Unlike previous infusion Fridays, there was no time for
sleeping in today. With a 9:15 am
appointment came the uncertainty of Seattle-area traffic. Would the carpool (HOV) lane require 2 or 3
people (deeming us ineligible to use it)?
If we’re unable to use the HOV (high occupancy vehicle) lane, then we’d
relinquish to the scenic route (twisting and turning through all the
neighborhoods). The difference is a 15
minute versus a 25 minute commute to travel the measly 6.5 miles to the
hospital. Not knowing our fate, we left
25 minutes early. Much like carrying an
umbrella in fear of rain, the fact that we left early ensured the 2 person
carpool lane was available and our rapid arrival.
Despite our 10 minutes to spare, the check-in line weaved
through the entry door, since there was only one receptionist checking in
patients. After receiving our stickers
assuring we aren’t sick, we didn’t wait long before the polite laboratory
technician accessed my port and drew blood to check the effectiveness of the
medications. Unfortunately, our
appointment with the doctor wasn’t until 10 am, so we had to wait 30 minutes in
the lobby before vitals were obtained, another 15 minutes to see the doctor and
30 minutes later (10:45 am), we finally reached the infusion center. My ANC (absolute neutrophil count) was 0.3, the lowest I’ve ever recorded, landing about 85-95% lower
than normal levels (normal is 2.0 - 7.3). After our typical, benign, uneventful exam
and lab results discussion, which often deviates to gardening topics, we agreed
to continue with chemotherapy again.
The infusion went smoothly and I
was delighted to discover a friend in a bay not so nearby. We talked until one of my bags needed to be exchanged
and then I returned to talk again. It
made the time fly by more quickly and before I knew it, it was nearly 2 pm and my
treatment was completed. Another one in
the books.
It’s getting much easier now. Chris and I come prepared with our books,
kindles, puzzle books, and even games to play together. He always gets his nap in, which is more
difficult with me because we have to verify my name and date of birth for every
chemo drug that is hung and so I would be interrupted quite often. Usually, I feel so wiped out afterward that I
will take a nap as soon as we get home.
But, I wasn’t going to miss the gorgeous sunshine this Friday. Instead, Chris and I went down to the
cafeteria where they make wood-fired pizzas and I had a pesto chicken one while
he ordered all-meat. We sat outside,
soaking in the sunshine while devouring our perfectly done, cheesy
concoction. This is not the hospital cafeteria
food of the old days.
I apologize for the decrease in
blog postings. It’s not that I haven’t
been inspired or have thoughts and experiences to share, but the clarity of my
prose has been lacking and I don’t want to publish either uninteresting,
uninspiring or lackluster work. That
being said, I have at least a dozen or more partially written works that I will
be trying to fine-tune in the upcoming weeks.
With my low ANC, I will be home, when not enjoying the fresh air. No meetings or gatherings are planned, so I
hope to get a few minutes on these overcast mornings to wrestle with my brain
and produce something readable and entertaining. Thanks for being patient with me and for your
continued support and prayers! God Bless
you all.
Keep your thoughts positive, because your thoughts become
YOUR WORDS. Keep your words positive,
because your words become YOUR BEHAVIOR.
Keep your behavior positive, because your behavior becomes YOUR
HABITS. Keep your habits positive,
because your habits become YOUR VALUES.
Keep your values positive, because your values become YOUR DESTINY. ~ Mahatma Gandhi
Love to hear from you even though you think your blog might not be interesting enough...love to hear about your day anyway! You are my inspiration! :)
ReplyDeleteThanks, Lori. I love hearing from you as well. Keeping in touch with people makes it not quite seem as long!
DeleteAnd you are GREATLY MISSED!!!!
ReplyDeleteGlad your back to blogging. I was starting to wonder if you were down.
ReplyDeleteNot down, just fatigued and busy.
DeleteJust read your latest post. Sounds to me like you have your head in the right mindset. Being busy is great!!! Helps the mind if not the body. I'm proud to know you and call you my friend!
DeleteYes, I missed your blogs too and was wondering how you are doing. It will soon be over and this will be behind you. Reading your blogs bring back memories for me. I treated my lymphoma for 4 months and the last one was in January of this year. Hopefully I'll be good for another 10 years. I love the cancer center at Evergreen and have had good experiences there. Excellent staff. I slept through my treatments because they had to give me Benedryl to ward off reactions to Rituxan. I brought crochet and word search puzzles and it didn't take long before I was in lala land. I regret not getting the port this time because I ended up getting clots in my arm. NOT FUN. Looking forward to your next blog. I love to read them and you are a great writer. We pray that God will continue to bless you.
ReplyDeleteI am thankful that I don't have to receive Benadryl. I am so delighted that you are doing much better and I hope that the memories that my blogs evoke are only the good ones!
DeleteHalf way - plus 1!!! You're on the down hill side of this race!
ReplyDeleteI'm happy to read your blogs. It's an interesting perspective to know what someone in your position is going through. Those of us on the outside do not always know what someone is going through nor what we can do to help. I continue to read your posts and think of you and hope you are doing better. I can't wait to see you back again! I missed you when I had to pop into the doctors office for sure!
ReplyDeleteLisa, thank you for your kind words. A kind word and just knowing that people are praying and thinking about you is exactly what most people need when going through a daunting journey. :)
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