Archive for May, 2010

My First Amazon Payment

Posted by: courtin Writing Life
27
May

Yesterday I got an email from Amazon saying I’d been sent an Amazon.com gift card redemption. I immediately deleted it.

There was no name and I knew no one I knew had mentioned they were sending me an Amazon gift card. It must be some kind of spam or virus or something bad. Hence, the delete button.

But then something nagged at me to go back and check it out.

Could it maybe be legit? Had I perhaps actually earned some money via my Amazon Associates program? That’s the only thing I could think of that would explain the gift card.

Incredibly, after going to check my AA account and learning that, yep, my balance had finally earned enough to merit paying me, I about busted out of my skin.

It’s nothing huge. All of $10.06.

I’ve had an Amazon Associates account for how long now? Since I launched courtneymroch.com back whenever that was. (I can’t even remember what year I did that. 2000? 2001? It seems I’ve had it forever now.)

After seeing where my fees came from, it’s all from my Haunt Jaunts blog. Amazing. It actually works.

No, I can’t buy much with it, but what a neat feeling to know it does actually work. I’ve read about other people making money that way for years, but until now I couldn’t say I ever had.

First time for everything!

I just have to get this out: I hate telling people what kind of cancer I had.

Don’t get me wrong. I never mind talking about my cancer. I’m not ashamed of it like some people are. I had it, it was a huge part of my life, and it always will be. It’s part of the Courtney package now.

However, everyone always wants to know what kind it was. It’s not their fault. That’s how society has conditioned us. We think of cancer by their labels. (And in some cases associate them by the celebrities that had them.)

  • Breast cancer. Very bad. Very sad when a woman gets it. Has the potential to be very deadly. Lots of ways to support the fight. Pink ribbons everywhere.
  • Lung cancer. The smoker’s cancer. Very bad. Very deadly. Basically a death sentence when you’re diagnosed. Not much sympathy. Everyone assumes you brought it on yourself with your bad habits.
  • Testicular cancer. For men only. a.k.a “nut cancer” or “what Lance Armstrong had.”
  • Prostrate cancer. Also for men only. Has the potential to be very deadly. Not discussed as openly as many others.
  • Pancreatic cancer. Bad news. Not curable. (a.k.a. the “Patrick Swayze one”.)

These are just some of them. The list goes on and on. (Unfortunately.) As do the way we associate them. (Also unfortunately.)

I understand doctors and researchers need to classify the different cancers because they all respond to treatments differently. But for the rest of us?

Cancer is cancer.

It’s scary. It’s life changing. It’s surreal. And it’s different for everyone. Both the treatments and how they experience it.

It’s driving me nuts that some cancers, like breast, are everywhere. It’s like some Pink Ribbon Club now. There are times I almost feel left out that I got lymphoma, a very common cancer in its own right, instead of freaking breast cancer because there’s no “club” for mine! (You don’t see lime green ribbons on products in every store from grocery to department to sporting goods, do you?)

But thanks to my family’s history, chemo and radiation I have plenty of opportunities to join that club at some point in the future. Great. (In case it’s not clear, I’m being sarcastic. I really don’t have any desire to become a member of the Pink Ribbon Club.)

But see there? Anyone who had breast cancer might now be offended. “What, my club’s not good enough for you?”

See what all this labeling has the potential to do? That’s exactly why I don’t like it and why it drives me nuts!

I know it’s a common reaction for nipples to get hard when they’re aroused or cold (which I guess is a form of arousal), but is it possible to suffer from a disease where they’re perpetually hard? If so, I have it.

I don’t know what to call it. How about headlightitis? My husband’s always turning his head as one hand  flies up to shield his eyes as he says, “Whoa! Can’t you turn those suckers down some?”

Would if I could, honey, but they haven’t invented the woman’s version of anti-Viagra for my sista girls.

However, bra manufacturers have come up with something: petals.

Some are peel-off stick-ons you can place right on your Ta Tas and wear under your bra. Some are built into bras.

I’m too cheap to buy the disposable stick-on kind. Made more sense to have them built-in. So I found some bras with the technology. Finally, something where my lady lumps would be nice and uniformly round underneath my shirts.

WRONG!

No sooner did I put on my new bra and cover it up with one of my tighter fitting Tee’s than I trotted down the stairs to show off to Wayne.

To my horror, there went the hand, the head turning sideways, the “Whoa!”

It can’t be. The petals were supposed to turn them off. Or at least dim them some.

I looked down. Nope. There were my two little familiar pointy Twin Peaks.

Impossible! I must have done something wrong. I checked to make sure the petals were positioned properly over my nipples. Check.

I threw up my white flag. Or, rather, my petals did. They knew when they were licked. They were no match for my nipples!

I Never Asked Why

Posted by: courtin Cancer Survivor Life
18
May

Something I see a lot of people doing when something bad happens to them is asking, “Why me?”

Long before I ever learned I had cancer I had resolved if anything bad ever happened to me, I would not go there –to the “Why me?” pity place.

I always thought, “How presumptuous can a person be to ask that question? What, did you think when you were born you’d get special privileges that would exempt you from suffering life’s tragedies just like everyone else?”

Yes, I always felt it was an extremely arrogant and self-centered question. And, should something horrendous ever happen to me, it wouldn’t even be worth whispering those words.

And I didn’t –not once at any stage in the “Oh shit, I have cancer!” process did I ever go there. I wasn’t even tempted.

However, ever since I’ve survived the Black Cloud’s wrath I find myself asking a “Why me?” question nonetheless. It goes a little something like this: Why did I survive when others don’t?

For example, the other night we watched the Survivor season finale. During the reunion portion of the show they paid tribute to former Survivor Jenn Lyon who died of cancer earlier this year. She was only 37.

Wayne immediately dove for the remote wanting desperately to change the channel. But he was too late. I saw it. Images of the beautiful young woman who once upon a time purposely subjected herself to enduring the elements for 39 days (if she could make it that far) with perfect strangers in a quest for a million dollar prize.

I tried and tried to hold back my tears, to not react the way I always do when I learn of a fellow cancer soldier losing his or her battle with the disease. Mostly I tried to put on a brave face because I knew Wayne would beat himself up for not having changed the channel fast enough to spare me from seeing it.

It’s his way of protecting me. I love him for it.

I could almost feel him holding his breath as he waited for the inevitable: the deluge that always follows. But, as it always does, it finally came.

And with it so did my string of “why” questions: Why her? Why not me? Why am I still here? Why are some cured and others aren’t? Why was I so lucky?

Then we had to staunch the flow of panic that also accompanies these events when I’m reminded of how lucky I am to have had 16 months, two weeks, and a day more with Wayne than I could have had if the alternative had happened.

I know I’ll never have an answer to any of my questions. I’m not sure I’d really want to know the answer anyway. But this is what I do know:

I know I’m here thanks to many factors: the scientists and researchers who invented the treatments that saved my life, those patients who went before me to perfect the treatments, the doctors and nurses who know how to correctly administer them, friends and family who lent their strength, support and comfort when mine was weak, and even my own Life Force willing me not to go out just factored in.

Most of all I know the “Why not me?” feelings I have is survivor’s guilt.

I know all of that, but it’s never enough to keep me from wondering it anyway.

Blessings to you and your life, Jenn Lyon. You accomplished whatever you were put here for faster than those who loved you would’ve preferred. I hope their memories of you provide comfort as they mourn your passing.