Morning all. I'm not sleeping at the moment. His snoring is getting worse and keeping me awake.
At the oncologists appointment yesterday she said she was very pleased with him. Apparently there has been a significant reduction in the primary tumor and his CEA marker has gone from 50 at the start of treatment to 9. She has now put him on Capecitabine pills starting 25th November after a break.
Does anyone have any experience of this drug at all? I have read some horror stories on line.
My husband is on his 4th palliative chemo cycle, following stoma surgery and radiotherapy. Oxaliplatin infusion on day 1 of each cycle, and then Capecitabine for the subsequent fortnight. It's alot of needles and tablets for my previously needle- and pill-phobic husband.
The Capecitabine makes him very nauseous. Strong anti emetics can only be used 3 days at a time. I'm afraid retching and vomiting would seem to be normal. Total energy drain and breathlessness. A raft of other side effects which play swapsies from week to week. Everyone is different. All you can do is take one day at a time. I wish your husband well.
PS it sounds like you need noise cancelling earpods. I listen to stories thru mine, to make the white noise.
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