Late last year, after unsuccessfully trying an Interstim implant, and after a long overdue MRI, my urologist told me that my bladder was "fibrotic".
He didn't, couldn't, or wouldn't tell me much else, and I'm still trying to get a handle on what it means to have a fibrotic bladder. Are the treatments for an IC bladder similar to any treatments for a fibrotic bladder?
After nine months on Elmiron it's rare for me to have much pain inside my bladder. By far the worst of my symptoms and the one that badly limits my life is a chronic need to urinate, up to fifty times a day. That need typically surfaces ten minutes arfter the previous urination, and gets painful pretty quickly. Attempts to regulate my voiding hasn't accomplished anything at all.
I'm also wondering if having a fibrotic bladder simply means that with a reduced ability to store urine, that there's simply no chance that I'll be able to lengthen the times between voiding and lead anything like a normal life again.
I stopped posting last year because I got very depressed about this and other news, and about the lack of change in my symptoms, but I hope everyone is doing well, and always appreciated the support I got on this site.
He didn't, couldn't, or wouldn't tell me much else, and I'm still trying to get a handle on what it means to have a fibrotic bladder. Are the treatments for an IC bladder similar to any treatments for a fibrotic bladder?
After nine months on Elmiron it's rare for me to have much pain inside my bladder. By far the worst of my symptoms and the one that badly limits my life is a chronic need to urinate, up to fifty times a day. That need typically surfaces ten minutes arfter the previous urination, and gets painful pretty quickly. Attempts to regulate my voiding hasn't accomplished anything at all.
I'm also wondering if having a fibrotic bladder simply means that with a reduced ability to store urine, that there's simply no chance that I'll be able to lengthen the times between voiding and lead anything like a normal life again.
I stopped posting last year because I got very depressed about this and other news, and about the lack of change in my symptoms, but I hope everyone is doing well, and always appreciated the support I got on this site.
Comment