On Monday morning I made my way to TOH to do my standard pre-session
blood tests and to meet with my Medical Oncologist to report on the reactions/side
effects over the last two weeks. The
first part was relatively simple as I renewed my friendship with the ladies on
the Cancer Centre “Blood Letting Unit”.
Nothing much new there with the exception that one of the staff members was
dropped by her husband of 40 years and she has never been happier. Things get pretty personal pretty quickly in
that unit. My regime of blood tests has been
adjusted for this session. It requires
some complicated instructions about a urine test. Firstly, I have never studied for a urine
test and secondly, I always thought I knew what I was supposed to do. Not so ......
After the visit to the blood unit I killed a bit of time
before meeting with the Dr. Robillard who was interested in my details of my
reactions and was somewhat disappointed that I had experience the side effects
that I did. In discussion she learned of
my aversion to drugs and she gave me good advice: “Take the drugs! .... and
drink more water” and my life may be better.
I considered myself told. My test
results were sufficiently good to allow me to go forward with Session 2. We also discussed my vacation plans to ensure
that this does not get in the way of my life and established plans. She noted our plans and agreed that we will be
OK to travel and put Chemo on hold for a short period. I thanked her for her good advice and understanding
and I went about my day.
Today I went to the Chemo Unit as scheduled and had a
slightly anxious feeling. I have no idea
why I was anxious and I had assumed because I did not sleep well last night. This was reflected in my Blood Pressure being
elevated above the level acceptable for one of the cocktail components. This resulted in a delay to the start as I
tried to relax and get my BP in the acceptable zone. That did not happen so a Dr. Consultation was
necessary and the Dr. decided to proceed but to also prescribe some BP meds for
me. Now this is not new to me. I have always had “white coat syndrome” when
in hospital but this time it did not abate with time. I now have a follow-up in two weeks to see how
that is going.
The actual Chemo was uneventful and of course the nursing
staff members are nothing but helpful in making me feel comfortable while
getting me out of there to fulfill their commitments to other patients. The
upshot is that I am a bit tired and just about to re-evaluate the drugs I have
been given and start a regime to ward off some of those nasty side effects. It is my hope that the plan will lessen some
of the inconveniences I experienced in Session 1.
I hope the week ahead is a good one for all of you.
I hope you blog is helping you as much as all the info is helping us to understand all that is going on. Also encouraging to hear that your team has options for you in your treatments.
ReplyDeleteThanks for sharing