CommunitiesProstate CancerWhat's active surveillance like for Stage I prostate cancer?

What's active surveillance like for Stage I prostate cancer?

JO

Community Member

a month ago

I have low-risk, Stage I prostate cancer and my doctor mentioned active surveillance as an option. From what I understand, this means regular monitoring with PSA tests, physical exams, and periodic biopsies instead of immediate treatment like surgery or radiation. The idea is to watch for any changes while avoiding potential side effects from treatment unless the cancer shows signs of getting worse. I'm trying to learn more about what this experience is really like from people who've been through it. If you've chosen active surveillance for similar prostate cancer: • What has the monitoring process been like for you day to day? • How do you manage any anxiety or concerns between check-ups? I'd appreciate hearing about your experiences or any insights that helped you along the way.

3 comments
Comment
CA

Community Member

a month ago

Active surveillance can feel overwhelming at first, but many find it becomes more manageable as they settle into the routine of regular monitoring. The community here has shared valuable experiences about coping strategies during the waiting periods between appointments, and connecting with others who understand this path can provide helpful perspective and support.

BO

Community Member

a month ago

Don't miss anything - my psa went from 3 to 4 & my pcp said “we need to keep an eye on this”… 19 months later, it was at 5.1, went to urologist & have a Gleason score of 8 - advanced prostate cancer - never miss a test, & good luck

TH

Community Member

8 days ago

The word “cancer” changes the way one thinks when they are told they have cancer. I had one of fourteen fusion biopsies showing cancer. My PSA was 12 and my Gleason score was 7. I chose 5 doses of high dose radiation instead of 30 doses of low dose radiation. After it was done it took it down to 5.9, so I chose 2 doses of eligard. The severity of the side effects of either one was unknown to me. I still feel the effects of the radiation, it seemed to have affected my muscles for bowel movements, it’s harder to hold them back and to finish when I am able to get to the bathroom. Needless to say I had to buy more underwear. That side effect has not gone away. After the eligard, it’s hard to explain but I no longer felt like a human being let alone a man. 8 months later I feel something like a human but I have no reactions as to my manhood. I see my oncologist next month. All I can say is the choices we make affect us for the rest of our lives, choose carefully.

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