I get a lesson in pill sorting. I now have one of those 2-dimensional pill boxes that have several pills in each compartment. I am still not quite myself, but fortunately, Gary is paying close attention, and he helps me with my pills for the next few days. He learns which ones I absolutely must take, and which ones can be postponed if my stomach says no way.
I have a visit from Dr. Hering who seems pleased with my progress. Dr Harmon comes in to check my incision and see how I am doing. My incision seem a bit red at the top, so he recommends putting some moist heat on it. Dr. Bellin, who helps me manage my glucose levels helps to create a regime to balance my insulin, glucose levels and carbs.
I am taken off all of the ivs which is wonderful, and I reattach my insulin pump. The amount of insulin that I am taking is already much lower than what I required before the transplant. I will no longer be taking Symlin, which is a drug like insulin that lowers blood glucose levels.
The theory is to rest the islet cells as much as possible at first so that the cells can become acclimated inside my liver. Then, hopefully, they will begin to produce insulin, and my pump will need to provide less and less. I can monitor my pump to see how many units I am using per day to assess how well the new islet cells are performing.
1 comment:
I am confused about why the islet cells were transplanted into your liver rather than pancreas. How does that work?
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