Prostate Cancer: A Doctor Discussion Guide for Patients and Caregivers
ProstateCancer:A Doctor Discussion Guidefor Patients and Caregivers

Every journey is different
Prostate cancer is a lot to take on. The symptoms – and the questions they raise – may feel too personal to talk about. But in conversations with your doctor, speaking up can make a huge difference in your care.
Whether you or someone you love was just diagnosed or has been managing this for years, no two cases are the same. The more your team knows about your body and your life, the better the plan they can build with you. So get personal. Say the awkward thing. Ask the hard question. This guide can help you get started.

Who’s on your team?
Treating prostate cancer takes a team. Your primary care doctor may have been the first to flag something, but a urologist and oncologist usually join soon after. Nurses, social workers, and mental health counselors can be part of the picture, too.
And sometimes the most important person in the room isn't a doctor at all. Patients say bringing a friend or family member to appointments to take notes and help sort through it all later makes a real difference. Remember, you don't have to do this alone.
What have you noticed?
Even the smallest change can be an important clue. Try bringing a symptom log to your next appointment.
In the last month, have you experienced any of the following?
☐ Bladder or bowel changes (control, frequency, or urgency)
☐ Difficulty achieving or maintaining an erection
☐ Pain in the lower back, hips, pelvis, or ribs
☐ Weakness, numbness, or tingling in the legs or feet
☐ Swelling in the legs or pelvic area
Have you noticed any emotional changes? How you talk about feelings of depression, anxiety, or stress can help give your doctor the full picture.

Your quality of life matters
Prostate cancer can impact every part of your life. When you talk to your doctor, share details about your day-to-day. Help them understand what is most important to you.
- For patients:
- “These side effects keep me up all night, so mornings with my kids are impossible.”
- “This treatment schedule means I’m missing an important weekly meeting at work. Are there any other options?”
- For caregivers:
- “How do we know if a side effect is bad enough to call?”
- “Are there any programs that could connect us to other patients and families?”