Prof. MD. Nihan Alkis

As a 67-year-old retired ship captain, I was preparing my affairs when diagnosed with myelodysplastic syndrome. Prof. Alkis's personalized hypomethylating agent therapy reversed my transfusion dependency completely. I've now sailed the Mediterranean twice since treatment, something I never thought possible.

As a 22-year-old competitive cyclist, my unexplained fatigue was dismissed as overtraining until Prof. Alkis discovered I had paroxysmal nocturnal hemoglobinuria. Her targeted treatment plan not only saved my life but allowed me to return to professional racing within a year, winning two national championships post-recovery.

My 8-year-old daughter's mysterious bruising was initially misdiagnosed as playground injuries. Prof. Alkis recognized the pattern of immune thrombocytopenic purpura immediately. Her gentle approach with pediatric patients and innovative steroid-sparing protocol gave us our vibrant child back without the side effects we feared.

Our family's genetic bleeding disorder affected three generations until Prof. Alkis identified it as a rare form of Glanzmann thrombasthenia. She coordinated care across five family members simultaneously, creating individual management plans that transformed how we live with this condition.

During my wife's high-risk pregnancy, Prof. Alkis managed her essential thrombocythemia with such precision that she avoided blood thinners until the final month. Our healthy twins were born without complications, and my wife's condition remains stable two years later under Prof. Alkis's continued care.