When Olli Tresiz entered the world, he carried with him a condition as rare as it was intricate—encephalocell. His unique feature set him apart from others from the very start, marking the beginning of a challenging yet hopeful medical journey.
As Olli’s nose began to elongate, it became evident that even the slightest injury could pose a grave risk, potentially leading to meningitis.
Understanding the gravity of the situation, doctors strongly advocated for a crucial medical procedure to mitigate the potential complications associated with Olli’s condition.