Total inability to have an orgasm post radiation

Posted by scottbeammeup @scottbeammeup, Aug 12 2:25pm

Since finishing radiation treatment two months ago, I've been completely unable to have an orgasm. I'm on Orgovyx for 2 more months, but still have good erectile function it's just that I can't finish either with or without PDE-5 inhibitors. I go at it until it's literally unbearably physically painful but nothing.

Is it possible the orgasm nerve was destroyed by radiation? A close friend recommended that I try a large dose of THC--has anyone heard of that? Is that part of my life basically over?

This was NEVER mentioned as a possible side effect of radiation OR ADT and I guess just one more thing to be upset about.

Interested in more discussions like this? Go to the Prostate Cancer Support Group.

@slick64

I had high dose Proton radiation with hormone therapy before the radiation. I had a total of 3 shots, the initial 2 were Firmagon, and that totally sucked, followed by one of Eligard. That was it, waited a few months , during which I was marked and fitted. In May 2023, I received the radiation. And while no complications, I had to learn how to hit the head and control my stuff. Slowly, the effects started to where off and I learned more of the effects and how long they could last, once I absorbed that, I became more at ease and optimistic. Doing the radiation was my choice, I was terrified to be cut and my surgeon stating that I wasn’t a good candidate for surgery. And my research discovered it’s just as good, if not better than surgery, if it’s an option. Once tested and diagnosed, my team worked hard and fast to get me treated. They genetically a core from my biopsy and my cancer was just over the line to aggressive. I was Gleason 4+3/7 stage one. My psa was nearing 6 and slowly rising, it’s now holding at .21 and my testosterone is coming back up. Hope this helps.

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First of all, thank you for taking the time to post a response. As you’ve likely learned, treatment for cancer, is it not a one size fits all proposition And I’m glad that you’ve had good results with proton therapy.

When I was first diagnosed in 2020 I absolutely did not want surgery. I was afraid of incontinence issues and sexual dysfunction, and I was unwilling to compromise even in the short term. My two top choices for treatment were proton radiation therapy and low dose radiation brachytherapy. I had private insurance at the time and my carrier Aetna wouldn’t even discuss paying for proton therapy. They also wouldn’t pay for any biopsy other than a 12 core random transrectal biopsy.

I opted for LDR brachytherapy and everything was great for three years until cancer returned with a vengeance in summer of 2023. Gleason 9 Stage 3. My prostate was removed in the salvage operation in January 2024 and I underwent seven weeks of salvage radiation that finished July 18 2024. I will be on ORGOVYX and generic Zytiga until April 2026 and my care team is optimistic that we can knock this into remission for several years and hopefully the rest of my life.

We are both blessed to live in an age where the treatment is largely so successful that we have the luxury of being concerned about sexual function.

Good luck on your journey!

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I have heard of this situation in my support group. The guy that had it , said it resolved itself in time. Body needs time to heal and such . Radiation. , generally, takes soem time to work too and drive down PSA number . Give it some time and walk / hike alot and keep active ! Keeping active and sauna's helped me recover - I do believe !

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@vancouverislandhiker

I have heard of this situation in my support group. The guy that had it , said it resolved itself in time. Body needs time to heal and such . Radiation. , generally, takes soem time to work too and drive down PSA number . Give it some time and walk / hike alot and keep active ! Keeping active and sauna's helped me recover - I do believe !

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Thanks. I walk my dog 3-5 miles every day and then cycle about 15. I always feel better while doing it, especially cycling which forces me to pay attention to something besides the negative thoughts that try to fill my head. Also do weights 3 days a week and yoga 1. Haven't thought about the sauna--may give that a try.

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@scottbeammeup

Thanks. I walk my dog 3-5 miles every day and then cycle about 15. I always feel better while doing it, especially cycling which forces me to pay attention to something besides the negative thoughts that try to fill my head. Also do weights 3 days a week and yoga 1. Haven't thought about the sauna--may give that a try.

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100% , you are doing the right thing for sure . Yes those negative thoughts are normal, so deal with them the best you can and divert your attention. Also , when you start going to the sun , bring in plenty of water and small micro sessions first ....then longer . I
The Sauna has many Bio-benefits. Read up on what "protein shock " therapies do , ridding your body of extra urea, salts and heavy metals , etc . I usually crave pickles after a Sauna ( common) to get my eltrolytes . BUT my point here is work your sweat glands in the sauna , but start slowly and work up to 15 minutes at 3 exposures per vision ! 🙂 . Also read up on the benefits of Sauna . Got use to it when I was working out of Budapest - very common . Looks of "Eye Candy " in those saunas in Budapest as well. Lovely gals ! 🙂

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I did a small bit of counseling and a cancer center and a surprising number of older men, past 65, had no sexual function at all. I personally haven’t had any since 2010. It’s what my life is and I have adapted to that. I’m not married and don’t have a steady girlfriend at the moment. Again, it’s something you have to adapt to because your body simply doesn’t respond that way anymore. It doesn’t stop closeness in a relationship, but you do have to find a woman who can look past sex as love .

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after my robotic surgery erection was not possible I tried MUSE and then trimix and trimix does work My orgams now are much more intense for some reasons, and because trimix stays active for over an hour, repeat performances are now the norm. my orgams are dry and have no ejaculate
the trimix takes some advanced planning so spur of the moment events are not possible

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@activesenior15

after my robotic surgery erection was not possible I tried MUSE and then trimix and trimix does work My orgams now are much more intense for some reasons, and because trimix stays active for over an hour, repeat performances are now the norm. my orgams are dry and have no ejaculate
the trimix takes some advanced planning so spur of the moment events are not possible

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That’s awesome! Good for you! I am meeting with a urologist that specializes in ED and going to investigate that. Wish me luck!

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Fellow warriors, you might this study report on the subject interesting.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3735091/

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@robertmizek

Fellow warriors, you might this study report on the subject interesting.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3735091/

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Thanks for that. At least I know now I'm not insane. I have my 3 month post-radiation PSA test in two weeks and am seriously considering stopping ADT after that so I can hopefully be "me" again by the end of the year.

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@robertmizek

Fellow warriors, you might this study report on the subject interesting.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3735091/

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Thanks for sharing that! Here's the money quote:


The role for hormonal treatment initially was restricted to men with metastatic and inoperable, locally advanced disease. Now it has been extended to neoadjuvant or adjuvant therapy for surgery and radiotherapy, for biochemical relapse after surgery or radiation, and even as primary therapy for non-metastatic disease.

So the article seems to be focusing on whether proactive ADT always makes sense for early-stage (non-metastatic) prostate cancer; it's not questioning it for advanced stages.

There's a similar debate over proactive chemotherapy for advanced cancer that's still responding to ADT (castrate-sensitive).

In both cases, the question is whether it's better to hit it hard right at the start, or to avoid interventions that affect quality of life until we're sure they're needed. I suspect the answer to both is "well, it depends…" 😕

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