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Author Topic: Weird Problem... Don't Laugh  (Read 2625 times)
Smeggy
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« on: November 11, 2011, 03:08:07 AM »

I have a weird problem…

From the beginning then!

Sunday I went to Sydney to have a stent put into my chest for better dialysis… Monday I was put under for it and then put on the renal ward after I projectile vomited on the nurse and missed my vascular surgeon. Given 2 panadoles and two 5mg of Endone (had it before, it’s magic).

On Tuesday morning, I couldn’t pee. Told nurses, Doctor's who said ‘yeah, you’re in renal failure.’ So I went to dialysis and had 3ltrs taken without problem and I still couldn’t pee. Went home, tried all through the night and at 6:35am on Wednesday I peed about… 367ml.

This repeated again on Thursday and this time I only had 181ml in my bladder but it felt full. I went to Emergency (more like dragged by my mother) but they couldn’t warrant a catheter to be used or anything, though did diagnose me for Urine Retention.

It’s not the kidney giving me trouble it’s the fact I can no longer pee on command and have now resorted to using the shower hose to help me actually go (yes, I know, disgusting, but I do clean it afterwards). Any ideas?

Oh, Endone was ruled out for constipation as I haven’t really eaten since Sunday. And I can’t get a urine sample for a UIT check either.

Please… I'm in horrible discomfort, and none of my Doctor's give a crap cause it’s not about the kidney.
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Whamo
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« Reply #1 on: November 11, 2011, 04:11:59 AM »

You're not the only one.  I am new to dialysis, and at first I could pee, but it has become a trickle.  It is disturbing, but it is a part of renal failure, isn't it?
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Cordelia
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« Reply #2 on: November 11, 2011, 04:17:35 AM »

 :grouphug;   Whamo,

My nurses tell me that eventually Dialysis dries you out over time. I've been on D for over a year though and I'm still peeing constantly though. 
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Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
Rerun
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« Reply #3 on: November 11, 2011, 04:21:35 AM »

Stopping the production of urine is normal for renal failure, but you should not feel like you have a full bladder either.  I think it is odd that you 'feel' like you have to go pee and that you 'feel' like you have a full bladder.  I would insist on a catheter to releave the pressure.  At that point if nothing comes out then you can address the issue of 'feeling' full.
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monrein
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« Reply #4 on: November 11, 2011, 04:49:27 AM »

You might have a urinary tract infection.  Important to find out and treat if necessary with antibiotics.  A Major symptom is the urge to pee and feeling like you still have to go once you have.  Also the feeling of pressure in the bladder.
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Pyelonephritis (began at 8 mos old)
Home haemo 1980-1985 (self-cannulated with 15 gauge sharps)
Cadaveric transplant 1985
New upper-arm fistula April 2008
Uldall-Cook catheter inserted May 2008
Haemo-dialysis, self care unit June 2008
(2 1/2 hours X 5 weekly)
Self-cannulated, 15 gauge blunts, buttonholes.
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Smeggy
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« Reply #5 on: November 11, 2011, 05:51:18 AM »

No, its not that I'm worried about urine production part, its that I can't empty my bladder when I *do* have a full bladder.

As I said to my doctor, ignore the kidney part, focus on the bladder.
« Last Edit: November 11, 2011, 05:52:47 AM by Smeggy » Logged

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boswife
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« Reply #6 on: November 11, 2011, 09:57:44 AM »

i say get to another dr.... I understand where your comming from and their is a definate difference in what youe eperiencing besides Kidney failure.  (imho) Very different feeling of full "bladder" vs just not peeing.  Please check it out...
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im a california wife and cargiver to my hubby
He started dialysis April 09
We thank God for every day we are blessed to have together.
november 2010, patiently (ha!) waiting our turn for NxStage training
January 14,2011 home with NxStage
jeannea
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« Reply #7 on: November 11, 2011, 10:02:47 AM »

You should find a urologist. The nephrologist doesn't know what to tell you. While it isn't fun to see a urologist, they have the knowledge you need. It could be related to your surgery (I don't know those drugs) or completely unrelated. But I would pursue it and find an answer.
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okarol
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« Reply #8 on: November 11, 2011, 12:45:25 PM »

You should find a urologist. The nephrologist doesn't know what to tell you. While it isn't fun to see a urologist, they have the knowledge you need. It could be related to your surgery (I don't know those drugs) or completely unrelated. But I would pursue it and find an answer.

I agree. Good luck!  :waving;
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
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