My surgery was successful in removing the visible tumor in
my colon. The goal of the chemotherapy is to attack the microscopic cancer
cells still remaining in the colon, as well as reduce the metastases in the
liver and lungs. My body needed time to recover from surgery before starting
chemo, as chemo will retard the healing. The surgeon and oncologist outlined a
minimum of four weeks before treatment could begin.
I was in the hospital four days post-op, then able to go
home. Our family and friends were instrumental in helping both Paul and I
during this post-op recovery, with many coming to stay with us to aid me while
Paul went to work. The surgery not only left me with a colostomy system, but a
5-in incision, a 1-in incision and two ½-in incisions on my stomach. These
incisions were held together by a total of 25 delightful staples. The staples
remained for two weeks, and really minimized my movement. Once they were
removed, my mobility and exercise increased pretty rapidly.
Of course, one if the first questions I had for my oncologist was, “What can I do?” Dr Torgerson and her team outlined the optimal diet to aid in my treatment, as well as encouraged exercise. I have adapted to a Mediterranean diet, which means I eat lean proteins (100g+ per day), avoid processed sugar, white flour, and focus on plant-based foods. My hydration is also incredibly important for both recovery, as well as the colostomy system. I have to consume 100+ oz daily that do not contain caffeine or alcohol, both of which I have removed from my diet. I started exercising daily. Initially walking only. Once I became more flexible and confident in my strength, I began biking as well (My new bike's name is Jolene! 😁).
In preparation of treatment, I had an outpatient procedure
to insert a port in my upper right chest. A port is a small plastic
disc about the size of a quarter that sits just under the skin. A catheter
connects the port to a large vein. My chemo medicines are given
through a special needle that fits right into the port. I’ll also have all
bloodwork drawn through the port.
As the treatment time drew near, my oncologist indicated I
was eligible to participate in an immunotherapy clinical trial. Immunotherapy
is treatment that uses certain parts of a person’s immune system to fight
diseases such as cancer. It does so by stimulating the immune system to work
harder or smarter to attack cancer cells, and giving the immune system
components, such as man-made immune system proteins. Immunotherapy has proven
successful for many metastatic cancers; however, it is not an initial standard of
treatment yet for my particular type of colon cancer. This is why I have to
participate in a clinical trial in order to receive it. I agreed to the
clinical trial, but this meant delaying treatment by one week. The
immunotherapy would be given in addition to chemotherapy, not as a
substitution.
First treatment session was Wednesday, May 9. I am scheduled
to have treatment every two weeks for a total of 12 sessions. The Tuesday
before, my oncology lab does bloodwork to ensure all my levels are up enough
for treatment. In the event some indicator is below the threshold, that particular
session will be delayed, most likely a week. There will always be two weeks in
between sessions.
For those interested in the nitty gritty, here are my
specific treatment drugs, with market names in parentheses:
- · Chemotherapy- FOLFOX (combination of 5-FU, Leucovorin, and Eloxatin)
- · Immunotherapy- Nivolumab (Opdivo)
- · Additional anti-cancer drug: Bevacizumab (Avastin)




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