Total inability to have an orgasm post radiation
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.
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I understand. The oncologist wants me to be on Orgovyx and Zytiga for 20 more months because of the aggressive nature of the cancer. I’m tolerating it well enough but if my quality of life degrades to the point that it becomes unsatisfactory I may have to revisit the issue.
I'm a sample size of one (so statistically highly unreliable), but my experience is that ADT and ARSI since 2021 have become easier to tolerate over time, not harder.
I guess that's lucky, since it looks like I'll be on them forever, barring any new medical breakthroughs.
Upate: I saw my general practitioner today. He recommended trying a supplement called "Horny Goat Weed" and said several of his patients have sworn by it. I've asked my oncologist if it's safe to take with Orgovyx and am waiting to hear back. A couple others have also suggested pelvic floor therapy so I'm looking into that as well.
Pelvic floor therapy (including kegels) can be a big help. If your insurance covers physiotherapy, you can find someone who specialises in pelvic floor recovery.
Is there data to support that this supplement is safe for PC patients to take? If so what's your source?
Thank you.
I don't have any data about this supplement. That's why I'm waiting to hear back from my Onco.
Well, I just read in a British journal that this side effect occurs up to 50% of the time in men who have radiation therapy and can be permanent. I feel really angry that no mention was made of this by either the radiation oncologist or the medical oncologist. Both did point out that ED was a common side effect but was treatable. Neither mentioned total, permanent loss of orgasm. I can't even find this mentioned in U.S. medical journals, just British ones. I feel like I've been deceived and lied to.
Guess I'm in the unlucky 50% and it is permanent. I too was never informed if this possibility when I had the 5 treatment SBRT. It could be explained away since I had it almost 4 years ago (9/2000). However, if I was told about the odds, I would have probably still rolled the dice.
Lucky to live in Phoenix Arizona and don't need to go to a sauna. I just walk out my back door at this time of year.
Really? 50%?
That doesn't seem right to me...
Could you give a link to that British journal?