Bladder Cancer

Has anyone tried ivermectin or natural treatments for metastatic bladder cancer?

I have bladder cancer that spread, on chemo but it's destroying my body. Has anyone tried ivermectin or other natural products.

What happens when bladder cancer spreads to muscle after TURBT?

Got my third turbt surgery. Apparently there still was 3 tumors on the top of the bladder. After biopsy my doctor informed me that it was now in the muscle. He stated that we need to be agressive about it and mentioned removal of the bladder. I will meet with him to discuss treatment. I am no ready for bladder removal. Do any of you guys went.to the same pass and if so what did you do? While being tired I am feeling fine otherwise.

What are the side effects of chemo before bladder surgery?

Hi, I'm new here. Just diagnosed with two aggressive types of tumors that have invaded the lymphovascular systems of the bladder as well. I am waiting for more scans to check for metastasis so they can do the final staging. I am told at minimum it will be weeks or months of chemo and then bladder removal. Just wondering if others in this situation have already started chemo and what kind of side effects there are.

What are the side effects of EV/Pembro treatment for bladder cancer?

I have been diagnosed with MIBC and starting on Monday with EV/Pembro. Anyone else taking this treatment? What side effects can I expect?

How do you cope with recurring bladder cancer pain and surgery?

Hello my name is Karen, im new here, i was diagnosed with bladder cancer since 2020, I’ve had 10 lazer surgeries since, was in remission for about 8 months, now it’s back😕 Dr stated I have to receive surgery again, I’m not happy, it’s hard, and I be in a lot of pain.The Dr don’t like to give me strong meds, Cancer sucks!

How has Myrbetriq helped with your overactive bladder symptoms?

I've been prescribed Myrbetriq (mirabegron) to help manage overactive bladder symptoms. My doctor explained it works by relaxing the bladder muscle to reduce urgent bathroom trips and frequent urination. They mentioned it might also help with bladder control issues that can happen with cancer or treatments. I'm aware of potential side effects like headache, dry mouth, and constipation, plus my blood pressure will be monitored since the medication can sometimes affect it. I'd love to connect with others who have similar experiences managing bladder symptoms. • How has your daily routine changed since starting treatment for overactive bladder? • What practical tips helped you manage symptoms or side effects?

Has anyone experienced severe digestive issues between cancer treatments?

I'm dealing with some tough digestive issues right now, including severe diarrhea, constipation, and abdominal pain, along with really bad fatigue. I'm not currently on active cancer treatment, but these symptoms are really affecting my daily life. My AI response suggested I contact my oncology team right away to get these symptoms properly evaluated. I'd love to hear from others who have experienced similar digestive problems during their cancer journey. • Have you dealt with severe GI symptoms when you weren't on active treatment? What was that experience like for you? • What helped you manage these kinds of symptoms day to day?

Why do I keep getting bladder tumors and what should I expect?

So, just found out that I have another tumor on the top of my bladder. Explaimg why I have have so much blood and clots in my urine. Need to jave another trust surgery. And God knows what. I am a optimist but this is really putting me down. I need you to get me up where I belong. Lots of love and take care. Life is great!

Has anyone had bladder removal and reconstruction for aggressive cancer?

Anybody had their bladder removed and a new one created? Oncologist is saying this is necessary and no way around it with an aggressive cancer. Is this an appropriate course of action? Is there anything else anyone has done in this case?

What does it mean when bladder mass cells aren't from the bladder?

I have had a mass removed from my bladder. I have been advised cells in mass are not bladder cells. In fact they have not given me clear information on where the cells came from. Labs are unclear. I feel like my Urologist is either not very educated on Cancer or they are not telling me something. Have referred me to oncology. Any advice?