I am my husband’s care giver and I don’t n... - Kidney Dialysis

Kidney Dialysis

2,808 members1,269 posts

I am my husband’s care giver and I don’t normally share

felizesperar profile image
11 Replies

Hi I am new to this site and to posting anything anywhere in general, but I have so many questions I thought I would give this a try.

My husband has been on dialysis for years and will always be on dialysis. He has many health issues but the most frustrating thing for him is not being able to control his bowels well. It’s embarrassing for him and a mess for both of us. Rock hard stool one day and runny mess the next. On top of that it is the dark toxic color only a phosphorus binder can produce. Sometimes the bathroom looks like a crime scene! It is really difficult to clean that stuff off the toilet! Ok I feel a little better just writing this. Maybe it will help some of you. Please share if you know what I am talking about! Thanks

Written by
felizesperar profile image
felizesperar
To view profiles and participate in discussions please or .
Read more about...
11 Replies
cs65 profile image
cs65NKF Ambassador

Has he spoken to his doctor about maybe changing the phosphorus binder? Tried one once that gave me really bad indigestion that felt like chest pains. I stopped it and went back to the Tums. Also, it helps to keep a well balanced diet - plenty of fruit and vegetables and meat, poultry and fish and try brown rice once in a while as well as Greek yogurt sometimes. The very bland diet we're on for kidney disease doesn't always give us what our bodies need. Some variety in your diet with moderate quantities helps.

felizesperar profile image
felizesperar

Hi thanks for the response! He is actually only able to take the chewable phos binders. So we are limited there. Her do try to vary his diet but we just can’t figure out any pattern at all!

Kbristow profile image
Kbristow in reply tofelizesperar

You may want to keep a log of what he is eating for now so his renal dietician knows how what to recommend. As you're varying the foods you may also begin to notice patterns of what foods might be causing more problems than others. Check with the dietician about more high fiber foods and a well balanced diet as cs65 suggests. I like to use chia seeds in my smoothies so you can ask about that. It's good to also stay away from processed and high sodium foods.

felizesperar profile image
felizesperar in reply toKbristow

Hi thanks for responding! Yes, I think we should track what he eats- I need him to agree, which can be a challenge- he is exhausted for a full day after dialysis and doesn’t want or feel able to do much at all. I try, but it needs to be a full list for it to mean anything. He also has to stay away from high fiber foods due to diabetic gastroparisis - slow bowels, Dutch to long term diabetes (since he was 6), he’s so between a rock and a hard place most days.

I will try to get him to start tracking his food! Thank you!

felizesperar profile image
felizesperar in reply toKbristow

hi- I wanted to provide an update to everyone- we started tracking his food, activities, medicine (extra stuff like stool softeners, vitamins, etc) Here is what we learned:

Natural stool softener in the AM and PM, AND Miralax, only every other day. This has significantly improved his bowel movements and frequency. We also are steering away from anything with an alfredo sauce - apparently really causes problems for his digestion! Thank you all, he is in such a better place now- and you have all helped!

cs65 profile image
cs65NKF Ambassador

I wonder is he should check with his nephrologist or dietitian about taking something like metamucil for fiber, or if his condition doesn't allow that?

felizesperar profile image
felizesperar in reply tocs65

Hi yes sometimes he takes that and stool softeners - I sometimes think he takes too much of that stuff. There are just so many variables.

felizesperar profile image
felizesperar

Hi yes he does that already.

mieka profile image
mieka

Does he take any type of a stool sofener? It may be that the frequency & dosage needs to be adjusted. I have had to play around with what stool softener & how much & when in order to find what works for me. Currently on Docusate capsule every other day. Any of the liquid softeners such as Miralax or Lactulose created a mess! Also - age & weight can make a big difference in what dose to take.

JJForDad profile image
JJForDad

My FIL has Sodium Bicar as his binder. It isn’t chewable but with what it is, may be worth asking the Nephrologist if it can be chewed. I think they crushed it for him when in rehab. But plz ck with doctor. What I’m saying could be way off base.

Good luck!

felizesperar profile image
felizesperar

Thanks for the suggestion! We will ask the doctor!

Not what you're looking for?

You may also like...

I am new to this forum, and would like to ask some questions on my fathers behalf.

My farther has been on self dialysis now for 3 years and has recently been very messed up with not...
Dad2020 profile image

So sad

Today I lost my first friend at dialysis. He was a charming gentleman who always made me laugh....
Frankie24 profile image

Tired

Like many of you I’m sure, but just speaking for myself, I am so incredibly tired of dialysis and...
Frankie24 profile image

My dad has CKD stage 4.

Hi, I’m so glad to have found this group. My dad has been told today that his kidney disease has...
Danidan25 profile image

Peritoneal Dialysis

I would just like to share my experience with peritoneal dialysis. If you haven't read my previous...
PUREkatniss profile image

Moderation team

See all
JessicaJ_NKF profile image
JessicaJ_NKFAdministrator
Cap21_NKF profile image
Cap21_NKFPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.