Tessa Evans, born on Valentine’s Day 2013, has captured hearts worldwide with her resilience and charm. Diagnosed with Bosma arhinia microphthalmia syndrome (BAMS), a rare condition affecting fewer than 100 people globally, Tessa’s story inspires hope.
Her parents, Grainne and Nathan, faced unexpected challenges when Tessa arrived without a nose. Despite normal pregnancy scans, Tessa’s condition shocked them. BAMS causes respiratory issues, preventing Tessa from smelling or breathing through her nose.
Tessa’s early life was marked by intensive care and surgeries. At two weeks old, she underwent tracheostomy tube insertion, enabling normal eating and sleeping. Pioneering cosmetic nasal implants at age two made her the first recipient.
“Tessa’s strength inspires me daily,” Grainne says. “Her zest for life and infallible courage are remarkable.”
Tessa’s journey hasn’t been easy. Implant removals and lengthy recoveries tested her family. Yet, Tessa remains upbeat.
“My BAMS syndrome won’t stop me,” she declared. “I’m excited for my new nose, but it’s awesome I don’t smell bad smells!”
Grainne praises Tessa’s growing energy and enthusiasm. “When she saw her new nose, she beamed with pride, saying, ‘Mummy, I love my new nose!'”
Tessa’s Facebook page, “Born Extraordinary,” overflows with admiration. Fans rave about her beauty, intelligence, and character.
“Her face may not be ordinary, but it’s exceptionally beautiful,” one supporter wrote.
Tessa’s story spreads joy and resilience, proving that challenges can’t define one’s spirit.
