At The Fault Line, Bravery, Memoir, Read, Support, writing

At The Fault Line

Today, Friday June 8, I am reading one of my recent essays at a ticketed event in Seattle. Eleven writers in my memoir group have crafted, honed and polished their words with grace and guts for the last few months. Writing a personal trauma story is a naked enough feeling. To read it in public takes exposure to a whole new level.

Last year, after my diagnosis and series of surgeries, three years of writing a manuscript went up in smoke. The questions came fast and hard, especially at night: do I bury my mother’s story, interweave mine, move on from past to present or take the story present to past? Do I even have the skills to do any or all of this? Do I want to?

When I finally wrote down the words which became my essay, “We Don’t Know Everything,” I felt there had been a nuclear explosion in my head; the collision of my story, my mother’s story, cancer information and understanding illness, all locking together in believable — and unbelievable — ways. All the pieces will be sharing, for lack of a better word, the radioactive fissure — the cracking of the fault lines —  that comes from speaking out on trauma. Eleven times over.

This is the second year of this event At The Fault Line. I hope we do this forever. The experience of professional coaching — by our mentor Tara Hardy —  speaking our words aloud into a microphone, into the atmosphere, into the ears of friends and strangers, validates our writing. And our existence. And our purpose.

Last year we sold tickets at the door. This year we have been sold out for almost two weeks. I am watching the seedling of a mighty tree of storytelling grow and grow and grow.

The stories will crack open hearts, from the mundane to the profound, from folding laundry to holding an Alzheimer patient. I am so proud of all of us.

Buddha

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Bravery, Carcinoid tumor, Health vs. Beauty, ovarian cancer, Women

Bravery: Not Always Pretty.

After the elective ovary-fallopian tube removal surgery that filled my abdomen with air, then sliced, diced, washed and scrutinized everything that could be examined in my abdomen — along the way my appendix didn’t look good, so the surgeon nipped that out too — the bloating had finally reduced enough on day four so that I could see my feet. In disbelief I howled my first complete sentence into the shower steam;

“WHO THE F DID THEY GIVE THE RAZOR TO?”

That was when I got my first laugh, bent over the sink holding a towel to my sutured belly. I needed that laugh. My belly was a mountain range of peeling steri-strips, yellow bruising up and down and around, my belly button full of stitches.

Thanks to two friends in the medical profession I had been linked up with a first class surgeon. April 20, 2017, was her first available surgery slot — a completely random date, for a straightforward elective preventative surgery  — which turned out to be more crucial than anyone knew. Two weeks into recovery, pathology reported that my female bits were all fine. But I only got half a victory lap. The appendix was filled with tumor.

The road back from this surgery initially required patience, sleep and helping hands. But most importantly, this one required, and still requires, bravery.

I am healing from round one and my work isn’t done. I have been overwhelmed and full of fear since the pathology report, the kind that makes your knees weak and your head disconnected, a paralysis that had me knocking things over when I bothered to even get off the couch. I did not know this fear, a bleak, dark, exhausting swamp that mired me day and night, that arrested my healing, my appetite and my sleep. I didn’t want to be alone, and then cringed when anyone saw me. This was ugly. This was not brave.

And then, last week, I went back to Mass General Hospital and met with my GI Oncologist and the next surgeon for round two. As we talked, I felt the anxiety rise out of me. Like a palpable, visible mist right off my shoulders. I suddenly realized I chose trust. As these two men looked me in the eye and laid out our game plan, I understood that after a life of being in control I could recognize when to give it away. I didn’t google, or argue, or faint. I asked questions and listened carefully. I brought a note taker.

The next day I received an email from a fellow writer and cancer survivor. She wrote me: You have to be a fighter. And I would add, to be a fighter, you need to chose your team to go to battle with you. And when I chose, and accepted, I got my first good night’s sleep.

As I move forward, this life changing surgery — now referred to as surgery #1 —  leads me in a few weeks to surgery #2. I choose to count my blessing; if I had postponed the first surgery until after my daughter’s wedding in September the situation would have been immeasurably worse. I will have deeper scars and take longer to heal. I have to ask friends and family to re-boot meals and help and support all over again (thank you). I will most likely marvel if not laugh over the new mountain range of scars and the price of spanxx.

Bravery isn’t pretty, but I am upright.

Though frankly, the guy in surgery #1 with the razor (had to be a guy) might have tried to do something about those stretch marks while he was down there.

To be continued.

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Nurse Olive never left my side.

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