Bladder Cancer Group: Introduce yourself and connect with others
Welcome to the Bladder Cancer support group on Mayo Clinic Connect.
This is a welcoming, safe place where you can meet people living with bladder cancer or caring for someone with bladder cancer. Let’s learn from each other and share stories about living well with cancer, coping with the challenges and offering tips.
Feel free to browse the topics, use the group search to find answers to your questions or start a new discussion.
Pull up a chair. Let’s start with introductions.
What type of bladder cancer were you diagnosed with? What treatments have you had? How are you doing?
Interested in more discussions like this? Go to the Bladder Cancer Support Group.
I should add that the doctor believes the cancer is directly related to my exposure to Agent Orange while in Viet Nam. The VA has given me a 100% disability as a result.
@portugalcass it sounds like you are following a good plan of treatment. They are looking and not seeing cancer which is good. The next step of a CT scan might show more, but planning on a biopsy under anesthesia would most likely give you an answer. The CT scan may also show any anal problem as well. My husband had bladder cancer and went through all these same tests to get a diagnosis.
How soon are you having these things done?
Hi many thanks for advice. Yes I feel as if my walk as dropped in my back passage. When I urinate there seems to be soreness and pressure As if I want to empty my bowels. But I don’t really. Want to. When in bed my feet get so hot and I sweat in between kegs it’s hard to get to sleep. I am now getting up to urinate 4/5 times a night. Only 2 months ago it was only once. Bear in mind I drink up to the time I go to bed. I am going this week for a ct scan. Then the week after they want to explore my bladder and do a biopsy. Of bladder. It’s a shock coz I am a very fit person. It’s hit me like a ton of bricks. Thanks for your advise it seems right. I will post the outcome. Of diognistics. Thanks Neil. .
Welcome, @archer72. The fear of recurrence is understandable. You're not alone in holding that fear sometimes top of mind and other times lurking in the background. I encourage you to start a new discussion about coping with the fear of bladder cancer recurrence.
Have you heard the term scanxiety?
- Scanxiety: How did you get through scanxiety https://connect.mayoclinic.org/discussion/scanxiety/
Makena, you mention persistent UTIs. How long ago did you stop BCG? Might that reduce the risk of UTIs? Will you start any other treatment?
Thank you for your response. Unfortunately I got the UTI from the tech inserting the catheter for BCG and catheter fell out before he put BCG in. He reinserted the same catheter. 2 days later after BCG I got Proteus UTI. 2 rounds of antibiotics and an E Coli too. Now I’m clear of infection. Have started on DMsnnose 1 tsp a day and cranberry pills. So far so good. I just had a clear scan and clear cytology. So now I start the 3 month clock of feeling relief and then a week before next scan the fear takes hold. I feel I am living 3 months at a time. I don’t know if anyone else feels this way. The doctor wants me to try to continue with maintenance BCG in 6 months after my bladder settles down from the UTIs.
Hi. I've just been diagnosed with bladder cancer. Aggressive and invasive. 51 yrs old. I have a new Urologist that found a dark spot on my bladder while I was in the hospital. (So much for my Urologist of 4 yrs) Long story short, I've been referred to another Urologist in the same practice that I meet with Monday. The Urologist that referred me said that it was best for me to have my bladder removed. I'm still in shock with cancer, let alone trying to function in life without a bladder.
@suka1, how did the appointment with the second urologist go? Did they offer additional treatment options?
well today is the day, i get to go in for the bladder check, see if c is back a bit nervous ,
Please let us know how you're doing.
Good luck today!!