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Posts Tagged ‘sympathy’

Third Game Plan

Marty Linsky is unimpressed with my ambition to join Donald Trump on The Apprentice and his slightly raised eyebrows indicate only marginal amusement with my stand-up comedy endeavors.  I had not planned to tell him about either during our informational interview, but now, over coffee in the Portland International Jetport, I seem unable to stop talking.

We had arranged for me to pick Marty up at the end of his training engagement and drive him here before his flight home to New York.   Since the moment he climbed into the passenger seat of my Jetta wagon, I have talked nonstop.  I blurted about adaptive leadership, the connections I saw with my consulting.  “I am a fish who has found my ocean!” I gushed. “Adaptive leadership is a perfect framework for all the diversity work I have done!”

I downloaded my entire career.  Domestic violence work to United Way to domestic violence again.  A stint with public radio and television before working for an AIDS organization.  Preaching the gospel of condom use across Maine.  A graduate degree in social work and building a nonprofit organization for gay youth.  By the time we stood at the American Airlines ticket counter, he had heard how the gay youth organization became the foundation of my organizational development consulting.  As we slid upstairs on the escalator to the coffee-deli bar,  Marty heard about my favorite consulting gigs – the seven weeks in Micronesia (they honored me with a pig roast when I left) and the four years with a college athletic department (Ramona has a lot of great sweatshirts now).  Somehow, I had refrained from actually tugging on his coat sleeve like a five-year old child and shouting “Notice me! Notice me!”

Now, sitting over coffee, I am telling Marty about The Apprentice and comedy classes.

The point of an informational interview is lost.  Marty should be the one speaking.  I should be the one listening.  Somehow, I know it’s the steroids. But I am powerless over my mouth.  I am beginning to suspect, but no one has told me, that steroids cause the equivalent of a manic PMS.   When I had a functioning uterus, I could count on every frustration or sadness being magnified for one week each month.  Big tears, big sadness, emanating from a real, but small kernel of disappointment.  Each month provided a hormonally-induced opportunity to examine and accept or discard what the kernel could reveal. Talking at Marty, I feel the sinking awareness that this steroid-induced mania is right this moment magnifying an anxious insecurity way larger than a mere kernel.

Marty listens patiently to everything.  His bright blue eyes, unnerving behind his spectacles, miss nothing.  He manages to convey detached yet empathetic interest.  He is intrigued by my culture change work with the college athletic department, so he asks questions about that.  I confess the crux of my call to him.  That consulting was fun at first – it  paid the bills and no one was getting beaten, thrown out of their homes, or dying.  I was good at it.  Competent.  “But now I’m bored.  I’m looking for more. Competence is not passion.”

An airport worker, in his fifties or so, approaches our table.  I finally stop talking.  “I noticed your ‘CHEMO BITES’ button,” he says awkwardly.  “May I ask what kind of cancer?”  My hand reaches up to my hat, fingers brush the button.  I’m so used to it already that I forgot it was up there.  I look at Marty, who smiles at me and sits back in his chair, interested in the exchange.  “Ovarian cancer,” I tell the man, “but my prognosis is excellent.  I should be fine.”  I always add the I should be fine. Ovarian cancer is a heart stopper and I don’t want people feeling more concern for me than they need to.  It’s hard to witness, over and over again.  His eyes well up anyway. “Really,” I assure him.

“My sister died of that,” the he shares.  “She suffered for years. She’d have liked that button.  God bless you.”  I reach into my coat and pull out an extra button for him.  Wonder if I should stand up and hug him or not, then choose to shake his hand from my sitting position instead.

“Does that happen often?” Marty asks after the man leaves us.

“All the time.”  My life is out of control, I want to say. I am supposed to be having a coffee about my career and instead I am comforting the bereaved and passing out CHEMO BITES buttons.  Instead I am being a good-cancer-soldier with a plucky, survivor attitude.  Instead I am nattering on about The Apprentice and stand-up comedy when I want to be, oh I don’t know, something different and better than this!   That’s why I called you!

I drink my coffee.  I’ve talked enough already.  I feel overexposed.

Marty returns the conversation to our work lives.  He has listened (what else could he do for the last forty-five minutes?) and informs me that his current career began in his forties.  He reminds me I am still young, there’s still time to explore and find meaningful success.  He tells me about the Kennedy School of Government at Harvard University and outlines their MidCareer Program.   It would be a good fit, he says, for where I am right now. Two hundred middle-aged students from all over the world, all on a path to discover what’s next, who enroll for a year to earn a Masters in Public Administration.  A degree they don’t necessarily need.  Just like me, many of the students already have advanced degrees.  It’s not the courses, he emphasizes, but the people and the connections and, literally, the world of opportunities that being in the program opens up.  It’s life changing.  Plus, he adds, as if life changing hasn’t caught my attention, there is more opportunity to study adaptive leadership.  Marty tells me I should really think about it.

After our coffee, when Marty gets on his plane back to New York, I think about it a lot.

© 2011 Cathy Kidman

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Morning Shift

When I wake up the morning after surgery, I see Dad, settled and dozing in the armchair next to my head.  His tanned bald head is tilted forward, chin meeting chest.   I understand two things without asking. One, that he and Mom, as if they were still married and not in the middle of their divorce, have come to an arrangement.  Dad will take the morning shift.  Mom will come in the afternoon.  Two, they devised this schedule without exchanging a single word.

I watch Dad for a few moments, grateful for his presence, and remember when it was me in that chair. Twelve years before, I had stolen into his hospital room early in the morning.  He had nearly died from an anesthesia complication.  At the time, I was not speaking with my family. In the late eighties, like every other middle class White girl with a liberal arts degree, I got a therapist. Sorting through the mishmash of my family dramas, I beat a messy two year retreat.  I am still working on making amends.

My then sister-in-law, Bruce’s wife, called me at work.  “Your father’s in the Intensive Care Unit. He’s going to be fine, but he almost didn’t make it.”

“Which hospital?”  I was on my way as I asked.

“No, don’t come. Your mother wants you to stay away. Showing up might kill him.”

My stomach fell as my throat closed.  “I bet you like telling me that,” I said nastily.

“No, I don’t.  I don’t know what else to say.”

“Fine. Thank. You. For. Calling.”  I hung up, the handset hitting the receiver.  My face burned.

The next morning, I snuck into his room, pretty sure I wouldn’t kill him.  I got up before dawn.  Stopped at the 24-hour Dunkin’ Donuts for caffeine.  Walked through the hospital corridors, fortified by an extra large coffee.  Kept an eye out for family members.  Arrived undetected at the ICU.  Admitted to the nurses that I am Merrill’s daughter, braving the possibility that my family had put me on a “do-not-let-in-because-it-will-kill-him” list.  They hadn’t.

Dad was lying in the hospital bed, framed by tubes and machines and IV lines. He was so far from the man I had been fuming at that I was suddenly crying. Grabbing tissues, I wiped my tears and runny nose.  Found the antiseptic hand sanitizer.  I’d be damned if my germs would do him in.  I pulled the plastic chair up next to his head, a determined squatter.  I was the first person he saw when he woke up.

Dad stirs in his armchair. Notices me awake. “Hi hon.”

“Hey,” I say quietly.  We share a comfortable silence.

“How are you?” he eventually inquires.

I will be asked this question over and over and over again in the coming years, but I don’t know that now.  It’s the question people ask and then fill in with their own stories, unless or until you set them straight.  How are you? She may die. How are you? She looks like hell. How are you? Must be hard without hair. How are you? I hope she doesn’t tell me the truth. How are you? She’s just going to say ‘fine’. How are you? I don’t recognize her, she’s gained so much weight. How are you?  Thank God it’s not me. How are you?  She’s lucky, I survived worse. How are you? Wonder if she can come back to work yet. How are you? Treatments are over, that must be a relief. How are you how are you how are you how are you.  I’m glad I didn’t know.

“I’m high,” I smile at Dad.  God, I love morphine.  “You’re here early.”

“Before work.  I saw the most magnificent sunrise on the way today, the colors were pinks and purples and yellows and oranges – just like a painting.  Did you see it?”

My hospital room is a two patient room.  The other patient, an older woman with advanced ovarian cancer and a piercing nasal snore, has the window view.  My view is the white curtain divider.  I look at Dad, look at the curtain, look at Dad meaningfully.  I’m not so high I miss the irony.  Dad chuckles. “Guess not,” he says, “but you missed a good one.”

© 2010 Cathy Kidman


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Another Flower Delivery

Flashes of yellow and orange bob above the window sill moments before the knock on the kitchen door.  ”Come in!” I yell from my horizontal post-surgery station on the couch.

This delivery woman has been here before and she brings this latest flower arrangement right into the living room.  She pauses at the doorway, taking it all in. There are flowers from other shops now, covering every surface and spilling out of the living room and into the kitchen and dining room.  Lilies, roses, daisies, Christmas cactus, house plants with unpronounceable names – they have been arriving daily, sometimes several times in a day, since my diagnosis.  Many accompanied me home from the hospital.  She moves a vase of lilies on the fireplace mantle to secure an advantageous spot for the new bouquet, a clear glass vase of bright Dutch tulips from a colleague.

Surveying the profusion of flowers again, she asks for the first time, “What kind of illness do you have?” as if this abundant overflow means that I am either an obscure, minor celebrity or my illness must be really, really bad.

“Ovarian cancer.”

“Oh.” Illness, not celebrity.  She weighs my response against the garden in my living room. Her face telegraphs that she wishes she hadn’t asked. “Ohhhh,” the extended syllable escapes, “I am sooo very sorry.”

No, no, I want to insist.  I get this many flowers because I have friends and a community of people who love me, not because they believe I am dying. And then I think, maybe I have these many friends and they believe I am dying. This gives me pause. Maybe I need to stop saying to everyone, “Don’t worry. It’s early stage. We caught it early. Great prognosis. Surgery went great. I’m fine. It’s just chemo.” Maybe I need to see what everyone else is seeing.

The words “Don’t worry” wilt on my lips and I acknowledge her sympathy with an awkward nod.  “Thank you for the flowers.” Rote courtesy kicks in as she sees herself out. “See you soon.”

© 2010 Cathy Kidman


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