What were your symptoms of Bladder cancer? Scared I have it.
Two years ago I started to have pelvic pain. Many ultrasounds later I dragged on by my gyneo who eventually changed her mind and sent me to urology. I’ve been peeing blood clots and have micro hematuria. Also been peeing mucus, white and black sedement. I still have pelvic pain.
Going to finally get a urinary and kidney ultrasound and a cystoscope come November.
I honestly am terrified and feel like I already have cancer and that it’s too late for me. That I’m destined to die.
Any stories or reassuring testimonies?
Interested in more discussions like this? Go to the Bladder Cancer Support Group.
Thank you so much! I can see why we all needed it shortened!
Transurethral resection of bladder tumor (TURBT
What do the letters stand for, please?
The surgery when they remove the tumor from inside the bladder
What is TURBT?
I went back for my cystoscope today 11th praise God no cancer go back in three months
for
Thanks doe drawing this to my attention I will ask for this to
be done
I would ask them to also do cytology on that urine specimen, that was the first test I had that was positive for cancer cells. I lost almost 3 weeks being treated twice for urine infections and having cultures, before they finally checked my urine for cancer cells.
My only symptom was gross blood in my urine; I mean bright to dark red blood. I was treated for bladder infections twice with antibiotics and forcing fluids. After the second failure of that treatment, I had a cystoscopy which was clear. Then I had a urine work up and that came back positive for cancer cells in my urine.. I think that was cytology.. not sure.
Since the bladder was clear, they did a scan of my abdomen which was positive for a tumor in my left kidney pelvis. Biopsy came back as Urothelioma in the pelvis lining.
On June 18th, 2025, I had my kidney and ureter removed. We thought that was going to be it, but the biopsy on my kidney after it's removal caused them to change my tumor from T0 to T3, from low grade to high grade and from noninvasive to invasive. Only 7% of kidney cancers are urothelioma, and that's what mine is.
I was stunned, all the doctors were so positive it would be a cure after removing the kidney. Suddenly, I am talking to an oncologist about treatment options. They are recommending chemo, but I also can opt to watch and wait. immunotherapy is not recommended for me due to some other health issues I have.