colon

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My oncologist is straight with me. He tells me the truth. I have made it clear that I want it that way.

I have stage IV colon cancer, and I have been in remission now for over a year.

So during my oncology appt today I asked him, “I know my cancer is a slow grower. It has stayed dormant before and then begun to grow after almost a year.” I already knew the answer to my question. “How likely is it that the cancer is staying dormant right now while I’m in remission, and will begin to grow again in the future?”

He said in his caring voice, “It’s very likely. But I have two colon cancer patients, stage IV, who are now years past their diagnosis. One is seven years out, no sign of disease.”

So once again I am faced with this prognosis: there is hope, but it’s not very likely. But it can happen.

So I can’t sleep.

It sounds to me like I am probably going to die from this cancer…but maybe–although it’s a stretch–maybe not.

Whom do I talk with about this? Cliff is worn out and needs sleep, the kids don’t want to talk about it and they aren’t my counselors anyway, I will wear out my friends if I talk about this stuff over and over. Everybody is too close. And I don’t have a counselor right now. So I am writing about it.

I paint too. Maybe all this sadness about dying a little too soon will find its way into an abstract painting one day. (Well, that will make it all worthwhile….)

It’s weird to think that in a year or two I could be not here with my family, but instead cremated and scattered.

Or I could be one of those oncology patients still walking around, and people are thinking, “What, she’s still here?”

It could happen.

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Painting

I took up painting over a year ago, then stopped during the summer of 08. In June 08 I was diagnosed with stage IV cancer and underwent surgery. Chemo in the fall and winter. Then during chemo I picked up art again and began learning in earnest.

Since people have asked to see what I do, I’ll post my work here now and then. I don’t have a particular style yet, as you will see; I’m all over the map. I’m drawn to abstract art, but so far I haven’t done much of that. Anyway, I’m so enjoying the challenges that I encounter in art.

I am just learning…about creativity, about process, about art in general. I love looking at other artists’ work. I absorb so much, and I enjoy seeing how they used color (or didn’t use it) and how they decided to compose the painting.

During my sixth colonoscopy earlier this month, my surgeon removed a flat polyp. No cancer, though! He’s keeping a close watch, and I am still on an annual colonoscopy schedule.

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Sixth colonoscopy

I have an appointment with my colon surgeon tomorrow. I am due for my annual colonoscopy. My first colon cancer spread to my lungs, and the doc says that I can always get new cancers, thus the yearly colonoscopy. Tomorrow he will give me the prescription for the prep and we’ll make an appt for the colonoscopy.

I have had five colonoscopies. One year I messed up the prep instructions, and the colonoscopy actually had to be rescheduled. I would rather not have that happen again; it’s pretty embarrassing not to be able to follow basic instructions.

So my sixth colonoscopy draws near. I’m not ready for this prep, not when I’m still dealing with the effects of my second bout with shingles. I was in the hospital for three days last week, sick, in pain, and throwing up. It would be nice to have a little respite before I have to deal with the nausea of the colonoscopy prep.

I should be valuing the colonoscopy because it means early detection. But I dutifully had a colonoscopy in 2002, and it was clear. Either the doctor (not my current surgeon) didn’t see the cancer or it hadn’t begun yet, because in 2005 I was diagnosed with stage I colon cancer. Then, even with annual colonoscopies and PET/CT scans every three months, I was diagnosed with stage IV colon cancer in 2008.

I feel like I should be cancer-free. I have been the poster-child for getting tested and being proactive. But still I got colon cancer, and still it progressed to stage IV.

So although I’m very grateful to have health care that covers colonoscopies, I have mixed feelings about actually having them. I have to deal with this anger and sadness every year. I did what I was supposed to do, and it didn’t matter.

Many of us have this story, whether at home or at work. We feel like we fell through the cracks somehow, and we feel alone. Of course, we are not.

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Hiking it out

I was so tired last Friday that I kept falling asleep during Reiki, which I don’t usually do. I think I was carrying around more stress about that CT scan than I’d hoped I would.

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On Saturday, Cliff and I celebrated the good CT scan results by going on a beautiful but tough (for me) hike. It was only a couple of miles, but we gained some good altitude. I took many rests, and Cliff was patient as always. He steadied me a couple of times when my balance wavered.

 

 

 

 

 

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There was a lovely stream by our path the entire hike upward. It kept crossing our trail. So nice to hear the gurgling as we hiked!

I told a friend about our hike, and she got us trekking poles from Sam’s Club today. I can’t wait to try them out!

Cliff and I saw my Univ of Colo oncologist this morning. Very good appt; he is so thorough and clear with his explanations. And it’s such a relief to have no evidence of cancer.

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Hurray — I already have the CT scan result, and it is all clear — no evidence of disease!

Bless that hospital radiology dept and my oncologist for getting me those results so quickly. It’s difficult to wait.

I kept reminding myself to remain quiet, to dwell in peace. But it’s like trying to keep a lid still over a boiling pot. (Sorry, that’s the only metaphor, lame as it is, that I can think of right now.) I would rather know what that test shows, and the sooner the better.

So I’m very happy. I’m off to Reiki now and Gail, my dear practitioner. Bliss!

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CT eve

It’s been a good week, although I’ve needed to keep reminding myself to breathe and be peaceful. My CT scan is tomorrow morning. Hopefully, I’ll know the results on Friday afternoon.

Because I felt better about the scan, I was able to enjoy a hike on Saturday with Cliff, and we went for a bike ride on Sunday. When I do those kinds of things, I’m exhausted for the rest of the day. But it’s so wonderful to exercise outside that it’s worth it.

I’ve been doing rough sketches this past week. I took a long fireplace-style matchstick and dipped it in ink and drew with it. It’s hard to control but certainly loosens you up! I sat on a blanket on the lawn in the shade, nestled the ink bottle in among the grass blades, and drew. Nice way to spend part of the afternoon.

The cat is asleep on my forearms as I type, so I’ll quit now, as this is getting uncomfortable (although the cat is snoozing quite comfortably — his head bobs up and down as I type).

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What is.

A CT scan is looming next week, and I have been dreading it. I’m not usually afraid of these cancer tests, but it has been five months since chemo ended, and I don’t know what’s going on inside me.

Well, that’s what the scan is for—to find out what’s going on. I still go into the chemo ward every other week for an infusion of Avastin, but that’s the extent of my treatment right now.

There are so many difficulties and tragedies in the world that it seems trivial to worry about a CT scan result. Yet, when something threatens our life, we are usually determined—instinctively—to fight it.

And I am.

Today during a quiet time I remembered this bit of wisdom:  “What is, is.”

And I realized that the scan in itself is nothing in fear. The results are non-emotional; the scanner is just recording what is.

I am making peace with what is. If cancer shows up on the scan, I will have treatment options. If it doesn’t show up, I will be relieved. The scanner is only recording what it sees.

And monitoring “what is” may save my life.

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Windy afternoon

I just finished walking the dog for a mile, with the crazy wind blowing my hair every which way. Then I poured a cup of coffee and sat out on the back patio, listening to the wind and feeling the gusts across my skin.

This is where I want to be in the world – in my neighborhood, in my backyard, in my own home. Maybe Cliff and I will do some traveling in the future if it works out, but if not, it’s okay. I love the beauty of the earth that is within my reach.

As far as my physical condition, the fatigue is lightening up a bit, thank goodness, but the neuropathy in my hands and feet persists. I need to be patient with that, because the docs said the nerve endings have to regrow, and that takes a while. We’ll see how much feeling is returned to my hands and feet.

I have been painting quite a lot. Last week I got frustrated and felt that I would never improve. So I took the powdered charcoal into the backyard on a windy day and threw the charcoal onto some watercolor paper. Then I poured water down it.

The papers kept blowing over, so I ended up with an interesting mixture of gray charcoal and brown dirt. I got most of the dirt off, but the little that remained seemed earthy and appropriate to me, so I let it be.

I created some things I liked and some I didn’t. But at least I have a place to start now, which is better than sitting in my studio and thinking dark thoughts about my art ability. I will post photos soon, but I have to finish the art pieces first.

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Chemo completed

cpmd-cabbage-104Source of my peace
   Spring of my joy
As always, I find your presence
   within myself
      and drink deeply of your hope.

Listening within, waiting, I have regained hope and happiness. Life is different now, to be sure, but again I reach into myself and the tranquility that has been worked within me over the years, and I rest in this sacred dwelling pace for love and peace.

Today—well, yesterday now, as it is 2:40am on Friday—I finished my twelfth and final round of chemo. I am so happy.  No more tubes and pumps, at least for a while. As the fatigue wears off, I will be able to start exercising, in earnest this time. “Listen to your body!”  the oncologists emphasize. I will listen, I promise.

But it’s hiking again, back to the gym and the elliptical, long walks with the dog as weather permits (and it often does), walks interspersed with race-walking (approved by the oncologists), and bicycling (with Cliff, in case of balance mishap).

It will be a couple of weeks—as this weeks’ chemo runs its two-week course—before I do much.  Still, it’s exciting to think about and start working up to day by day.

Thank you ALL for your support!!!!!  And thank you, my heartlings — Joanna’s and Evan’s friends — including Douglas in Paraguay.

Well of joy, spring forth!

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Midway

I’m halfway through chemo – six rounds done, six to go. I should be wrapping chemo up around January 2009.

In the meantime, I am prepping today for a colonoscopy tomorrow. The oncologist told me just because we’ve taken care of one malignant site doesn’t mean there might not be more in there. So tomorrow morning my surgeon will take a good look at my insides again.

I am truly grateful for good health care and for alert physicians. But having a colonoscopy during chemo is a little tough. I am feeling the cumulative effects of chemo now – some loss of balance, shakiness, fatigue, and the ever-present neuropathy in hands and mouth. Today I am fasting and will be drinking the vat of liquid this evening for internal cleansing, which will leave me even shakier.

Oh, and a mammogram on Friday. I know these tests all vitally important. That’s why I’m having them done.

Still . . . all I want to do is curl up in bed and rest, so I will do that this afternoon. Weariness and gratitude coexist here.

Outside my window, the temperature is dropping and the wind is up. Leaves are sailing off the trees like snow.

And now thunder is booming. Lovely.

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