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I am so different than I was, now with a knowledge of medicine and death that feels like a burden. I know what it is to be on the other side of bad news, to envy the physicians who could weave in and out of my mother’s day while I felt stuck. I have, at times, found myself unable to forgive the most human instincts in the people I love. I have held the hand of the most important person in my life, knowing our time together was somewhere between fleeting and borrowed.
There is a price caregivers
pay for being strong.
We do what needs to be done,
but the longer our emotions are
suppressed for the sake of our
loved ones, the harder it is
to connect with them.
We are the front line for that person, and having a bad day just isn’t an option. But when that person is gone, and there are no insurance companies to argue with, no rushed drives to the emergency department, no little fires to put out at home ...
... you find that you are wholly
unprepared for the inevitable.
There is a newfound freedom to, quite simply, feel, and you find yourself unable to feel much of anything.
I was a first-year medical student when my mom was diagnosed, and I took a leave of absence to be with her and the rest of my family. My return to school was enveloped in the fear that my loss would make me “less than” within the uncompromising walls of a hospital.
To my surprise, every single day I am
surrounded by physicians and students
who themselves struggle with grief.
I hear it in the way our voices change and become harder, more clinical when we talk about our negative outcomes—the way our snarky comments about people not taking care of themselves make it feel just a tiny bit easier when we watch them suffer. Although I am not excusing this behavior, I find myself unable to look at my colleagues from some sort of moral high ground. After all, at times I viewed my own mother as “stage IV cholangiocarcinoma” to survive the most trying time of my life.
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