Prostate Cancer - Wife

Former Member
Former Member
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My hubby was diagnosed with prostate cancer last week and it has hit us hard. Hubby is 55yrs, I'm 50. We have six children, with three children still living at home aged 16, 14 and 13.

The consultant who gave us the diagnosis was awful. As we sat down to hear the results of my husband's biopsy, the first thing he said was..... 'right we have the results of your biopsy and with this type of cancer we recommend surgery'! We both sat there mute and in shock thinking .... what?....wait!...what cancer?....slow down! but he was talking so fast we couldn't get a word in edgeways. After about 5 minutes he ushered us out of the room and said 'the nurse will explain more'. We left the room following the nurse like lost sheep. I must admit the nurse did a better job at explaining but when you're in shock, it's hard to digest everything. 

There was a lot of information to take in. My husband's PSA is 14, (the consultant said that's high but when I pursued this forum i'm seeing people with psa's of over 100). His MRA scored 3 (whatever that means) and his Gleason is 9. 


We have young children to break the news to but how can we when we're not sure what's going on? (our older children now know).

Moving forward, we are at the 'staging' point. My husband had a bone scan, 3D scan and CT scan of his head yesterday. He has another scan on Sunday to see if it has spread to his lymph nodes. They will then call us in to discuss treatment. They have offered him the choice of having either a prostatectomy or RT but recommended the surgery because of his age.

My husband wants to go for the surgery and i'm happy to go with his decision but that was based on the short conversation we had with the Nurse. From the leaflets and information I've read both will have lasting effects. Sorry to be graphic but we're both relatively young-ish with a healthy sex life....OMG!! The possibility of ED or incontinence is scary. In saying that, I'd rather him take the treatment and be here for many years to come, as opposed to having a rocking sex life for a few years and then him to succumb to cancer because he didn't take the treatment offered.

So many thoughts, so many hurdles, so many decisions...... THIS IS TOUGH GUYS.... i'm not gonna lie, this is tough.

  • Former Member
    Former Member in reply to Barnman

    Hi Barnman,

    Thank you for sharing your journey with me, it sounds a though you're at around the same point as my hubby. Please let me know how you get on.

    Wishing you all the best!

    J33

    ps. I wasn't sure whether to laugh or gasp at the insensitive question the medics asked you....Scream

  • Haha thanks j33 yes we were quite surprise too but luckily we are not shy types. He then went on to mention pumps, pills and injections to address the challenge. Well good to know upfront I guess. 

    Best regards BM 

  • Hi I am due to have brachytherapy in about a week and I am really concerned about the after effects to my sex life. I have had the hormone injection and my sex drive is dwindling . The thought of noWearygetting an erection again is driving me mad to the extent that I’m googling life expectancy if I don’t have treatment Weary

  • Hi I have signed up for the mighty hike with macmillan to motivate me to exercise to try and counter the effects of hormone treatment , lots of countryside walks to train .

  • Hello    Well first off let me say I hope the brachytherapy goes well next week. Please share your experience of this with us please. There are a couple of other Community members waiting for this operation.

    As for the erections - when does your Hormone Therapy finish - something to look forward to!!  Grimacing

    Best wishes - Brian.

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  • Waiting for the bone scan was the worst, overthinking about worse case scenario luckily mine was clear the only symptoms I had were frequency of toilet visits. Of all the side effects it’s the effect on our sex lives that bothers me the most it’s almost like it’s taken your manhood away, I have even started cooking vegan food and drinking white wine, is this the point of no return. 

  • Hi Millibob they have said I will need hormone treatment for two years WearyWeary

  • Hello Trifle

    The HT will give you the gift of erectile dysfunction for the full 2 years plus probably a further 6-12 months whilst it works it's way out of the system.

    Mrs Millibob and myself have found other ways to "amuse" ourselves and to be honest with her support it's brought us closer together. (Only 12 more months to go for me!!).

    Best wishes - Brian.

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    Strength, Courage, Faith, Hope, Defiance, VICTORY.

    I am a Macmillan volunteer.

  • Hi Trifle

    Good name for the time of year, always partial to  a big bowlful.

    On a more serious note,  HT will have an effect on sex drive def which will  continue for some months after HT ends, 

    But it should come back eventually that's the good news.

    U don't give any stats so difficult to help further ie PSA, Gleeson , what does MRI say although I presume confined to the gland if u r having the brachy.

    Good luck with the brachy , let us know

    best wishes 

    Steve

  • Hi Joyful,

    well, I might as well weigh in with my two penn’orth.  Click on my name to see my bio history and progress to date.  I was PSA 13, so just under your hubby’s score. I think, at his relatively young age, he would be a good candidate for surgery  - but ONLY if they’re sure it isn’t breaking through the prostate capsule.  So it depends how close to the edge it is.  That said, it usually starts growing in the peripheral zone, so it may well be close / bulging / through the edge.  However, I’ve gone for brachytherapy boost - there is a link to a presentation about it in my bio. It has consistently outperformed all other treatments at the 15 years after treatment date.  Yes, that’s not a typo.  15 years after treatment. Don’t despair about Gleason 9 - if the radiotherapy kills it, it doesn’t matter what number it was!  AW.