Devastated by support group meeting: I'm doing everything wrong

Posted by fritzo @fritzo, 2 days ago

Just absolutely devastated last night during a PC support group meeting. I thought I'd share with the support group (via zoom) that my RP surgery is in four days and was hoping I might get a few words of encouragement before the big day. Instead, this support group session was an informational meeting on Focal Therapy from an expert.

To me, what followed was 90 minutes of medical information with the slant that RP surgery is absolutely a terrible thing to do as first treatment if you can do Focal and that people should start with Focal therapy and not suffer the barbaric side effects of surgery (I'm informed, I know what they are).

I was a zoom participant and my audio was turned off and I never had the chance to say, "Hey guys, I'm doing surgery in few days and now you've got me convinced that everything I'm doing is wrong." I was despondent because I thought I had my mind made up and now experts were saying that was not the right thing to do.

It was a rough night.

Let me explain: This meeting turned out to be entirely a presentation by a director of a Focal Therapy program where they offer five different focal therapies. His program was loaded with fantastic information.

But, one of his key messages that I was taking away is that Focal Therapy for those that qualify is that you don't have to unnecessarily suffer the indignities of impotence and incontinence if you choose focal therapies...or at least much less risk. They assess your case and then pick the most appropriate focal therapy. Later, down the road, if your PSA starts going up, you still have the full option of RP. But, another key theme is that you really want to avoid RP because of the horrific side effects. So, explore this new, modern approach that is the forefront of treatment that is Focal Therapy.

At the end of the session, the moderator saw I was waving my arms (my audio was muted from the feed during the entire session) and leaned in to see that I wasn't waving goodbye...I was upset. He could kind of hear me. At first, the discussion was like if you're not 100 percent confident with your decision, then contact your doctor and get more info and if not confident, cancel the surgery....even it it's as late as rolling in the operating room.

However, he very graciously got my phone number and called me directly, which I'm super appreciative. We were able to talk more. At first, it was an assessment of whether I would be a candidate for Focal Therapy (contained to one lobe of the Prostate, no spread). So, yeah, I probably could be a candidate. But, then I think he realized that an entire session on Focal and how glorious it is with no opportunity for "support" from the group for those at a surgery turning point could have left me "conflicted' just days before my surgery.

I reached out to a PC buddy who was really helpful. He shared his journey and some of his thought. The turned out to be a real lifeline.

I'm still conflicted, but thinking I'm going forward with my surgery. Holy smokes, that was not what I needed from a "support" group days before surgery to be convinced that I'm doing the absolutely wrong thing.

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

Profile picture for clevelandguy @clevelandguy

@ctsenior
The new one incision hole surgery is suppose to dramatically lessen the amount of nerve damage. There are lots of men who have had surgery that have recovered and have a useable member. I would not take the risk on focal therapy because long term data does not support its use. “Need for Retreatment: About 20% of men may require additional treatments (either a repeat focal session or whole-gland treatment) within 5 years. “. (From the Cleveland clinic). Surgery cure is about the 91-95% range. Sad to say there are no guarantees, but more based on a case by case by competent surgeon and oncologists.

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@clevelandguy Yeah, the one incision approach sounds ideal. And, that's really good to know about Focal. It's good that it's an option and I sure hope that it gets better and better as they figure out what works and what doesn't. Much appreciated!

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Profile picture for brianjarvis @brianjarvis

My view on this is a bit different.

First (as you have just found out), there are different types of “support” groups out there. Many do offer “encouragement,” and will nod “yes” and agree with everything I say. (I have not found those to be useful.)

Others provide “support” in providing the latest diagnostic and therapeutic information, for me to then digest and consider, and (perhaps) to discuss with my medical team to see if it would improve my treatment outcomes (I have found those to be very useful.)

And finally, other “support” groups have their own agenda, either to promote (or demote) a particular treatment or protocol, or simply to be critical of whatever path others have chosen. (I have not found those to be useful.)

(I regularly attend two in-person support groups, and irregularly attend five virtual suppirt groups.)

That said, if you’re already that close to getting a prostatectomy, there shouldn’t have been anything said at that Zoom meeting that you hadn’t already known about and already considered in making your treatment decision.

> you should already know all the facts about RP.

> you should already know all the facts about focal therapies.

> you should already know all the facts about (external and internal) radiation therapies.

At this point, this close to going under the knife, there should have been nothing that expert could have said that would make you conflicted or despondent because you thought you had your “…mind made up and now experts were saying that was not the right thing to do.” So, regardless of what that Focal Therapy expert said, you should have already looked into that option and known (at least most) of what he was saying.

I would simply ask you to consider whether you’re confident that the treatment choice you’ve made is the right one for you? If the answer is “yes,” then absolutely go for it. If the answer is anything other than “yes,” then you probably need to step back and think this through. (When I decided to have proton beam radiation therapy, I had spent at least a couple of years accumulating information and evaluating treatment options. When I finally made my decision, that was it. As much as anyone can be certain, I was confident that was the right choice for me,)

Even though I didn’t have focal therapy (because of the nature of my disease, I was not a candidate), I do sort of agree with his one point —> If you’re not confident with your decision, then contact your doctor and get more info…..

This is an important decision you’re making; possibly the most important decision you’ll ever make. And, you’ll have to live with this decision for the rest of your life. It’s not possible to be 100% certain, but you should be as certain on this decision as you have ever been on any decision you’ve ever made. Again, if you’re good with it, go for it.

Exactly 5 years ago today (April 19, 2021), I started my 28 sessions of proton beam radiation; I had already had my Eligard injection and the SpaceOAR Vue insertion. I was confident it was the right decision for me then; today (5 years later), I’m still convinced (and relieved?) that everything has gone as well as we had expected and planned.

Good luck as you proceed on your journey.

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@brianjarvis Hey Brian, which of the virtual support groups do you find you like the best?
(there are no local support groups in my area, so it is virtual for me)

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Profile picture for clevelandguy @clevelandguy

@fritzo
Hi, From the information I have read the success rates of both surgery and radiation are about the same. Both are in the mid 90% for localized process cancer. It’s more of a case by case depending on lots of factors. If you have cancer contained in the prostate and you have an experienced surgeon you should be fine. Sad to say there are no guarantees.

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@clevelandguy Yeah, no guarantees in life for sure. But, gonna roll with those 90 percent odds and try and beat the house.

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Profile picture for dinu @dinu

@fritzo ,

also after the surgery those groups are very helpful. Just cause you had surgery does not mean that the problem is gone. Depending on your surgery outcome you may end up with additional radiation or ADT treatment.
Just like me. I am waiting for the official pathology results from the surgery, hopefully this week I will get the results and then the plan moving forward can be defined. I am still continuing my ADT which i started before the surgery, but it will most likely be augmented with RT.

Looking forward to hear back from you once you get back from surgery.

Stay strong and be positive!
Dinu

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@dinu Dinu, wishing you good news and the strength to handle anything that is to come.

Uncertainty seems to be the one certain thing we can count on during this journey. I think the other certainty is that there are really good people we never knew before who help us all get through. Safe travels!

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Profile picture for wheel1 @wheel1

@fritzo
I am so happy to hear of your wife. I am sure that you were quite frightened as I would be, way more for your spouse than you could ever be for yourself. It is so true to keep the ball rolling as new treatments continually reach the opportunity for all of us to continue to just keep the ball rolling.

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@wheel1 Yeah, my wife is currently a basket case because she is used to being the patient, not me. I've had to keep a stiff upper lip so as not to pull her down to much. So, thankful for this community so I can fully vent.

Ball is definitely rolling, but I might just be Indiana Jones in Raiders of the Ark
https://tenor.com/bDWht.gif

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Profile picture for wheel1 @wheel1

@fritzo
It sounds like your surgeon is still ahead of the game with this surgical approach similar to the goals of Retzius sparing technique. It is unfortunate so many surgeons are old schooled. I still hear about open prostatectomies. I first started sharing about the new technique I was getting prepared for close to two years ago and it had been around but most knew nothing about it. Your surgeon seems also intent upon minimizing side effects from the surgery and is up to date on newer techniques. I think you will be find and hope you update quickly after your surgery. Best of luck

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@wheel1 Can't tell you how much of a deep dive on surgical approaches, but had not learned of the one-incision approach until you're earlier post on it. Wish I had seen it earlier, but I think I'm still with a good team. (Northwestern) Thanks much!

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Profile picture for guybe @guybe

@surftohealth88 Good note about "promoting". And even without that crass motive, we can never forget that our doctors are human, subject as professionals to the need to know "facts" and hold onto them, sometimes before they deserve the name or in the face of (at least initial) counter evidence. It's just human, especially among people who are esteemed for a particular body of knowledge. One "tell" that this is happening may be when we observe enthusiasm - an emotion - come into a doctor's recommendation. I appreciate professionals who give me objectivity and leave the emotion to me and my loved ones. We have plenty as it is.

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@guybe So true, we have plenty of emotion already....just most of it is suppressed most of the time. But, this stupid disease can force it to the surface.

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Profile picture for Jeff Marchi @jeffmarc

@fritzo
I was at the UCSF conference today and Dr. Cooperberg gave a talk about focal therapy

He said this in November

At the 11/1/2025 PCRI conference the following was said by Matthew R. Cooperberg, MD, MPH Urologic Oncologist UCSF

What about focal therapy?
* The energy modality matters much less than the accuracy of the imaging - which is not there yet.
* Overall focal therapy is associated with minor side effects, but high rates of recurrence both in- and out-of-field.
* Focal therapy is not really a replacement for surgery or radiation; it is better considered an adjunct to active surveillance

He reinforced it today. He felt that people who had more than a 4+3 or had lesions in both sides of their prostate should not even consider it. Here’s a bunch of information from his today’s presentation.

Some information from today’s slides

UCSF Results: first 135 HIFU patients
• 54% recurrence (41% in-field)
• 4% progression by 1 year, 16% overall
• IPSS (urinary obstruction) 6 before, 6 after
• SHIM (erection function) 16 before, 13 after (p=0.11)
• Major drivers of recurrence: GG3, high Decipher

Trade-offs
• Overall focal therapy is associated with minor side effects, but high rates of recurrence
• Inadequate energy delivery?
• Inadequate field of treatment?
• New cancer development?
• Others?
• Understanding the high recurrence rates and trying to improve them is a major area of research focus.
• Focal therapy does not burn bridges: RP, RT, even additional focal therapy are possible if necessary

Summary thoughts
•Focal ablation has a growing role for very carefully selected cases.
• Side effects rates are low but recurrence rates are high. GG3 and high Decipher are warning signs, as are high PSAD and bilateral disease.
• Focal therapy is an adjunct to active surveillance; additional treatment may well be needed down the road, but these treatments are still possible after focal.

University of California Consensus
1. Focal therapy must be acknowledged to be investigational
2. Focal therapy should be done under trial or research protocols as much as possible
3. Candidates should have at least 10 year life expectancy, GG2 or low-volume GG3, stage T1 or 2, and PSA < 10 or PSA < 20 and PSAD
< 0.15
4. Candidates need an MRI-guided confirmatory biopsy before treatment
5. Follow-up biopsy at 12 months is essential

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@jeffmarc
Just read thru this again. Reminds me why I am glad that I was not eligible for HIFU. Tulsa Pro is much more precise due to the MRI guidance. I met all the criteria under the California consensus and remain very happy with my choice.
This is great information for men to keep asking questions and researching whatever treatment is recommended.

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Profile picture for fritzo @fritzo

@ctsenior Yeah, from what I hear, it's seems like it's 90 percent of RALP men end up limp. And, yes, I have been a bit obsessed about that. Thanks for the advice...good to have options for sure.

I'm 63, but I think of myself still as young. I know others look at my gray beard and probably think otherwise. I almost think Focal would be great for old men too...because if you want to kick the can down the road a bit and then do the heavy recurrence treatments, you still can.

If you're old, you probably aren't a candidate for surgery, so Focal might be great and then follow with radiation/ADT when it comes back.

Based on the info shared by @jeffmarc (thank you again!) from the UCSF Prostate conference on this Friday; UCSF finds on recurrence with focal was really staggering. "Overall focal therapy is associated with minor side effects, but high rates of recurrence both in- and out-of-field."

This bullet point from the presentation really seemed like a shocker....the UCSF Result for their first 135 HIFU patients was: "• 54% recurrence (41% in-field)."

Recurrence is higher than 50 percent, so that means you will have to follow with surgery/radiation/ADT or whatever choice you have. So, I'm guessing it does buy you time, but perhaps spread becomes worse. I don't know.

I really do appreciate that reality check. Yeah, dick at half or no mast, coming up. Sucks. But as a long-time buddy of mine told me this week who has complete ED but is cancer free after eight years , his decision was to chose life over cancer Hoping to do the same...

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@fritzo If you choose radiation vs. RALP, there is only a small limp dick possibility. But radiation entails ADT which is no fun.

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Profile picture for fritzo @fritzo

@brianjarvis Hey Brian, which of the virtual support groups do you find you like the best?
(there are no local support groups in my area, so it is virtual for me)

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@fritzo Virtual support group meetings that I sometimes attend:
> Each Wednesday: 7:00PM (ET): an independent support group (I like this one because it’s not affiliated with an institution; they can speak more freely and openly.)

> 1st Wednesdays: 7:00PM (ET): Affiliated with Zero. A good one for beginners; a bit too warm & fuzzy for me, but I do stop in once in a while to listen for anything new.

> 2nd Wednesdays: 1:00PM (ET): Affiliated with Mayo Clinic. Always informative.

> Last Wednesdays: 7:00PM (ET): Cancer Support Center (Cincinnati/Northern Kentucky). A good place to tell your story and listen to others’ stories.

> 3rd Mondays: 5:30PM (ET): Ackerman Cancer Center. A small group; most attendees have had proton radiation (like I had). They serve pizza to the in-person attendees; bring your own if you’re virtual.

> 4th Mondays: 4:00PM (ET): Duke University. Well moderated.

Also, Zero, PCRI, AnCan, and other groups hold other regular virtual sessions or sponsor conferences.

Each month I search Eventbrite for free upcoming virtual PCRI presentations worldwide; I only listen in on those (unless I’m asked a question).

And I attend two local in-person support groups and sometimes a third one.

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