CKD and Sparkling Mineral Water
Posted , 10 users are following.
My husband is Stage 4 CKD, GFR 19. Since getting the shock news, he has stopped drinking alcohol. He never drank much alcohol anyway. He now drinks mainly his favourite mineral water, which is sparkling San Pelligrino. He drinks 1-2 litres of it a day. As it is sparkling, does it cause any harm to his kidneys, or is it OK please.
1 like, 9 replies
diana50966
Posted
Drink water instead - Kidney Health Australia
www.kidney.org.au/kidneydisease/drinkwaterinstead/tabid/703/default.aspx
Kidney Health Australia position paper. ... Note: bottled mineral water contains salt which can lead to fluid retention, swelling and even increased blood pressure ...
Your husband needs bi carbonate of soda, you will find lots on internet to support it helps to stabilise kidneys start now!
Diana
diana50966
Posted
Also you should note: Oral sodium bicarbonate has been shown to slow progression to end stage renal disease in individuals with stage 4 chronic kidney disease and metabolic acidosis (plasma sodium bicarbonate levels 16-20meq/L).[24]. This is from Wikipedia.
Change his diet now.... To kidney foods... They love grapes red, lettuce, cucumbers, beet root, celery, red peppers, use fermented rice miso for flavouring and garlic. Stay away from seeds, and granary bread.
My husband is at stage4/5 , I research constantly...he is now taking Ayurvedec medicine along with other western. Suggest review Husbands present medication if on anything, and reduce what ever or delete anything unnecessary with Dr.
He has Only been on Ayurveda medicine 11 days, will have new blood,tests in less than 2 weeks, will post
results.
One last thing, suggest you could be his,donor, takes about 6 months to get through all the tests, start them ifyou are both young and want to do this as last resort.... I did it for my husband, we matched, but he has otherconditions that presently prohibit this operation.
All the best.
Diana
diana50966
Posted
Diana
Tommo781
Posted
rosalava87771 Tommo781
Posted
I see I'm 4 years late on this question but several sites say plain carbonated water - flat water with no additive except carbon gas appears to be good for you. How is your husband doing, I hope well.
rosalava87771 Tommo781
Posted
Sodas are bad because of the phosphorous and sugar, but "Noncola carbonated beverages were not associated with chronic kidney disease (0.94; 0.4-2.2)." https://www.ncbi.nlm.nih.gov/pubmed/17525693
bernard03571 Tommo781
Posted
bernard03571
Posted
helen54849 Tommo781
Posted
Hi,
Any bottled water is bad as it contains sodium, I don't have salt due to having had CKD all my life, I spent the last two years on PD and had my transplant in September last year.
Regarding the need to adjust your husbands diet and take bicarb unless you have been told to do this by your husbands doctor then don't. (I asked my doctor about studdies I had seen on line and he said it was rubbish it would make it worse, As they kept me in stage 3 from 13-37, I trust what they say)
It all depends on what your husbands blood results are, so the lower the blood bicarb level, the higher the blood acid. You would not take bicarb unless his blood bicarb was less that 20 normal levels being between 20-26. Regarding lowering potassium, if his levels are between 3-5 and you reduce his potassium through food it is as bad as his potassium being too high ie he would be at risk of a heart attack. If you lower his phosphate through diet and it is within normal range any thing over 0.75 if you make this lower he is at risk of going into a coma. So this is why it is important you do not change his diet unless a Doctor tells you to as it is very dangerous. Avoid salt and low salt, ready meals and ibuprofen. You more than likely know this already, oh and don't believe everything you read on the internet! If you are ever unsure of anything then it is best to ask the doctors who are caring for your husband. He is getting to the point now where they will start discussing doners and dialysis. I had a live doner, the work up took two years as what you have to bear in mind when the testing process starts the doner is often told of issues with themselves that they didn't even know they had. I was told it took 6 months, but in reality it is a lot longer in the UK due to waiting lists etc. Even if you have a live doner you still have to go on the transplant list incase a more specific match comes up that will be better. All sorts of thiings have to match, blood group is just one of them, antibodies are checked as people have different antibodies that are not compatable. They also test your kidney function and project what it is likely to be when you are around 85. If there are any issues the doner pairing is stopped, and after you have gone through all of the tests in the uk you are interviewed by the human tissue authority and they decide if they are going to give the go a head and allow the licence for the transplant to go ahead.