My last MRI showed lesions "typical of MS" and last weekend I had a 24-hr period where I couldn't urinate (well, maybe a
littleLittle noses decongestant
Little tummys dribbling during bowel movements, but nowhere near a
normalNormal saline flush output).
Then the next day it was fine, although I continue to have a slight burning sensation where I imagine my bladder to be, although no burning during or after urinating.
My questions are:
1) Could MS cause this, even if it's only for a day?
2) How long can I have less than
normalNormal saline flush urineCalcium - urine
Calcium urine test
Chloride - urine
Cortisol - urine
Electrolytes - urine
Glucose test - urine
Hcg in urine
Ketones - urine
Kidney - blood and urine flow
Lh urine test (home test)
Ph urine test output without risking damage to my kidneys?
3) Now that I'm back to
normalNormal saline flush, would anything show up on tests if I go for tests? (I'm a
littleLittle noses decongestant
Little tummys tired of tests).
4) I sometimes have to stop and start several times during urination to feel like I've really emptied my bladder. Is this part of the same issue?
5) Is the bladder emptying function also controlled by the autonomic nervous system? (I already have problems with bowel, eye focusing, heart rate, and body temperature, which I think are all controlled or influenced by autonomic nervous system)
I am a 45 year old caucasion female with no bladder problems up to now, apart from a few UTIs 25 years ago. I don't drink coffee or sodas, and I try to drink lots of water.
Thanks for your help!