Kidney disease can feel overwhelming. These guides explain what your tests mean, what your treatment options are, and how to live well alongside CKD — written by kidney doctors for patients and the families who care for them.
A simple explanation of kidney function, why your doctor monitors it, and what early changes mean.
How kidney function is measured, what the stages mean, and what you can ask your doctor about your result.
The first questions to ask, lifestyle changes that matter, medicines that protect your kidneys.
Salt, potassium, phosphate, protein — what to add, what to limit, and how to enjoy food again.
ACE inhibitors, ARBs, SGLT2 inhibitors — why your doctor prescribed them and what to expect.
Practical planning for holidays, long flights, fasting during Ramadan, and managing work demands.
How HD works, what a session feels like, how to prepare your fistula, and how to live well between treatments.
Home-based dialysis through the abdomen — who it suits, daily routine, and avoiding infections.
From the waiting list to the surgery to life with a new kidney. Living donor and deceased donor explained.
A respectful conversation about supportive kidney care without dialysis — what it offers and who it suits.
All patient guides will publish in both English and Arabic. Arabic versions are written, not auto-translated, by an Arabic-speaking clinician — keeping medical accuracy without losing dignity in the language patients actually speak at home.