Tag Archives: mitotane

Excuses

Managed to get through the worst part of the day—taking my morning medicine, all 13 pills. I know there are those who take more pills than that but I used to take only three: one for my acid reflux, one for my high blood pressure, and one for my seasonal allergies. Still, those extra ten are magic and I try not to forget that.

It’s Father’s Day and Steve has gone golfing, his usual game at 6:30 a.m. on Sunday. It’s supposed to be my time to write. So far I have watched CNN, some HGTV, and back to CNN for Sonjay Gupta, then read the HGTV magazine, taken my medicine, texted Jesse, and now DIY is playing in the background as I finally sit down to write.

Are you getting tired of my excuses yet?

I am.

While I was painting the guest bedroom yesterday, I had some great ideas about my book (“Anne”). Unfortunately I couldn’t just put down the paint brush and dash to the laptop to get them recorded but that is exactly what I should have done as today they are just sort of vague but there’s enough of them left to work with. Except I just got another text from Jesse and she and the kids are on their way over so we can go to breakfast….Interesting that we are going out to a Father’s Day breakfast without either of the fathers…oh, and that I have already eaten a glazed donut and two pieces of raisin toast.

Magic Pills

It’s 5:30 in the morning and I’m rolling out of bed so that I can join my husband on the couch for coffee, CNN, and the weather before he heads off to work at 6:30. When I was working it was all I could do to get out of bed with enough time to perform my morning rituals and arrive at work by 8.That included eating breakfast in the car during my eight minute commute to my job!

You’d suppose that as soon as he heads out the door I would be firing up my laptop and start pounding away on my novel, the one that I have committed to finishing before I, well you know….

This is the novel I started back in 1986, a mere 27 years ago, definitely a lifetime ago. The one that my mother has asked repeatedly if she will be able to read it before she dies and now that is no longer the question we ask. So now, almost seven months after my surgery and a month following my retirement I am doing just that.

It’s so true what “they” say, those seasoned writers like Stephen King, you need to write every day as once you get out of the habit of writing it is nearly impossible to force yourself back into it. My daughter, the yoga instructor with a successful blog, allows herself fifteen minutes to tackle any project. If that is all that she can manage, she has at least achieved her goal. If she gets so wrapped up in it that she works on it until she absolutely has to stop, she has the satisfaction of knowing that she has far exceeded her expectations. It makes sense when you apply it to writing because once you’re fifteen minutes into your project ,you’ll probably not be able to stop. But still. Isn’t the hard part sitting down and starting, committing to those first fifteen minutes?

In addition to firing up my laptop, the hardest part of my morning is opening the refrigerator and taking out the milk container without looking at or smelling the food then extracting from the kitchen cupboard the pills that now sustain me. It’s hard because I feel fine before I’ve taken my pills after I’ve eaten my breakfast. Because I’ve decided that they are magic, the actual act of swallowing them doesn’t seem to cause any problems.

One In A Million

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That’s me.

No, I didn’t win the lottery.

I have Stage 2 adrenal cortical carcinoma (ACC), an ultra rare, aggressive cancer with a grim prognosis that strikes .5 to two people out of a million annually. This is one time when you don’t want to feel special. I had surgery the day before Thanksgiving 2012 to remove my right adrenal gland, kidney, a piece of my liver, and resected my inferior vena cava (what in the world is that, I wondered. It’s the artery that returns the blood from my legs to my heart. Who knew?)

Not only did I miss Thanksgiving dinner, which I would normally have hosted at my house, but a Thanksgiving day trip to Atlantis in the Bahamas with my middle daughter and her family. We did make it there the end of March 2013 and it was a wonderful trip. Funny how when I was recuperated and able to eat normal food I craved turkey dinners, whether at a local restaurant or in frozen dinners due I am certain to being deprived of a real Thanksgiving dinner. I am not certain what I did eat for Thanksgiving dinner on the day following my surgery as the day of and most of the day after have disappeared from my memory. A good thing, I am told by my family who were unlucky enough to be there with me and forced to endure their Thanksgiving dinner in the hospital cafeteria. I no longer crave the turkey dinners as my cravings change constantly—what I absolutely had to eat a short while ago I no longer desire.

Except for carbs.

For the last few years my husband and I have tried to follow the South Beach diet principles and now all I want to eat are things off limits on South Beach: all carbs, including bagels, cinnamon raisin bread, pumpernickel, pasta, even the occasional toaster streudel.

Vegetables? No thank you.

It sounds as though all that ACC has done is impacted my eating habits. Nothing could be further from the truth. I am lucky in that my cancer is stage 2, even though the prognosis is that I have a 51% chance of living five years. I had several options for treatment, one of which was to do nothing, just wait for the results of my CT scans every three months. That didn’t really thrill me.

I am used to taking action, to being in control.

A remote second opinion from the University of Michigan recommended Mitotane, a DDT derivative, taken in pill form daily for three years. Although my oncologist at Dartmouth Hitchcock Medical Center did not support my decision, I went with the U of M recommendation. Rumor has it that only 20-30% of ACC patients benefit from Mitotane—how am I to know if I am one of those? Clean CT scans only prove that the cancer has not returned, not that the Mitotane has kept it from returning. Mitotane has extreme side effects, which prevents many patients (are there really many people making this decision?) from taking the drug. Because it also kills your other adrenal gland, you need to take hydrocortisone, which I have difficulty tolerating even though it does fuel my appetite and apparently my energy level.

The biggest decision of my life was to retire at the age of 58. (Sorry, Steve, marrying you wasn’t really a decision, it was a given.)

On the day I returned to work from medical leave after my surgery I gave my notice. That wasn’t part of our plan, just like cancer wasn’t. Steve was supposed to retire this year at 63 and I was to continue working until I was old enough to draw Social Security. So much for plans. But who wants to keep working, no matter how rewarding, when death looms on the horizon? Sure, we’re all going to die at some point but by the time you reach my age you assume you’ve got another 30 years ahead of you, especially when your mother is still alive and kicking—and I do mean kicking—at the age of 85. And I thought I could produce a lot of novels in those 30 years.

Now I am hoping just to finish the writings that I’ve already started.

Yes, writing is my dream and what better time to try to realize your dreams than when death is no longer just a concept but a very real possibility?