An Ordinary Day
Tomorrow
at this time, I will be at Hopkins for my five-year brain tumor MRI and
neurosurgery appointment. They will make me sign a bunch of consent
forms, then give me a sedative, before putting an IV in my arm. It will
be my right, because that is the one with the "best" veins. I always
ask them to please not talk about my veins, because it makes me queasy.
They always do, anyhow.
I will be strapped down so I cannot move my
arms, and then a Hannibal Lecter-type mask will be locked over my face.
I will be told not to move, and to keep my head still. As soon as they
tell me this, my nose will start to itch, it always does. I will be fed
into a tube, where the banging, clanging, will go on for an hour.
It
will be loud, it will be cold. I will refuse a blanket (eww, hospital
blanket!) and try to think positive thoughts, although my mind will
wander to the injustice of how this became my life, why I am here, my
fears, my hopes, and eventually, how RIGHT NOW my nose REALLY itches and
I sort of have to sneeze.
The MRI will end, and still sedated, I will
wait for the neurosurgeon. I'll be told by a nurse to go get a cup of
coffee or some lunch, but I'm still queasy, from the sedative and the IV
and all that vein talk, so I will wait, with the book I brought
unopened on my lap.
The neurosurgeon will arrive, he will measure the
tumor on the screen and compare it to past scans, ask me about my
symptoms, check my reflexes, ask me some questions, "Who's the
President? Subtract 7 from 100, keep going ... Remember these three
words, watch, pen, ball ... OK, what were those words?" (Maybe I should
be studying now?)
It is routine - my twelfth visit - yet, it never is.
Because you never get used to being slapped in the face by your own
mortality. It never feels "normal" to confront a potentially
life-limiting illness in your 30s (my doctor does not enjoy the word
"terminal").
When I was first diagnosed, the five-year survival rate
was 32%, or maybe 50%, depending on what you looked at. "You are a
statistic of one. That is all," said the neurosurgeon. I thought that
was bulls^%t, because it was MY statistic of one, not his.
My son was
four, I was worried he would never know me. He'd have fuzzy memories,
of course, but if I were gone, he would never REALLY know me, as a
person.
Scariest of all was that thought of putting my son through the
sudden death of his mommy. Or the opposite, a gradual decline, a long
goodbye, diminished vitality, and then a slow death. Which was worse?
Did it matter? I could not control this.
So here I am, five years later,
and my nine-year-old boy knows me. I still have the same worries, and
more. Facing a serious illness is, in a word, devastating.
Emotionally, physically, financially. Every possible facet of my life
has been shattered by me being sick.
Even my decade-long marriage has
been a causality. Sometimes people fall together during a crisis, and
sometimes they fall apart. We were the latter. We had plans - law firm
partnership for me, share in the Hamptons, 2.3 kids, a golden retriever
... not this. Not this!
And, yet, even amidst all the devastation, I
am still here. I am still standing. I am still fighting. I am still me,
in all the important ways. I am funny (sometimes inappropriately so), I
am an excellent writer (and working on getting a book published this
year), I am a caring, involved mom, I am a loving and empathetic friend;
I am a terrible cook, I am awful at math, I am always ten minutes late
for virtually every moment of my life, I have little patience.
I am both
incredibly strong, and extraordinarily weak, sometimes in the same day.
Sometimes in the same hour. In short, I am human.
My son still has
his mom, and he knows these things.
Last night, we had a completely
ordinary Tuesday, I picked him up from school, we went out for macaroni
and cheese, we walked to the library to pick up some new Thea Stilton
(him) and Jodi Picoult (me). He laughed, I laughed. It was happy, it
was easy, and I was content.
Here's to five more years of perfectly
ordinary days, and then five more after that.
Wish me luck.
7 comments:
I wish you so many things, the least of which, is luck.
Ever since you posted that your scan was coming up i have been watching, waiting to hear. Your post made me cry.
When i was pregnant with my daughter they told me i had cancer. When she was 6 weeks old, they removed it. When she was 4 months and 18 months old, i had radiation.
I don't have to worry about the cancer anymore, turns out i had a good kind. I understand how you feel, not knowing how much of their lives you will get to see. I wouldn't wish it on anyone.
I wish you so much more than luck. I wish you many many years with your son, good health for as long as you can stand it, and defying medical odds (because i believe that if anyone can, it's you)
tomorrow i will be thinking of you, sending you healing thoughts and wishes, and will be watching, waiting to hear.
I wish you all the luck!! Can you bring your own blanket?
I'll be thinking of you and praying for a miracle! Hey, it could happen, you know!
My wish for you extends beyond mere luck. I wish you many, many multiples of five years to spend with your son. Many, many multiples of five years where you are healthy and happy and know joy. Luck is for things like getting that book published, which I wish you much luck with.
Hoping for good news. Or at the very least, news that is not bad. Much love to you and your son.
From one of the people on the internet
I wish you the blandest day possible, where they tell you everything looks fine and send you home on just another Thursday. :)
Thinking of you today and sending my very best wishes. xo
Intending that the news was/is good for you, that you are getting some exciting news about your book project and that you are experiencing many, many more years of living... for the highest and best good of all concerned, so be it and so it is!
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