Cancer Support and Caregivers Who Are Trail Blazers!

[DapperButch]

Originally Posted by JustJo

Ugh...so many things have been discussed that she and I BOTH got this wrong. It is a stomach tube, but it is located between the stomach and what's left of the small intestine, and is to control outgoing rather than incoming.

Evidently it will help them clear blockages, and also allow her to cirucumvent the intestine entirely (at will) when she is feeling discomfort.

So...now she is hooked up to 3 bags....TPN in through the PIC line, the original ostomy bag and now the new one....that I don't even know what to call.

Her TPN is increased to about 20 hours a day, and she will never be off of it.

She is feeling like a monster....with every step of food intake and digestion being controlled by valves and clamps and bags and needles.
On the plus side, this blockage was cleared and she is no longer having any pain.

The chemo will start later this week...since the latest scan shows that the liver lesions are now 11 mm and 8 mm, respectively....when they were so small they didn't even show on a scan a few months ago.

Oh, Jo this so sucks. I feel so terrible for her.

It is this kind of stuff that worries me (about me). Yes, the CAT scan I had a month ago said there were no tumors. This was really meaningless to me due to the above. That is what my eating (most often successfully), vegan is all about. The hope is that eating in this way (plus doing some other things), will make my body less hospitable to cancer. The hope is that those small tumors don't grow. I am aware, however, that no matter what I do, it could still happen. Additionally, I am aware that there are people who have undetectable tumors that never grow no matter how they eat or what their lifestyle.

You remain in my thoughts, Jo.