Posts Tagged ‘partners’

Kenneth Lourie

A Life Worth Living, Still

January 3rd, 2013 - by Kenneth Lourie

It might be my age (as in getting older), or it might be the fact that I have cancer (you think?), but my brain and the related physical and mental tasks it coordinates are not exactly working at peak efficiency.

Don’t get me wrong, I’m not exactly “Forrest, Forrest Gump,” but plans are not easily made and when they are made, not so easily or successfully carried out. Whether it’s a drive to an unfamiliar destination, time spent with semi-unsuspecting (about me) acquaintances, or overnighting away from home (and out of my routine: alkaline water, pills, asparagus, baking soda, apple cider vinegar, etc.) as a few examples, what once seemed like ordinary and manageable acts of everyday-type life now present previously unfamiliar hurdles. Talk about making something out of nothing. Everything is something, even if it’s nothing. And that’s a change – for the worse.

Unfortunately, knowing this – and accepting it, hasn’t lessened the burden and inevitability of living with it. I’m always relieved when whatever, wherever, however, we (meaning me) finish what we’re doing: get to where we’re going/solve the problem we’re needing to solve/arrange the schedule we’re attempting to arrange, and complete our miscellaneous activities. I can then settle back into what’s familiar and relatively uncomplicated. If I’ve been there and am accustomed to doing it, it gets done, without much ado.

However, if I haven’t been there – literally and figuratively, getting there – and back, becomes increasingly more difficult. I don’t necessarily want to blame this behavior on my age or my underlying problem (“NSCLC”), but at least if I blame it on something that makes sense – to me, I can live with the consequences of this preferred inaction. And the more I understand the reasons for certain “inaction,” the less stress I’ll feel. And the less stress I feel, the better off I’ll be; as a cancer patient, first, and as a reasonably intelligent adult second (no comments from the peanut gallery, please).

I guess what I’m trying to do is what Jerry, Elaine, George and Kramer were competing to do years ago on a particularly memorable “Seinfeld” episode: master my own domain; trying to control the uncontrollable. However, if any set of circumstances is likely uncontrollable, it is the physical, mental, emotional and spiritual effects one experiences after receiving a terminal diagnosis. You’re either ready for its demands or you’re not. It’s not like – at least for me, there was really any preparation or expectation that your life – as you knew it, was over.

I suppose there’s a handbook somewhere. (Maybe there’s even some training or a class – Cancer 101, you can attend.) And though I can certainly appreciate the benefit and power of the written – and read word, a terminal diagnosis with a “13-month to two-year” prognosis requires – in my opinion, a more personal touch, one with a one-to-one/face-to-face-type connection.

When the diagnosis is stage IV-serious, it’s best to leave nothing to chance and/or misinterpretation. As much as you – as the patient/”diagnosee” think you’re hearing and/or reading what’s being said or handed to you concerning the facts of your case, the shock of what you’re learning will not only cloud your judgment, but rewire your brain, emotionally speaking. It’s hardly another day at the office. In fact, it’s like no other day you’ve ever had at your office or any other office. The assimilation – or rather the attempted assimilation of your diagnosis, prognosis, treatment options, schedule of diagnostic scans and doctor appointments, best and worst case scenarios, will forever change the way you process information and plan your future.

What I’m finding out is, the longer I survive, it’s the emotions I feel about having cancer more than the facts of having cancer that are causing me the most problems.

One I can live with, the other is living with me. And it’s not of my own choosing, either.

Share your thoughts with us below. How do you live with the emotions that accompany being a cancer survivor?

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“This column is my life as one of the fortunate few; a lung cancer anomaly: a stage IV lung cancer patient who has outlived his doctor’s original prognosis; and I’m glad to share it. It seems to help me cope writing about it. Perhaps it will help you relate reading about it.”

Mr. Lourie’s columns can be found at www.connectionnewspapers.com. (key word, Lourie)

Read Kenneth Lourie’s 1st LUNGevity blog post & bio.

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Juhi Kunde

The Magic of Applause

July 11th, 2012 - by Juhi Kunde

I have a confession: I write poetry. And this summer, I took a big leap and entered the poetry contest at the local County Fair.

Apparently, the Fair doesn’t notify winners ahead of time.

That would be too humane.

Instead, they make you hunt for the plaza where the poetry entries are displayed. And once you’ve stumbled onto the plaza, they make you wander through the displays seeing countless ribbons attached to other people’s work.

You hope. You pray. Maybe one of your entries will have a ribbon next to it. Okay, probably not a big ‘first prize’ ribbon, but maybe a small ‘honorable mention’ ribbon.

I hunted for my entries. Ultimately, I discovered that I lost. Or, at least, I didn’t win.

With the dull ache of disappointment still clinging to my stomach, the poetry reading began. Winner after winner stood up and read their work. Many poems were exceptionally-crafted and a few were mediocre. Nevertheless, I clapped with as much enthusiasm as I could muster.

Then it was my turn. I had agreed to read my work when I felt confident of victory. But now, I had to present my poems, which were apparently worse than mediocre. I wanted to cry.

But I stood up, walked to the microphone and explained that it was my first time reading my poems in public. And do you know what the other poets did? They clapped – loudly and enthusiastically.

Miraculously, the ache in my stomach disappeared. I actually felt uplifted as I read my poems. And I am ready to try again.

I think there must be magical healing powers in the support of our peers. Even hugs from my family couldn’t soothe my raw feelings the way that round of applause did.

The nods of encouragement. The supportive smiles. They have impact and strength.

Poets can get that strength from other poets. Lung cancer survivors can find that strength in other survivors.

Whether it is a golf outing in Illinois, a mocktail contest in Pennsylvania or one of the many Breathe Deep events that are held nationwide, every LUNGevity event is an oasis of support and healing.

These events are critical wells of strength for survivors and caregivers. By embracing the magic of applause at every LUNGevity event, we can help each other persevere.

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