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Hope

Who knows how many voices created the cacophony that filled the waiting room that night? Words, wails and whispers gave sound to the gamut of human experiences and emotions. But as I listened, I heard one clear, unwavering note that floated above the clamor.

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Green, White and Sterile

The young, black-haired waiting-room receptionist, in a voice that is pleasant and professional but too loud, instructs those of us who are waiting–grey-haired and balding, strangely like me–where we should go for the next phase of our lives. So many are told to go to the critical-care waiting area that I worry that young black-hair knows no other destination. I have an urge to educate her about the “everything’s fine, no need to worry” waiting area and to speak a little more softly, but I think twice about it since, like all the people working here, she seems so powerful, and we, right now, are just weak, worried wait-ers.

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“Hug Lady, Pretty Dress, Crying?”

I am sitting in the all-too-familiar waiting room of my local emergency department on a Saturday night in July. I am here with my daughter, Ashley, who is nineteen but could pass for a typical twelve-year-old—until she starts to talk. Ashley has a rare genetic disorder. On the good days I laugh and say that she will make a great ventriloquist because she talks without ever moving her lips. This is not a good day. She has a fever, a wet cough, and she snuggles up against me.

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Seeing is Believing

For months I spoke, but no one listened. Not my dad’s primary care physician. Not the physician’s assistant. Not the nurse. I described the “attacks” my ninety-six-year-old dad was experiencing: loss of awareness of his social and physical environments; inability to stand on legs that had turned rubbery; skin that looked pasty and felt sweaty. “Give him orange juice,” I was told. “His sugar has probably dropped a bit. And don’t worry.”

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