So much has
been written about the stages of grief over the years. It’s interesting to me, and I have found some comfort
reading about generic Grief because the information sometimes serves at times to let me know
what may be coming down the pike emotionally for me and at other times to reassure
me that what I am feeling/thinking/doing is Normal (whatever Normal is).
One of the
many things that I did not know about before we were in the thick of things
ourselves after my dad’s illness was Anticipatory Grief. Somewhat ironically, I actually learned about
it after we’d been launched into full-blown Grief after my
dad’s death, but even in that context I was able to recognize the accuracy of
what I was reading about it in terms of what my family went through while my
dad was sick.
Something related to Grief that I
haven’t heard anything about, though, is the watchdog mentality of a person who is caring for someone with a catastrophic illness, an emotional state that can even extend into the time period after the death of their loved one. It’s an odd habit that can easily find footing, morphing into almost an addiction of
sorts, the waiting for something bad to happen, the unwelcome sense of dread and fear, the impending sense of doom. That Waiting for Disaster kind of thinking makes sense when a person is caring for someone who is critically ill; what doesn’t add up, though, is when that feeling lasts even when the sick person isn’t around to need help anymore.
I don't think there's a term for that extended expectation of catastrophe; perhaps Foredoom is a good way to label it. From talking to so many people who have gone through similar situations like my family did after my dad's diagnosis, I can tell you that it's real - and that it's not that uncommon.
At times, when that Foredoom takes hold, it can feel almost shocking when things go
well, and what’s even stranger than that is the way it feels disconcerting, maybe even reckless, to try to drop the Worst-Case Scenario kind of
thinking, the sleeping with one eye open, the constant monitoring of the cell
phone just in case someone needs me for something critical. The thing about it that hooks us, I
think, while we are caregivers in a critical situation, is the feeling of being needed, perhaps even in a life-or-death type of way,
and of feeling like we have some control over things that without us, we
imagine, would go spinning out of control.
When that caregiver role is gone for us, it’s a loss
that adds to the chaos, the directionlessness, and the grief of the loss of our
loved one. The sting of the realization
that we did our best and still weren’t able to FIX things weighs so heavily on us and makes
us wonder “What next?” It makes us
question whom we are, what we are supposed to be doing, and how we are going to
cope with the changes that have been forced upon us.
Sometimes, I’m learning, that sense of
vigilance remains, long after it makes sense. Maybe we've become so accustomed to the noise that we don't know how to cope with the quiet. Maybe it’s our psyche’s way of punishing ourselves for not being able to save the
person we loved - or for living still when he isn’t. Maybe it’s a result of
clinging on to the idea that we have any control over anything in life, even long after
we should have realized how crazy and misdirected that thought is. It’s like being “on call” was the thing that
gave us direction and meaning, and, now that that’s gone, those of us still here
are left adrift, unable to relax or unwind but so, so exhausted and confused
and disoriented.
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