And I hope that I won’t have to move home.

 

© Christopher Morrison 2002

 

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