I had my oncology review on Friday, and following low blood counts, there has been a change in my chemo regime. The IV drug (Oxaliplatin - nasty side effects) has been cancelled and I proceed with oral chemo only (Capecitibine - very few side effects for me). If my blood counts continue to be low then the whole lot may now be cancelled.
But for now - after one cycle of capecitibine only - my bloods have recovered to an acceptable level. I picked up my tablets for the next cycle this morning (cycle 5 of 8) in record time and even better had my PICC line removed.
It is a relief to no longer have to plan around the bad weeks (caused by the tiredness, nausea and pins and needles side effects experienced with Oxaliplatin). Over the past few weeks - when I have either had weeks off while my blood recovers, or have been taking tablets only - I have been well and active. Great to know that there can be more of the same from now on.
Some people had mentioned an injection available to boost white blood count, and some people may wonder if it is a problem that I will no longer be having all the drugs that were originally recommended.
I asked about the injection. This is very useful for improving neutrophil count, but has no effect on platelet production. I was having problems with both. Also, my chemo is adjuvent - ie post-surgery. On the last scans there was no evidence of cancer anywhere other than the area which has since been completely removed. This means my chemo is precautionary. Having had three cycles of both drugs and now continuing with capecitibine only, I should still be on a very effective treatment. And it is better not to put further stress on my bone marrow.
Now I must dash off as it is P's sports day. A few days ago I wasn't sure if I would manage to get to this. So happy to be able to go now. x
