Keeping in mind that this blog is being written in large part for current and future folks facing pancreatic cancer, I am including the ugly part of stage IV PDA (pancreatic ductal adenocarcinoma)
It has been 7 weeks since I read my MRI outlining the tumor in my pancreas and "mets" in my liver and lymph node. Friday the 13th (Nov) is burned in my memory and truly a bad date, lol I decided to not continue chemotherapy and my oncologist immediately turned me over to Hospice.
So my biggest challenge besides the abdominal pain is unrelenting diarrhea. Food just passes on through.
The diarrhea does not stop at night time. I've soiled my bed on a number of occasions. That is just not pretty and is upsetting. I have been prescribed pancreatic enzymes (Pancreaze) to help digest my food. By its self it did not help any. Then I was prescribed Lomotil, a schedule 5 medication that slows the intestinal activity down. Together these meds have slowed the diarrhea and frequency. My appetite is definitely way off and finding food I am interested in eating is difficult. I am forcing myself to eat something during day, although my appetite is higher in the evening. I just can't eat anything at night with out night time diarrhea.
I have been lucky so far in that my bile ducts are not blocked so no jaundice as of yet. There all kinds of complications I am facing. As I deal with these I will include this in my blog. Hospice is trying to switch me from oxycodone to methadone. Using methadone for pain control is kind of a new thing and I am highly skeptical. I am of the belief that if something is working, don't change it. Keep in mind that the life span for someone with stage 4 PC with out chemotherapy is 2-6 months, with 3 months being the average. I have a couple of good reasons to make it to 6 months, but remember life is what happens while you are making other plans. So time will tell.