I said I had no major side effects from dose 1 of Erubulin. Spoke too soon, havnet been sick or anything, but the fatigue is awful. I have been mainly horizontal since Sunday - just about walk dogs round a short circuit and then lie down again. Housework, what is that? Have managed to make myself a veg stew today, so maybe been a bit more vertical today. No doubt by Friday morning I will feel fighting fit, just in time for dose 2 on Friday afternoon. I know fatigue isnt the worst side effect i could have, and many have and are having much worse, but it does sap positivity.. Still I get next week off so am really hoping that full energy returns for a while.
Full sympathy to anyone going through worse, or the same.
Thanks Stuart. I am sure your fatigue is of a different order- so no apologies needed for short response. Sleep is demanded.
Love
Di
xx
It seems fatigue is a big side effect of most anti cancer meds. My pazopanib causes fatigue. It’s a weird fatigue as some days I seem to be able to plod along all day quite happily other days I do a little then need an afternoon nap. Hopefully as your body gets used to it the fatigue will ease a little
Richard
be safe, be nice, be you
What a shame OBS, I hope it will not be as bad after dose 2 and you get a full week the following week.
Richard (Remoh) is right though, fatigue is a common factor with many meds for pain and cancer. The Occupational Therapist tells me it is our body protecting itself, so if we feel like a nap, we should have one and on a day it is not so bad, just try to pace ourself. It is very frustrating!
Love Annette x
I certainly do listen to my body - it wont let me not! I love snoozing to be truthful. snuggled up under a blanket on the sofa with radio 4 burbling away. Today I felt 70% normal - went to hosp for bloods and PCR test. Walked dogs twice ( I do manage that most days). No doubt , as I said before, i will feel 100% tomorrow and then go for second treatment in the afternoon. And it all starts again. I hope my body will gradually get used to it, and second time isnt worse than first. But whatever it throws at me, hopefully I can cope. I find being on the chemo unit strangely comforting - I went 3 weeks out of 4 for 2 years so I sort of missed it in the 2 years on oral treatments. Does that make me weird? Thanks for yout thoughts.
xx
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