The A to Z Blogging Challenge calendar looks like this:
But in my mind’s eye, until this evening, the calendar looked like this:
If I’d paid attention, I’d have noticed I was supposed to post yesterday, a Saturday, instead of taking the day off.
If I’d paid close attention, and counted, I’d have seen that my April calendar provides for only 22 letters, four fewer than the official calendar assigns spaces to, and also four fewer than are found in the alphabet. I was embarked on an A to V Challenge.
When I realized I’d gone wrong, I considered dropping out. After all, I’ve breached the rules, failed to post as required.
But it’s a glitch, not a transgression, and a blog challenge isn’t a life-and-death matter. So I proceed.
Two weeks ago, my radiation oncologist used the word remission.
Nothing has changed. My most recent CT scans show the same results as those done in December 2016, three months after I completed radiation treatments. The bone scan, my first, was also clear.
The oncologist, although he’s now smiling as if he means it, continues to be conservative. Stable is the word he uses. “As long as you’re stable…”
The radiation oncologist has always been more upbeat, possibly because she isn’t in charge of my case, possibly because she has a cheerful nature. A year ago, she was calling my scans awesome. I liked that word.
Remission, though, has a certain ring to it–a medical ring.
For two years, I’ve been living from scan to scan, and that won’t change either. The challenge continues: to live with past, present, future all at once; to wrap my mind around the contradiction–I have cancer, I had cancer, I . . . what?
The next CT is scheduled for early June. Scan to scan.
Read more posts dedicated to the letter G by clickingAtoZ.
For several months, William has been taking insulin injections.
The good newsis that he cooperates, mostly. If he’s downstairs when shot time comes around, David grabs him and puts him on his lap; I give the shot. If he’s upstairs on the bed, that’s different.
David goes up first and pets him. I follow a minute later. When he sees me, he starts to get up. David positions him so I can scruff him. Sometimes before I get hold of him, he lunges, and David has to redouble his efforts. Then I give him the shot and we pet him and tell him he’s a good kitty, something he already knows, and that’s that. In short, he doesn’t mind the shot, just the temporary loss of free will.
The most difficult part is scruffing him. There’s not much to scruff. Sometimes I have to try several times to pull up enough skin so the needle doesn’t go too deep. The veterinarian has trouble, too.
The other good newsis that in all the time I’ve been sticking a needle into him, I’ve stuck it into myself only three times.
The second other good news is that have I never injected myself with insulin.
The really, really good news is that I always stuck myself before, or instead of, sticking him.
Except for once last week when the needle went through his skin and into my thumb. As I said, there isn’t much up there to scruff. Since them, I’ve aimed more carefully.
The best news is that his blood sugar is down and he’s back to his old self, wrestling with Ernest (William starts it); staying downstairs more; playing with the Filthy Pink Mouse; grabbing my hand, holding on (claws), and biting my fingers. Sometimes he just licks my hand. That’s icky, worse than the biting.
It’s been a calendar year since I was diagnosed with breast cancer.
My good news is that I finished chemo (the evil drug) at the end of May and now am much stronger. I said many times during chemotherapy that the side effects were mild. Now I realize that during that time, I felt pretty rotten. I was weak. The feel of water on my skin was unpleasant. I couldn’t walk more than five or ten steps without stopping to rest. I lived on Benadryl to keep my hands and arms from itching. But I still believe I had it easy.
In June, I had lumpectomies (I didn’t know you could have surgery twice within one week). In September, I went through radiation, twenty consecutive days, weekends and Labor Day excluded, smiled cheerily at the technicians, let them admire my cute socks, lay perfectly still for a few minutes while they zapped me, and drove home.
The hardest part was getting the gown tied correctly.
On the last day, in the hallway outside the radiation room, one of the techs asked if I wanted to celebrate. I said, “Sure.” He brought out a small cardboard box and the three of them threw confetti at me.
If I seem to be making light of the experience, I suppose I am. In part, that’s because it’s what I do. It makes better copy. In part, it’s because I didn’t go through the hell others go through. In part, it’s because I have to.
Within days after the last radiation treatment, I slid into depression. The radiation oncologist said she’d seen it before, and I needed a goal: travel (just did); creative activity (got one story with an editor, working on another one); gardening (no place to plant and I kill everything anyway); talk to a therapist (already do); exercise? (oh d*mn).
Before it ended, I heard myself thinking, I’ll buy the package of 300 stars instead of the one with 1000. I might not be around long enough to use 1000. Every time, I immediately countered that with, Stop it, you can’t think that way, buy the 1000.
Radiation might have caused the downhill slide, but I believe it stemmed from the feeling that I wasn’t doing anything to help myself heal. Three months without the chemo drug, I felt all right. I no longer had to report at 8:00 a.m. for radiation. There were no technicians to impress with my brave, cheery attitude; nurses didn’t seem impressed. Taking a pill every morning took no effort. Periodical infusions to boost the immune system had weeks ago lost their luster. I wasn’t working at it.
Hearing, or telling myself, Cheer up! didn’t help. As all depressives will tell you, it never does. It makes us want to cuss or, better yet, to kick the sunshiny idiot adviser in the knee.
My other good news is that by Christmas I was on the mental mend, thank goodness. Because the scariest part was that depression and big T-cell boosting smiles don’t coexist.
My second other good news is that my latest CT scan, done in early December, shows the lesion in each lung and the two lymph nodes that were radiated in September have decreased in size so much that they wouldn’t show up on a PET scan. The radiation oncologist’s pronouncement: “Awesome.” Indeed. The oncologist is pleased and said he hopes I am, too. Yes, I’d say I’m pleased. The next scan is scheduled for March.
I continue to juggle a positive attitude and uncertainty. The next scan may be clear. The lesions and lymph nodes may show metabolic activity again. Problems may show up elsewhere. I’ve been having pre-cancerous tissue removed here and there for the past fifteen years. Cancer is the Curse of the Wallers. It’s in the other side of my family, too.
But I’m here, and I had an excellent report, and I keep on keeping on.
Which makes everything I’ve written here not just good news, but the best.
P. S. I have hair again. Shirley Temple and then some. I don’t know what I’m going to do with it.