James had an overnight pass
last night. It was a well-needed reprieve from the hospital (and the hospital
is among the worse places to be with a non-functioning immune system). We have
no structure or routine (or space of our own), but there is something to be
said for the freedom to move at your own pace.
Tonight, I had to leave him
in the hospital again. It is the hardest in the evening. I feel his absence the
strongest. We will both have long nights. James will be awoken each hour to
have his vital signs taken. His IV medications will be complete in the middle
of the night. He will wake to the beeping of a machine, search for the call
bell in the dark, and wait for a nurse to disconnect him. There will be
continuous movement in the hallways and bright lights at all hours. James will
listen to his body. He will be able to fall back asleep with ease after each
disturbance.
I will have the company of
Ophelia by my feet, but I will still feel the loneliness of a dark and empty
apartment. She will remain close with each and every change of position and
will not stray with my diminishing hopes of sleep. Insomnia has a tendency to
feed into cycles of further insomnia. I will get into bed with the fear that I
will be awake to hear the evening traffic slow to silence, and still be wide
eyed with the rise of the sun. The bright lights will eventually seep in
through the curtains, and I will welcome the streetcars and sirens as a signal
to the end of this nighttime torment. I will start another day with forever darkening
circles under my eyes. I know that I will eventually fall asleep. How long can
I go without rest? Perhaps, I will sleep tonight. Regards, I will try (and
Ophelia is already warming the bed).
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