I'm interested in conversations about and I want to talk about
Know exactly what you want?
Show search

Notification

Error

early docetaxel chemo 6 sessions

User
Posted 09 Apr 2016 at 05:23

morning peeps


was wondering apart from myself who else has had the early staged chemo, and what has been the follow up treatment, mine has been so far zero


last onco apt which was 6 weeks after last chemo told me that they would refer me back to urologist at my local hospital, even though my 1st onco said they would not do this, its now been 7 weeks and not a bean, spoke with urologist nurse answer was I don't know anything either


gave me a piece of paper though saying being referred back to urologist, don't know if I am on 3mth or 6mth visits, asked onco secretary but answer is I need to deal with my local hospital


referral letter to urologist says mets in right acetabulum and left ischium previous letters say mets in


left and right ischium,  left sacroiliac joint(SIJ) and right acetabulum


so don't understand what happened


going to see my GP to try and understand what is happening and for a referral to another hospital, some of you will know which one


regards


nidge


 

run long and prosper
'pooh how do you spell love'
'piglet you dont spell love -you just feel it'
User
Posted 10 Apr 2016 at 02:46
I wish you the best. Hopefully, you might find this link helpful:

http://community.macmillan.org.uk/cancer_types/prostate-cancer/f/142/t/68691
User
Posted 10 Apr 2016 at 18:55

Hi nidge
We too was wondering on this as to what happens after
my husband has just had his 5th chemo a few days before he had his 3 monthly hormone injection which we had a good talk with the specialist nurse we asked these questions about what happens next she told us that after chemo finishes you still get appointments at intervals to visit western park to see oncologist to see how things are going
The 3 monthly injections can be done by GP or we can carry on going to urology dept at hospital a PSA test would be done just before injection to check the level
If we decided to go to GP and wasn't happy we could at anytime be referred back for hospital for them to do PSA & hormone injections
My husband was told by his oncologist as his PSA levels have been coming down all the time he's had a test he won't need a CT scan so it sounds to us if PSA levels go up then that's when something else is needed that's why it's checked every 3 mths
Hope you can make sense of this and helps a little I know all hospitals aren't the same but ours are fantastic
Yorkshire lass

User
Posted 10 Apr 2016 at 19:17

hi yorkshirelass
thanks for the reply I was being looked after by Weston park oncos albeit at Donny, have tried to give them the benefit of the doubt but it seems that if you go to Sheffield you seem to get better info
regards
nidge

run long and prosper
'pooh how do you spell love'
'piglet you dont spell love -you just feel it'
User
Posted 12 Apr 2016 at 09:45

Hi Nidge,

Have finished the chemo and had all the scans. I have been advised no further treatment except the HT and then check up in four months time. I am really pleased but it seems strange after all the recent activity!!

Steven

User
Posted 24 Jun 2016 at 23:52
Hi all,

I'm not yet on Docetaxel but I'm due to start it sometime in the next month, after a few other tests have been done, and wanted to know what sort of side effects I could expect. It'd be good to get a few tips on how to handle any side effects, too.

I've looked at some information booklets about it, and I have a print out the oncologist gave me, but I'm interested in hearing some personal experiences of this drug from others who have already been on it because I've learned before that as good as printed info is, it's never as good as getting a real life account.

Thanks

Jim
User
Posted 25 Jun 2016 at 05:42

hi jim
I had few side effects, the worse one was the fatigue this built up the more chemo I had due to the red/white blood count being hit hard, picked up an infection but it soon cleared, as treatment progressed I did not go out as much, also had to stop working for 4 months
I did work for the first 6 weeks of chemo starting and mine is not a manual job, but deal with money all day onco was worried of picking up infection from the money
its just something else that hits us all different
on your visits take something to keep you occupied, also a bottle of water and a snack, I did get offered a sandwich and tea, but whoever went with me only got tea, I took my own tea decaff green tea
the steroids will increase your weight, I wrote on each box in BIG letters what each one was and when to take, also put it on my phone diary
the anti sickness pills I never needed

some of the things I carried and still do
small battery fan for the hot flushs
electronic thermometer as you need to be aware of any major increase
small hand gel
you will get a card to carry with an emergency contact number on it
purchased a small man bag to put everything in

the chemo nurses are WONDERFULL

hope some of this helps

regards
nidge

run long and prosper
'pooh how do you spell love'
'piglet you dont spell love -you just feel it'
User
Posted 25 Jun 2016 at 06:17
Hi Nidge
After chemo I had 6 big doses of radiotherapy to the prostate as my onco said there was "some evidence" that even though like you I have mets bashing the mother ship could reduce PSA increases initial severity. After that I had a MRI about 3 months later to compare with the MRI pre treatment. It was good news for me as it said " there are no visible signs of cancer" my lymphs had shrunk from a cancerous 3.5 cm to normal size of less than 0.5 cm. I was then on 3 monthly PSA checks but then it rose from 0.3 to 4 so they started me on Abbi which seems to be working as now back at 0.5. I asked about another scan but they said they don't do any more until PSA is increasing. That does worry me a bit as I have read about further spread without an increase in PSA but onco said as my presenting PSA was so high (342) that my cancer appears to be closely linked to PSA whereas some men have a PSA of 1 and get PC and in that case they would scan more as only way to see what was really happening.

Hi Jim, I was very lucky on docetaxl, side effects, hair loss 50% , taste buds dented ( tongue went black for 4 days initially), fragile nails and skin on hands/feet ( used nutrogena a hand and nail cream twice daily which improved things), numb feet ( still no feeling a year on, most other side effects gone), hot flushes ( still here now and worse but may be hormone invoked rather than chemo I guess), don't sleep very well, nose bleeds whilst on chemo ( I say nose bleeds but really I would wake with nostrils full of dried blood that's all). I did feel sick on day 4 of first chemo so doc said take anti sick pills for 6 days as they are otherwise harmless so I did and never felt sick again. I did not put on weight although my face puffed up due to steroids, I also ran most days and did a couple of marathons whilst on weeks 13 and 15 of chemo. I stopped working because I could as I was 49 and my employer left me on full pay, if they had not done that I could have gone in most days to a desk job I think although mentally I was not in a good place then so if you are like me i would recommend not if you can avoid it. I also had an occasion when my temperature rocketed due to injections to stimulate red blood cells, went to a&e and was on antibiotics through a drip within an hour plus lost of morphine as I had a bad reaction to the blood cell injection but all delt with over 1 night.

An advantage of early chemo is that you can have it again later on( and again) when the cancer returns, I am pleased I had it and all the above were minor niggles rather than real issues.

I feel good now 18 months on , still running , still working ( but part time as mental stuff still my issue).

Kev

Edited by member 26 Jun 2016 at 08:31  | Reason: Not specified

Dream like you have forever, live like you only have today Avatar is me doing the 600 mile Camino de Santiago May 2019

User
Posted 25 Jun 2016 at 10:48
Hi Nidge and Kev,

Thanks for all those tips. That's exactly the sort of info I was after!!

Which thermometer did you get? My Macmillan nurse said I should get a good ear thermometer from the local pharmacist but I don't have a clue what a good one would be.

Luckily I no longer have to worry about work. My employer was not the understanding sort from Day 1 when I first got the diagnosis almost 3 years ago. I look back now and wonder why I ever fought to stay on coz it's great not having to set the alarm anymore.

Jim
User
Posted 27 Jun 2016 at 17:01

Hi Jim,

Like Kev and Nidge, I was dx last may and started HT and then early Docetaxel Chemo which started in Oct and finished in Feb, 6 rounds. When I first knew about it and looked up all the side effects it scared the bejesus out of me, however didn't turn out all that bad.
Choose to use the cold cap so kept all the hair on my head but all body hair disappeared over session 3-4, only thing noticeable was no eyebrows. I kept working throughout although I took fridays off but the tiredness does catch up with you and ended up taking cat naps in the car if I suddenly needed to. I did put on some weight but kept an eye on diet and was a bit puffy due to steroids etc. The flushes and night sweats were an annoyance rather than anything else, and these unfortunately have continued 4 months done the line. I didn't have any change in taste and nails seemed ok. They gave you a scored card to fill in over the three week cycle and out off 20 odd SE I really only had tiredness and bit of nausea.
The chemo sessions themselves were fine and I just brought a knapsack with book, ipad, pineapple chucks (supposed to keep taste buds), water etc, just enough to keep me going over the 4 hours. However spend most of time chatting with others and nurses, who were all fantastic.

Hope it helps and good luck for the treatment.

Steven

User
Posted 27 Jun 2016 at 19:56

jim
its a kinetic non contact thermometer got it off amazon

regards
nidge

run long and prosper
'pooh how do you spell love'
'piglet you dont spell love -you just feel it'
 
Forum Jump  
©2024 Prostate Cancer UK