I am going in for a Urodynamics study this afternoon, and I'm very nervous about this test. I know they use a small catheter, but I've never had one while awake before... Then next week, an office cysto. It seems like ever since I saw my Uro, my symptoms have gotten worse. Is it in my head? Is it the stress of not knowing what is wrong that is causing my symptoms to get worse? Or...
It seems like the weather here, in Las Vegas has gotten bad... Windy and it even Rained the other day (Rain? What's that?)... My allergies are bothering me more in this past month. I've read that IC patients have Mast Cells in their bladders. Are my symptoms related to my allergies? Allergies are VERY common in Nevada!
My Uro put me on Enablex, it doesn't seem to do a thing for me... It's been 2 weeks. Right now, I wish a toilet was sitting right next to me in my cube at work. I find myself going to a different bathroom each time so the same people don't see me LOL. And when I get back to my desk, I still feel like I gotta go...
Thanks for letting me rant
It seems like the weather here, in Las Vegas has gotten bad... Windy and it even Rained the other day (Rain? What's that?)... My allergies are bothering me more in this past month. I've read that IC patients have Mast Cells in their bladders. Are my symptoms related to my allergies? Allergies are VERY common in Nevada!
My Uro put me on Enablex, it doesn't seem to do a thing for me... It's been 2 weeks. Right now, I wish a toilet was sitting right next to me in my cube at work. I find myself going to a different bathroom each time so the same people don't see me LOL. And when I get back to my desk, I still feel like I gotta go...
Thanks for letting me rant

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