Hi, what are peoples experiences of filgrastim injections? I had my first chemo last week and have been doing the injections since, last night I suddenly had body aches all over and so had to go into a and e, after a very long night they have decided it is a side effect from the injections, has anyone else had this? When did it start and how long did it last?
I’m on EC for the first 4 cycles and then docetaxel for the last 4, which ones are you having? it would be good if I don’t have so many for the last 4 cycles but at least now I know what to expect and can get on top of it, the worst pain was only really for a day and my actual side effects from the chemo have been pretty minimal (feeling spaced and tired for 2 days post chemo) so as far as cancer goes I’d say I’m doing pretty well so far!
I had 3 ec, followed by 3 docetaxel and finished 4 weeks ago, similar to yours.
It really is a take each day as it comes, some cycles seemed easier than others. Rest when you need to, keep on top of pain which allows you to sleep better and it will be over before you know it x
I’m on AC first 4 then onto paclitaxel for next 4. It seems most people are on docetaxel. I’m up and down with side effects, today is a better day
Well done Cupotea for making it through. Are you having surgery next?
Being at the beginning it feels like such a long way to go so it’s nice to hear from people on the other side of it. At the moment I’m looking forward to my next treatment but I’m sure at some point it will turn and I’ll start dreading them!
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