EC Round 3 - the doldrums

1 minute read time.

When I first started chemo, a doctor described it as standing at the top of the stairs and being knocked down. Each time you climb back up, only to be knocked down again. But each time it’s a bit harder and you don’t get quite so far up the staircase before you are knocked down again 

I am now on day 8 of cycle 3, and it does feel as if it’s been a bit harder this time around. The sleeplessness from the steroids was a bit worse; 3 nights of being awake from 2am, eventually getting up at 4, going back to bed at 5, but not sleeping again until 6. The gut problems have been worse - I don’t think I have had a normal motion since the chemo went in. On Sunday I sent my other half to buy some Lactulose as I had so much pain with wind, but couldn’t get anything out. Of course that took me too far the other way, with obvious consequences. This is the first time I have found I needed to return to bed after breakfast on each of days 5, 6, 7, 8. Exercise has been a distant memory (other than the Aqua class I managed on day 2), largely because I have been afraid to be too far away from a loo. The lack of taste has been worse than last cycle, even plain water tastes unpleasant. Everything needs to be spiced, or herby, or on certain fruit spectrums, or a little sweeter or saltier than would be my usual taste.

I do feel I am now starting to turn the corner. We managed lunch in a cafe yesterday. I managed to drive to a meeting this afternoon. I guess Immodium and possibly Lactulose need to be my friends for the rest of the cycle, but past experience says I will get through this. And only 1 more EC to go before I switch to Paclitaxel. At least the bone marrow stimulation pain hasn’t been too bad this cycle. 

Anonymous
  • Hope you are feeling better.  I've just had week 2 of Paclitaxel, I'm finding it much easier than Ec, especially as I'm having it weekly.  Only do 2 days of sub cut injections, no oral steroids and also managing some gentle running xx

  • They told me I wouldn’t need the injections on Paclitaxel. I hope that’s the case when I get to it. I will also be weekly. I managed a little gentle running this morning but I am a long way off where I was just 8 short weeks ago pre chemo. 

  • I used to find a prune at bedtime was great for the gut issues. I didn't find a problem with my gut with paclitaxel. It does get harder with each one, but exercising stops you falling further and it sounds like you are doing a great job of what you can, when you can. Only one more to go after this one. It helps if you don't have the steroids attacking your thigh muscles and messing with your sleep too! For me, paclitaxel was better, and I hope you find the same xx

  • Hoping so too. Although as it happens the rest of this cycle has so far been better than the other two

  • Hi Codfish

    I really hope your side effects from the chemo have lessened by now and your life has regained a little normality. thuinking of you very much x