Hi Elenamae
I started EC chemo 14th January, and will be having 4 cycles of 3 weeks each. I believe EC is very similar to AC, my chemo nurse said it is also known as AC, I hope I have got this right.
My treatment was in the morning, and apart from feeling a bit heady I was fine until I started feeling a little queasy during the evening. I felt very sick overnight and this continued until mid afternoon the next day, when it eased. By the third day I was only feeling a little queasy again, but this continued to ease off. My medication is going to be altered for next time, so it shouldn’t be as bad.
I was very tired days 4 - 8, spent much of these days in bed and I was still quite heady, but has improved since then. Last few days I have been almost back to normal - just have to pace myself.
I also had the Neulasta injection the day after - it didn’t help having to trek back to the hospital when I was still feeling very rough, but I have arranged for this to be done by a nurse at our local surgery next time.
From what others have said, and my own experience oncs are keen to keep SEs to a minimum, and I have a review before each treatment, to adjust meds as necessary.
I also had constipation problems, which again with a change of meds will be better next time round.
I also had an odd taste in my mouth for the first few days after, but this has almost gone now. I have been fending off cystitus, which is a side effect of the Cyclophosphamide by drinking lots. I have been suffering from hot flashes - have got myself a chillow to help with those. (but this had started before my treatment anyway).
I did use the cold cap - am just waiting and watching to see when/how much hair I will lose in the next week or so. Scalp very tight at the moment.
I know all this sounds a lot, and at the end of wk 1 it did feel as if everything seemed to be hitting me one thing after another, but I have felt well for a few days now, and should be ok until my next round as long as I don’t overdo it. I am working part-time, but I work from home so am just doing what I can when I feel ok. I have learnt some ways to cope better with the SEs next time round.
I have been able to go out for a walk most days, only short walks at first - but am now back up to an hour a day.
As Rhian says, it is do-able. If I can help any further please do PM me.
All the best
Chris