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Stage 3 Kidney Disease and Diet: What can I eat?

Kidney & Bladder | Last Active: 2 hours ago | Replies (759)

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@rosemarya

Hi All,
This morning I am thinking about all of you who have been participating in this discussion. You have mentioned and shared about kidney disease, diets, GFR's, shingles, and so many more topics that are affecting your own health journeys. While I am not experiencing kidney disease, I am living with a kidney transplant and I am interested in hearing from you about how you are doing with your dietary needs.

How are you doing? How are you able to manage your numbers during this current era of 'healthy at home' restrictions? What advice do you have for someone who is just beginning their own life with Stage 3 Kidney Disease?

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Replies to "Hi All, This morning I am thinking about all of you who have been participating in..."

@rosemary My best advice is to listen to your nephrologist and follow guideline set for you. If your dr does not offer the information you need, ask! Also there is information on rsnhope.org or National Kidney Foundation. Basically limiting phosphorous-, sodium- and potassium-rich foods, maintaining healthy blood pressure and weight, will assist you in keeping optimum health. Each person is unique, each case has its own nuances. In these days of healthy-at-home, you may have to be more creative, but it can be done!
Ginger

@rosemarya As a volunteer mentor who has been following this thread for quite a while, you have already seen what we are going through. My strongest suggestion to you is to identify, if possible, the cause(s) of your kidney disease and build your life plan from there. Secondly, read labels and know what you are ingesting--find out what those words you cannot pronounce actually are. And lastly, make sure you can live according to your plan for life. If you cannot see yourself eating this way 10 years from now, you need to do some adjusting.

For instance, my kidney degeneration is caused by oxalates and has been greatly impeded by my adherence to a low oxalate diet. Additionally, I still maintain: 1) a low carbohydrate diet from long-term brittle diabetes; 2) low fat diet after finding out I do not assimilate fats; 3) low dairy diet; and 4) low fiber diet after diagnosis of gastroparesis, gastric retention and rapid transit. There is some crossover between the diets, but as you can imagine my diet is quite limited. However, after six years it has become habitual.

When I look at a recipe or menu I first look to see if it includes anything I cannot eat. With the current emphasis on healthy eating you might think it would be easy, but, here is a list of current popular trends that I cannot use:

any green leafy vegetable (includes spinach, kale, lettuce, etc.)
root vegetables (potatoes, yams, sweet potatoes, beets, turnips)
smoothies (dairy base)
nuts (except walnuts)
peanut butter
all berries (except strawberries)
high fiber fruit (apples, pineapple, etc.)
raw vegetables (salads, carrot sticks, celery, radishes, etc.)

Also, in my opinion, sugar is sugar. Honey, agave, cane sugar, stevia, molasses, brown sugar, raw sugar, and whatever other trendy names they are using now; all convert to dextrose, which I count as sugar.

I had to reset my mind about food. I had used it as a socialization tool. Now I have learned to eat for sustenance. If I am not hungry and a meal is not overdue, I don't take a pastry with my coffee just to make the other person/people feel more comfortable. I may have a fruit cup if one is available.

Blessings to you on your journey.