My family and I arrived on Friday morning at the UAMS Cancer
Institute for the routine blood work required before meeting with Dr. Makhoul’s
nurse practitioner, who was filling in for him while he attended a medical
conference. We reported to the infusion
waiting room, as usual.
Marla Crider having celebratory dinner with brother Marion and sister-in-law Carolyn. |
While dressing earlier that morning, I made the decision to
wear a scarf and huge flower as my head cover. It was the comfortable choice for
the long day ahead of me. While I was waiting to be called for the blood draw,
a lovely black woman tapped me on the shoulder and asked me to tell her how I
tied the scarf and secured the flower to it.
Her goal was to duplicate the effort for Sunday church. Our conversation made me feel more confident
about wearing scarves in public, rather than the hot wigs that had become a
part of my everyday work attire.
A few minutes later, a nurse of Asian decent called my name
from the infusion room door. I followed
her inside, where I stepped on the scales for my twice monthly weigh-in. I had lost another pound but was still within
the limit of no concern. The nurse
escorted me to an empty recliner and said she would be the one accessing my
port for the blood draw. It was our first nurse/patient encounter; therefore, I
would have to caution her about my port-on-nerve malady. The nurse said she wanted to try something
that might eliminate the discomfort I usually experience. She instructed me to take a deep breath and I
complied. Simultaneously, she quickly inserted the large gauge needle into the
port. It was a flawless and painless
procedure. It made perfect sense; taking
the deep breath expanded my diaphragm and lifted the port from atop the nerve.
I was almost giddy with the outcome. She
quickly finished her task then taped the dangling port lines to my chest in
preparation for the chemo treatment.
My family and I departed for the appointment with Dr.
Makhoul’s colleague. The waiting room
was filled to capacity. It was going to
be “one of those days.” Almost an hour
had passed when the nurse practitioner finally arrived in my cubicle to tell me
that my blood work was in the “normal” category, indicating that I would not
have to endure another Neulasta injection in the belly to help stimulate white
blood cell production. She asked if I would be receiving my first treatment of
Taxol that day. I nodded my head in the
affirmative. She warned me that the most common complaints about the drug
included flu-like symptoms, bone and muscle aches and tingling of the hands and
feet. I thanked her for the details and
departed for my first one-on-one with the toxin.
After only a minor delay in the infusion waiting room, a nursing
assistant summoned me. It was time to
experience a new chemo adventure – Taxol. Carolyn accompanied me with the
intention of helping pass the time during the three-hour, intravenous process.
As soon as I occupied the recliner, the male version of Florence Nightingale,
aka Mr. Nurse Ratched, approached my chair and said, “You’re here for your
first Taxol treatment, right?” “Yes,” I
replied. “Bring it on.”
“Get comfortable because you’re going to be here a while,”
he responded. I pulled out a book of
crossword puzzles and settled into my chair.
In his loud, booming voice, Mr. Nurse Ratched started rattling off all
the things that could happen with Taxol, such as hives, swollen tongue,
breathing issues, and low blood pressure to name a few. He explained that I would be given Benadryl
intravenously along with the Taxol to counteract any possible allergic reactions. “The Benadryl will probably make you sleepy,”
he warned me (for someone who sleeps
very little, I welcomed the possibility). Before he hooked me up to the drugs,
he brought me six pills to take – the anti-nausea cocktail that included more
steroids. As soon as I swallowed the meds, Mr. Nurse Ratched injected Benadryl
into my port and proceeded to hang the bag of Taxol on the pole next to me and dialed
in the rate of drip. “If you’re going to
react, we will know shortly,” he said.
Carolyn watched me closely to see if she could detect any
changes as the Taxol dripped into my veins.
Instead of making me drowsy, the Benadryl just blurred my vision. Then I started giggling as if I had consumed
one glass of wine too many. There was an
internal battle going on in my system between the abundant steroids and the
Benadryl. Apparently, the steroids were
winning because I wasn’t sleepy… darn it. Mr. Nurse Ratched continued to check on me to
ensure I wasn’t reacting to the Taxol.
For the next three hours, I read and worked crossword
puzzles, while Carolyn and Marion alternated sitting with me. Fortunately, there were no signs of an
allergic reaction. What I did notice was
a tingling feeling in my right breast accompanied by little sharp jabs… a
sensation not experienced with the previous chemo drugs. Could it be that the
Taxol had already found its way to the cancer cells in my breast? After all, the drug is known for reducing the
size of malignant tumors. The tingling
continued throughout the treatment.
Carolyn and I were chatting away as the last of the Taxol
dripped from the bag. Suddenly, a small,
white feather floated from above and landed in my lap. “The chemo is either causing you to molt or
it’s a sign from above,” Carolyn remarked.
We started laughing. The feather
was from my festive flower affixed to my scarf.
It was the perfect way to end the three-hour ordeal.
Since I didn’t experience any allergic reactions to the
Taxol, I knew that new side effects could be a possibility the first few days
after my treatment. I awoke the
following morning with slight tingling in my hands and feet, which is
considered a common response. The feeling subsided within a few hours. The next day, fatigue and digestive issues
were the side effects du jour. After taking medications throughout the day to
deal with the diarrhea, a new condition cropped up – severe bone pain in my upper
spine, hips, knees and shins. I was so
uncomfortable during the night that I had to take pain medication and place
pillows under my knees to take some of the pressure off the joints. I went to
work on Monday morning but the pain was ever-present. I checked the side effects on the Internet
just to confirm that what I was experiencing was normal…and it was. The pain lasted two more days. The days
following I felt great. Well, maybe
that’s an exaggeration. I did feel
pretty good and actually had some energy.
The fatigue was still present but only at night. I was even sleepy at normal bedtime hours;
however, the night sweats continued to wake me up and disturb my slumber. After two and a half months of chemotherapy,
I was accustomed to the minor inconveniences associated with ridding my body of
cancer.
About ten days after the Taxol infusion, I decided to check
the size of the mass in my right breast.
It was significantly smaller and could no longer be felt along the outer
tissue, which was very exciting. The Taxol
was responding exactly the way Dr. Makhoul said it would and after only one
treatment, too. There is no question that the Taxol causes more issues than the
adriamycin and cytoxan cocktails taken during the first four treatments;
however, I felt confident that it was going to eliminate the tumor completely
and make it easier for the breast surgeon, Dr. Klimberg, to do her job. There
is no question in my mind that the positive results of chemotherapy far
outweigh any of the pesky side effects. And
with only three more treatments to go, I’m determined to persevere.
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