Hi everyone
My OH received news in March 25 that his annual MOT at the GP showed a PSA of 77
We were 'gobsmacked' as he hadn't had any issues at all but suddenly our world turned to chaos and within 5 weeks he had had a CT, Biopsy, MRI and had 2 Urology appointments.
His Gleason was 4+ 3 =7 , T3, N0, M0
They put him in CPG 5.Locally advanced
All this sounded so bad to us, but the Urologist was confident it was curative and would start Hormone Treatment straight away, followed by Radiotherapy
He started Bicalutimide tablets on 18th June and had his 1st Hormone injection on 2nd July
Met the Oncologist today and Radiotherapy will start in mid October for 4 weeks, 5 days a week.
I must say that all medical staff have been absolutely brilliant but one thing we would like to know from people who have gone through this Treatment.
Consultants have given us a list of side effects he might have on Hormone Treatment but fingers crossed, after 5 weeks he has had nothing at all.
Thanks
Dear Worriedwife
you certainly know how to give everyone in this forum perspective & hope .
hugsst hugs to you both.
liz & OH
Sorry to hear of your OH’s diagnosis @Cal58 and yes, your world does head off in another direction for a while.
If it helps, I started Zoladex LA therapy late last year and for the first two three-monthly injections I thought I’d got away with almost no side-effects. After the third, the hot flushes became more often and more pronounced, but only last for a minute or so. Some days I get more than others and sometimes I wake in the night due to hot flushes and have to cool off. They are very manageable.
My memory for names and dates seems to have dipped too although that was never one of my strong points anyway...! I was told these side-effects are quite normal.
I have just finished the four weeks of weekday radiation treatment your OH will be starting in October, after 8 months on Zoladex.
Wishing you both the best of luck with your journey through this.
Whittaker you have sparked my interest now with those comments. Since my HT & RT my right foot and both thumbs have become painful. I've attributed this to arthritis but maybe the treatment has had some effect on these joints.
My last three month HT implant was October 2024 but the side effects are still very present. Time alone will tell.
Rod
Certainly looks like your pathway will lead to a cure, it won’t be all easy but a great job is getting started, we are all different and respond in different ways so it’s difficult to say just how it will go in your case. Earlier on during my Ht I had quite a few hot sweats but these have become less as I have continued these days I have more problems with shoulder and muscle pain and some swelling in my feet and lower legs!!Just hope you don’t get to much of anything on my last treatment now yippee just remember it Is doing a great job! Very Best Wishes David
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2025 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007