Monthly Archives: August 2019

“Moving On”

A phrase I hear a lot now is a variation of “there are no words I can say to you right now.” I completely understand that sentiment. There really aren’t words that we can use to convey the depth of sorrow, empathy, sympathy, loss, love, and common human togetherness that we feel when someone, whether it’s one we know and love or a complete stranger, is suffering from the loss of a loved one. In a way, those words convey all of these feelings, like the phrase is a magic spell to bind emotion into language, itself incapable of conveying it, in a short, succinct, and meaningful way. I appreciate it when people say that to me, because there are simultaneously no words and not enough words that can truly soothe a suffering heart.

Of course, it’s a real shame that there are no words. Every human being who has lived in the history of this planet is either dead or will be. We should probably have come up with words by this point. But I understand the difficulty, especially now in an age when “thoughts and prayers” is a phrase that conveys a complete indifference to the actual suffering of people. (Fun side note: I received a card from coworkers after Julienne was in the hospital for two weeks with her second collapsed lung. All but two people used the phrase “thoughts and prayers.” The other two? “Prayers and thoughts.” What a world.) Both no words, and not enough.

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Julienne

Julienne Gede Edwards left the world on August 8th, 2019, just before 11 am on a bright morning as she lay in her bed. It was where she’d wanted to be at the end. As it happens, despite having a lot of people in and out of the house during her final days, she and I were alone. I was holding her hand and reading The Ocean at the End of the Lane aloud, her favorite book and the one she’d asked me to bring to hospice with us to read to her. I checked her oxygen levels as I did periodically, to make sure that she was getting enough to her blood. The last week of her life required a lot of oxygen so she wore her nasal cannula as she’d done for over a year by that point, as well as a mask that she hated over her nose and mouth to give her additional air.

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