Beauty Found and Shared

I did not know or even follow Lisa Bonchek Adams as well as most other breast cancer bloggers I follow/interact with. So while her death saddened me, my reaction has skewed more toward first anger, and now strengthened resolve. Anger that her message of not losing a battle seems to be lost on so many, that so many articles and even comments and tweets have relied on that stupid battle cliché. Strengthened resolve to speak up and out more in criticizing euphemisms, to be brutally honest in communicating to any and every person that death is a potential result of cancer. No matter how unpleasant it is to say the D words (death, die, died), my conviction is stronger than ever that using those words is a crucial part in moving the conversation about cancer forward.

I’ll write more posts about all of those topics later. Today I am going to do what Adams always advised her followers to do—the finding beauty and sharing it thing.

I admit, not being a sentimental type, I kind of blew off her tweet exhorting folks to find and share beauty. I’m not one for the inspirational quotes. I am a sarcastic curmudgeon, and like snarky quips and memes. But I will take a break from my natural state, just for this moment.

Yesterday was an awesome day for me. In spite of still so many posts about Adams on social media, while I was out in the world, everything just worked so well! Just a few days ago, my beach town had suffered yet another ice and snow storm with freezing temperatures that road crews and residents are simply not equipped to handle. I was frustrated at having to walk dogs while slipping and sliding on ice. But yesterday the warm hints of spring finally took root. Snow melted rapidly. So many neighbors were out and about: walking, playing ball with their kids, or just driving with the windows down.

Pond Still Frozen

I’m not a fan of springtime, I’m allergic to every plant, ever. But nothing is in bloom just yet, so I was able to walk outside without discomfort. I’ve mentioned before that I live in a beach resort area. Warmer weather brings the tourists and traffic snarls (until a brief shining moment on Labor Day). But they had not yet arrived as of yesterday. Sure the ticks bearing Lyme Disease are waking up, the mosquitos (our regions unofficial “bird”) are going to stir. The next few months will heat up and all these irritations—bugs, pollen, traffic—will make me (and other locals) grumble.

But yesterday, this one day, was perfect.

There were other things, silly things, that made the day awesome: I finished appointments early, I found a grocery item the first place I looked (living in rural areas means some healthy foods are hard to come by—Whole Foods is over 2 hours away). No, these aren’t big things; no one announced a cure for cancer and I did not win the lottery. But the day just “clicked” for me.

It may not seem like a big deal to anyone reading this. But, for me, it was a good day (again, cue the phone to start playing Ice Cube’s “It Was a Good Day”). So I’m sharing it.

Curmudgeoning will resume on this blog soon I’m sure.

Need Help Finding Deleted Post   

Early August 2013, I reblogged and/or linked to a post by my tumblr buddy lux-fiam called On Loving a Sick Body. (On WordPress, here.) She deactivated her tumblr account some time ago, and has no copy of the text of that post. She contacted me last night wondering if I have or know of anyone who might have the text of that post. We think we saw in some comments that someone was posting it on a thyroid cancer site or Facebook page.

Does this post sound familiar to anyone? Or better yet, does anyone have any advice on finding posts that have been deleted (nothing is ever really gone from the internet, right)?

Any help with this would be much appreciated. Thanks!

–Cancer Curmudgeon.

The Next Time Round

Sometimes I forget that there are actually people out there who do not understand that metastatic breast cancer is usually fatal. Laurie Becklund’s video, in which she mentions how someone gave her a “get well” card upon hearing of her metastatic recurrence, reminded me of an upsetting incident that happened last summer. (For anyone who does not know, Becklund died Feb. 8.)

I’ve written often about the ever present fear of cancer, that I’ll never be “over” cancer, and how that sometimes that fear is a bit more pronounced. Last summer, after a “suspicious” mammogram that led to an MRI, and various other symptoms, I was in a state of higher anxiety about recurrence than usual. When discussing the fear, someone said to me that it would not be as difficult the second time round, because after all, I knew what to expect.

I was unable to respond. In the back of my mind, I was afraid I would sound like my usual self, always determined to see the bad side of a situation. Now I could kick myself for that. I think everyone views me that way anyway, even when I choose not to express my “negative” thoughts. But more importantly, I regret not taking the opportunity to explain what causes me fear. And yes, this person, given their profession, should’ve known better than to dismiss any fear.

It is so odd that anyone would think a second round of cancer would be easier, simply because a patient has been through it before, and knows what to expect. I want to say “yes, I HAVE done it before, I know what to expect, and that is precisely why I am so anxious—because it was horrible!!!!” I remember reading an article while in treatment, written by a caregiver, who said that over time, all the memories of chemo and its awful side effects fade. True, I don’t really “remember” how awful I felt, only because I’ve never felt so bad/sick/tired before or since. But the knowledge that it was the worst over-a-year-long experience of my life has not faded at all.

At any rate, recurrence will probably not be much like the first time round. I expect there to be variables. If it is a simple, early stage recurrence of the same cancer in the same place, I’d have a mastectomy—very different than the lumpectomy I had last time. That’s just for starters. There would be no radiation. And what drugs would get used—and would they impact me differently, given my body is not as healthy as it was going into cancer that first time? Those are just the thoughts off the top of my head.

The biggest issue is that recurrence can be in a different place, because the cancer would have metastasized. That is a completely different scenario. Metastasis is real possibility, and it troubles me that 1) some folks refuse to acknowledge or are simply ignorant of that and 2) treatment and outcomes for metastatic cancer are NOT comparable to the first cancer experience. Sometimes I wonder, with all the positive survivor culture that saturates everything, if some people mistakenly took home the message that breast cancer at least, never causes death.

For me, the fear, obviously, is death. Right now, even though I’ve had cancer, I can hang on to the idea that maybe I won’t get it again, and that I will reach an old age and die of something else. Metastatic cancer would put limits on that idea. Would I have to abandon the idea of reaching age 80, 70, 60, even 50?

Yes I’m aware of the anecdotes, of the many women who have lived well beyond that five year from metastatic diagnosis mark. And I am aware that many would prefer not to be viewed as a dead woman walking—would prefer to concentrate on living. I’m not discussing that, merely stating that I know such a diagnosis would severely limit the likelihood of reaching old age. Because I think there are so many who do NOT know this.

I do not know how I would handle a metastatic recurrence. One of the socially UNacceptable lessons I learned from cancer is that it is useless for me to say I’d know what I’d do or how I’d feel if a situation were different. I do know that I do not want to know.

I think this knowledge of limited life span should be enough for anyone to understand why a recurrence is such a huge fear, such a cause of anxiety. It should also explain why I cannot count on previous experience. The idea of “you’ve done cancer before, so you know you can do it again” concept does not apply to a metastatic recurrence scenario—at least for me.

Of course there are many other differences that I am thankfully only aware of because I read other bloggers who describe them. Differences like, frequency of doctor visits and scans, being in treatment permanently, switching to a new drug every time the current one stops working, and I’m sure there are more. How can these things even compare to that first cancer experience? For me, they do not.

Even worse, the incident last summer reinforced for me the awareness that most people do not even understand that treatment for Stage 4 (when a cancer has already metastasized by initial diagnosis—see note below) is vastly different for those of us who “caught it early”. The experience is different for ALL the “metsters”, regardless of if metastasis was found the first, second, or third time round. Thankfully I am not in that group, so I do not have the right to try and describe it. I’m guessing anyone who reads my piddlin’ blog already reads blogs by those who can articulate the experience. (Anyone who has other blogs or sites communicating the metastatic experience, feel free to leave links in comments, if you are so inclined).

I wish I’d brought up all these points to the person who tried to assure me that since I’d done cancer before, I knew what to expect, and that should reduce my anxiety. It only heightened my anxiety. That person is no longer in my life (for other reasons). I’ll make sure all those who do remain in my life, or enter it in the future, understand that the next time round, would not be the same for me, at least. Metastatic cancer is a completely different animal in CancerLand, and I’ll try to do my part to make that clear to those who just do not “get it”, to the best of my curmudgeonly ability.

Note: See here for explanation of difference between Stage 4 and metastatic breast cancer. Also find in this article information about how statistics and data do not accurately reflect metastatic recurrence. Another note about deaths not always being attributed to MBC: “Another quarter-million Americans are estimated to be waiting in the wings. I say “estimated” because no one is required to report a metastatic diagnosis. Death certificates normally report symptoms such as “respiratory failure,” not the actual disease. We are literally uncounted.” from As I Lay Dying by Becklund.

Addendum: I rarely write about MBC because I can only speak for myself, and only write from my POV–so I never want to come off as someone worried & whining about what MIGHT happen, when those with MBC are worried about what HAS happened. So I hope everyone with MBC who reads this understands that is the spirit behind the post.

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