Unfortunately my mother is learning the ramifications of not taking in enough fluids. She is one week post-radiation/chemo. She did not have a PEG tube inserted prior to start of treatment (big mistake). And she is lucky to get down 1 nutritional drink a day.

Yesterday I realized that she had to get some fluids in her so found out about home infusion. She started today and will receive for the next 2 days. Fortunately scheduled to see a doctor Monday so we'll have to address this.

Along these lines, we both are wondering if it's really necessary at this stage to have a PEG tube inserted. We are looking at other alternatives. One suggestion was TPN (total parenteral nutrition) done via a central line and pump. Has anyone had experience with this? Would appreciate comments on pros and cons vs. PEG tube.

Thanks in advance.

Cynthia