Thanks Ck x
Don't know if I've mentioned this before.....but I had a craving for sausage sandwiches, round about midnight! Weird.
I remember my chemo nurse said to me at the start.....just eat what you fancy, whenever you can. She said you need to take on the calories, mainly making up for those days when you really don't want much. Fortunately, I didn't suffer from sickness at all. Unfortunately, I carried on eating as if I did need to eat extra! Consequently, every time I went for my weigh in, I just put on more and more weight! Oh well, it was the least of my problems at the time.
Good luck with all the tests SueW. I am going for a wig fitting on Thursday afternoon myself. The other salon I went in only had one longer haired wig to actually try on but they have ordered some more in. Hair has started to shed more at Day 4 post chemo. Awful heartburn here (wasn't given anything for this symptom) seems stuck in my back and still can't eat much, I start to hiccup, so sticking with plain things, though I did manage to make an apple and berry crumble for the family today, then tried a spoonful and heartburn reared its head so gave up. Drinks are a problem too, used to love my cups of tea and coffee but can only sip warm water or the coconut water when my neck swells with the bone injections. Sleep is eluding me, awake around 2.30 am most nights but don't feel tired in the day strangely. I am trying a home made beef stew tomorrow, wish me luck probably one spoonful and it is back to the dry cracker. Can't believe how hard it is to enjoy food or try to eat it. Best wishes to all
Hi runnerbean good luck for Thursday & Friday. My work is the same just take each day at a time. I was planning on self certificating for first 7 days if need be, then working from home 2nd week and maybe go in the 3rd week. I guess that'll depend on how I deal with the treatment. In some ways wish I was signed off for the whole thing as it makes things easier and less to worry about!
Hi chaffinch I'm also having fecx6 followed by radiotherapy and tamoxifen. I've also always found dolls a bit creepy. Went for wig consultation last Friday in case can't tolerate cold cap/ it doesn't work, they didn't have any to match my curly hair so they agreed to order 3 for me to choose one. She did show me one which did look ver much like dolls hair, but the other one she showed me was really good. Not sure if they'll be any good but it does give another option. I also booked look good feel good session. Good luck for Wednesday.
Just wanted to welcome Karana to the thread. Sorry that you're here, but we try and help where possible.
I had chemo last year, so if you have any questions please ask. I may not know the answer, but I can point you in the right direction of who to ask!
Good luck with your forthcoming chemotherapy karana23. Had my first fec last Thursday (they sit with you to put that in with a tray of large syringhes) only took a couple of hours and yes just turned up as I normally do, I don't wear alot of makeup anyway but put a bit on along with some lip gloss.
Me again...I know this maybe a really stupid question but those of you that have already started your chemo did you turn up looking how you normally would on a day to day basis, as in wearing makeup, jewelry etc, I was thinking definitely comfy clothing but just wasn't sure about my face lol!! Xx
Hi Meesh....no decided against the cold cap...I hate the cold!!! Have got quite short hair at the minute so have decided that it wouldn't be as traumatic as it wld be if I had lovely long locks, still a bit scary though!! I wore a sea band while on a boat trip on my last holiday as I suffer terribly with motion sickness so will stick that on....being sick doesn't freak me out too much but I hate feeling dizzy xx
Hi everyone....I'm starting on Wed (4th) 6 sessions of FEC...been ok about it all up until this weekend then been having a few panicky melt downs!! Off shopping today...any suggestions of things I may need 😊 Xx
Chaffinch17, I know what you mean. Sleep has been a bit on and off for the last week. I now just feel like I doze from about 1:30am and there's no sleeping after 5am. Hopefully it will be better once we've started and not so anxious.
SueW good luck with appointment today, hope all goes well.
I'm off to work in a bit, no idea how I'll keep focussed today and that's without chemo brain!
The injections seem to depend on your type of chemo and which hospital you go to. I had them days 3 through to 7 ( that also seems to vary! ) and are given to boost your white blood cells, which helps fight infection. They are worth having, although they can initially create joint pain. Sometimes you have to do them yourself, but I was too much of a chicken, so a friend did them for me!
Thanks Patchwork Girl and Ali49 for the feedback on your first treatments. It's encouraging that you're both doing well and feeling better, even despite your sickness Patchwork Girl. Does everyone have injections? They never mentioned any injections but I've found through this process that they like to drip feed you with bad news rather than give it to you in one hit, so guess I'll find out Tuesday. I'm booked in for 9am and have been told to have a bit of breakfast beforehand, any recommendations of what to eat prior to treatment?