What is the average age of the gentlemen on here?

I'm a 52 year old hispanic; I was diagnosed in June of 2022 with prostate cancer, there were no previous cases of prostate cancer in my immediate family. I went to the ER one day for some abdominal pain, the doctor did an MRI of abdomen/pelvic area and found that I had an umbilical hernia but noticed on the MRI that my prostate was slightly enlarged which tends to occur as we age anyway; she said she'd order a PSA test as I hadn't had one before that I was aware of. The PSA came back high at 29; I then saw my primary doctor who did a digital rectal exam and was able to feel what she thought may be a nodule, she referred me to a urologist. The urologist also felt the same nodule and scheduled me for an ultrasound needle biopsy in which 9 of the 14 samples taken came back as cancerous, the highest Gleason scored being 4+4=8. I had not been exhibiting any signs/symptoms of prostate cancer that I was aware of. Due to my fairly young age and aggressiveness of my cancer, the urologist recommended and discussed w/me a Radical Prostatectomy; she also referred me to Mayo Clinic for a 2nd opinion as well as to a radiation oncologist and medical oncologist for their opinions. The radiation oncologist recommended radiation and hormone therapy, the medical oncologist said both RP and radiation/hormone therapy were viable options. All doctors explained to me pretty thoroughly I believe, the side effects and pros and cons of all; it was a lot of overwhelming information as you all know. In the meantime, the urologist scheduled me for an CT scan of abdomen and a bone scan. I asked the radiation oncologist about a PSMA scan and he said that it was actually newly available in Santa Fe, NM where I live; after a bit of back and forth with my insurance, I was approved for a PSMA scan. The CT, bone scan and PSMA all came back fine. In my consult with Mayo, in which they had all my records, the two Urologist's I spoke to via zoom also recommended a RP. After much research online, many questions to doctors and many sleepless nights, I finally decided on a Da Vinci robotic radical prostatectomy which my urologist/surgeon would perform; I also asked for an MRI of prostate before the surgery at the recommendation of the Mayo Clinic urologist to see if any spread outside the prostate was indicated; the MRI came back fine. I had a RP on Aug. 18, 2022 which went well; yes, recovery was painful and catheter was awful and I did get a MRSA UTI which took 3 rounds of antibiotics while I had the catheter and more antibiotics after the catheter was removed. After the surgery, the 7 lymph nodes removed came back negative for cancer as well as all the margins of the prostate. The Gleason score went from a 4+4=8 to 4+3=7. I did have trouble urinating after the catheter was removed in which the stream was weak and quite thin, felt like I was urinating through a pinhole. From my research I told my urologist that I felt I had developed a stricture, I was sent to PT for pelvic exercises, etc. to help with urinary incontinence and to see if my urinating issue would improve. The physical therapy did seem to be improving the urinary incontinence; however, I was still having issues urinating and one morning, I couldn't pee and panicked. I had to manipulate the end of the penis which allowed urine to come out slowly. (during the time of trouble urinating, the stream would also sometimes shoot in different directions.). My urologist scheduled me for a cystoscopy which is done in the urologist office; however, the urologist was unable to insert the scope into the urethra, she tried stretching urethra with metal devices as well as a wire device but no luck. ugh! She said she thought it may indeed be a stricture and scheduled me for surgery a few days later as she'd have to put me under to do a cystoscopy and MRI of the urethra. After the surgery, she found that I actually had developed a meatal stenosis which was causing the urinating problems. (meatal stenosis likely caused by the catheter). The stenosis was stretched out and so far I've been able to urinate fine; if it returns, the urologist said she can do another surgery which should correct it. I had my PSA test in November, 3 months after the surgery which thankfully came back as undetectable. I'll have another PSA test now in Feb. which I'm hoping and praying will also be undetectable. I'm still having some urinary incontinence 5 months after surgery but it's improved a lot. I use maybe one pad/day and I've been able to go without a pad some days as well. I believe the physical therapy and continuing the stretching of pelvic area muscles and the Kegel exercises have helped me. I also do walking daily and am hoping to get back to playing tennis. I unfortunately still have erectile dysfunction and at 52 years old, yes, it sucks but I'm dealing with it and am hoping for improvement. I've not yet tried pills, injections or penis pump but will be discussing with urologist. Sorry for such a long rant and maybe too much information but the more information we have, the better I believe. When I was first diagnosed I felt so lost and would have been grateful for any information from people that had dealt with prostate cancer already. I wish everyone well with their journey through this awful cancer.

I'm a 52 year old hispanic; I was diagnosed in June of 2022 with prostate cancer, there were no previous cases of prostate cancer in my immediate family. I went to the ER one day for some abdominal pain, the doctor did an MRI of abdomen/pelvic area and found that I had an umbilical hernia but noticed on the MRI that my prostate was slightly enlarged which tends to occur as we age anyway; she said she'd order a PSA test as I hadn't had one before that I was aware of. The PSA came back high at 29; I then saw my primary doctor who did a digital rectal exam and was able to feel what she thought may be a nodule, she referred me to a urologist. The urologist also felt the same nodule and scheduled me for an ultrasound needle biopsy in which 9 of the 14 samples taken came back as cancerous, the highest Gleason scored being 4+4=8. I had not been exhibiting any signs/symptoms of prostate cancer that I was aware of. Due to my fairly young age and aggressiveness of my cancer, the urologist recommended and discussed w/me a Radical Prostatectomy; she also referred me to Mayo Clinic for a 2nd opinion as well as to a radiation oncologist and medical oncologist for their opinions. The radiation oncologist recommended radiation and hormone therapy, the medical oncologist said both RP and radiation/hormone therapy were viable options. All doctors explained to me pretty thoroughly I believe, the side effects and pros and cons of all; it was a lot of overwhelming information as you all know. In the meantime, the urologist scheduled me for an CT scan of abdomen and a bone scan. I asked the radiation oncologist about a PSMA scan and he said that it was actually newly available in Santa Fe, NM where I live; after a bit of back and forth with my insurance, I was approved for a PSMA scan. The CT, bone scan and PSMA all came back fine. In my consult with Mayo, in which they had all my records, the two Urologist's I spoke to via zoom also recommended a RP. After much research online, many questions to doctors and many sleepless nights, I finally decided on a Da Vinci robotic radical prostatectomy which my urologist/surgeon would perform; I also asked for an MRI of prostate before the surgery at the recommendation of the Mayo Clinic urologist to see if any spread outside the prostate was indicated; the MRI came back fine. I had a RP on Aug. 18, 2022 which went well; yes, recovery was painful and catheter was awful and I did get a MRSA UTI which took 3 rounds of antibiotics while I had the catheter and more antibiotics after the catheter was removed. After the surgery, the 7 lymph nodes removed came back negative for cancer as well as all the margins of the prostate. The Gleason score went from a 4+4=8 to 4+3=7. I did have trouble urinating after the catheter was removed in which the stream was weak and quite thin, felt like I was urinating through a pinhole. From my research I told my urologist that I felt I had developed a stricture, I was sent to PT for pelvic exercises, etc. to help with urinary incontinence and to see if my urinating issue would improve. The physical therapy did seem to be improving the urinary incontinence; however, I was still having issues urinating and one morning, I couldn't pee and panicked. I had to manipulate the end of the penis which allowed urine to come out slowly. (during the time of trouble urinating, the stream would also sometimes shoot in different directions.). My urologist scheduled me for a cystoscopy which is done in the urologist office; however, the urologist was unable to insert the scope into the urethra, she tried stretching urethra with metal devices as well as a wire device but no luck. ugh! She said she thought it may indeed be a stricture and scheduled me for surgery a few days later as she'd have to put me under to do a cystoscopy and MRI of the urethra. After the surgery, she found that I actually had developed a meatal stenosis which was causing the urinating problems. (meatal stenosis likely caused by the catheter). The stenosis was stretched out and so far I've been able to urinate fine; if it returns, the urologist said she can do another surgery which should correct it. I had my PSA test in November, 3 months after the surgery which thankfully came back as undetectable. I'll have another PSA test now in Feb. which I'm hoping and praying will also be undetectable. I'm still having some urinary incontinence 5 months after surgery but it's improved a lot. I use maybe one pad/day and I've been able to go without a pad some days as well. I believe the physical therapy and continuing the stretching of pelvic area muscles and the Kegel exercises have helped me. I also do walking daily and am hoping to get back to playing tennis. I unfortunately still have erectile dysfunction and at 52 years old, yes, it sucks but I'm dealing with it and am hoping for improvement. I've not yet tried pills, injections or penis pump but will be discussing with urologist. Sorry for such a long rant and maybe too much information but the more information we have, the better I believe. When I was first diagnosed I felt so lost and would have been grateful for any information from people that had dealt with prostate cancer already. I wish everyone well with their journey through this awful cancer.

I'm a 52 year old hispanic; I was diagnosed in June of 2022 with prostate cancer, there were no previous cases of prostate cancer in my immediate family. I went to the ER one day for some abdominal pain, the doctor did an MRI of abdomen/pelvic area and found that I had an umbilical hernia but noticed on the MRI that my prostate was slightly enlarged which tends to occur as we age anyway; she said she'd order a PSA test as I hadn't had one before that I was aware of. The PSA came back high at 29; I then saw my primary doctor who did a digital rectal exam and was able to feel what she thought may be a nodule, she referred me to a urologist. The urologist also felt the same nodule and scheduled me for an ultrasound needle biopsy in which 9 of the 14 samples taken came back as cancerous, the highest Gleason scored being 4+4=8. I had not been exhibiting any signs/symptoms of prostate cancer that I was aware of. Due to my fairly young age and aggressiveness of my cancer, the urologist recommended and discussed w/me a Radical Prostatectomy; she also referred me to Mayo Clinic for a 2nd opinion as well as to a radiation oncologist and medical oncologist for their opinions. The radiation oncologist recommended radiation and hormone therapy, the medical oncologist said both RP and radiation/hormone therapy were viable options. All doctors explained to me pretty thoroughly I believe, the side effects and pros and cons of all; it was a lot of overwhelming information as you all know. In the meantime, the urologist scheduled me for an CT scan of abdomen and a bone scan. I asked the radiation oncologist about a PSMA scan and he said that it was actually newly available in Santa Fe, NM where I live; after a bit of back and forth with my insurance, I was approved for a PSMA scan. The CT, bone scan and PSMA all came back fine. In my consult with Mayo, in which they had all my records, the two Urologist's I spoke to via zoom also recommended a RP. After much research online, many questions to doctors and many sleepless nights, I finally decided on a Da Vinci robotic radical prostatectomy which my urologist/surgeon would perform; I also asked for an MRI of prostate before the surgery at the recommendation of the Mayo Clinic urologist to see if any spread outside the prostate was indicated; the MRI came back fine. I had a RP on Aug. 18, 2022 which went well; yes, recovery was painful and catheter was awful and I did get a MRSA UTI which took 3 rounds of antibiotics while I had the catheter and more antibiotics after the catheter was removed. After the surgery, the 7 lymph nodes removed came back negative for cancer as well as all the margins of the prostate. The Gleason score went from a 4+4=8 to 4+3=7. I did have trouble urinating after the catheter was removed in which the stream was weak and quite thin, felt like I was urinating through a pinhole. From my research I told my urologist that I felt I had developed a stricture, I was sent to PT for pelvic exercises, etc. to help with urinary incontinence and to see if my urinating issue would improve. The physical therapy did seem to be improving the urinary incontinence; however, I was still having issues urinating and one morning, I couldn't pee and panicked. I had to manipulate the end of the penis which allowed urine to come out slowly. (during the time of trouble urinating, the stream would also sometimes shoot in different directions.). My urologist scheduled me for a cystoscopy which is done in the urologist office; however, the urologist was unable to insert the scope into the urethra, she tried stretching urethra with metal devices as well as a wire device but no luck. ugh! She said she thought it may indeed be a stricture and scheduled me for surgery a few days later as she'd have to put me under to do a cystoscopy and MRI of the urethra. After the surgery, she found that I actually had developed a meatal stenosis which was causing the urinating problems. (meatal stenosis likely caused by the catheter). The stenosis was stretched out and so far I've been able to urinate fine; if it returns, the urologist said she can do another surgery which should correct it. I had my PSA test in November, 3 months after the surgery which thankfully came back as undetectable. I'll have another PSA test now in Feb. which I'm hoping and praying will also be undetectable. I'm still having some urinary incontinence 5 months after surgery but it's improved a lot. I use maybe one pad/day and I've been able to go without a pad some days as well. I believe the physical therapy and continuing the stretching of pelvic area muscles and the Kegel exercises have helped me. I also do walking daily and am hoping to get back to playing tennis. I unfortunately still have erectile dysfunction and at 52 years old, yes, it sucks but I'm dealing with it and am hoping for improvement. I've not yet tried pills, injections or penis pump but will be discussing with urologist. Sorry for such a long rant and maybe too much information but the more information we have, the better I believe. When I was first diagnosed I felt so lost and would have been grateful for any information from people that had dealt with prostate cancer already. I wish everyone well with their journey through this awful cancer.

Layperson response.

Mixed bag: RP recovery excellent; surgical margins clear; lymph nodes & seminal vesicles clear; surgeon optimistic.

Unfortunately, postop pathology reported Gleason grade 9; extra prostatic extension (EPE), which I understand as cancer cells outside prostate but within surgical margins, indicating aggressive cancer characteristics.

1st 90 day PSA a very disappointing 0.19 (repeated 0.18).

Rad Onc recommended radiation to pelvic floor (38 txs) and 4 mos hormone therapy. Begin tomorrow with Orgovyx. Radiation next Friday.

However, 2 friends with 7s doing great post RP w/ PSAs below 0.1.

Hopefully difference is aggressive nature of my cancer vs theirs, and hopefully your🤞🙏

Best wishes.

I am 56 and diagnosed with Gleason 7 (4/3) in September 2022. Had RP on November 3, Pathology looked good, nothing found in 6 lymph nodes or seminal vesicles. Now, awaiting my 3-month post RP PSA check Even though the post RP pathology looked good, I am quite anxious for my PSA check, praying for PSA to be undetectable/near 0.
Question, has anyone been in my situation (clear pathology post RP), only to be surprised with increasing PSA?

Happy New Year and hope everyone had a wonderful X-Mas/Holiday Season.

Honestly I do not like the Lupron. It is what was recommended for treatments. I have had 2 of the 3 month injections. The 2nd injection hit me hard. My muscles are sore. My bones ache. My libido went straight to zero. Testicles are a lot smaller than usual. I do have a little bit of the "Hot Flashes" but not too bad. This is taking it's toll on me. I am very active and hands on. It doesn't take much to run out of energy, and my leg muscles get sore and tired very quickly. Hopefully this all starts to recover after this last shot wears off.