Today has been a much better day than either Monday or Tuesday, and possibly even better than yesterday, although yesterday turned out to be pretty good. I had just a bit of nausea this morning – maybe the new medication is helping to resolve that discomfort – and I have been able to eat throughout the day. I didn’t want anything other than saltine crackers and carnation instant breakfast to start, but Cathy made some really good fried potatoes after our walk, which hit the spot and started me on a good eating trend. What would I do without her?
Cathy and I have both been working at home for most of the day today. I prefer these days to the days like yesterday, where she had to go into work for most of the day. She had everything set up for me before she left, so of course I survived, but it just is not as much fun! There is something special about being with your best friend, even when you are in separate rooms working on different computers!
One of the things I struggle with on occasion is low blood pressure. I’ve been struggling with it the past few days. I’m not sure why I have it, whether it is due to medications or possibly the disease (I read that severe pancreatitis can cause low blood pressure, so perhaps a tumor on the pancreas can do the same). The low blood pressure makes me more tired and lethargic than I’d like to be. Otherwise, it is not a big problem. I’ll ask about it the next time I am at Piper for treatment.
I go to Piper tomorrow for a routine blood draw at 11:45, followed by my first post-treatment CT scan (they are scheduled for every two months of treatment). This scan is critically important. It will tell us whether or not the tumor has responded to the chemotherapy. That, in turn, will determine next steps in the treatment. If the tumor is responding by either staying the same size or shrinking, then we’ll keep going with the current regimen of chemotherapy drugs. If it has increased in size, we’ll move on to a different regimen. My first choice, of course, is that the tumor has been reduced in size, thus allowing us to continue with the current regimen for another two months and hopefully another four months (four cycles). After that, we thenwould definitely move on to the different regimen (in turn, for another six months or cycles, assuming some success with shrinking the tumor).
Unfortunately, we will not know the outcome of the scan until next Thursday – ugh! At that time, the blood draw prior to chemo will include the monthly measure of the cancer antigen CA19-9. You may recall that this value decreased last month relative to its baseline value – a very good sign! I guess they want to present the new CA19-9 results along with the CT scan results at the same time … Still, I’m going to ask if they might read the scan sooner and let me know before next Thursday, just so we aren’t on pins and needles for almost an entire week. They have been very reassuring and have told me not to be nervous, but …
Regardless of when we get the scan results, please send good thoughts and vibrations our way tomorrow. This is a real milestone in our treatment and we could use some really good results! Thanks!