Spent the day with Mitchell in the ER. After a miserable night at home, I convinced him to go in. Long story short...The ct scan they did today showed "significant" growth in numbers and size of lesions in his liver and a handful new metastases in both lungs as well as growth in those already present. He was finally admitted late this evening. The plan is to reintroduce liquids and food and then his meds and see whether or not he can tolerate them. Not sure how long his stay will be.
Although I am not surprised at this news, it leaves me feeling hostility toward health care in general. Perhaps if the insurance company would pay for scans at regular intervals for Mitchell, the oncologist would know in a more timely manner that a protocol wasn't working. I also realize that chances are slim to none that we will beat this cancer...Knowing that, shouldn't Mitchell be given the opportunity to extend his life while battling this disease as much as is medically reasonable? And have a reasonable quality of life at that?
The longer we are in this, the more medicine seems to be random shots in the dark and less science and logic based on evidence. No one seems to really know anything with any kind of authority.
No matter where you go, there you are. Thoughts and rants and rambles about where I am.
Showing posts with label results. Show all posts
Showing posts with label results. Show all posts
Friday, October 8
Tuesday, August 17
more love-hate
Mitchell's MRI was read this morning, and everything is clear in his brain. WHEW! The headaches are definitely being caused by the abraxane.
On a negative tip, the oncologist and a specialist have had an opportunity to compare Mitchell's last CT with the most recent PET scan. The experimental treatment is not working. His tumor markers have elevated since beginning the new treatment....So it's back to the drawing board so to speak. The abraxane/avastin has been discontinued as of this morning. Mitchell was supposed to have treatment on Friday, but it is being put on hold until Dr. Brown can consult with a colleague to decide what the next steps are.
On a negative tip, the oncologist and a specialist have had an opportunity to compare Mitchell's last CT with the most recent PET scan. The experimental treatment is not working. His tumor markers have elevated since beginning the new treatment....So it's back to the drawing board so to speak. The abraxane/avastin has been discontinued as of this morning. Mitchell was supposed to have treatment on Friday, but it is being put on hold until Dr. Brown can consult with a colleague to decide what the next steps are.
labels:
change,
chemotherapy,
colon cancer,
life as we know it,
meh,
PET scan,
poop,
results,
scans,
things i don't like,
treatment,
update
Monday, July 6
again
This morning Mitchell had another PET scan; the results for which will be read tomorrow morning by the oncologist. I hate the anticipation of these appointments. The closer it gets; the more nervous I become.
labels:
chemotherapy,
colon cancer,
family,
results,
stuff i don't like,
vomit
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