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For families and carers

Supporting someone on dialysis

Most of caring for someone on dialysis is not medical. It is logistics, food, noticing, and conversation. Here is what actually helps with each of them.

The week has a new shape

In-centre haemodialysis is usually three sessions a week, about four hours each (NIDDK). That is the treatment. The day is longer: travel there, weighing, observations, connecting, four hours in the chair, coming off, pressure on the needle sites until the bleeding stops, then travel home. For many people a four hour session is a six or seven hour day.

Then there is the recovery. Feeling washed out afterwards is very common, sometimes for a couple of hours and sometimes for the rest of the day, and it is worse when a lot of fluid has been removed. In practice this means dialysis does not take three half days out of the week. It takes three days out of the week, and gives some of them partly back.

Plan the life around that shape rather than fighting it. Put the things that matter, the family lunch, the grandchild, the good hours, on the non-dialysis days. Stop treating a dialysis day as a day when other things can also be achieved.

Transport and getting there

  • Work out the whole journey, not the session. Ask the unit what time they need to arrive, how long they will actually be there, and whether the return trip can be arranged before you set off.
  • Ask the unit what transport support exists. Ask the renal social worker too. Do not assume there is none, and do not assume there is some.
  • Build a backup driver into the plan from the start. A dialysis session is not an appointment that can be quietly rescheduled, and a car that will not start on Monday morning is a clinical problem.
  • If they dialyse on a different island from the one they live on, that is not a detail, it is the central fact of their week. Documented haemodialysis units in Seychelles are on Mahe and on Praslin, which are separate islands, so plan travel around the chair, not the chair around travel.
  • Keep something warm in the car. Dialysis units are cool and the blood is cooled on the way round, so people often come out cold.
  • Pack the bag the night before: medicines list, something warm, headphones, a book or a tablet, and whatever snack the unit allows.

Cooking for a household when one person is on dialysis

This is where families do the most damage with the best intentions. The instinct is to take away everything on a photocopied list of forbidden foods. That instinct is out of date, and it is dangerous.

There is no single kidney diet. Current nutrition guidance moved deliberately away from blanket restriction towards advice individualised to blood results, dialysis modality and remaining kidney function (KDOQI Nutrition in CKD, 2020). Blanket restriction produces a miserable, narrow diet and it produces malnutrition, and malnutrition kills far more people on dialysis than an occasional banana does.

So the goal is not a safe list. The goal is to get a renal dietitian, take them a real food diary and the latest blood results, and cook to the plan they give you. What follows is what to understand so that conversation is a good one.

Salt is the lever that moves everything else

If you change one thing in the whole kitchen, change the salt. Guidance is less than 2,300 mg of sodium a day, which is roughly under 5 to 6 g of salt (KDOQI Nutrition in CKD, 2020).

Here is why it matters more than any other single lever. Salt drives thirst. Thirst drives drinking. Drinking drives the weight they put on between sessions. That weight has to be dragged off in four hours, and dragging it off fast is what causes the blood pressure crashes, the cramps, and the washed-out feeling afterwards. The most useful fluid advice is almost never "drink less". It is "eat less salt, and you will want to drink less".

Most salt is not in the salt cellar. It is in processed and takeaway food, bread, cured and processed meat, stock cubes, sauces, crisps and salted snacks. Cooking from scratch is the single highest-yield thing a household can do, and it benefits everybody at the table.

Protein goes up, not down

This one catches families out badly, so read it twice. Before dialysis, protein is often restricted. Once dialysis starts, protein needs to go up, roughly doubling, to about 1.0 to 1.2 g per kg of ideal body weight per day for people on haemodialysis and on peritoneal dialysis (KDOQI Nutrition in CKD, 2020). Dialysis removes amino acids, and peritoneal dialysis loses protein directly into the drained fluid.

People who carry the old pre-dialysis low-protein rules into dialysis become malnourished. If the household has spent two years carefully keeping the meat off his plate, that has to change on the day dialysis starts, and it should change on the dietitian instruction, not on ours.

Fish is excellent protein and it is the Seychelles staple. It is not free of potassium or phosphorus, so portion size still matters, but do not let anyone talk them out of protein.

Phosphate, and the tablets that deal with it

Phosphate builds up in kidney failure, and over time it pulls calcium out of bone and deposits it in blood vessels, the heart and the eyes, which raises the risk of heart attack and stroke. It also drives the itching (National Kidney Foundation).

The most useful fact about phosphate is that not all of it is equal. Phosphate added to food as a preservative or a texture agent is almost completely absorbed. Natural phosphate from plants such as beans, nuts and grains is bound up and poorly absorbed, and the phosphate in animal foods sits in between (National Kidney Foundation).

So cutting the processed food with phosphate additives is far higher-yield than cutting the lentils. Read ingredient labels and look for anything containing "PHOS". Dark colas, processed cheese, processed and enhanced meats and convenience foods are the usual culprits.

And never solve a phosphate problem by cutting protein. The highest-phosphate foods are often the highest-protein foods, and they need the protein. That is precisely why phosphate binders exist.

Potassium, and why the modality changes the answer

Potassium sits in a narrow safe window. Too high can cause a dangerous heart rhythm, and too low is also dangerous. But current guidance does not set a universal limit: it says intake should be individualised to keep the blood level in the normal range (KDOQI Nutrition in CKD, 2020).

And it depends enormously on the modality, which almost nobody tells families. People on haemodialysis, especially across the long weekend gap, are the group genuinely at risk of a high potassium. People on peritoneal dialysis often run low, and some are told to eat more potassium, not less (NIDDK). Getting this backwards is a real risk in a household that has absorbed the standard advice from somewhere else.

A cooking technique that genuinely helps, if the dietitian has asked you to lower potassium: boil vegetables and starchy staples in a large volume of water and throw the water away. It leaches potassium out. We are not going to publish a percentage, because we could not verify one for the local staples, and your dietitian can tell you how much it is worth in your case.

One warning that matters in any kitchen, and especially in a self-catering apartment or a rented villa: most low-sodium salt substitutes are potassium chloride. They are marketed as the healthy option and they are hazardous in kidney failure. Read the label.

The food that is actually on a Seychellois table

Renal diet leaflets are written for temperate countries. They warn about potatoes and bananas and say nothing about the food that is actually on a Seychellois table, which is why we have set out the numbers below.

Coconut is the headline. Coconut water is sold everywhere as a natural health drink, and for someone on dialysis it is a double hit: it is a fluid, and it is a potassium load. Coconut milk hides the same potassium inside a curry, where it is invisible on the plate.

Breadfruit and cassava are traditional staples and they are high in potassium, breadfruit being roughly in avocado territory. Neither appears on any imported diet sheet.

The good news is real and worth saying: not all tropical fruit is a problem. Papaya, mango and pineapple are all lower in potassium than a banana, and pineapple is notably low. There is more to say yes to here than most people think.

What is actually in the local food

Higher potassium foods commonly eaten in Seychelles, milligrams per 100 g
Higher potassium: take care with thesePotassium, mg per 100 g
Breadfruit seeds, raw941
Avocado, raw (California)507
Breadfruit, raw490
Banana, raw358
Coconut meat, raw356
Avocado, raw (Florida)351
Cassava, raw271
Coconut milk, raw263
Coconut water, from the nut250
Lower potassium foods commonly eaten in Seychelles, milligrams per 100 g
Lower potassium: the safer local choicesPotassium, mg per 100 g
Papaya, raw182
Mango, raw168
Coconut water, ready to drink, unsweetened165
Pineapple, raw109 to 137
Potassium and phosphorus in yellowfin tuna, milligrams per 100 g
Fish, the staplePotassium / phosphorus, mg per 100 g
Yellowfin tuna, fresh, raw441 / 278
Yellowfin tuna, fresh, cooked527 / 333

Source: USDA FoodData Central, Foundation and SR Legacy datasets, retrieved 13 July 2026. These are food-composition values, not a diet plan. Potassium and phosphorus allowances are individual: they depend on blood results, remaining kidney function and dialysis adequacy, and they must come from your own renal dietitian. Use this table to have a better conversation with the dietitian, not as permission or as prohibition.

Fluid, and the heat

We are not going to give you a number. Fluid allowances are individual: they depend on how much urine they still pass, their dialysis modality and schedule, and their blood results, and the renal team sets it. Anyone on the internet who gives you a millilitre figure is guessing about your household.

What we can tell you is that fluid is not only drinks. Soup, gravy, sauces, ice, jelly, ice cream, yoghurt and juicy fruit all count, and so do melons, grapes, oranges and tomatoes (NIDDK). In a resort or at a family lunch, the iced drinks, the sorbet and the fruit platter are exactly the trap.

And the heat here is not a licence to drink more. Kidney Care UK is explicit that there is no one-size-fits-all advice on fluid in hot weather, and that fluid restrictions, diuretics and blood pressure medicines must never be changed without the kidney team, even in extreme heat. Heat cuts both ways: sweating plus fluid removal can tip someone into dehydration and collapse, while drinking to thirst in tropical heat can tip them into fluid overload. It is a conversation with the unit, and the answer is theirs, not ours.

Spotting problems early

You will often see it before they do, partly because you are looking at them and partly because people adapt to feeling awful. Two habits are worth building.

First, learn their access. If they have a fistula or a graft, there is a buzz you can feel over it, called the thrill. It should be checked several times a day. If it weakens or disappears, that is a same-day emergency call to the unit, because a clotting access may still be saved if it is treated within hours (National Kidney Foundation).

Second, know what a missed session actually costs, because families are the ones who quietly enable them. In a European cohort study, in the 48 to 72 hours between a missed session and the next scheduled one, the death rate rose from 4.86 to 51.9 per 100 patient-years and hospitalisation rose from 0.58 to 2.1 per year compared with normal attendance. Missing the first session of the week, the one after the long weekend gap, was around twice as dangerous as missing a mid-week one (BMC Nephrology, 2020). If they are about to miss a session, do not agree that it will probably be fine. Ring the unit.

Looking after the access, every day

  • Feel for the thrill, the buzz over the fistula or graft, several times every day. If it stops, treat it as an emergency.
  • Wash the access with antibacterial soap every day, and always before dialysis.
  • No blood pressure cuff on that arm. Ever. Tell every nurse, doctor and paramedic who reaches for it.
  • No blood taken from that arm, and no drips into it.
  • No tight sleeves, no watch, no bracelets and no rings on that arm.
  • Nothing heavy carried on that side, and no sleeping with the head resting on it.
  • Keep gauze or a clamp within reach at all times, in case a needle site bleeds.
  • Bleeding from a needle site that lasts more than 30 minutes should be reported (National Kidney Foundation). Bleeding that will not stop with firm pressure is an emergency: press hard, do not let go, and call for help.

The access is the lifeline of haemodialysis. Protecting it is one of the most concretely useful things a family can do.

When to seek urgent help

Some things cannot wait until your next session. If you recognise yourself here, act now.

Call your local emergency number now

  • Bleeding from your fistula, graft or catheter that will not stop with firm, continuous pressure

    Blood loss from a dialysis access can be rapid and life-threatening. Press hard, do not let go, and call for help.

  • Chest pain or tightness, or pain spreading to the arm or jaw

    This can be a heart attack. Heart disease is the leading cause of death in people on dialysis.

  • Severe breathlessness, especially lying flat, waking up gasping, or coughing pink frothy sputum

    Fluid on the lungs. This can be fatal and may need urgent dialysis.

  • Collapse, fainting, a seizure, or new confusion

    Could be a dangerous drop in blood pressure, a dangerous potassium level, a stroke, or dialysis disequilibrium.

  • Palpitations with dizziness, or a very slow or very irregular pulse, especially after a missed session

    Suggests a high potassium level or an abnormal heart rhythm. Severe hyperkalaemia can stop the heart.

  • Sudden weakness or numbness of the face, arm or leg on one side, or sudden trouble speaking or seeing

    This can be a stroke. People on dialysis are at high risk, and treatment is time-critical.

Contact your dialysis unit today

  • The thrill (the buzz you can feel over your fistula or graft) is weak or gone

    The access may be clotting. This is time-critical and it may still be saved if it is treated within hours.

  • Fever, shaking chills, or suddenly feeling very unwell, especially if you have a catheter

    This can be a bloodstream infection. Catheters carry the highest infection risk of any access.

  • Cloudy drained fluid, tummy pain, fever, nausea or vomiting on peritoneal dialysis

    Treat this as peritonitis until proven otherwise. Do not wait, and bring the drained bag with you.

  • Redness, heat, swelling, tenderness, pus or discharge at any access or exit site

    An access or exit-site infection needs to be seen, not watched.

  • A cold, painful, numb, weak or pale hand on your access side

    Possible steal syndrome, where the access diverts blood from the hand. A strong thrill does not rule it out.

  • You have missed a session, or you are about to miss one

    Missing dialysis is dangerous, not merely inconvenient, and missing the session after the long weekend gap is the most dangerous of all. Call the unit. Never just skip.

  • New swelling of the ankles, face or abdomen, or new breathlessness on exertion, or a bigger weight gain than your unit agreed

    Fluid is building up. It is far better to be reviewed early than to arrive with fluid on the lungs.

  • New or worsening low mood, hopelessness, or thoughts of harming yourself

    Depression affects roughly a quarter of people on dialysis. It is treatable, and it is linked to missed treatments. Tell someone today.

Whatever else is happening

  • Carry a card or wear an alert saying that you have kidney failure, that you are on dialysis, and which arm carries your access. No blood pressure cuff, no blood tests and no drips in that arm.
  • Tell any doctor, dentist, pharmacist or paramedic that you are on dialysis before any treatment or prescription.
  • Avoid anti-inflammatory painkillers such as ibuprofen, diclofenac and naproxen, and check every over-the-counter medicine and supplement with your kidney team or pharmacist.
  • If in doubt, ring the unit. Dialysis units expect calls. They would far rather answer a question than admit you in an emergency.

This list is general information, not a diagnosis. It cannot cover everything, and it does not replace your kidney team. If something feels wrong and it is not on this list, ring the unit anyway.

Talking about the things you are both avoiding

  1. Say the first sentence badly rather than not at all

    Almost every family waits for a good moment to talk about fear, dying, or what happens if the treatment stops working, and the good moment never comes. You do not need the perfect words. "I do not know how to ask you this, but I think about it" is enough to open a door.

  2. Ask, then be quiet

    Ask what they are most afraid of, and then leave the silence alone. Most people fill it. The fear is often not the one you assumed: it is more often about being a burden, about losing dignity, or about what happens to you, than about death itself.

  3. Do not rush to reassure

    The reflex to say "do not talk like that, you will be fine" is love, but it lands as a door closing. It teaches them to keep the frightening thoughts to themselves, which is the loneliest place in this illness. You are allowed to say "that frightens me too" and stay in the room.

  4. Separate the medical question from the human one

    Some of what they are asking is answerable by the kidney team, and should be written down and taken to them. Some of it is not a medical question at all, and does not want an answer, only company.

  5. Talk about what they want, while talking is easy

    Advance care planning is part of good kidney care, not an admission of defeat, and it is far kinder to have the conversation on a calm Tuesday than in a crisis. Ask the unit how to start one. Doing it early gives them control at the exact moment they will otherwise lose it.

  6. Let them talk about the ordinary things too

    They are not only a patient. Sometimes the most useful thing you can bring into a four hour session is gossip, football, and a family argument about nothing at all.

Sources

  1. Hemodialysis, and Eating and Nutrition for Hemodialysis (NIDDK)
  2. KDOQI Clinical Practice Guideline for Nutrition in CKD: 2020 Update (KDOQI, American Journal of Kidney Diseases, 2020)
  3. Phosphorus and your diet, and Hemodialysis access: caring for your access (National Kidney Foundation)
  4. Hospitalization and mortality following non-attendance for haemodialysis (BMC Nephrology, 2020)
  5. Living with kidney disease: stay safe in the heat and in the sun (Kidney Care UK)
  6. FoodData Central, Foundation and SR Legacy datasets (retrieved 13 July 2026) (USDA)