I'm on a journey. After experiencing some degree of nocturia for some time I approached the GP. I had a DRE which found my prostate to be smooth and Initial PSA in late December. was 5.99 going down to 5.5 a month later and subsequently up to 6.25 after a further month. This finally triggered a fast track referral to the local urology department. It felt like the initial DRE seemed to have triggered more acute urological symptoms of frequency and urgency alongside the regular waking in the night. I felt lucky to get a cancellation with urology and was seen within 2 weeks of the referral.
I was retaining urine and a further DRE was felt to show a benign prostate with a degree of enlargement and inflammation. I was treated for prostatisis with 2 weeks of antibiotics and commenced on Tamulosin. There were some positive charges but my symptoms got worse again when the course finished. My PSA was up to 8 when repeated and I had a MRI scan which has shown 2 lesions one a 2 the other a 5 and am now going to have a biopsy.
Being a 5, I'm definitely very worried. 62 and loving life! I know I have to wait for the biopsy but need to share. My wife is incredibly supportive and I know I need to be positive but it's not always easy.
I have an ache in the pubis area which did resolve when taking the antibiotics but has now returned. I'm conscious everyone here has a journey and I take comfort in sharing mine. Thank you.
Hi RAS1961 , sorry you have joined our club. Following your PIRADS 5 it is likely that PCa will be found but with your other symptoms that may not be definite. Unfortunately a biopsy is required to identify exactly what is going on and if PCa then how aggressive it is.
You are young and that is definitely in your favour. Waiting is the hardest part but you have no reason to think that you cannot be cured, so try and enjoy life and stay positive. I am sure others will be along, but take heart from the numbers of guys on here who have had a really bad prognosis at the start and are still around years later and enjoying life. Please feel free to ask any questions. Best wishes to you both. David
PSA quite low and I assume any tumour confined to the gland so potentially curable
So after biopsy assuming it be PC you'll be started on a treatment plan.
I know it's the waiting that's the worst part but it does look like a low key affair.
Best wishes
Steve
Hello RAS1961 - Another warm welcome to the online Prostate Community - we aren't a bad bunch! The first post by David2017 has stolen my thunder as I totally agree with his post.
I will just add a link to Prostate Cancer UK's splendid booklet "How Prostate Cancer is Diagnosed".
https://shop.prostatecanceruk.org/our-publications/all-publications/how-prostate-cancer-is-diagnosed
I do hope reading this eases your worries as a positive attitude and family support is half the battle.
If I can do anything else for you please let me know.
Best wishes - Brian.
Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm
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Hi RAS: I was similar to you- When they told me PIRADS 5, I thought my world was crashing down. However, I went through the diagnosis (made friends with every medical secretary/ booking person I could and politely pushed for any cancellation for biopsy (and got one). I went on to consider all options and started my treatment within the NHS guidelines. Check out my bio (and main thread if you have lots of time to read it!). AW
Thank you so much that my friend. Had a read through your story as well. You have definitely been on a journey! I have it in mind to chase them for biopsy appointment and ring them tomorrow.
I have taken great comfort from replies. It really helps. Robert.
An update. Had my biopsy on Friday. 3/05/24. I'd been very nervous but overall the experience wasn't too bad. The Consultant went through my MRI. He felt it could be contained but noted an area of protrusion. He indicated he could feel this when doing a DRE prior to the procedure. This wasn't there before, unless it had been missed.
I felt a little elated after the biopsy, possibly due to feeling as if I knew more. This feeling has deserted me now as the worry creeps back in. I know I have to wait for the results but have sympathy with everyone who has been in this negative limbo place before me.
Recovery has been unproblematic after the biopsy but I have a nagging ache between my shoulder blades which is disconcerting. Not painful nor restrictive, but there. I'm trying not to think to much into it.
I haven't had a repeat PSA so nothing further to add. Getting hot in the night but I've always been a warm sleeper. Will have to open the window!
I'm prepared, not necessarily happy, for PCa result but hoping for a treatable outcome. I continue to work as a nurse part time. It provides some distraction as when idle, ones mind wanders!
I want to thank you for your warmth when I first posted. I will do my best to keep you updated If it's ok to do so. I'm happy to be pointed in the right direction if I should post elsewhere.
Robert
Hello Robert (RAS1961)
So there you go - one little step nearer to a full diagnosis - that's the hard part of the diagnostic journey over - the hardest bit is waiting for the results.
From what information we already know I am sure whatever your biopsy results are there will be a "curative pathway" to look forward to.
Please post your results on this thread - and anything else for that matter. Every time someone posts on the thread it get's "bumped" back to the top of the forum.
Remember it's OUR Community and YOU are a most welcome member (even though you would rather be somewhere else!!).
Best wishes - Brian.
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