New diagnosis at 50
Well, I got the news... About 4 weeks ago my Dr told me I had PC. Since then I have, and still go through all the emotions, sad, mad, angry, denial etc... I also have researched my diagnosis, treatment options and next steps(to include reading this forum). I thought I would jump in here with you nice folks instead of just being a tourist. With that being said here is my story. I am 50, My father passed away from PC when he was 72, he was diagnosed at 60 but chose to ignore his disease and also got bad/no info from his provider. My last PSA was 3.9, MRI and biopsy came back with 4/12 cores positive, one less than 10% the other 3 less than 1%, all 3+3 Gleason 6. Had a Polaris report done that puts me at very low risk with a molecular score of 2.2. My Dr is great, and without his proactiveness I probably wouldn't know I had PC. His recommendation is active surveillance, which I fully understand. I don't know if I have the bandwidth to do this.. Im a pretty anxious person by nature so wondering what my cancer is doing seems like a stretch for me. Given my family history I never want to be playing catch up with this disease when I had the chance for probably a cure early. So i'm leaning towards removal, not sure when but in the future. My question(s), Is, am I missing anything? Anybody have a similar story? My Dr said the info that 20-30% of post removal biopsies coming back a higher score is dated and skewed? Feel free to recommend, comment on anything I might have missed etc.. thanks, Pete
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@xahnegrey40 Oh Man, what a terrific post!! If your father had married my mother, they might have produced a whole different species entirely; one that was impervious to tobacco carcinogens: Homo Cigarettis😂.
He sounds like quite a guy and hopefully you too will look back on all this when you’re 101 as well! Best,
Phil
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1 ReactionI was just recently diagnosed with 3+3=6. Waiting on genetic testing to come in to help guide my next decision. My doctor is proposing active surveillance, but like you, I am finding it hard to live with. Not to mention, I still have blood in my semen from the biopsy that was 6+weeks ago and I can't imagine having to continue doing biopsy's and having the blood for this long afterwards. Once I get my genetic marker test back, I will meet with my doctor again. I am also planning on meeting with another doctor to get a second opinion. I feel overwhelmed and not sure what to do. I am glad that I found this board.
@rybread
A large number of doctors do not consider a 3+3 cancer.
You could get a second opinion on your biopsy. Here’s info on a couple of highly respected doctors who do it.
Dr. Epstein biopsy
https://advanceduropathology.com
Dr. Zhou
Send an email to Ming.zhou@mountsinai.org to inquire about a second opinion and ask for his specific instructions for the process.
For a few years, they even stopped testing people for PSA because too many people were being treated when they’re only a 3+3. We now have a lot of advanced cases because of that decision back in 2012.
As for active surveillance, here is some information from some doctors, but discuss who should or should not do it. The second video is from the same doctor that does second opinions.
Here is a video with Dr. Laurence Klotz, one of the experts on active surveillance. He can give you answers as to why you would or would not be a good candidate for active surveillance.
Here is a video by Dr. Epstein discussing active surveillance and more
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1 Reaction@rybread
Listen to jeff Marchi..you are in very good shape..just get PSA test every 6 months...and relax and enjoy life.
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1 Reaction@mtcoastie, checking in. There's so many phrases in your post that I'd like to pull out like the words "lucky and grateful". Yeah, that might be feelings you can feel at some point. But in the moment of hearing the news that you've got cancer and reading the information to sift through to make decisions about your life -- lucky and grateful are not top of mind, right?
"Damned if you do, damned if you don't." True...maybe. But decisions have to be made with the best information you have at the time. Luckily (damn, there's that word again), you have support here and the guidance of your medical professionals.
So, now my question. How are you doing with the treatment decisions? How are you doing with the emotional roller coaster?
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1 Reaction@mjp0512
Love the simile:)
Hello,
I was 46 when I was diagnosed. I am 65 now. Biopsy resulted in 3+3 Gleason. Had my prostate out Gleason was 3 + 4. 17 years of undectable PSA last year posted a 0.1, so now getting more sensitive tests.. bouncing around .1 for the last 18 months. Dr. says I shouldn't worry.
I had an "open" surgery not robotic at Mayo by a highly renowned surgeon. Bladder control very little issues. Sexual function reduced significantly.
I am thankful I had access to testing at an early age.
All the best to you. It's rough stuff at times, but you will have good days ahead.
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5 Reactions@keywest19
My husband had targeted biopsy and was 4+3 pre RP. After surgery pathology showed 4+5 - so... Have no idea what that doctor is mumbling about lol . Some doctors are just full of air, honestly ...
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2 Reactions@colleenyoung honestly, this site is invaluable...not only does it let us PC victims connect with others, but lots of great info here and ways to compare your treatment with what others get..and lastly, of course, lots of hope and even some levity !
thank you for the moderation and keeping order..I have found all the guys here to be very empathetic and courteous with their comments and opinions !
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1 Reaction@stu6060 thank you for the response! Did you immediately have the surgery? Or did you do active surveillance for a little while?