Afternoon all
so today was the day for my radical prostatectomy. Arrived at Castle Hill Hospital at 6:50am and got taken through to the surgical lounge. Following seeing nurses & doctors regarding the op I was taken down in theatre just after 9.00am and was on the ward for 1:30pm, a little late but this was due to having to be given painkillers for the sensation of needing to urgently empty my bladder even though I have a catheter fitted, apparently this sensation will pass by tomorrow.
i was very sleepy from then until now (4:30pm) and still am so I’m going to sign off now before I drop my phone. The main thing from this is I’m still here and will still be here for years to come, after the surgeon popped his head in and told me that he got it all as planned with no complications.
Next job for me is to become a first time grandad at the end of this month so this cancer was no way going to beat me.
Best regards to you all, I’m going back to sleep
John
I said I wasn’t going to post again until I had my catheter removed but… op day +3 I’ve just had my first bowel movement in 75 hours & 12 minutes - it left me with the feeling of needing to pee again like at the beginning… but just this simple thing has made me feel so much better, almost instantly
I’ll be back later next week after the catheter removal to report on that and how I’ve been
Best wishes & good luck to you all
John
Good Morning John
Well that's some good news - everything is working well now. Don't worry about the catheter removal - it's painless and it's such a great feeling knowing you can pee again (I should know - I had one for 10 months !!)
Thanks for keeping us up to date.
Best wishes - Brian.
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Thanks for these posts .helpful to know what might be coming .whilst still waiting for a date my surgery looks like being in August due to waiting list at the Freeman ,Newcastle. this has been going on since my PSA test reading of 17 on 19/4 )
MRI was non diagnostic due to hip replacements so straight to biopsies . 16 out of 21 positive . 3+4 so a Gleason 7 .
told that due to biopsies nerve saving was not recommended !!’ Oh well , better to be here for , hopefully, longer
Well done John a great positive response to the surgery. I am now19 weeks post op and apart from the ED which is the next hurdle to over come I'm pretty much back to normal. Walking an average of 16,000 steps a day, playing tennis, doing yoga, pump classes but crucially doing pelvic floors daily. So to echo your message we can beat this thing. All the best BM
Hi Magpie
pretty much the same as me, diagnosis given on April 5th with 13/18 Gleason 7 (3+4) but I got to save the nerves on one side so Viagra will help my ED given time apparently. But you’re correct overall what matters is being here at the end of this, if there are prices to pay….take my money.
All the best for your op next month
John
Hey Ras
Im just saying it as it happened to me and how I feel my experience has been, everyone’s will be different in some way but if my journey has helped you make a decision, im chuffed for both you and me
Ill be back on here next Wednesday pm following the removal of my catheter removal.
My posts are not recommendations but simply telling my story, maybe not for everyone, but if it helps someone to clear the fog of what way to go because of the way I write, I’ll keep on posting my journey.
Best of luck Ras
John
Hello John (JohnyBoy)
Everybody has a different journey but we all want to get to the same destination.
The more people who document their personal journey, the more informed those who follow later are.
Crack on John, you are doing a grand job.
Best wishes - Brian.
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I am a Macmillan volunteer.
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