There are a variety of versions of
the story that gives this blog its name. The pony is the constant in
all of them. A man is on his way to a party when he comes across a
young boy shoveling ass over tea kettle at an enormous mountain of
manure. The man asks the child if he wouldn't rather go with him to
the party than shovel all that poop. The kid says, “No way man.
With all that poop... there must be a pony in there somewhere.”
Tuesday, June 10, 2014
Look who got an A+
We had another positive clinic visit
this week.
I actually got an A-plus from the
doctor for the way my blood work has progressed. That's right A-plus,
and I didn't even study.
The subject of remission finally came
up. I had been reluctant to ask, just in case. I mean, not knowing
was better than being told I wasn't in remission. It reminded me of
the last time I was out of work. Whenever I had an interview, I
dragged my feet on following up to see if I got the job. As long as I
didn't know, I had hope, and in the second year of being unemployed,
hope was hard to come by. The more the rejections piled up, the
longer it took me to do the follow-up calls.
The doctor here felt the blood work
showed amazingly quick progress. He did, though, point out that there
are other aspects of the multiple myeloma that he wasn't prepared to
address. Those would have to wait until we go back to Dana Farber in
Boston next week. Fair enough. We'll take the successes we have and
drag them along with us to face the next bits.
We had a revelation while we were at
the Alfond this week: We don't really have any idea how to deal with
processes involved in my getting healthier. I had been sick and
getting sicker long enough that we knew so many of the medicines I
took, the procedures to be done, and so on, that we were able to
address it all pretty easily.
But now, so much has changed. It sort
of ties into what I was saying recently about not having specific
tasks ahead of us to get through. Now the treatment plan is in
something of a state of flux. There are nutrition restrictions; when
can they be lifted? There are medicines to take until a certain point
in my recovery; when is that point? I have to avoid crowded places
and anyone who visits me in our home has to wear a mask and gloves;
how much longer before each of those restrictions can be lifted?
Another thing that has popped up takes
me back to when I was first sick. I didn't know what my cancer was
going to do; what is was going to feel like. So each little pain,
each physical anomaly caused me to wonder if that was because of the
cancer. The trouble with the speculation at that point was that I'd
never paid much attention to my body, so in most cases I couldn't
tell if something was always like that, or was it something new that
could be cancer-related.
Now, I find that speculation has been
turned on its ear. I know to a great extent what the cancer feels
like, though virtually nothing is certain.
For example, after mentioning recently
that I was pain free for the first time since I got sick, the pain in
my ribs, which had previously been my constant companion since day
one, returned. Currently the pain is dull, except for when I probe
with my fingers to try to determine the extent of the problem. Then
it hurts a lot, reminding me of course of the old vaudeville joke. A
man goes to his doctor, who asks the man what's wrong. He raises his
arm above his head and says, “Doctor. It hurts when I do this.”
The doctor wastes no time telling him, “Don't do that.”
Rib pain hasn't always meant something
bad. At first, it usually meant the myeloma has caused some damage
which brought on pain. But as I gave myself injections designed to
build up my stem cells prior to the transplant, I had the worst pain
of all as my bones, literally, became crowded as healthy cells fought
for room with the cancer cells.
Good pain, if you will, was also the
result of an intravenous bone densifier that I was taking, as well as
my white blood cell count improving and fighting for space.
When I brought it up at my appointment,
my doctor, who has always told me what was really going on, admitted
that he wasn't sure. He allowed that it could have been ay number of
things, all to do with the effects of the transplant or some other
aspect of treatment. He wasn't too worried about it because almost
any issues would have shown up in the blood tests. So, I don't worry
about it either. So, there.
Continuing to heal will obviously have
its own challenges, its own moments. And that's okay. The journey
continues but I like the scenery better on this new road I'm own.
The next challenge is Sheri
reacquainting herself with driving in Boston. She's been practicing
being unthoughtful to other drivers and, of course, she has been
pounding the horn, regardless of what the circumstance might be; some
days before we even get out of our own driveway.
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