Recently diagnosed & scared

So bottom line is muscle invasive requires bladder removal plus potentially the prostrate and lymph nodes.

I have read a little but damn the more I read the more it scares the shit out of me. Sorry if I am imposing on the community.

Thank you. Makes sense!

Thanks again Alan. I am dealing with my PCP for the other issues. Although my Urologist/surgeon who did my TURBT is highly regarded as a surgeon it seems that everything else goes through his PAs. My PCP is up to speed and reacts quickly. He noticed on my blood work last week that my blood sugar was 147 where right before surgery it was 90. He sent me for some follow up labs to make sure there isn’t any issue.

A couple of quick questions. Is radiation ever done on a bladder that is non muscle invasive? And visa versa with a muscle invasive bladder is radiation ever chosen instead of removal of the bladder?

Somebody test my rationale. If there was spread of cancer to other parts that aligned to the perceived pains, swollen and aches that I have then something would have been potentially identified on my CT scan. Since most symptoms started post diagnosis minus the original urination issues. Sorry to ask you to play psychologist.