Tag Archives: yoga

Thank goodness for NaNoWriMo

My "almost" done quilt

My “almost” done quilt

Gearing up for NaNoWriMo—National Novel Writing Month—when I am committed to writing the first draft of a 50,000 word novel in 30 days. Starting November 1, less than a week from today!! I did it once, in 2011, and that was while I was working full-time.

Shouldn’t be so hard to write about 1,667 words a day now that I’m retired, right? Unfortunately, I’ve turned into one of those retired people who can’t imagine how I even managed to fit work into my busy schedule….lunch with the ladies from my writing group….Pilates once a week and yoga sometimes…..submissions for my writing group…..noontime walks with Judy….How did I do all those things and work?

Let’s see—I do more laundry than I used to….I vacuumed the other day….I take more naps….and, um, has much of anything else changed?

I am writing this blog—that’s new, something I committed to after my surgery. I took a quilting class at Seams Sew Easy Fabric Shoppe and am sort of close to having a finished product. (Thank you, Chrissy Steeves, for your patience!! I’m not done yet…) I spend more time at DHMC at doctors’ appointments and I go with my mother and Steve to their appointments. And I’ve made more of an effort to do things for friends who could use some help. (Mainly I make batches of turkey chili.)

I try really hard to write more. I was working on my umpteenth revision of “Anne,” after vowing to complete that version before the start of NaNoWriMo. Well, that never happened. Not even close. But I worked at it, every day, which was good preparation for NaNoWriMo. Then our wonderful vacation to Arizona disrupted the flow. Totally worth it, however.

The big change is in my attitude, in my approach to the daily tedium of life. I’m less hyper, more relaxed, as others have felt free to point out. Yet sometimes I wonder if I shouldn’t be the opposite. With my adrenal cancer diagnosis and the remote chance that I won’t live to be 90 years old, shouldn’t I be more amped, more energized, more productive? Shouldn’t I try to cram as much living into every day, every hour, every second? Nah, I think I’ll just take it as it comes, do what I feel like when I feel like it.

Thank goodness for NaNoWriMo.

It’s always nice to come home

I love this place even though I am a rock 'n roll kind of girl!

I love this place even though I am a rock ‘n roll kind of girl!

Just spent ten days in Arizona on vacation with our daughter Joy and her family. I thought I would find time to work on my blog and on my book, to think about adrenal cancer. I didn’t end up doing any of that. OK—I did spend some time thinking about ACC, how could I not? It’s my life now, even in my Facebook news feeds. Listened to a podcast from MD Anderson of a Stage 4 ACC survivor on the trip home from Boston. Encouraging!

We were busy all of the time and I loved every minute of it. Especially the constant warm temperatures (90’s!), blue skies, and sunshine, which I blame on preventing me from sleeping. That would have been a good time to write but I didn’t–blame it on Ken Follet’s long book, “World Without End.” I can only dream about writing a book that keeps someone up until 2 a.m.

Vacation with the grandkids is always go, go, go. Football practice. Football games. Shopped at the malls, so many to choose from, so close, not like at home. Celebrated Joy’s birthday. Skipbo marathon with Haley. Yoga with Joy .

Breakfast at Liberty Market with Haley followed by the splashpad while Joy taught a class at Gilbert Yoga. Lunch at Queen Creek Olive Mill. Dinner at San Tan Flat—a blast and I indulged in one of their awesome margaritas. Not all on the same day–but we do tend to eat out a lot while we are on vacation!

Went on a trail ride at MacDonald’s Ranch in Scottsdale with rattle snakes, a rabbit, a coyote, and a runaway horse—Haley’s, not mine! My horse, Holiday, and I were a perfect match. Nice and easy……My buddy, Holiday.

Swam in the pool fully clothed with Haley. Hiked a new trail (to us) in the San Tan Mountains. Toured the Phoenix Zoo.

Met with Dave and Toni Bellin, travel agents (yes–they do still exist!) at Sunrunner Travel to plan our trip to Hawaii. (So exciting!)

Finally arrived in Boston after a disappointing boarding of our flight in Baltimore on Southwest. After several elevator rides elicited the assistance of a Massport employee to find our truck in the Logan parking lot. Rain and 47 degrees when we finally headed out onto I-93.

Vacations are great but it’s always nice to come home.

What a difference a day makes

But does it? Yesterday was supposed to be my routine three-month scan at DHMC. Confirmation that I am one of the 20-30% of ACC patients who respond to mitotane. Whose cancer is kept from recurring by enduring the side effects of a DDT derivative.

We were disappointed that the CT scan report was not available by the time we met with my oncologist but we were pleased that he was able to bring up the scans on his computer.

We weren’t so pleased when he pointed out the arrow the radiologist had inserted next to the cyst on my thyroid. A new cyst? No, he was able to show us that it was on the April CT scan. It just happens that July is when the new batch of residents arrive with a fresh perspective on old problems.

The issue is that neither of us remembered hearing about a cyst on my thyroid. (And when I got home and reviewed the prior CT scan reports I found no mention of a cyst there either.) My oncologist “reassured” us that people have thyroid cancer and die of other causes without ever knowing they had it.

Somehow that was not reassuring. Seems as though that is what we’ve read about ACC. But it’s not my situation.

And the lesion on the liver. Another shocker. I can’t seem to find that in the prior CT scans but daughter Joy thinks that has been there right along.

The scan should have been read by today. My oncologist goes on a two week vacation next week. (My cancer has been a series of timing issues.) Luckily I see my endocrinologist next week. She should be able to address the thyroid cyst. She will address it.

And then there’s the atypical mole on my back, circled in black marker by my oncologist. It might not be so bad if I hadn’t already had two melanomas removed (11 years ago).

Am I worried? Not really. I know liver issues can be addressed in many ways. I probably won’t die from thyroid cancer. The mole, if a melanoma, most likely will be Stage 1 and require no further treatment other than removal.

I am disappointed. We had already decided that we were not going to overreact if anything new came out of the CT scan. Take our time and weigh our options. But deep down I was confident that there would be nothing new. And now there’s a thyroid cyst. And a liver lesion. Supposedly these aren’t new. Except they feel new.

So is today really any different than yesterday?

This morning I started a gentle yoga class. Not looking for a physical experience. Looking for the serenity to accept the things I cannot change. And the courage to change those I can.

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