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Wednesday, November 5, 2014

Radiation will start on Friday

We went to the radiation oncologist's office on Tuesday and they "mapped" Marshall for his radiation. They said he will have five treatments starting this Friday (then Monday, Tuesday, Wednesday and Thursday). So I reserved a room at the Springhill Suites for those nights. Our housesitter will be able to be here for those 7 days.

The morphine was really holding the pain at bay but yesterday was a bad day for Marshall so when he finally went to sleep I didn't want to disturb him and I skipped his 10PM morphine pills. Today he slept until about 4:00. I woke him up four times for his scheduled medications and he went right back to sleep. When he did get up he was in really bad pain again. I think that's my fault for missing last night's dose. So we won't miss any more.

He also had some nausea this evening. He tried to eat a sandwich but couldn't. So he hasn't had hardly anything to eat in three or four days. They tell you to have good nutrition (and drink a lot of water) in advance of the radiation treatments. Supposedly it makes things go easier. So we did fairly good on the water, but not on the nutrition part. It's so hard to do everything we are supposed to do.

He went back to bed around 10:00 right after his 10:00 morphine pills. The radiation oncologist sent me an email saying that Marshall should also be on an anti-inflammatory so along with the morphine I gave him some Aleve. Tomorrow we will be picking up the anti-inflammatory that the doctor prescribed (something called Salsalate).

Tomorrow also we will see Marshall's primary care doctor to get the oxygen thing set up. He needs portable oxygen for these trips to Denver. When we went to the hospital on Tuesday, the only thing we had was those great big oxygen bottles and when we got to the hospital they didn't have any of the wheelchairs available that had a slot for the oxygen tank so we had to carry it. We looked very odd with me pushing him in the wheelchair and him carrying a big oxygen tank in his lap. This time when we go to Denver we are going to lug the big oxygen generator along with us, too. Might as well be prepared for the oxygen needed for his CPAP machine.


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1 comment:

  1. Thinking about you and all that is happening. Sending lots of (((((HUGS)))))
    Sharon

    ReplyDelete