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Author Topic: Help! The taste in my mouth is getting to be too much!  (Read 3745 times)
paddbear0000
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« on: December 10, 2008, 09:07:38 PM »

 ???  ???  ??? As I briefly mentioned in another post, I've been having some mouth issues lately. The last time I had my creat checked (about a month ago), it was3.7 and my function was 14%. I am not on dialysis yet. I've been getting a weird taste in my mouth that seems to fluctuate in intensity for the last week or so. I've been reading old posts about similar things, but they don't quite seem to fit. The taste is kind of a sweet metallic taste. Has anyone else gotten this same sensation? A lot of posts seem to mention a bleach and metallic taste.

Also, it sometimes gets unbearably dry. Is this interchanging taste/dry mouth normal before needing dialysis? I have tried every flavor and brand of gum out there, plus hard candy and drinks, but nothing helps. It's so bad, that I have to fall asleep with gum in my mouth after brushing my teeth, just so I can sleep. I don't have any swelling or itching. Nor do I have much nausea (but I'm not sure whether it's kidney or gallbladder related).

I've also been having bad tremors off and on as well. Can this be a sign of worsening function too?    ???  ???  ???
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« Reply #1 on: December 10, 2008, 10:28:09 PM »

Here are a couple of threads, if you haven't seen them:
http://ihatedialysis.com/forum/index.php?topic=8485.0
http://ihatedialysis.com/forum/index.php?topic=5795.0
http://ihatedialysis.com/forum/index.php?topic=8040.0
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« Reply #2 on: December 10, 2008, 11:00:53 PM »

Yup, it's normal, all of it. Mine was a taste like chewing on pennies.  Most of it will disappear when you start dialysis.
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paddbear0000
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« Reply #3 on: December 11, 2008, 12:16:50 AM »

Thanks okarol! Yeah, that sucking on pennies description sounds about right.   :P
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« Reply #4 on: December 11, 2008, 04:26:07 AM »

I hate to say this Paddbear but it sounds as though you're nearing dialysis starting time.  I started with better numbers than yours but I couldn't take it any more because of the symptoms.
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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
paddbear0000
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« Reply #5 on: December 13, 2008, 01:39:41 AM »

Ok, another question related to this...Is it common for the taste to come and go? The dry mouth too? It seems to get worse about 1/2 hour after eating, particularly if I eat meat (turkey and seafood is all I'm eating meat wise lately due to my gallbladder issues). Also, could one experience these symptoms without nausea and vomiting?
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Diagnosed type 1 diabetic at age 6, CKD (stage 3) diagnosed at 28 after hospital error a year before, started dialysis February '09. Listed for kidney/pancreas transplant at Ohio State & Univ. of Cincinnati.
G-Ma
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« Reply #6 on: December 13, 2008, 02:36:15 AM »

I started dialysis at 16% and yes all of the above, nausea, vomiting, horrible taste, dry mouth and hated food.  I couldn't swallow anything for 6 weeks which is why neph started dialysis when he did.  I feel so sorry for anyone who is on this path and still going through all that nasty sh....
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monrein
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« Reply #7 on: December 13, 2008, 04:38:53 AM »

Ann is right paddbear.  Your symptoms are classic, even without the nausea.  And protein can definitely be the culprit, which is why the pre-dialysis diet is low-protein.  We can't eliminate the breakdown waste of the protein because our kidneys aren't working.  The nausea can come and go or be a constant thing.  Depends on the person and the amount of function left I think.  The taste drove me the  craziest of all the symptoms and sometimes it felt as if I was swallowing a mild acid that was burning my tongue and throat.  It occasionally returns now when I'm really in need of a dialysis run.
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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
paddbear0000
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« Reply #8 on: December 13, 2008, 07:30:46 AM »

I don't have the burning sensation you are talking about. Does that always happen when one starts getting teh metallic taste?
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I HAVE DESIGNED CKD RELATED PRODUCTS FOR SALE TO BENEFIT THE NKF'S 2009 DAYTON KIDNEY WALK (I'M A TEAM CAPTAIN)! CHECK IT OUT @ www.cafepress.com/RetroDogDesigns!!

...or sponsor me at http://walk.kidney.org/goto/janetschnittger
********************************************************
Twitter.com/NKFKidneyWalker
www.facebook.com/profile.php?id=1659267443&ref=nf 
www.caringbridge.org/visit/janetschnittger

Diagnosed type 1 diabetic at age 6, CKD (stage 3) diagnosed at 28 after hospital error a year before, started dialysis February '09. Listed for kidney/pancreas transplant at Ohio State & Univ. of Cincinnati.
monrein
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« Reply #9 on: December 13, 2008, 07:33:07 AM »

No, this stuff is always a little bit different for everyone.  I didn't always get the burning but got it often enough that it drove me nuts.
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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
boxman55
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« Reply #10 on: December 13, 2008, 08:33:17 AM »

I get the burning tongue every so often salty foods even a little salt really does it. dry mouth also comes and goes. I have been on dialysis for 28 months. Mouth wash before I go to bed sends me through the roof...Boxman
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« Reply #11 on: December 13, 2008, 10:29:25 AM »

I hardly ate red meat at all just before dialysis.  I couldn't stand the taste of it.  All I wanted was sweets, bread and fruit.
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« Reply #12 on: December 13, 2008, 11:57:26 AM »

I was living on toast, jam and a little cream cheese, pre-dialysis.  Even that didn't go down well.
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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
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« Reply #13 on: December 13, 2008, 07:15:35 PM »

For over a year and a half before I started dialysis, my breath often smelled/tasted strongly of ammonia. For two months before dialysis, I got that burning tongue sensation, but usually eating or drinking something made it go away. A couple weeks before dialysis, a caught a bug and got so dehydrated/uremic that I could hardly talk - breathing in my own breath hurt my throat. Not only that, but something in the dynamic screwed up my mouth so much that I caught thrush and could hardly eat while I was in the hospital.
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3/2007Kidney failure diagnosed5/2010In-center hemodialysis
8/2008Peritoneal catheter placed1/2012Upper arm fistula created
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9/2008Began CAPD4/2012Buttonholes created
3/2009Switched to CCPD w/ Newton IQ cycler            4/2012HD catheter removed
7/2009Switched to Liberty cycler            4/2018Transplanted at UCLA!
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