I have Gleason7 (3+4) PC and am due to start 20 Radiation treatments on 5th October. I am thinking of taking 1/2 day holidays from work to cover these. I am hoping that the side effects will be minimal. Work is like therapy to me and I want to keep working as much as possible.
By the time of my first Radiation treatment, that will be my 31st medical appointment this year. It's not just the Cancer, I have a load of other pre-existing conditions.
In myself I feel fine physically, but mentally is another thing. The hormones have taken over.
It is the money situation I am more concerned about rather than my health. Sick pay is a no-no, just the £90 odd quid for SSP.
I have tried applying for benefits, but "I am working and have my own property" and am ineligible for just about everything. PIP is a joke, by the time I get a decision...
Hi Steve
For me the effects of RT took a while to kick in. In the beginning all OK then in week 3 things got tiring. I had a ticket to a football match that week and was so tired I coudn't get off the sofa to go (it was a european night too!) . The mini-enemas also became more effective by the end (it may also have been a side effect of the RT) and having a loo nearby was essential. So, given how important work is for you, I recommend late afternoon appointments as - for me - it was easier to cope with work after a night's rest. Also, if you are driving yourself to RT it might be worth seeing if there is a free patient transport service (just the hassle of car parking etc was taking a toll by the end) - having a lift on one or two days could make a difference.
Best of luck with the long term effect of the RT - I'm almost three years on now and the cancer status could not have gone better (began with Gleason 9 / PSA 141, now PSA too low to measure and a lot fitter and healthier than for years) I hope you have good results too.
Stevie
Hi Stevie,
Being a Newcastle fan, it could be a blessing not being unable to go...They could even win!
I am trying for as late in the day as possible so I can still go to work. There is the option of free transport, it's a company called "Daft as a Brush". They are supposed to be good, they wait for you at the hospital to take you home.
Glad to see you are getting fitter and the old PSA is virtually non-existent.
Steve (SteveCam)
Are you having the fiducal markers inserted to your prostate first ? I am due to start my 20 sessions of RT to my prostate 1st week of October but I have to have the markers inserted first which I am not looking forward too as I have been told it is a similar procedure to the prostate biopsy which I was not pleasant. I am also having 2 sessions of RT to my chest to reduce breast swelling and pain.
Regards
Paul
"Diagnosed March 2021 at 38 years old with stage 4 metastatic prostate cancer, my journey so far is on my profile"
Thank you Steve, that is good to hear. I'm also anxious regarding the side effects combined with the current ones on HT, the fatigue mainly as I've only just in the last few weeks felt able to get on top of it.
Regards
Paul
"Diagnosed March 2021 at 38 years old with stage 4 metastatic prostate cancer, my journey so far is on my profile"
I think that HT side effects r worse than the RT.
I didn't have too many problems with the RT and most people say the same.
Worst part was severe constipation which started midway thru and lasted for a couple of weeks after treatment finished. But it's something that can be coped with.
Steve
Having the markers inserted was really not so bad as the biopsy but I had no big problems with either. I had no side effects from the Radiotherapy apart from one night about half way through when I was up all night peeing every few minutes. I had no bowel problems - which was a surprise as the cancer was near the capsule and pushing against the rectum so I expected bowel problems. Others had bowel problems and all sorts of other problems - we are all different and react differently. I certainly had no more fatigue with the RT than from HT.
Good Luck
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