In her spare time, Stephanie works full-time, and then some, as an attorney. She has published articles and delivered talks in arcane fields like forensic evidentiary issues, jury instructions, and expert scientific witness preparation. She attended law school near the the banks of the Charles River and loves that dirty water; she will always think of Boston as her home. You are welcome to take a look at her Facebook author page, or follow @SMartinGlennon on Twitter and @schnitzelpond on Instagram. Bonus points for anyone who understands the Instagram handle. All content on this blog, unless otherwise attributed, is (c) 2012-2023 by Stephanie M. Glennon and should not be reproduced (in any form other than re-blogging in accordance with the wee Wordpress buttons at the bottom of each post) without the express permission of the domain holder.
For several days I have found it impossible to capture the light.
Before sunrise, as the beagles happily disrupt the neighborhood with their hopeful howling (whatever is upwind for them every morning never gets any older for them than does the thrill of having the same old thing for every meal), I see vivid, wavering lines of yellow which I cannot seem to replicate in a photograph.
At sunset I see streaks of bright pink at peach and try, but fail, to capture them with the camera Jim gave me. I know he could have done better.
And in between, during daylight, the sky has shifted wildly, cleaved between storm and sunshine, winter and spring.
Over the same period my dreams have shifted. They are always about Jim, but for the first time I have had dreams in which Jim is not sick, has not yet been diagnosed.
For well over a year, since his diagnosis, I never had a dream in which my subconscious was not acutely aware that Jim was sick.
The scenes in these recent dreams are of things I can never fully recapture.
These dreams are so stunningly ordinary as to be extraordinary, and they bring me some peace: we are sitting with the children laughing and watching a movie, going to a band event, walking in the woods, even swatting at the zombie-like mosquitoes which sometimes mysteriously appear inside our house even in deep winter in New Hampshire (and tended to escape above the reach of a five-two person but within the leaping reach of my six-fourish spouse). Before dawn one day I trudged around the yard cleaning up after our dogs, among the endless tasks which have fallen to me alone. But in my dreams that night, Jim and I were cleaning up together.
These dreams bring back, if briefly, the family life in which I know Jim would want our memories to dwell.
(c)2012 Stephanie M. Glennon
“Has anything else changed?”
The way my husband lived with dying somehow took away all my lifelong fears—all but the fear of his suffering and of his death, and of life without him.
He planned a final family vacation for us during his last season. Short months before his diagnosis he had finally coaxed me onto a plane with our daughters, and I was still white-knuckled with terror of flying. Although he wisely did not forewarn me that each leg of the final family-of-six trip would involve four separate plane rides, I discovered that after four decades I was no longer afraid of flying.
He needed someone to be able to give him subcutaneous injections at home when he no longer could do it, and he needed carefully-mapped sequences of injections through his port. I discovered then that I no longer was afraid of needles. How could I be, after what he had been through?
He needed to know I’d be able to handle the complicated finances for getting four children through college, and I very nearly conquered my fear of his elaborate financial computer system.
He was not afraid of his own death. I never got there, but, as he told me, the two of us are made of different stuff.
The World Still Out There
More than a year ago, after my husband was diagnosed with pancreatic cancer, I began writing. At first I wrote about appointments and logistics, then immense disappointments and more logistics. Eventually I wrote much more as I waited at appointments, and waited by my husband’s bedside. Some people who read my expanding missives, posted for a private community within a larger site (Lotsahelpinghands), began identifying them as blog entries. They suggested that I share them with a wider circle.
I’d like to start here, now, long after the end of the medical portion of this ordeal. Today marks exactly one month after what would and should have been my husband Jim’s birthday. In honor of him on that occasion I gave a talk at the hospital where he was the first Chief Medical Officer. It was about our family’s experiences in the treatment of a dying physician, and about the treatment of seriously ill patients (physicians or not) known well by a treating physician.
Before speaking to the group of physicians I circulated some of what I have written for my children.
The day after the talk, a physician who had been there and whom I did not know wrote to say he works with nursing home patients. He thanked me for sharing our experiences and helping him to “open a door” that he said is easy for physicians to keep closed, even–and maybe especially–among the constant presence of dying and death.
His comments give me hope that the worst of our experiences can lead to some good.