Next chemo on 20th august , I've never felt so ill , even had pins and needles in my Tongue .. Hands and feet .
Hi , I had my second chemo 12 days ago for my p... - My Ovacome
Hi , I had my second chemo 12 days ago for my ppc , carbo and taxol .. This time the fatigue has totally wiped me out ime dreading the
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Elft63
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Dear Elft, I'm really sorry to read you're feeling so ill on Carbo-Taxol. Have you spoken to your CNS nurse to see if there's anything they can give you to relieve the symptoms? It might also be worth checking with them, or the nurses at Ovacome whether you will necessarily feel as bad next time. It might at least help you get through it if you feel the side-effects might not be so bad another time.
Sending love and hugs to cheer you up. xxxx Annie
Hi Elft63
It's horrible to have to go through, but it's worth it in the end. I used to feel at death's door for 3 or 4 days during the 2nd week, then much better by the 3rd week. I think you get used to it once you know when to expect the bad days. It's important to tell your oncologist about any symptoms of peripheral neuropathy, in case they need to reduce the dose. I hope the treatment weeks will fly past and you will start to feel better very soon. Wishing you all the best, Gx
Hi Elft,
Poor you I send you my sympathy as I know just how you
are feeling. It effected me exactly the same and I didn't feel
well until the middle of the second week after chemo.Hope
you have got lots of help because really all you can do is
get lots of rest and lazy days in bed with books etc, if you
can manage to concentrate on reading. I also had terrific
pains in my knees and feet...so bad it made me cry.
My friends got me through the number of chemos I had
left. We used to go out for a meal on my good week and
I got lots of encouragement from them for the next
session. Do you have an appointment with your
oncologist the week before your next chemo is due, as
this is the time to tell them how you have been affected
and if your dose can be adjusted then they will try this
for the next session.
Sending you a hug (((((((x))))))
hope you feel better soon
Angie xx
Angie .. Such relief to know someone had the same symptoms as me .. I also get terrible pain in my knees , ankles and hips this usually comes after this restless leg and body thing I get .. It took me 10 days to recover last time , I like you cram everything in the good week I have .. I see my oncologist the day before my chemo every time so will speak to her thanks
Watch the pins and needles, and make sure the onc now s as taxol can cause permanent nerve damage to hands and feet. I felt like Ii was walking on hot coals after my second treatment, so he stopped it straight away. I still have problems with them now.
Hope you feel better soon.
Love n hugs
Viv
On my first paxi/taxol/carbo I too thought I am not doing this again agonising joint pain sickness constipation the whole lot, returned to onc. he could not make it out read my notes to see they had forgotten to give me STEROIDS he was livid with the staff, but he gave me much stronger anti sickness and constipation tablets. The next session so much better I nearly sailed through but the tiredness is unbelievable now finished all 6 sessions and in my fourth week still tire going up stairs or hills out of breadth, ok walking on the flat, sure they will give you something stronger to see you through your treatment, I really wish you well.love Jenny xxx
Oh dear poor you. The second time around is definitely worse than the first treatment, I remember that going downhill and I also had the nerve issues. Somehow the feet don't surprise you (by the way watch your step - theres a numbness too that you may not even notice but its enough to trip you occasionally) but the mouth thing doesn't seem logical and is so un ignorable. Do not ignore, mention to the doc as they can sometimes dial back dosage of taxol a bit and improve things without removing it from the regime
Love
Sue xxx
Hi....I think the symptoms you describe are pretty much par for the course, but you will get through it, even though I was told to report neuropathy I must admit was very reticent to do this as I didn't want them to stop the chemo, (so I carried on) I have had carb-taxol twice and on both lines my symptoms were bad, but I am still here and this was my choice, I am sure you can get help with the symptoms though...best wishes love x G x
Oh yes and I also got the tongue sensation too xx
Thank you everyone for replies , looks like the symptoms I get are what nearly all of you get , the pins and needles in my mouth is defiantly connected to the weird taste I get ( thankfully so far it goes aft a few days ) and yes I did notice this strange sensation when walking I have tripped on occasions . In a strange way it's a comfort to know others have done this chemo journey .. At the time you really do think your not going to do it again ..love to you all xx
Hi sorry you have been so poorly but also relieved that you are the same as me. I am just waiting to see oncologist and was thinking of packing it in. I am having single agent carbo. Will message you when I get home later from laptop. You will get better later this week take care xxx
Hi sorry you feel like this . Please talk to consultant and nurse . There is so much they can do to help with the side effects. You may find it falls into a pattern and you have a couple really crap days and then feel better. You will get through it. Chin up and hope feel better soon
Ally x
I was in hospital 2 wks. ago couldnt breathe with fluid in right lung. They drained over 6and a half litres out. it was not a pleasant experience to say the least. I have just started today my 4th. round of chemotheraphy. They are giving me carboplatin on its own this time, on a 3 weekly cycle, as i had 18 weekly taxol last time which ended last october Will keepyou all posted as to how i go.xuna.
I am sorry to hear that. I must have been lucky. Never really had a problem except for the metallic taste which wasn't great. Had six rounds 3 yrs ago. Then last year I had a reaction to the carbo on my second round. So you just never know how it's going to go. I have heard they are working with Manuka honey here in nz as a post chemo treatment. To boost your immune system. Will see what I can find out. Regards chris (I also have PPC 3 yrs this month since diagnosis)
