Tag Archives: Chemotherapy

The Chemo Diaries Round Seven: Maintenance Begins

Last Wednesday I had another CT scan to see how the initial six rounds of chemotherapy played out. On Friday I finally got around to looking at the images on my computer, whisking through cross sections of my body to try and get an idea of what was going on in there. On Sunday night I finally remembered the web site to check for the imaging results so I could read the reports. Then on Monday I went in to consult with my oncologist about what the reports actually meant and to verify what the next phase was going to be for my treatment.

We had anticipated that the tumor would likely not be gone. The previous scan in February had shown a distinct reduction in the tumor size, but not an overwhelming reduction. It seemed highly unlikely to me that it would shrink away in less than two months. So seeing it present on the scans and reading in the report that it was, at best, only marginally smaller was not a huge surprise. I was happy to read, however,

Continue reading The Chemo Diaries Round Seven: Maintenance Begins

The Chemo Diaries Round Six: Cycles End, Cycles Begin

Going into the final round of what I term Phase One of my treatment, I am reflecting a bit on two coincidences that have given me plenty to ruminate on. One of these is the fact that of one of my high school friends who I have not seen in far too many years informed me recently that her spouse is also going through chemotherapy and, interestingly, was just about a week ahead of me in the treatment schedule. The other coincidence of merit this week is that my neighbor will be starting her own chemo treatments at the same time I go in to complete my initial run of this badass toxic cocktail before moving toward a kinder and gentler maintenance schedule.

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Ready for my hook up, Nurse!

Neither of these coincidentally timed treatments are for the same cancer, which would have been too weird for believability anyway, and we probably won’t share identical side effects across the board or react too similarly to the drugs, but there is still a commonality of experience that cannot be denied. My friend from high school is one of those rare and thoughtful people who is cursed with the right balance of kindness and patience to really place herself in the center of care giving. It feels weird saying this, but I would not wish that upon anyone, as great a gift as it is. This goes back to my issue with patient guilt, perhaps; I feel lacking when I cannot help those suffering worse than me or I feel guilty about not suffering as much as them, and this extrapolates to me not wanting others to suffer as a result of my condition or being forced to take care of me. Continue reading The Chemo Diaries Round Six: Cycles End, Cycles Begin

Alternative and Complementary Cancer Treatments: Good, Bad and Ugly

An article by Victoria Stern, MA published on the Medscape website in September, 2014 details information on many complementary and alternative cancer treatments. Because not all my readers are likely to have subscriptions to Medscape, and because the article is rather long, I am going to summarize a lot of it here. The comments and opinions below are my own unless cited, and I am not a doctor; the information on studies and data comes primarily from the Medscape article and it, along with Medscape in general, is worth reading if you sign up.

The takeaway on complementary vs alternative treatments remains consistent with what I would refer to as, Continue reading Alternative and Complementary Cancer Treatments: Good, Bad and Ugly

The Chemo Diaries Round Five: Egg Counting

It’s that old adage of counting them before they are hatched. That’s probably what I should have been considering yesterday, one might suggest, because I did go out running around as though everything were back to normal. Not entirely, of course, but enough; so today, which is the fifth day of my fifth round, I woke extra wiped out. Although to say that I “woke” that way is being kind of generous. Really, I simply had not slept. Continue reading The Chemo Diaries Round Five: Egg Counting

The Chemo Diaries Round Five: Hiccups in the System

Side Effects and Annoyances

It only took about fifteen minutes for the hiccups to begin. By the time I sat in the car and turned on the ignition, I could feel them coming on. But the good news was they only lasted a few minutes and by the time I had pulled out of the parking structure after my infusion, they were all but gone. Hiccups are an odd addition to my routine over the past month or so, and they really came on strong the week after Round Four, though I had all but forgotten about them since. After returning from the infusion this time, they only popped up a few times, as though to remind me that I shouldn’t be complacent about the effects of the chemotherapy, even though I generally feel just fine on infusion days. Continue reading The Chemo Diaries Round Five: Hiccups in the System

Sitting in the chemotherapy infusion room.

The Chemo Diaries Round Five: Infusion Day

Okay, coming in for round five of six may not be quite as sexy as spending time with Seven of Nine, but it isn’t without its perks today. For one, check out today’s accommodations! I may have to squeeze in a nap, just to take advantage.

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Plus, apparently I have managed to gain ten pounds over the past month or so, perplexing the medical staff who are now curious about my diet and exercise… Let’s just say, it hasn’t been my exercise, and maybe that is part of it. Continue reading The Chemo Diaries Round Five: Infusion Day

Guilt of the Patient

Genuinely, I sometimes wonder when I hear stories of other cancer patients who are suffering so much worse than me with their treatments, whether I should feel guilty about how well I appear to be doing, comparatively. It is an irrational reaction, of course, as I am not responsible for how other people respond to their chosen treatments, nor do I have any level of control over their physical health either before or after their cancer was discovered. Yet it pains me to hear these stories and realize that there is so little I can offer to ease the suffering.

In many of these cases, the patient remains upbeat, even happy, throughout the story. Tougher than I, these characters. Stronger of will, because they endure more by choice, determined to lick their adversary. And lick it they shall, because these are cancers that, even far along, can now be cured or, more practically speaking, be diminished to the point of near eradication. And this, in spite of the heavier toll paid for the intense beat down of the chemo cocktail, makes me feel a little jealous. And that jealousy makes me feel guilty, too.

And then along comes my friend, Carlos. A refuge from El Salvador, Carlos came to California with the hope of finding some treatment for his leukemia. He is a slight fellow, but only on the outside.
Continue reading Guilt of the Patient

Survival Rate Statistics and What They Don’t Tell You

The other day I was having a discussion and it came to light that statistics had been bandied about quite early in my post-diagnostic journey. Now, I’m no stranger to statistics, but odds are that, whether you realize it or not, most of you are. That is not to say you have never heard any quoted or identified yourselves among some figure cited here or there… The truth is, one way or another, we are all statistics. And that means, well, virtually nothing. Moreover, even if one out of ten of us understands that even if the median reader gave up two sentences ago and clicked off this page, some readers will actually read most or maybe even all of what I am typing up here, this understanding is still only a basic understanding of a type of statistical qualifier and hardly bridges the gap between acquaintance and friend.

Which is all just a very wordy way of saying that statistics should only be read when one is prepared to interpret them, and while interpreting them it is important to remember that they often cannot highlight a “truth” without refined analysis. Such is the case with the statistical survival rates of adenocarcinoma, my particular flavor of cancer.

By the time I had received my diagnosis, Continue reading Survival Rate Statistics and What They Don’t Tell You

February 2015 Video Update

Here is a quick video I threw together this morning so that you can see my general physical appearance after passing the halfway mark on my current treatment schedule.  No, my beard was already that gray… However, I’ll admit, my face does look a little “fuller” than it did this time last year. This isn’t a beauty contest, Folks!

Maximizing Your Cancer Benefits

While it may seem oxymoronic to use the term “benefits” in conjunction with a cancer diagnosis, the fact is that there are going to be some options that open to the cancer patient and ways to take advantage of them which might not be immediately obvious. And the best way to maximize these benefits, of course, begins with an early diagnosis. Just like everything cancer related, the earlier the diagnosis the better, though no matter how late the diagnosis comes it will always be better than an even later one.

Because cancers tend to move at varied rates, it is important to know whether a cancer is of the slow and steady variety or if it particularly aggressive. The options available for an aggressive cancer are naturally slimmer, largely because that cancer needs to be attacked right away. But this can, in its own way, be liberating. When our set of choices is reduced to the bare minimum, it frees us up to focus on other things. There is somehow, amazingly, less to worry about. I do A or B, it works or it doesn’t. There is no waiting or wasting time, just getting into action and rolling with it.

And focusing, then, on what really matters. Continue reading Maximizing Your Cancer Benefits