Showing posts with label Janice Throup. Show all posts
Showing posts with label Janice Throup. Show all posts

Thursday, January 17, 2013

MOM'S GOT CANCER - CHAZ SALEMBIER RECALLS GETTING THE NEWS AT THE AGE OF 8

THE WHY? FOUNDATION - TOUCHSTONE THURSDAY
 


written by Chaz Salembier 
Eight months was still a lot of time, I remember telling myself. With fuzzy kid-logic – in which hours are days and days are months – I had convinced myself that this was such an infinitesimally small problem that like an ant under my shoe I shouldn’t give it a second though. In fact, I should ignore it. Elephants in rooms, after all, only exist if you let them. So I turned a blind eye toward it. In the 90’s, when soda was cheap and video games were starting to make it possible to live lives you never thought existed, it was easy enough to distract myself. Out of head, out of mind. Eight months was a long… long time.

I hated school. I mean, really, what kid didn’t, but school was school. I remember spelling it “skool” in my book reports as a juvenile middle finger to my grade school teachers – you can’t get to me. You can’t teach me (belligerent eye roll). My mother drove me to school every morning. It was a short drive, maybe two minutes, short enough that most days I had to walk. But two minutes is an awfully short time. Short enough that it’s difficult to convince my mother that my stomach is feeling particularly grouchy. I complained heavily, with plenty of nasally whine and, sighing, caving under my insistence; she drives past the front door of the school and takes me home. I play it straight, don’t blow my cover, on my way home, which is key to finagling my way out of another day of classes.

There was no official family announcement that I can remember. As an eight year-old, the finality of death was still a relatively new concept and one that still seemed absurd. I didn’t even quite know what was happening to my mother. She had leukemia, I knew, something nasty to do with her white blood cells, but most of her disease was nothing more than whispers behind closed doors. I don’t know if my parents were trying to keep me in the dark intentionally, to protect me, or if I genuinely didn’t understand. All I know for certain is I didn’t know for certain.  

We arrive at home, and I’m told to lie in bed, which I do because, hey, lying in bed is better than sitting at a desk. My mother brings me a bowl of soup and, to pass the time, she reads to me. This is not an uncommon sight at my house – me lying in bed, my mother in the chair next to me, some wild, large, philosophical fantasy novel, with enough imagery to keep my impatient and TV-trained brain occupied. Today, it is the final book in the Chronicles of Narnia. I sip soup and listen to her read The Last Battle, as Aslan – the great a noble lion and quite unsubtle metaphor – judges all of those who have fought in the great battle. The good guys are invited to join him in His country and, with that, Narnia comes to an end. Father Time calls the stars down from the skies, he puts out the moon and the sea washes over the land. Narnia is no more. My mom has read this book to me a few times. She always pauses at this part.

Around this time I started seeing Mrs. V, an older woman who looked as though she was plucked from someone’s garden. She invited me to her office once a week during school and, at the time, I was none too concerned why as I strutted room to the envy of my classmates. Mrs. V and I would sit in her small office where I would fill out puzzles, draw, and do visual word challenges. I thought I was pretty damn special at the time. As though I might be just awesome enough to play for an hour a week with Mrs. V while answering her trivial and banal questions about my family. I would later learn that Mrs. V was a grief counselor, who was preparing me for the death of my mother.

I spend the rest of the day walking around with my blanket around my shoulders, trailing after my mother like the world’s most annoying jet stream. My stomach feels fine. It always does. And she knows this. Yet I’ll pull this stunt a few more times over on my mother in the coming months. Each day on the short car ride to school I’ll groan and complain with the bravado of a Shakespearian actor on his deathbed. And day, I’ll wait in bed for my bowl of soup and whatever fantastic book has been dug up from our basement library. What I won’t admit at the time, however, is that this isn’t about skipping class, the joy of knowing my classmates are stuck doing math workshops in Home room, or playing coordinated tunes on hand bells in Music. No, staying home from school isn’t so much about “school” as it is “home.” Because home is where mom is. And any day more I get to spend with her is a better day than one spent away. Because these days go by so, so very quickly.

Eight months became weeks, became days. For reasons that she can explain better than I, eight months came and went with little ramification. Throughout the rest of my childhood, I was told not to get my hopes up, not to expect her at my baseball game come next spring, or to welcome me home from my driver’s test, or even at my high school graduation. But as I write this, having graduated from not one but two educational institutions, she is skiing somewhere in western Colorado. This past summer, she was told that one more year of recession and she can stop taking her medication. Suddenly, the rest of her life seems like a long… long time.



In 1995 Chaz’s mother, Janice, was diagnosed with Chrinic Mylegenous Leukemia and given less than a year to live. Proving cancer was messing with the wrong lady, Janis is currently happily taking on the world and enjoying every moment of every day. To read the short story THE BLAST CELLS written by Janice about her cancer experience please click the link below.

http://thewhyfoundation.blogspot.com/2012/08/the-blast-cells.html

Thursday, August 30, 2012

THE BLAST CELLS



In 1995 Janice was diagnosed with Chronic Mylegenous Leukemia and given less than a year to live. Proving cancer wrong on a daily basis, Janis is happily married, a proud mother and enjoying every minute of every day.

A Short Story By Veteran Cancer Fighter Janice Throup

The blast cells—the bad guys, the ones that were going to kill me—were perfect circles with little purple halos from the dye they used to stain them. The good cells—the ones that had matured properly—were misshapen. They looked aged and tired in comparison with these new little babies who hadn’t yet differentiated.

I was struck silent. This was not what I had expected. I was diagnosed with leukemia in the days when the Pac-Man visualizations were popular. You were supposed to imagine Pac Men (from the old video game) eating the bad cells. I’ve never been very warlike, so the exercise had no appeal to me, but I thought maybe I should take a look at the enemy.

My doctor, already frustrated with me because I had refused the only real chance of recovery (a bone marrow transplant) was persuaded to let me look at my marrow in exchange for my promise to him of more bone marrow biopsies (“just a little prick” he called them, but they seemed horribly invasive to me). Perhaps the deal appealed to the scientist in him. He left his other patients waiting and took me down to the bowels of the hospital to see my blast cells through a microscope.

I felt something shift inside of me when I saw these purple wonders. They looked so harmless. It struck me that they were just trying to live their little cell-lives. I mean, something had gone wrong because they weren’t following the normal pattern of white blood cells, but they looked … well, happy.

Chronic Mylegenous Leukemia doesn’t hurt. At least in the beginning. Because nothing hurt, I was, at first, disinclined to believe my diagnosis. When my doctor pressed upon me the seriousness of my condition—“only 2% of people with your condition are still alive in two years”—I began to feel betrayed by my body. It had always served me well and I had always loved it. I had studied ballet, taken up mountain climbing, been a star yoga student. And now, in the very marrow of my bones, it was trying to kill me.

But there in the hospital basement, as I looked at those little purple baby cells, I felt overwhelmed with Love. I simply couldn’t get my mind around these babies being the bad guys. They were young life, full of promise, full of beauty. I felt myself falling in love with them, and all of a sudden, my body and I had a reconciliation.

Along with this feeling of invasive Love there came a flood of all those wonderful corollary consolations—the certainty that everything was just as it should be, that I could relax and let life unfold as it would, even if it led to death.

It didn’t. Now, I’m not saying that my attitude brought on healing (though the timing might lead one to believe so). I am saying that for me, acceptance gave me my life back—gave me back the feeling that neither my body nor life was against me. And I realized that the enemy wasn’t Death—it was Fear.

“Perfect love casts out Fear.” Didn’t Jesus say that? It’s true. And maybe, just maybe, when Love prevails, cells realign themselves. Or they don’t but that’s OK too, because what we’re about on this planet is learning how to love. And if that lesson comes through illness, even through terminal illness, it’s still OK as long as we learn it. 


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