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Author Topic: Smelly Urine  (Read 5484 times)
BeachLover
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« on: August 11, 2009, 11:01:44 PM »

Why is my urine so foul? I am at 3.9 and still not in dialysis yet. I have notied I am urinating much less and it smells terrible. Is this the way it will be from now on? IMy appetite is dimoniishing and I feel weak and tired and out of breath. I am anemic but on Aranesp. Recently they have upped my dose a lot.
Will the odor get better when I start D?
This isall getting bad and I am losing my spirit. I yearn to feel well again. \Thanks
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Hanify
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Hadija, Athol, Me and Molly at Havelock North 09

« Reply #1 on: August 12, 2009, 01:47:21 AM »

Yes bad urine is a sign of bad kidneys.  It will probably get better after dyalysis - I think most of us have clear pale wees.  Oh, the things we share on IHD!
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Diagnosed Nov 2007 with Multiple Myeloma.
By Jan 2008 was in end stage renal failure and on haemodialysis.
Changed to CAPD in April 2008.  Now on PD with a cycler.  Working very part time - teaching music.  Love it.  Husband is Paul (we're both 46), daughter Molly is 13.
Des
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« Reply #2 on: August 12, 2009, 07:48:54 AM »

My pee smells like amonia..... eeuw. It is mostly darkish... I think it is the bleeding in my cysts. Not sure.

My breath also smells and I'm not even on D yet. oh ya and food tastes like .... well ... nothing. everything is tasteless.

Hang in there .... it is all the stuff building up in your system making you feel so bad.

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Please note: I am no expert. Advise given is not medical advise but from my own experience or research. Or just a feeling...

South Africa
PKD
Jan 2010 Nephrectomy (left kidney)
Jan 2010 Fistula
Started April 2010 Hemo Dialysis(hate every second of it)
Nov 2012 Placed on disalibity (loving it)
peleroja
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I have 16 hats, all the same style!

« Reply #3 on: August 12, 2009, 07:52:31 AM »

Oh, the things we share on IHD!

Not just on IHD.  We share similar stuff in my renal support face to face group.  I guess when you have a common illness, the entire body and its various processes is just fuel for the conversation!
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monrein
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« Reply #4 on: August 12, 2009, 12:22:43 PM »

My pee smells like amonia..... eeuw. It is mostly darkish... I think it is the bleeding in my cysts. Not sure.

My breath also smells and I'm not even on D yet. oh ya and food tastes like .... well ... nothing. everything is tasteless.

Hang in there .... it is all the stuff building up in your system making you feel so bad.

Hopefully your breath will improve once you start D.  Mine did.  Pre-D my mouth always tasted like I'd just downed a big gulp of bleach from a rusty metal can.
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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.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
Sunny
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Sunny

« Reply #5 on: August 12, 2009, 07:01:11 PM »

My urine was smelling odd lately too. Turns out I have a UTI (urinary tract infection) for which I am on antibiotics. Just make sure that is not the problem. A simple urine dip test at the doctor office can rule it out.
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Sunny, 49 year old female
 pre-dialysis with GoodPastures
Jean
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« Reply #6 on: August 12, 2009, 11:28:32 PM »

I think that is my problem also. Did the urine specimen and if I have one, will know by Monday I am sure. ( My Dr. reads slowly)And, will also let you know. I am one of the rare ones who have no other symptoms when I have one,no burning, no stinging. I am grateful for that.
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One day at a time, thats all I can do.
Tallons5
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« Reply #7 on: August 13, 2009, 11:10:42 AM »

I too have the same issues am always self conscious and after using the bathroom I spray cleaner hoping to cover up the smell I am waiting on results from labs right now, last few days have been in more pain during urination also it has been so foamy I have since learned it is caused by protein in the urine don't understand how I could be losing so much protein when I don't take in very much, Oh and I have been very active the last few days we are in the process of painting our house there is much to do to get ready and am determind to do as much as I can! perhaps that has something to do with it.
again you are not alone, there is comfort in that I have found.
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paul.karen
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« Reply #8 on: August 13, 2009, 11:35:44 AM »

beachlover your at 3.9?  What?

Sounds like you should be on dialysis a few months ago.
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Curiosity killed the cat
Satisfaction brought it back

Operation for PD placement 7-14-09
Training for cycler 7-28-09

Started home dialysis using Baxter homechoice
8-7-09
monrein
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« Reply #9 on: August 13, 2009, 12:06:17 PM »

Most likely his creatinine, Paul.   My urine had zero smell before I started D...It was purely water, no toxins etc.   Important to see about UTI's that can travel upwards and potentially cause trouble.
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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.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
silverhead
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« Reply #10 on: August 13, 2009, 09:42:31 PM »

We are convinced that the cause of Sharon's kidney failure was from untreated UTI, she had several bouts of it, and I'm sure she built up some tolerance to it, anyway it caused a lot of scarring in the Ureters leading to the Kidneys, it blocked the flow and her Doctor at the time never tested her for UTI, just treated her for bad back pain, finally took her into the ER and they quickly caught the fact her Creatinine was at 11, by then both Kidney's were to far gone to save.......
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Do not argue with an idiot. He will drag you down to his level and beat you with experience.
monrein
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« Reply #11 on: August 14, 2009, 06:50:11 AM »

That's what happened to me at 8 months old, an UTI and reflux (ureter valves not developed enough to stop backflow)  sent infected urine up into the kidneys causing a whack of grief.  A simple antibiotic at the right time would have been nice but alas in Jamaica in 1953 they said I had PKD. 
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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.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
Hanify
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Posts: 1814


Hadija, Athol, Me and Molly at Havelock North 09

« Reply #12 on: August 14, 2009, 03:48:54 PM »

Oh Lord.  I sometimes feel sorry for myself, then I come onto ihd and realise the amazing strength people show through years of trials.  8 months!!
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Diagnosed Nov 2007 with Multiple Myeloma.
By Jan 2008 was in end stage renal failure and on haemodialysis.
Changed to CAPD in April 2008.  Now on PD with a cycler.  Working very part time - teaching music.  Love it.  Husband is Paul (we're both 46), daughter Molly is 13.
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