Just Diagnosed With Prostate Cancer

What treatment did you choose for Stage IIB prostate cancer?

I was recently diagnosed with Stage IIB unfavorable intermediate-risk prostate cancer. My oncologist explained that I have several treatment options available, including different types of radiation therapy (external beam or internal seeds) combined with hormone therapy, surgical removal of the prostate with lymph node examination, or careful monitoring. They mentioned that the best approach will depend on my overall health, preferences, and specific cancer characteristics. I'd love to connect with others who have faced similar treatment decisions for Stage IIB prostate cancer. • What factors helped you decide between radiation, surgery, or monitoring? • What do you wish you had known when weighing these treatment options?

What helped you choose between active surveillance and treatment for low-risk prostate cancer?

I was recently diagnosed with low-risk, Stage I prostate cancer. My doctor explained that I have several treatment options available, including active surveillance (careful monitoring), surgery (radical prostatectomy), and different types of radiation therapy like external beam radiation and brachytherapy. It's reassuring to know that all of these approaches are considered equally appropriate for my situation, but I'm still trying to figure out what might be the best path forward for me. I'd love to hear from others who've been in a similar position with low-risk prostate cancer. • What factors helped you decide between active surveillance and active treatment? • If you chose treatment, what was your experience like with recovery and daily life afterward?

What's the difference between active surveillance and observation for low-risk prostate cancer?

I have very low-risk prostate cancer and my oncologist mentioned two monitoring approaches: active surveillance and observation. From what I understand, active surveillance involves more frequent check-ups with PSA tests, exams, and periodic biopsies to closely track any changes. Observation uses less intensive monitoring with visits up to once a year and focuses more on symptom management. I'd love to hear from others who have been in a similar situation and what your experience has been like with either approach. • If you chose active surveillance or observation, what has your monitoring schedule been like? • What factors helped you decide between the two approaches?

What does a Gleason score of 6 mean for my prostate cancer diagnosis?

Recently diagnosed. I think my Gleason score was 6 . My PSA has risen from a 5.9 to 7.3 in a 6 month period. Looking for answers / knowledge/ information. My day has been filled with nothing but anxiety and panic attacks to the extreme. I don't know where it came from but holy Jesus can't shake it.. praying for all because it helps.

Why did my cancer come back and what should I do next?

Hello, My cancer has returned!

Should I choose surgery or radiation for Gleason 7 prostate cancer?

I just started ADT therapy and I just saw my radiation oncologist try to get a second opinion about whether to do surgery or radiation.The doctor was nice and he told me either way you can go by looking at my chart and all my PET scan results he didn't see a problem with either one. He said that with radiation and be a little longer a little more dragged out then the surgery. And he told me the side effects of both. He says my Gleason score is 4+3=7 and my low PSA of 8 doesn't think it's spread so he would not automatically do lymph nodes. Still up in the air about both. Anyone has or knows a similar situation like mine to give me some advice.

What are the best treatment options for Gleason 4+3 prostate cancer?

Just diagnosed. I have a 4 + 3 Gleason Score. Have appointments with a medical and radiation oncologist at Dana Farber in Boston scheduled in a couple of weeks. I am thinking either prostatectomy or seed implantation. But will speak with the oncologists and see.

How long is normal to wait for an oncologist appointment after diagnosis?

Just diagnosed. Stage 4 and spread to my lymph nodes. Oncologists seemed to be backup. The soonest they can get me in is end of October. Seems way too long and I’m freaking out a bit. Anyone else still waiting? Is this normal??

How can I support my sons after prostate cancer diagnosis at 89?

Writing for my husband who was Just diagnosed and can't do for himself. Age 89 and prostate cancer has spread. Want information on quality of life ahead, what to expect and how to helpour sons to deal with their own life and health of their prostate in future.

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