We are back from the hospital. Mom's vomiting is under control with the use of a drug called Reglan. She did vomit a bit after we brought her home so that probably means that she needs a steady stream of the anti-nausea medication rather than just before meals.
Apu and I have had to devise a charting system for when she takes her meds.
Upon discharge we talked about a home nurse aid that would come periodically to check on mom. The family meeting was good, constructive.
The doctor feels that the experimental therapy described by Dr. Stephen Cantrell is not optimal for my mother because the interferon is a very harsh, toxic drug. She just overcame this hump in the road, and that's the last thing we need right now. (http://spotlight.vitals.com/2009/10/dr-stephen-cantrells-melanoma-self-cure-helps-his-patients/)
He wanted to start on chemo as soon as this week but I think we should wait so that she can regain her strength then start the chemo 1 a week for 3 weeks then off one week.
After a cycle or two of the treatment he wants to get another CT scan to see how the cancer is responding. The goal is to contain the cancer in the pancreas, and to improve the quality of life, decrease the pain and symptoms due to the cancer.
This is excellent news for now. It hasn't spread to any of the other organs, it is not metastatic.