Am I doing this wrong?
Posted: Fri Oct 21, 2011 1:48 pm
Hello,
I have a question. For the past year or so I have had overactive/painful bladder issues. So I went to a urologist, two of them in fact. These two urologists came up with totally different plans about how I should be treated. I didn't feel like I was getting any positive results with the first urologist. The new urologist wants me to go on an overactive bladder medication indefinitely and have the pressure in my bladder checked. I have been on overactive bladder medications, the side effects are horrible. This course of treatment just doesn't sound right to me. I have had every test from cat scans to bladder scopes to see if I have cancer, etc. Both urologists agreed my symptoms are probably due to MS. Does it have to be this way? Can't my MS Specialist just treat me for this or refer me to a urologist that has lots of MS experience? I am tired of going from doctor to doctor to try to solve MS symptoms. It just seems like this has been a lot harder than it had to be. How does your MS doctor handle new symptoms like this? Any advice would be appreciated.
Alicia
I have a question. For the past year or so I have had overactive/painful bladder issues. So I went to a urologist, two of them in fact. These two urologists came up with totally different plans about how I should be treated. I didn't feel like I was getting any positive results with the first urologist. The new urologist wants me to go on an overactive bladder medication indefinitely and have the pressure in my bladder checked. I have been on overactive bladder medications, the side effects are horrible. This course of treatment just doesn't sound right to me. I have had every test from cat scans to bladder scopes to see if I have cancer, etc. Both urologists agreed my symptoms are probably due to MS. Does it have to be this way? Can't my MS Specialist just treat me for this or refer me to a urologist that has lots of MS experience? I am tired of going from doctor to doctor to try to solve MS symptoms. It just seems like this has been a lot harder than it had to be. How does your MS doctor handle new symptoms like this? Any advice would be appreciated.
Alicia