New Options...I guess you'd call it options...
I'm afraid this is how things will be. Take the fluid out, back the fluid comes.
I would have to say that Dad doesn't have as many symptoms of the reaccumulation of fluid...as he did last time.
We went to the oncologist today.
Basically she said she thought the fluid was reaccumulating because of "cancer". I really think that Dad thought his cancer was, well, gone. Because of all the radiation, the chemo, the procedures he's undergone and the side effects of these things he had forgotton one thing. He has cancer. Cancer AND side effects of those other things.
The oncologist gave us three options. One...a different type of chemo, Two...consult with a thoracic surgeon who could put Dad in the hospital for several days, insert bilateral chest tubes, drain both lungs, "scar" up the pleural spaces and MAYBE this would work to keep the fluid from reaccumulating, Three...go on as we have been, still getting monthly Zymeda, draining the lungs as needed.
I don't know, for some reason I had convinced myself that the fluid was related to, perhaps, the radiation or chemo. As we were about to leave I thought to ask the Dr. this question. She said, No...the fluid is not caused by these things. She seemed sure. I still question it. I don't think she likes me. I don't think the nurses like us either. I hate that place. I see them visiting with other patients, caring, asking questions, touching, making eye contact...and then...they seem very very different to us. I wonder why.
Anyway, we have to talk about our options and figure out what to do now.