I've had a neurogenic bladder all my life, but wasn't diagnosed until I was 18. I currently use pelvic floor control to keep from leaking primary (meds dried my mouth out to much!). My biggest thing with this condition is no one has ever been able to tell me why I have a neurogenic bladder. if anyone has experience with a situation similar to mine I'd love to hear more about it!
hi!! i have neurogenic bladder too, my detrusor muscle doesnt work at all. They couldn’t find a reason for why everything wasn’t working right. Do you know what the beighton hyper mobility score is?
I'll have to check my bladder study to see if it's on there!
i private messaged you!
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