Prostrate-Night Urinating Problems/Symptoms(Autonomic)
Posted , 7 users are following.
I have had problems with urinating. I have to go several times a night and I'm lucky if I can get 1 0z out-with the attendant problem most times that I cannot go right away.
So far-this description is fairly typical of common problems with this condition. But what I am about to describe is atypical so I thought I'd share. My alarm system that tells me I have to go includes both a feeling in the bladder but also profuse sweating from the waist up to the point where my top(T-shirt) gets totally wet and my mouth goes dry-I mean totally dry.
I had already posted once on this forum if anyone experienced these same very unpleasant symptom, and there was no response. I also got a referral to Board Certified Urologist. Ihave Type 2 diabetes and I asked the Urologist the following question. The question was: Have you ever had a patient who had the sweating symtom and susequent really unpleasant dry mouth when I felt the urge to go. His answer was "NO". His diagnosis was my Type 2 diabetes aggravated my over-active bladder & prescribed oxybutynin. For my condition it should NEVER be prescribed as is shown in the link I have provided.
My other post to this forum about these symptoms, as I mentioned, went unanswered so I thought my condition was rare or peculiar. A fairly good Google search on night time over active bladder yield little if nothing on my problems.(I should mention;my problem ONLY shows when I'm lying down(supine position) There is practically nothing(zero) on thne Internet EXCEPT for this which was a bull's eye:
http://www.dana.org/Publications/GuideDetails.aspx?id=49997
This article at this link explains exactly what I have been suffering from for almost 8 years. I am going to go see in Boston to a "neuro-urologist" who deals with "Autonomic diorders" of the bladder. This article was where I found the admonition to NOT use the oxybutynin if you had my symptoms.
I finally have some hope & I hopes it might help anyone experiencing fairly similar symptoms. And I also think it is a perfect example of how important it is to be your own advocate!!
0 likes, 10 replies
ianC al03909
Posted
Perhaps it was the very rarity that failed to get you a response. Guys here are very helpful.
But now you've posted this, anyone else will get help too.
You are totally right in being your own advocate. Most of us would agree with that - me in spades when my first 3 specialists said there's nothing they can do, so go home & die (7 years ago). Huh.
And your case also shows the immense benefit the Internet is now. Hurrah!
al03909 ianC
Posted
In my forty's I went back to school & became a lawyer in the State of Maine. This was in the early '90s when the economy in merry old New England was horrible, and so I closed the doors on my own "practice"-if you could call it that-which does get me to my point about being your own best advocate. In the short time I practiced law-I would hear about malpractice cases(not mine as they take a ton of experience).
It was absolutely scarey-some of the stupid mistakes doctors or hospitals make. I am not talking about the one's that make the newspaper-rather the ones that don't!
I know lawyers are not particularly well liked; believe me- lawyers make mistake that hurt clients or are some times dishonest. As it is with truck drivers-pick a vocation. But some times people misplace their trust in a doctor; after all-they walk on water -don' they? And again-I cannot tell you enough good things about the Dana Foundation-the link I provided in this thread. Anything that has to do with the brain & I-not my internest or urologist figured out that my problem had to do with the signaling system to my brain re; the symptoms I was having. My deep background in electronics helped to under stand what was going on with me when my 2 doctors had not. All parts of the brain are some how related tol the micro processor or computer (human) brain. As a piece of trivial & extremely interesting to me-the human heart (pump & transceiver(or in networking terms-heart=router or bridge router) the hear sends more messages to the brain thany other human organ. Sorry for my verbosity but I am by nature-a learner & (hopefully) have some thing of value to share with others!
david91143 al03909
Posted
Good luck
David
pete25515 al03909
Posted
Hope all goes well.
pete25515
Posted
Good luck,
Pete.
bruce19007 al03909
Posted
david91143 bruce19007
Posted
This is my story too! I had L4-5 and L5 -S1 compression incident which has left my left foot and part left leg paralysed. I have had 'flow' problems too and have had a Foley inserted twice in the last 10 months. I don't think my problem is the prostate but have been prescribed tamoslusin (Flowmax). It really messed me up. I would rather try relaxant medicateion (or intermittant catheter for problem times) - but what is your experience? Have you had success treating the damaged nerve rather than the prostate?
Thanks'
David
bruce19007 david91143
Posted
DarrenUK al03909
Posted
not sure where to go now or what to do? Urologist doubts I have an enlarged prostate and gp did the fingers test and said I have. Intermittent catheters are helping totally empty my bladder but still waking up to pee in the night and leak through the day.
bruce19007 DarrenUK
Posted