I'm getting into the habit that the first
thing I do when I wake up in the morning is to reach for the phone and check
the temperature.
You'd think 9 degrees would be freezing
(well, it is) and that I would bundle up to go outside, but to let
the dogs out and then stand on the patio to take a photo it's fine, even in
my stocking feet, though I wouldn't want to stand there for a very long
time.
The snow is all still on the ground, but
there are bare patches now. Still the trees are laden with snow and
look so pretty,
This afternoon, I watched a bunch of these
birds trying (mostly unsuccessfully) to fly in the wind which is blowing
large amounts of snow off of the roofs.
They finally gave up and a bunch of them
grouped together among the branches of this bush. It was difficult to
see them in the viewfinder of my camera, so I was only able to get one at a
time, but there were actually at least four all huddled together, nestled
down as far as they could get in the leaves, feathers fluffed up to insulate
them against the wind.
Peach also spied a fox on the ground opposite
the house, but I didn't get there in time to see it.
There is also a lot of static electricity in
the air.
With all this cold weather, we were off to
the Cancer Center for treatment #2 this morning. This is how you dress
to go out in 9 degree weather.
This was a frustrating morning. The
anti-diarrheal meds seemed to kick in yesterday afternoon and she was
actually able to eat.
but then the diarrhea was back again.
This is all so overwhelming for everyone, especially Peach, who only
discovered a breast lump a little over a month ago and has since had
numerous scary tests and procedures, including having her breast removed and
now she is having toxic chemical pumped into her body with uncomfortable,
painful, terrible side effects. She has lost about 20 lbs in this
time.
And Bob, god love him, wants so much to help,
but doesn't understand what is going on and all he knows is he wants a magic
pill to bring his wife back. She is trying to hard to hold everything
together, but it's so difficult.
The one big thing she has going for her is a
support system. I am here, of course, but so are her daughter, son-in-law,
grandson and his fiancee. At least two of us are with her for every
exam and every procedure. This morning there were four of us and the
nursing staff seemed surprised at the size of her entourage, but were
welcoming and brought enough chairs for all of us.
Kris got an appointment for her with her
therapist, which I hope will help a lot in letting her have a safe place to
deal with the emotional side of all of this.
In the "shelter from the storm" category, the
doctor heard about all of her symptoms (and saw that her temperature was
slightly elevated) and decided not to give her second chemotherapy
treatment today. Instead he is trying meds to cure the diarrhea first,
so that we won't have to worry about adverse after effects of the chemo this
week. I hope that will give her a chance to stabilize and get a bit of
strength back before she gets Round 2 next Monday.
1 comment:
Some of us need longer times between treatments. My own symptoms were much milder, but evidently my blood work indicated that there was just too much. Doctor changed me from every two weeks to every three weeks.
Sending all good wishes.
Post a Comment