Decision made. I’m pT3a, N0 M0 (see my profile for details ). My extensive research points to a combo treatment of HT / RT / Brachy (NHS and NICE approved). MDT met again a couple of days ago and their recommendation (without my input) was the same. I had a consultation at Addenbrookes yesterday with a top prostatectomy surgeon and he agreed with me that my decision was the best one, as surgery would carry at least a 30% chance of recurrence. So I collected my prescription on way out! I took my first bicalutamide tablet taken this morning…..so the treatment is underway. Just over 62 days (NHS target) since GP referral so well done to them after a thorough diagnosis. I feel like a weight has been lifted from my shoulders with regards to timelines (chasing the NHS, politely!), but I’m under no illusion that the next few months of treatment will present challenges. My wife and I are a strong team and we intend to take everything in our stride and, hopefully, this curative pathway will prevail. Here we go…..wish us luck!
Nurse took my bloods yesterday morning and by this morning my PSA reading (amongst other blood counts) had already been processed, ready for my hospital consultation appointment on Monday.
My PSA has gone down to 0.07!
Great news, as it’s less than 2 months since radiotherapy ended. The nadir (lowest reading) is usually after 18 months, so all going in the right direction, especially as I still have a prostate gland.
I will open a bottle of bubbly this evening to celebrate.
Maybe i should wear a tuxedo, as I always wanted to be “007” AW
Hi Alpine Wanderer,
That PSA reading is certainly something to celebrate. Make sure you open the bubbly carefully otherwise you might end up with a black eye lol.
Enjoy.
Great News AW - All is going well and I hope you are sharing that bottle with Mrs AW !
I must confess to being a tad jealous here. Of course it's the bottle of fizz but I am 12 months post RT and can only get my PSA down to 0.33!! and my nadir reading is in 2 months time!!
Never mind, I will join you in raising a glass tonight. - it's nice to know that there are a few "good news posts" around the Community today and long may it continue.
Thank you also for all the support you bring to the Community in helping other Community members - it's not gone un-noticed.
Kind Regards - Brian
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Love it. We'll be raising a glass with you this evening before we have to go dry during treatment. Long may it continue down. OK 007 - Live and Let Die - long may you live and let the cancer die.
Excellent News and still sufficient time to drop further!
Hi AW, very encouraging reading. Will definitely have a beer tonight to toast you. David
Best wishes, David
Please remember that I am not medically trained and the above are my personal views.
Millibob - you’ve forgotten your own (correct) advice. Your PSA is still dropping after 12 months! The PSA figure is immaterial. As you know, some PCa can occur with low PSA figures, and some PCa causes very high figures (especially if metastatic). Therefore, the most important aspect is whether the PSA is increasing (at whatever level) or is decreasing (at whatever level). So no need to be jealous - we’re all different, fighting our own brand of PCa. Hope this clarification helps. AW
Hi Dedalus, so far the side effects are minimal, initial burning when I peed but drinking plenty and using Tamsulosin has eased that. I am deficating more frequently but not in quantity but with plenty of wind. No accidents in either way so far. My treatment coincided with my next ht injection so the sweats are a bit of a problem. I have no loss of energy , carrying on a very productive life as normal despite getting up 3 or 4 times a night. I did have the nodes done too as that was the lottery and I lost that but.
I will keep you briefed
ToFo
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