Don’t let anyone tell you that starting a
new life is easy. It is not. It feels like Howard and I have just begun
our lives together and have to begin to set up a routine that fits us.
I hardly know where to begin.
Most of the last ten years have been spent
taking care of Mother. Although five of
those years I was working, the last five have been trying to make sure all her
needs were met. The hardest part was
adjusting to the fact that I am no longer the person I was ten years ago and
have to really struggle to take care of myself, much less trying to care for
another. I say this part was the hardest
because she has yet to understand how MS works.
I know that is a common problem for those of us with MS.
There are so many aspects of my life that
have changed in the last few years. One
of the scariest ones, to me, is the loss of my comprehension. I really become agitated as I search for the
words to say what I am trying to get across to others. It is a fear I share with many of you. Searching for the word for the picture I have
in my brain is often like putting that camel through the eye of a needle that
Jesus talks about!
Many people have told me not to worry
because it is just a part of aging. I
appreciate their encouragement, but they have no clue as to what is going on in
my brain and body. Yes, we all age every
day, but with MS is often is a quick thing rather than a gradual thing. To suddenly go from being able to comprehend
anything put in front of you, to struggling with the simplest of things is a
change that is not understood by most people.
It is frustrating, frightening and no medication known can change it or
stop it. It is something we have to
learn to adjust to and go on with our lives.
It is not easy.
People that are not around a person with
MS on a daily basis are often shocked at the change. The MS patient often has lost a lot of
mobility, speech, comprehension and the ability to emotionally handle the
things that were not a problem in past years.
Most of us have lost a lot of “friends” this way. It really hurts when that happens.
I say all this to relay to you how I feel…………….although
it is a dream come true for us to have a home to ourselves again after so long,
it is really hard for me to adjust to it with all the changes MS has brought to
the table after ten years. I have the
same hopes and dreams, but more and more of them are beginning to be out of my
reach.
No, I don’t feel sorry for myself. I am just trying to be honest and face the
fact that some of the things I dreamed of doing when I retired have to be rethought. Some of those things will have to be discarded
and replaced with things more in my reach.
So far, I am finding that there are many things I can still do (MOST
days) and enjoy. I am learning to enjoy
new things that I never really thought about before. All in all, I am adjusting to a new life
pretty well.
But, as Ringo once sang:
1 comment:
I totally understand about allowing our dreams to float away as we progress. I often think, "If only I could walk better, I'd [fill in the blank.]" or "If I had the use of my hands, I'd..." I don't have the cognitive difficulties you have, and I'm grateful for that. But who knows what may be the next thing I lose. Can you tell that I hate this disease?
Post a Comment