Would anyone recommend using Botox to their bladder to reduce urine frequency?
I have had boxtox in the bladder for many many years now. I can honestly say it's one of the best things I have ever done to help prevent anymore terrible things MS does to us. I was constantly have uni's as I wasn't able to empty properly. I would highly recommend. It has been an absolute blessing for me. :)
Check your prostate
I also did botox in my bladder with bad results. My mother, on the other hand, thinks it's wonderful.
Well I've gone from catheters putting crushed up Ginger pan in my bladder at night Botox interstim device which is a pacemaker on my rear end connected to my sacral nerve and now my body has taken over again and so the end of the month I'm going to go to my urologist to talk about an SP maybe that will fix me for good haha I just love this jungle that you have to slash and cut and Wade your way through in life with the darn disease. But I'm not giving up my pitbull's dog got her jaws locked and I'm shaking away and nothing's going to get me to let go!
Keep on fighting my mighty warriors💪🙏🏻
Depends on how fast I can run before a needle reaches my bladder. Depends on how absorbing my underwear are. It just depends! 😊🦋