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Author Topic: Binders - how quickly does the use of Tums change lab values?  (Read 3194 times)
Deanne
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« on: July 09, 2012, 07:32:37 PM »

Confession time: I was really bad about not taking Tums while my parents were visiting. I'm pretty new to needing to take a phosphorus binder and I'm only supposed to be taking them with my biggest meal for now. It's hard to get into new mealtime habits and especially so when my parents were a distraction. I'm trying to get back on track and be consistent. My next neph appointment is at the end of the month so I'll get my labs run in about two weeks. If I'm really consistent with Tums, will that be enough time to show the difference?
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Deanne

1972: Diagnosed with "chronic kidney disease" (no specific diagnosis)
1994: Diagnosed with FSGS
September 2011: On transplant list with 15 - 20% function
September 2013: ~7% function. Started PD dialysis
February 11, 2014: Transplant from deceased donor. Creatinine 0.57 on 2/13/2014
Cordelia
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« Reply #1 on: July 09, 2012, 07:38:41 PM »

I remember when I started taking Tums, my labs showed a huge difference in about a week, pretty quickly actually, for me.

Good luck!
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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
Whamo
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« Reply #2 on: July 10, 2012, 09:06:34 AM »

I just got my labs, and for the third month in a row, they were all in the target range.  I use the "antacid tablets" I get at Target that are Tums clones, and they come in assorted berry flavors.  It costs $2.50 or something like that for 96 chewable tablets.  They're cheaper than eating binders, and a lot more palatable.
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Willis
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« Reply #3 on: July 10, 2012, 10:58:32 AM »

Tums (or clones) worked great for me but then my calcium levels went through the roof. I still have trouble controlling my phosphorus but the combination of high calcium and high (or close to high) phosphorus causes horrible itching over my entire body. I use Fosrenol as a binder now and it supposedly doesn't add any calcium. Now if I can just control my craving for cheese!  :P

 
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Cordelia
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« Reply #4 on: July 10, 2012, 12:34:28 PM »

Have you tried Brie cheese, Willis? Its like half the amount of phosphorus I think that regular cheese.
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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
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