I often wonder if I should really play up the disabled card
and get a few perks. Yet I know that’s not how I operate, and I opt for the ‘try
to look normal’ approach, and I shove all the disabilities aside. I’ve seen how
both can work against me.
My kids are very aware that I’m becoming far less able to
accomplish simple routines. It isn’t discussed, but they just step in when
needed. I also detect their shying away from any discussion about it. I guess
that’s normal – kids really have a hard time seeing their parents decline. I swore
my father really wasn’t that bad after he suffered two strokes. I turned a
blind eye to all the routines he could no longer finish. I preferred to think
that he had a small setback, and he’d be back to himself one day. I refused to accept
how seriously ill he was, and when he died, I was devastated.
I did the same thing with my mother at first. I couldn’t
allow myself to see that she was really slipping, and that her dementia was
taking over her life. I got angry – how dare she get old, how could she be
acting this way, and where had our close relationship gone? Once I finally
accepted that the mother I knew was not this person, and when I came to realize
that things would never be the same, I started to deal with the situation. I see
her nearly every day now, and I look into her blank eyes. Most of the time she
knows me, but at other times, she’s in another world.
I think my children have had to go through similar
processes, and I may have added fuel to that fire. By pushing myself, and
trying to keep things as normal as possible, I probably built up a false hope
for them. I couldn’t continue the charade indefinitely, and now I try to act
more realistically, for all of our benefits. It’s sad, but that’s life.
I may have also led others down the same path of denial. At my
mother’s nursing home, they know I’m disabled, but they don’t understand how
bad it is. Yesterday, they asked me to help my mother since she can no longer
use her hands. They were painting brush strokes in rhythm with Strauss waltzes.
I’m right handed by nature, but I’ve become left handed by necessity, and now
even that side is becoming less functional. So, instead of telling the activity
staff I couldn’t help, I just dived right in. Having been a painter in the
past, I understood the components, but now I need more than just knowledge. In my
mind, I can see the color mix, I can feel the way a brush should execute
strokes, and I can envision the finished product. But what I get as a result is
far different from what I imagined. Of course, it looked much better than what
the residents were producing, and the staff admired it. But I kept wishing I hadn’t
shown myself how bad I’ve become.
So, in the end, I still keep thinking – should I still be so
vain as to not allow others to see my weaknesses? Should I continue to pretend?
Remember the words in “Whistle a Happy Tune?” When I fool the people, I fear I fool
myself as well. I moved the comma to show my thinking on it.
Peace,
Muff


9 comments:
You're not going to believe this, but tomorrow's already scheduled poem is sort of about this. Great minds?
Judy
Interesting question? Most people already have insight into the fact that we are different by watching us move, they just fail to speak up to avoid making an uncomfortable situation even more awkward. In the end we all look like fools.
Judy, can't wait to read it!
Rae, when moving, it's obvious about me, but if I'm just sitting, you really can't tell that I'm a gimp!
Peace,
Muff
Hi Muff,
I don't really understand what you mean by playing the disability card.
I don't think you need to share the severity of your disability with anyone you don't want to.
Personally, my disabilities can't be overlooked by others. They are right out there for all to see, as plain as the nose on my face.
I have no problem as far as vanity goes, being disabled is my "normal". I neither flaunt it or hide it. I am still very proud of who I am, and how I how I appear to others.
Fooling myself is not an option. I know all too well what my limitations are. Facing them helps me deal with them in an effective manner, so I can build on what I still have, find new direction, and live my life the best I can, hopefully with joy and purpose.
I think we have to handle our situation in the way that is the most comfortable for oneself.
I gave up the pretending and false impressions. I am who I am. I can only do what I am able to.
Sometimes I think I place to much importance on what I think others think and forget that many of these perceptions are my own.
If I act like my new normal is a bad thing then other respond in kind.
I don't understand the part about playing the disabled card? Are you saying that you either try and look normal or your playing the card?
I really don't know how to comment, 'cuz I haven't walked in your shoes. My thought would be do what you're comfortable doing, and don't worry what the rest of the world thinks.
Muff, how would you say you are going through your stages of grief (The SEVEN stage model: 1. denial/shock, 2. guilt/pain, 3. anger/bargaining, 4. depression/reflection/loneliness, 5. the upward turn, 6. reconstruction/ working through, and 7. acceptance/ hope)? Linearally, hopping around, or some other way?
Karen and Jan,
I think by the disability 'card' I mean letting it all show and just allowing others see how bad I really am. I am vain, though, and it just doesn't work (for me.) I prefer to act as 'normal' as possible and be a part of the 'normal' world as much as possible.
Muffy, thanks for your support!!
Webster, I waffle among all those stages, but I don't stay in the acceptance phase too long. And hope? Gone!
Peace,
Muff
What I found over time, as I tried to hide behind my happy face so no one could see the pain, and that I felt like crap. The amount of energy I wasted doing this cost me time, so my visits got shorter and shorter. It was pointed out to me by my brother, he said; "The people who know you best see through your mask and wonder why it is your trying to lie to the people who love you just the way you are." Funny thing was no one noticed I stopped putting on my happy face, learning that most people tend to see what they want to see anyway. My visits got longer after I stopped wasting all that energy putting on that happy face.
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