Tessa Evans’ story showcases incredible resilience and medical breakthroughs. Born on Valentine’s Day in 2013 without a nose due to the rare Bosma arhinia microphthalmia syndrome, Tessa has inspired hope worldwide. This condition affects the nose, eyes, puberty, and potentially the brain, with only 100 cases recorded globally since its first documentation in 1981.

Her journey began with a tracheostomy at two weeks old, followed by becoming the youngest recipient of a cosmetic nasal implant at age two. Innovations like 3D printing and medical tattoo artistry offer Tessa a chance for a more permanent nasal structure, reducing future surgeries. Despite challenges, including her inability to smell—a vital safety concern—her family’s unwavering love and pursuit of solutions continue to transform her life.

Tessa’s courage has driven awareness and inspired similar treatments for others. Her story, shared through the Facebook page “Tessa; Born Extraordinary,” followed by nearly 10,000 supporters, highlights the power of determination and medical innovation. Tessa’s life is a testament to overcoming adversity and shaping a brighter future for those with rare conditions.