The Baby No One Expected to Survive Is Now a Beautiful Princess

Tessa Evans was born on Valentine’s Day 2013, a moment of love and shock for her family when doctors revealed she had no nose, the result of an extremely rare condition. Only about 100 such cases exist worldwide, leaving her parents facing fear and uncertainty from the very beginning. The family’s life became a maze of appointments, consultations, and questions without easy solutions. Yet in the midst of uncertainty, hope began to take shape, as doctors introduced a pioneering plan that could change everything…

Tessa Evans arrived on Valentine’s Day in 2013, a day the world usually associates with roses, hearts, and love. Her family remembers her first moments with the same warmth—her tiny fingers curling, her lips forming the faintest smile. But alongside that joy came shock. Something about their newborn daughter was startlingly different. Tessa had been born without a nose.

Doctors quickly diagnosed her with Bosma Arhinia Microphthalmia (BAM) syndrome, an extremely rare condition so uncommon that only around 100 known cases exist worldwide. For her parents, the news was overwhelming. How could their baby, so beautiful and so fragile, face such an uncertain future? In those early days, no one could offer a clear answer.

The family’s life became a maze of appointments, consultations, and questions without easy solutions. Yet in the midst of uncertainty, hope began to take shape. Medical experts saw Tessa not just as a patient, but as a pioneer. They believed her story could rewrite what was possible for children born with this condition.

Using advanced technology, doctors turned to 3D printing and medical tattoo artistry to create a groundbreaking solution: a nasal structure designed to grow with her. This innovation meant Tessa wouldn’t have to endure endless major surgeries. Instead, her “nose” could be gradually reshaped and updated as she matured, giving her both a natural appearance and a chance at a more normal childhood.