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Author Topic: Frustration with Urination  (Read 5639 times)
Whamo
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« on: July 14, 2012, 07:33:49 AM »

I had a fistula surgery two days ago, and I am having a hard time urinating.  I get the urge to go, but I can't, most of the time.  If it does come out it's a trickle.  I'm wondering if this is a temporary thing because of the surgery or if that's it from now on.  I hesitate to use lasix because I don't want to make it any worse.  It feels horrible to need to go, and have it :Kit n Stik; :Kit n Stik; get stuck somewhere.
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jbeany
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« Reply #1 on: July 14, 2012, 12:01:00 PM »

It may be your kidney reacting to the anesthetic.  Unfortunately, the drugs tend to lower kidney function even more than it already is.  It can take a while for the crap to clear out of your system, too, so things may shift back into gear in a few days.  If it were me, I'd try a single dose of Lasix to see if it made me more comfortable.  Have you called your neph about it?  It might be wise to rule out things like bladder infections as well.
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"Asbestos Gelos"  (As-bes-tos yay-lohs) Greek. Literally, "fireproof laughter".  A term used by Homer for invincible laughter in the face of death and mortality.

cassandra
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« Reply #2 on: July 14, 2012, 04:23:50 PM »

Solid advice Whamo, the narcotics, pain meds, contrast fluids, stay in your system circling around, doing no good to any of your organs. Take the Lasix, call your neph!

good luck, love Cas
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I started out with nothing and I still have most of it left

1983 high proteinloss in urine, chemo, stroke,coma, dialysis
1984 double nephrectomy
1985 transplant from dad
1998 lost dads kidney, start PD
2003 peritineum burst, back to hemo
2012 start Nxstage home hemo
2020 start Gambro AK96

       still on waitinglist, still ok I think
Whamo
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« Reply #3 on: July 15, 2012, 10:01:19 AM »

Thanks for the advice, but I have a twist to the story to add.  Well, I could not sleep for two days after the surgery.  My stomach kept getting harder and bigger.  Last night I was in deep pain, and freaking out.  My wife said, "Let's go the ER."  Well, Loma Linda's ER was full, plus two helicopters worth of critical patients had just landed.  I waited for an hour before they saw me, evaluated me, and said you're up front on the list, but you're still going to wait.  So I waited two more hours, freaking out in pain, sitting in the wheelchair.  Some gangster homie who got shot was there with his crew, and looked like he was hurting even more than me.  Finally, at two in the morning I saw a doctor, and she was sharp.  She put a cath on my penis and drained out two liters worth of fluid.  It was instant relief.  I got home at three AM and enjoyed a night of sleep.  But now I carry around a bag to store my urine, and the cath i still there.  My wife, a nurse, says the more often I empty the bag the bigger chance for infection.  I see my regular doctor Monday to have it removed and/or evaluated.  What a night!  The co-pay also cost me $100. 
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jbeany
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« Reply #4 on: July 15, 2012, 01:04:02 PM »

Yikes!   :cuddle;  Hope this gets better soon.
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"Asbestos Gelos"  (As-bes-tos yay-lohs) Greek. Literally, "fireproof laughter".  A term used by Homer for invincible laughter in the face of death and mortality.

cassandra
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« Reply #5 on: July 15, 2012, 03:08:27 PM »

me too, good luck Whamo, and lots of love Cas
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I started out with nothing and I still have most of it left

1983 high proteinloss in urine, chemo, stroke,coma, dialysis
1984 double nephrectomy
1985 transplant from dad
1998 lost dads kidney, start PD
2003 peritineum burst, back to hemo
2012 start Nxstage home hemo
2020 start Gambro AK96

       still on waitinglist, still ok I think
LarryG
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Grateful to my donor, I feel great!.

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« Reply #6 on: July 15, 2012, 07:51:39 PM »

I am not sure what the cause and reason of your renal failure. I know with me when I first diagnosed with ESRD I could urinate and as time went on I just stopped completely. I had the urge and the body was willing but not even a trickle. Only dialysis could remove my fluids until I received a transplant.
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LWG
Diagnosed ESRD Jan 2008
Wegener's granulomatosis
Uncontrollable Hypertension
AV Fistula inserted Jan 2 2009
Transplant waiting list University Illinois Chicago Division of Transplant.
Angioplasty and Coil placement to limit Blood Flow from Fistula Jan. 18 2011
Transplant by living donor March 28 2011
Whamo
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« Reply #7 on: July 16, 2012, 08:46:46 AM »

This is just my wife's speculation, but it makes sense.  When I was out cold for the fistula surgery they might have put a catheter on me.  Somehow that damaged my urinary system, and when they removed it my ability to urinate went too.   This pumped by blood pressure up to 190, even with BP meds, as well as filling up my bladder.  I knew at some point this would happen when I got on dialysis.  I just feel so strange with a bag on my leg, a huge bandage on my arm, and a catheter on my chest. 
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jbeany
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« Reply #8 on: July 16, 2012, 02:32:16 PM »

I am not sure what the cause and reason of your renal failure. I know with me when I first diagnosed with ESRD I could urinate and as time went on I just stopped completely. I had the urge and the body was willing but not even a trickle. Only dialysis could remove my fluids until I received a transplant.

Larry, most people gradually lose the ability to make urine as their ESRD gets worse.  I don't think that's the problem here, though.  It seems to me that if it was his ESRD getting drastically worse that fast, he'd likely make no urine at all, not fill up his bladder without being able to release it.

Whamo, hopefully, it's some kind of nerve issue that will repair itself soon.  Have you called to find out if they used a urinary cath during surgery?
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"Asbestos Gelos"  (As-bes-tos yay-lohs) Greek. Literally, "fireproof laughter".  A term used by Homer for invincible laughter in the face of death and mortality.

Whamo
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« Reply #9 on: July 17, 2012, 06:23:34 AM »

I meet with my surgeon this morning.  I am not a happy camper. 
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billybags
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« Reply #10 on: July 17, 2012, 07:37:43 AM »

Oh Whamo, that sounds painful.   I know ladies pay to go to the loo but that is taking the pi** 100 dollars.   Can't find the sign for  dollars.            Why are you not a happy camper.
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Whamo
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« Reply #11 on: July 17, 2012, 09:10:50 AM »

How would you like to walk around with a plastic bottle of urine on your leg?  A bandage stretching from your elbow to your armpit?  A chest catheter?  All at once.  I feel like I'm becoming the Mummy.
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billybags
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« Reply #12 on: July 18, 2012, 03:56:44 AM »

Whamo, you make me roll. Hope things are getting better. The mummy I like that.
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jbeany
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« Reply #13 on: July 18, 2012, 12:59:27 PM »

I meet with my surgeon this morning.  I am not a happy camper. 

What did the doc say?  Anything useful about the problem?  Or a lot of fuzzy muttering about side effects and risks?
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"Asbestos Gelos"  (As-bes-tos yay-lohs) Greek. Literally, "fireproof laughter".  A term used by Homer for invincible laughter in the face of death and mortality.

Whamo
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« Reply #14 on: July 19, 2012, 11:04:51 AM »

My surgeon said they didn't put a cath on me during the fistula surgery.  The fistula thrill is good, but it's sore and painful.  It will heal.  I see my "Family Doctor" today where I will probably get a referral to see a Urologist.
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Whamo
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« Reply #15 on: July 20, 2012, 05:23:15 AM »

My "Family doctor" visit ended like I thought it might, with a referral to a Urologist on Monday.   But, thanks to my wife, I got a little torture.  Before they took off the catheter they injected my penis with 250 ml. of saline.   This is not a pleasant sensation.  Then I tried to urinate, and only 50ml came out.  What to do?  They put a new catheter on, and made the referral to the Urologist. 
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billybags
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« Reply #16 on: July 20, 2012, 06:01:07 AM »

Whamo, If I was a man I would be going "WOOOOOOOOOOOOO"   I bet that was painful. Hope you get on alright on when you see the Urologist. Keep your chin up. I was going to say Pecker but is is not appropriate is it.
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cassandra
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When all else fails run in circles, shout loudly

« Reply #17 on: July 20, 2012, 06:25:42 AM »

I'm so sorry Whamo this sound absolutely horrendous.
Wishing you a bearable weekend, and all the luck in the world on Monday, I sure hope they can sort it out.

love Cas
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I started out with nothing and I still have most of it left

1983 high proteinloss in urine, chemo, stroke,coma, dialysis
1984 double nephrectomy
1985 transplant from dad
1998 lost dads kidney, start PD
2003 peritineum burst, back to hemo
2012 start Nxstage home hemo
2020 start Gambro AK96

       still on waitinglist, still ok I think
peaches94
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« Reply #18 on: July 31, 2012, 10:59:49 PM »

Im sorry u r having so much trouble, i deff feel for u. I dont know if this will help or not but if ur like me any info is better than none at all. My husband has issues with certian types of meds, especialy Morphine, that do that to him no matter how hard tries or how bad hes gotta go nothing happens. May not be your problem but i jsut thought id put it out there as somethin to maybe think bout. Again im sorry i know it really stinks to feel like that. Hope things get better for u.
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"Live everyday as if it was ur last, no regrets, fill it with love and happiness."
malaka
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« Reply #19 on: August 01, 2012, 10:21:37 AM »

Frustration with urination? Don't get p.o.'d. 


Call the doc.  Something ain't right.
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ACRViper
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« Reply #20 on: September 11, 2012, 04:18:55 PM »

How would you like to walk around with a plastic bottle of urine on your leg?  A bandage stretching from your elbow to your armpit?  A chest catheter?  All at once.  I feel like I'm becoming the Mummy.

I have a SP catheter, but I don't wear the leg bag-hardly ever. I just clip clip it shut at the end of the catheter line with a plastic blood line clip from dialysis and then put a zip tie over that to make sure it doesn't pop open. (!)

Then I just open it up and relieve myself every few hours.

If you are going to be faced with long term catheter use, check into having the catheter inserted into your stomach area, or to be more specific-into your bladder.

Much better than you having the catheter where it is now...!

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On dialysis for two years now.
I have been in the Philippines for the last year
Only need dialysis 2x a week
I am not on any kind of water restriction
Overall, I am very healthy, not symptomatic etc
62yo
Whamo
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« Reply #21 on: September 11, 2012, 08:05:09 PM »

I'm back to normal these days.  Well, if you call dialysis normal.
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Big E
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« Reply #22 on: September 12, 2012, 10:32:24 AM »

Whamo, sorry you had to through so much pain, but I'm you're doing better now. Waiting hours in the ER to be seen is no fun--I've been there.
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PKD diagnosed June 1996
Started in-center hemodialysis May 2010
Darthvadar
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« Reply #23 on: September 12, 2012, 11:44:29 AM »

Whammo, I don't have KF (yet), but I've been there...

I'd my knee replaced using epidural anaesthesia, and my bladder closed down... Had to be cathetherised... Not nice, not dignified, but a nessessary evil...

Now if I could regain some semblence of bladder control, I'd be laughing... But as I've Ehlers-Danlos, I have to expect some of life's little 'joys'... Hope your doctor's appointment went well...

Darth...
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Cared for my late mum, Elsie who had Kidney Failure... Darling mum died on July 15th 2014... May her gentle soul rest in peace....
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