Hi my name is Peter
I was having treatment for an overactive bladder with prostate blood test as part of treatment which came back at 7.7. I then had an ultrasound, GP said I had enlarged prostate but nothing of concern. Has MRI scan as part of pathway which has revealed lesions on prostate rated 4 and 5. Having a biopsy, no noted signs of other lesions throughout body. Notes 66.9% chance of prostate cancer and really worried and having bad anxiety and not sleeping, I have the constant peeing which I thought was my over active bladder no pain peeing small leaking and sometimes stop and start to finish,I've pretty much resigned myself to having prostate cancer and finding very tough to deal with like everyone with the horrible disease, any helpful advice would be much appreciated
Kind regards
Peter
Hi ya
No I'm not on hormone treatment as been told I'm meeting the urology team and surgeons after the pet scan,
I'd prefer beam radiotherapy and hormone treatment to surgery as I have a over active bladder and a enlarged prostate so could do without any more issues,
I'm 56 so would the preferred option from the specialists be surgery if anyone knows
Regards
Peter
Hi Peter-
Sorry to hear your results. Will you meet the urology team and surgeons on the same day as your PET scan on 22 Nov, or will that be a separate appt and if so do you know the date ?
Following MRI, I am also currently assessed as T3a. Biopsy result appt next Wed 20 Nov. May receive PET scan in due course. Have received preliminary heads-up that surgery is likely to be my primary treatment.
(No medical expertise; just an amateur on an unwelcome learning curve)
Hello Peter Psb2024
With your results I would think you would be ok for either surgery, HT/RT or brachytherapy. If you meet a surgeon they will press for surgery, an oncologist will press for the other two.
I would make a list of the pros and cons for each treatment as they affect you and go for the option that suits you best. Use trusted sources like Macmillan, Prostate Cancer UK and this Community for your information (not Dr Google).
I hope this helps. Feel free to ask anything, however trivial.
Best wishes - Brian.

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Hello Peroni
I think the post above to Peter (Psb2024 ) possibly applies to your situation too. Feel free to ask any questions.
(No medical expertise; just an amateur on an unwelcome learning curve)
That's s contender for "best new strapline 2024" - Magic - .
Best wishes - Brian.

Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm
Strength, Courage, Faith, Hope, Defiance, VICTORY.
I am a Macmillan volunteer.
Hi ya
Thank you ,Had my biopsy it's not that bad it definitely wasn't as bad as I thought it was going to be, meeting urology team and surgeons after PET scan ,as Brain said way up whats best for you treatment wise,hope everything goes well for you .
Peter
Hi ya hope your all doing well
I have my PET CT scan next Friday, was just wondering the kind of time frame for getting the results, as most guys and wife's/partners have been through this terrible wait.
I've been told by the clinical nurse specialist it's to rule out bone metastases, my GP and and couple of members on here have said that is rare for bone metastases with my Psa of 7.7 psa density of 0.15 no spreading in the pelvic area lymph nodes bladder colon ,but I'm still thinking the worst for some reason it don't half mess with your brain, I know many on here have been through this awful wait
Thanks
Peter
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