Hi all,
Had colon cancer removed and now need to have chemo.Anyone with similar experience?
Hi all,
Had colon cancer removed and now need to have chemo.Anyone with similar experience?
Colon cancer removed in August, starting chemo in October. Feeling a little "cheated" as was orriginally told cancer was contained within colon but have now been told it's in a couple of lymph nodes. Felt knocked sideways by the surgery and worrying that I'll be similarly wiped out by chemo.
Hi Sfuc,
I had op abroad as it was emergency but treatment was great.Im back here and now worried if the chemo will be properly done here.Literally told the GP and hospital doctors that it's about my life here and having appointment next Tue regarding chemo.Do u know how many lymph nodes?
Hi Denise,
Same here.Depending how I will be feeling after chemo I'm always here to listen especially that for me I don't want to worry family even more so it's easier to share my worries in the group
Hi
I was in your position 2 years ago.
Four rounds of chemo, oxaliplatin & capecitabine.
You don't lose your hair with this chemo.
I'm not going to lie, this is strong stuff and you will feel rough especially on the day of your intravenious one. Does wierd things with your nerves, for example if you sneeze, your face stays screwed up for a while after, you shouldn't touch cold things, metal or definitely not go near the freezer. Also with me I found the first mouthful of any food sent the nerves in my teeth off and was quite paiful. Came round pretty quick on week off before starting it all again.
Just cross the days off untill it is all finished and you can get back to normal.
Good luck, hope you have someone at home to look after you well, to control what tablet to take when.
Hi,
Can I ask about the stage u was diagnosed with and is it all clear now?
I can't see any reason why chemo wouldn't be done properly here but currently have no personal experience to base that on! Where did you have your surgery?
Cancer found in 2 out of 19 lymph nodes. I've been told that finding cancer in so few of a relatively large number of nodes is a good sign.
I hope your appointment goes well - take someone with you if you can (I don't mean if they'll let you, more if you have someone who can attend). I was able to have my husband present at the appointment and he took in some of the information that I might have otherwise forgotten or missed. The Macmillan nurse also gave me a useful booklet so hopefully you'll have a similar experience. Let me know how it goes.
Hi,
I was on holiday in Poland and had it over there.Everything went smoothly and a week from colonoscopy I had the op.cancer found in 5 out of 17 nodes and was told to start chemo max till 6 weeks after op.Also had already arranged for chemo last week in Pl but was assured I can continue here so obv came back as my family and work is here.I just hope the despite having everyth done abroad the doc here will accept the documents as I know from the experience that they need they like to have the evidence from here.Not sure if I want anyone to go with me as they panic more than me
I was never told the stage and daren't ask. spread second time to 1 out of around 20 lymph nodes. 2 years on and a clear ct and colonoscopy.
Stressful! I'm happy to send you the list of questions I asked if it helps? You should try to write everything down, if nothing else it'll give you a moment to process what's been said. If you are attending on your own, ask if you can review what's been discussed afterwards with an experienced nurse. Ask this in advance of your appointment so you can't be fobbed off on the day.
What were your symptoms. I have had a lot of mucus in my stool and had blood a couple of times .