Prof. MD. Mehmet Tasdemir

Our newborn's prenatal ultrasound suggested multicystic kidney disease. Prof. Tasdemir initiated in-utero consultations and prepared a birth plan coordinating nephrology, urology, and NICU teams. The condition self-resolved by six months, but the family support system remained for other expecting parents.

Our 14-year-old competitive swimmer, Elif, developed sudden proteinuria during national trials. Local doctors suggested rest, but Prof. Tasdemir identified a rare exercise-induced glomerular condition through specialized stress tests. His tailored hydration and medication protocol allowed her to compete safely three months later, winning a regional championship while maintaining perfect renal markers.

As Syrian refugees, we feared seeking care for our 3-year-old son's unexplained kidney swelling. Prof. Tasdemir not only provided treatment without bureaucratic delays but discovered a congenital ureter abnormality missed in two countries. His team created Arabic-language care instructions and connected us with support groups, transforming our crisis into hope.

My 17-year-old daughter, diagnosed with lupus nephritis during exam season, faced potential dialysis. Prof. Tasdemir pioneered a novel combination therapy avoiding steroids' cognitive side effects. She completed university entrance exams on schedule with improved kidney function, now studying medicine inspired by his holistic approach.

After earthquake displacement, 5-year-old Ali's chronic kidney disease management collapsed. Prof. Tasdemir located the family in temporary housing and established a mobile treatment unit, later securing permanent housing near the hospital. The model now serves other displaced children with special medical needs.