I finally met up with my new Oncologist, Dr. Taub. I like him much better. He is very clear with what his treatment plan. He is aggressive and he is clear about what he can do, and what he can't do.
I say we are back to square one, because Dr. Taub is starting a new chemo routine of high dose chemo given once every three weeks. It is cancer specific, and attacks the malignant cells, but not the healthy cells.
Dr. Taub didn't hesitate to up my pain medicines, and finally my pain is pretty much under control. There's not much we can do for the nerve pain, but I am going to start a combination of B vitamins that is suppose to help.
I am having an access port put in this week. For those who aren't familiar with ports, this is a semi-permanent way to give fluids and draw lab specimens, etc, without having to look for a vein every time you need access. It goes through a large vein into the heart. This is how I will get my chemo without burning up all my veins. After I finish chemo, they can take it out.
I thought the other Oncologist, Dr. Zafar, was radiating both my pelvis and the tumor. Guess what, not so. She was just radiating the pelvis. We will probably start radiating the tumor pretty soon, because Dr. Taub was a wee bit irritated that she didn't do that.
I asked Dr. Taub if I could travel, because I really, really want to go home. He says travel is very risky and he doesn't recommend it. I may go anyway.
We have figured out a way that Juan can travel without me, between treatments. That makes him happy, because he is super homesick.
It seems that after a rocky start things are finally coming together.
I am blessed.