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Showing posts with label memory. Show all posts
Showing posts with label memory. Show all posts

Friday, December 7, 2012

The Same as a Broken Leg?

I don't think so.

I was just telling someone that my scans were clear.
He was telling me how much of a blessing that is.

He obviously didn't know how I have been feeling.

I tried to explain to him what the situation was.
I tried to explain that my mind may be affected for
a long time to come.  I tried to explain that just
because chemo was over didn't mean that suddenly
everything was OK.

He tried to tell me that I often sound fine.  That I
had to be fine, and now I could just move forward.

When I tried to tell him that he didn't understand,
that even though I could function in some ways,
there were things that are extraordinarily difficult.

He turned around and said that when someone
breaks a leg they don't just "sit there."  They get
up and and do something.

When someone breaks a leg?

It is NOT the freaking same thing.

Someone else I was talking to was looking online
to see what he could find out about what I am
dealing with.  He found something I didn't even
know about:  PCCI Post Chemotherapy Cognitive
Impairment.  According to good ole Wikipedia,
it can last up to 10 years!

While there are things I might be able to do to
help myself over the long run, over the short run
it is incredibly frustrating to work so hard to do
some things that before were practically effortless
for me.

I have always appreciated my brain.  I have often
been quick-witted and able to remember things.
Now it is very difficult, and it is even difficult
to read things, and retain what I read.

I had heard about "chemo brain," but it was never
explained to me like this.  Would I have wanted
to know?  Would it have changed the way I did
things?  I don't know.  But what I do know is that
this recovery may very well be more difficult than
the recovery from cancer.

This - in some ways - is much harder to cope with
and harder to accept.  I read that "many" people
think that when the chemo is over they will just
be able to get on with their lives.  So apparently
I am not the only one who thought that.

How the fuck am I going to deal with this?  It is
so hard to do anything.  On top of that, I heard
of one woman who had it so bad she had unpaid
bills piling up and didn't care.  I am not quite there,
but I can relate to the lack of caring.  You have to
care to do things - especially when it takes extra
care to do them, or they don't get done.

People talk about the fight with cancer.  This
feels like a much bigger battle to me.

I want myself back.

That sounds so tame compared to how I really
feel.  I am sobbing as I type.  I feel like I am in
this really strange state.  It is one that I think only
another who has had this could relate to.

If you know someone who is being treated with
chemo, please understand this is all too real.  It
is not stress.  It is not made up.  It is fucking real.
And it will change the person in ways that s/he
has absolutely no control over.

I have told people around me that I don't always
remember things.  I probably repeat myself more
than I want to.  I sometimes get lost mid-sentence.
I forget the simplest of words.  I can't always
communicate as effectively as I would like, as
I sometimes lose my way to where I was going.

At the same time, it would seem to those on the
outside looking in that it is no big deal.  That I am
just fine.  As I have explained before, I am
functioning mainly from my right brain.  I have
always been right brain dominant.

But the right brain is more intuitive.  It is easy
for me to write these blog entries when I DON'T
think.  But the problem comes when I do.

For me to plan my life, for me to plan work and
negotiate the things I need to for work, it is an
incredible challenge.   I wonder if those treating me
ever thought about how much it would challenge
me, given my circumstances.  I don't know that
it would have changed a thing, but I am in a very
different situation than most.

I don't have family supporting me.  No husband.
No kids.  I didn't have a job when this happened.
No benefits.  No disability.  I have the "wrong"
kind of cancer to get much of the help that is
offered.

Sure you can treat me.
But, hell...now freaking what?

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Tuesday, September 18, 2012

Not feeling well and frustrated

The last two nights I haven't slept well.

One night I was constantly getting up to go
to the bathroom.  The other night I woke up
with what I think was a bad gas attack.

If you have never had one, it makes you think
something is really wrong, especially if you
have a port.  I kinda know better, given how
I first felt when I came home from the hospital.

It was something that was all too "usual" then.
I was actually thinking last night that I am not
exactly sure when it stopped happening.  I
was also thinking about how grateful I was
that it had stopped.

Funny how life is.

In the midst of something nothing else matters.
But once it is gone, so might the memory of
the misery be gone, too.  In a way I would say
that is good.  In another way, though, the
contrast is often where the appreciation will
lie.

I was told that I may want to be careful how
I managed my energy.  I was told that if I
over did it, I might find myself down for
a length of time.

I think I over did it in the last couple of days.
I felt horrible last night.  I thought I might even
entertain staying in bed today.  It is the perfect
day for it, actually.  Overcast and stormy.  The
perfect weather for me.

But what did I do?  I got out of bed and
got creative and did a few things.  As great
as that may be, I am frustrated because I need
to do some things that require me to think and
it is next to impossible.

It is odd not to be fully functioning.  It is odd
to know that there are things I could do before
that are incredibly difficult now.  I saw a video
yesterday with someone who had no arms.  She
never had arms.

She was showing how she does things.  She
learned to use her feet as arms.  She doesn't
know what it is like to have arms, and doesn't
know what it is like to lose them.

I am not sure why I am saying this, except
to observe how when you don't know what
is possible, you don't necessarily miss it.

I hope that things will get back to normal
when all is said and done.  I really am
missing how it feels not to have this cloud
in my head.  It is like a blanket, but
unfortunately not one that comforts.

A few people have also made comments to
me recently about me and what is next.  Before
all of this I didn't have answers, and I certainly
do not now.  As much as I would love to have
the ability to plot my next path and strategize
and do all those wonderful things that healthy
people do, I can't.

At the same time, there must be some things
I CAN do, which is why I am likely spending
the time I am being creative.  One of my newest
works is like a doodle, of sorts, and someone
told me that there is the thought that when one
doodles, it is because the mind is in an "idle"
state.

Yup.  That fits.
I do feel like
I am going
no where fast.