Practice Hugs
Will this be
the last time
she remembers me?
As the disease continues to slowly claim my mother’s mind as its own, she stops recognizing first her friends, and then her family, in public. This starts innocuously enough: we are strolling around the grocery store and she walks off with strangers; or we visit a restaurant and she tries to sit at other patrons’ tables. Outside the familiar context of her house, she has a hard time remembering who she is with or how we know her.
Over the last few months, my mother greets me by standing at
a distance, apparently not sure if she knows me. Once I smile at her and set my hand on her
shoulder, she smiles back. This
development should not surprise me, as I know this hesitation is part of the
progression, but it gnaws on my soul. My
mother no longer sees me as her daughter, and my family is pretty sure she just
sees us as friendly faces.
There is a feeling of completeness when we are together as a
family; my sisters, mother, father, and I, much like the announcer at hockey
games yelling “full strength!” when players emerge from the penalty box and
rejoin their team on the ice. Even when
we aren’t doing anything particularly important or exciting, a missing member
of the family is noticeable. Lately,
even when we are all together, on holidays and Sunday afternoons, the dynamic
plays toward someone missing, and I realize the absent one is my mother, even
though she is sitting right next to me. The
feeling of “full strength” has eluded me for a while now, and this realization begins
manifesting itself from an unexpected rationalization.
I notice my sister draining the dishwater from the sink and
neglecting to rinse the bubbles and residue down the drain. On several occasions I think, Mom’s not going to like this when she gets
home, as she was the one who lectured me about preventing rings in the sink
years ago. The thought then immediately
shifts to, no, wait, Mom’s here, and she
won’t notice, before finally settling on, why are you thinking about this?
You are an idiot. I learn
quickly that if I pick on myself, I don’t dwell as much on the painful
realization that started this thought-process in the first place.
This immense sense of loss is partially due to the lack of
connection with who my mother is becoming.
She looks at me and smiles, but I often question if she knows who I
am. She sits to the sidelines when we
play board games or watch movies, or cook dinner, and I worry that we are
inadvertently alienating her. I wonder
if she feels alone, even when she
probably does not know what that means.
Her dwindling ability to understand words makes this even more
complicated, as we are no longer able to explain that we love her and are here
to support her. How can we explain this
to someone who no longer recognizes her own name?
This soul-gnawing gives way to anxiety as I think about the
time she will reject me as even a friendly face.
Months ago, my mother stops giving hugs, even when my
sisters and I say goodbye. We open our
arms and ask, “Hug?” but she just smiles and clutches her magazine. After too many failed attempts to get her to
understand, I finally lean in and wrap my arms around her shoulders. She laughs.
I let go, look her in the eye, and say, “Thank you.” She laughs again, and then taps her fingers
on the sides of my stomach. I hug her
again, and this time she hugs back. I
rest my chin on her shoulder and she pats me on the back. On some days we do several of these practice
hugs before she hugs back, but sometimes she does not react at all.
My mother’s ending is not going to be a surprise—the disease
will continue stealing her brain until her body can no longer function and she
leaves us for good. I know the day is coming when she will have no
recognition of me at all, either as her daughter or just a friendly face, but
every time I wrap my arms around her and rest my chin on her shoulder, I hope
that she will feel loved, even when
she no longer remembers what it means.
Comments
Post a Comment