Tag: Skin cancer

Saguaro Scars

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I don’t expect to live 150 or 200 years, the span of a saguaro cactus. Yet it inspires me to follow its lead. To reach for the Sonoran sky. To transcend the inevitable scars of life that appear on exposed appendages. Perhaps perpetuated by a thirsty woodpecker. In my case, it’s a spot of invasive squamous cancer cells on my left hand. A patch that’s beginning to heal.

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The temperature gauge in my Sonata read forty-one degrees as I pulled into the Omni Dermatology parking lot at eight this morning. Chilly for us desert rats. Though my Midwestern sensibility reminded me of January mornings in arctic Illinois when the cilia in my nostrils froze as I shoveled snow and inhaled subzero oxygen.  A badge of honor for what I endured to earn a living.

Kind Claudia greeted me. Amanda’s replacement for the holidays. First treatment of 2020. Number eleven of twenty overall. More than halfway home. I handed her my blended bifocals in exchange for a less stylish pair of protective goggles, blue flak jacket and matching collar. Ready for another round in the radiotherapy barcalounger.

Claudia applied cool gel for the ultrasound. More flecks of green gremlins on the screen than before. Healthy cells populating where the darkness had been. Cheering from the sidelines. Newfangled therapy bowl game. All that matters is the final score.

Next stop. Secured square metal plate with a hole in the middle. Taped and surrounding the culprit. Quiet conversation with Claudia to hold us in place. No pain. Just procedure. Left hand gripped the padded recliner. Magical mechanical machine lowered tight on my hand like an intimate crane from construction crew captain Claudia. Excused for forty-five seconds. Out of the room.

Just the two of us: me and the humming machine. Less-sinister HAL from 2001: A Space Odyssey. Cold comfort. Scanning the wall through blurred vision. Amanda’s family photos. Notes and files on her desk. Radiation warning sign. Authorized personnel only.

Away-less-than-a-minute Claudia. Three sessions in our week-long radiotherapy affair over. Goggles and gear gone. Blue windbreaker and bifocals with me where they belong.

Back in my Sonata. Two degrees warmer than twenty minutes before. Ten new minutes in the car. East on Indian School Road. South on North 68th Street. Home in time to help Tom fold the laundry on January’s first Thursday.

I’ll do it all over again Monday. Next time, Amanda will greet me. Saguaro scars and all.

 

Standing in the Light

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On this marvelous Monday in the Valley of the Sun–basking in the afterglow of a weekend of holiday performances with my gay friends here in Phoenix–I’m struck with this truth-seeking irony. After stepping out of the shadows in my thirties and forties and standing in the light in my fifties and sixties, I’m finally comfortable in my skin. Yet, I find myself being treated for a spot of invasive cancer on my left hand.

Tom escorted me to treatment #4 this morning. Like the first three, it was pain-free. Just the rigmarole of driving back and forth, wearing a protective flak jacket and goggles, and applying Aquaphor ointment and sunscreen religiously. I can handle that.

Escaping the darkness of an inauthentic life was much more complicated. At fifty-one, I remember the fright of auditioning with Windy City Gay Chorus (WCGC) in Chicago. Even back then, Tom encouraged me to sing again, though it had been decades since I’d performed on stage. I needed a fun, affirming and creative outlet away from work and parenting responsibilities.

In March 2010, a giant door swung open before me. I mysteriously and joyfully found myself singing with WCGC. Later that year I went on to perform in my first holiday concert with the renowned gay chorus … one of the founding gay choruses in the United States. At that point, I couldn’t have imagined I would develop lifelong friends there. Men and women I would share the stage with for seven years. Friendships Tom and I have carried with us across the miles to Arizona.

Now a new chapter standing in the light of the western sun. After yesterday, I’ve completed ten consecutive years of holiday performances. Seven as a tenor two in Chicago with Windy City followed by three more with the Phoenix Metropolitan Men’s Chorus (not withstanding a brief blip as a baritone).

Here in Arizona in a new choral community, I’ve befriended another sixty or so men of all ages and backgrounds. Some of them have stood by me (literally) while I recovered from a mild heart attack. For others, I have willingly given hugs and a listening ear as they fight to create whole and meaningful lives no matter whether their families of origin love and accept them or not.

On stage yesterday in my black tuxedo and red bow tie, grateful for the friends and family members who came to see us perform, I gazed out from the top riser into an enthusiastic audience of four hundred or so. Like a Rubik’s cube with all the right answers aligned, the clarity of the last ten years clicked into place.

The Phoenix Women’s Chorus, a talented group we perform with from time to time in Arizona, was singing on the apron of the stage. They repeated this lyrical refrain from “Stand in the Light”, a song written by Stephan Moccio and Lauren Christy (arrangement by Roger Emerson).

To stand in the light and be seen as you are.

This phrase captures the essence of why I sing with a chorus of gay men. Why I need to be a part of this community in an uncertain world sometimes fraught with surprising discrimination. More broadly, why the LGBTQ choral movement continues to matter for those of us who lived in the shadows for too long.

We must continue to step out of the darkness and sing for those less fortunate. With proper protection and plenty of sunscreen, we must all stand in the light and be seen as we are.

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December, Dermo and Dormancy

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You might think that excellent reports on a Monday from my cardiologist (“your blood pressure is good; your heart is strong; come back to see me in eight or nine months”) and gastroenterologist (“the polyps we removed during your colonoscopy were benign”) would be cause for celebration. You would be wrong.

At the end of the first Monday in December, I didn’t feel happy or relieved. I found myself in a funk. That’s because my dermatologist called on the same 3D-December Monday (cardio, gastro and dermo, oh my!) to confirm “the biopsy showed that you have¬† a patch of invasive squamous cell carcinoma on your left hand.”

Oh well, two out of three ain’t bad.

After I got off the phone with a skin cancer specialist, who explained the treatment options and assured me that my condition isn’t life threatening, Tom held my hand. He told me more of what I needed to hear. That everything will be okay. That we will get through this latest blip together. That it’s nothing compared with what happened in St. Louis on July 6, 2017. All for the chance to start a new life in a warmer home. To explore our sixties in the wide-open west of possibilities.

After all of this Monday mayhem, I needed to salvage some semblance of normalcy to the day. I needed to feel the fresh, creosote-laced air racing through my lungs. So I took a long walk alone. Along the cross-cut canal. Past the Papago buttes. Five thousand steps on a sunny-but-gauzy day restored my hope. It gave me comfort to see that none of the elements (not sun, not wind or rain) had affected these giant boulders. They were here long before me. Skin cancer or not, they will stand long after I’m gone.

In a separate attempt to rescue my day, I returned home to move our desert roses (aka adeniums). It was time to bring them inside to prepare for dormancy. I do this every December. I suppose, unlike the buttes, all of us living creatures need a little protection from the elements on certain days. Time to retreat. No water. No sun. Time to rest. Time to heal and rejuvenate.

Now it’s Tuesday. December continues in the Sonoran Desert. The sun is casting long shadows at sharp December angles. The adeniums are beginning their winter slumber in our sun room. Their leaves will fall soon and their branches will be bare. But new leaves will reappear in the spring after I carry my favorite desert flowers back outside to feel the warmth of the sun. To grow and bloom again.

Next Monday I will begin my own version of winter dormancy. It will be flecked with cancer treatments and holiday gatherings. Rather than surgery, I’ve opted for twenty pain-free sessions of superficial radiotherapy over the next several weeks. The procedure has a ninety-five-plus percent cure rate.

This course of action will allow me to continue my normal day-to-day activities … writing and exercising … and sing in two holiday concerts with the Phoenix Gay Men’s Chorus on December 14 and 15. Being on stage and performing alongside my gay friends will bring me joy. Tom will be in the audience. My son Nick will be too, along with his girlfriend Aida, her two children and about a dozen other friends I didn’t know in 2017.

Late in January 2020, I expect to receive good news from my dermatologist. Something positive and life affirming. Something like what the cardio and gastro folks have already told me. Perhaps that the Superficial Radiotherapy Treatments (SRT) have fully eradicated the skin cancer cells on my left hand.

Whatever transpires, I am a fortunate guy. Tom and I will begin a new decade in our Arizona home. Faithfully smearing on sunscreen and wearing broad-brimmed hats. Continuing to follow all of our doctors’ orders. Writing, healing and growing together. Watching our desert roses bloom and fade in our less-than-certain sixties.

What more could I ask for?