My Cancer journey continues.
Status: Stage IV Colorectal with Mets in the left lung and posterior pleural wall soft tissue. Inoperable, incurable, and seeking palliative care while I can.
I went in to have my first round of palliative chemo today to find that my freshly installed medical port isn't working. It looks kinked on today's x-ray, compared to last Thursday.
Backstory
For anyone just tuning in for the first time:
From ~2015-2020 I kept going into the VA with complaints of lower back pain and occasional red stool water. Lose weight, here's some hemorrhoid cream, was the docs response.
2020, age 40, was when my bowl movements started getting very painful. After a year of hearing me complain, Mrs went into the doc appointment with me and gave the doc an earful. Late summer of 21, I finally got a endoscopy which had a 7 cm tumor just inside my rectum.
That winter I had radiation treatment and pill chemotherapy. Spring of 22 I had a foot of my large intestine removed, with an ileostomy.
Summer of 22 was chemotherapy. Infusion and oral. It sucked.
Fall of 22 my ileostomy was reversed and I officially was in remission.
Periodic CT scans showed growths in my lungs in 2024. I went to the VA for treatment, and they referred me out locally for surgery. The doc they referred me to said that he'd basically need to cut my back from down by my mid side, up, and around the ... Umm... Around the ... (He turned and looked to his medical assistant) scapula?. Yes scapula!
Soon afterwards I went to MD Anderson. They got me in April and June for lung lower lobe resections.
In November of 25 a new spot was found growing in my left lung by CT. In December another in the soft pleural wall tissue, found via PET scan. Early January determined it wasn't surgically viable.
MD Anderson said that it also wasn't a good candidate for any medical trials.
That should bring us back to getting my port last week.
Status: Stage IV Colorectal with Mets in the left lung and posterior pleural wall soft tissue. Inoperable, incurable, and seeking palliative care while I can.
I went in to have my first round of palliative chemo today to find that my freshly installed medical port isn't working. It looks kinked on today's x-ray, compared to last Thursday.
Backstory
For anyone just tuning in for the first time:
From ~2015-2020 I kept going into the VA with complaints of lower back pain and occasional red stool water. Lose weight, here's some hemorrhoid cream, was the docs response.
2020, age 40, was when my bowl movements started getting very painful. After a year of hearing me complain, Mrs went into the doc appointment with me and gave the doc an earful. Late summer of 21, I finally got a endoscopy which had a 7 cm tumor just inside my rectum.
That winter I had radiation treatment and pill chemotherapy. Spring of 22 I had a foot of my large intestine removed, with an ileostomy.
Summer of 22 was chemotherapy. Infusion and oral. It sucked.
Fall of 22 my ileostomy was reversed and I officially was in remission.
Periodic CT scans showed growths in my lungs in 2024. I went to the VA for treatment, and they referred me out locally for surgery. The doc they referred me to said that he'd basically need to cut my back from down by my mid side, up, and around the ... Umm... Around the ... (He turned and looked to his medical assistant) scapula?. Yes scapula!
Soon afterwards I went to MD Anderson. They got me in April and June for lung lower lobe resections.
In November of 25 a new spot was found growing in my left lung by CT. In December another in the soft pleural wall tissue, found via PET scan. Early January determined it wasn't surgically viable.
MD Anderson said that it also wasn't a good candidate for any medical trials.
That should bring us back to getting my port last week.
