Tessa Evans, a bright and charming 10-year-old from Ireland, has captured the hearts of many with her extraordinary story. Born on Valentine’s Day in 2013, Tessa was diagnosed with Bosma arhinia microphthalmia syndrome (BAMS), a rare condition that affects less than 100 people worldwide.
Tessa’s condition means she was born without a nose, and as a result, she cannot smell or breathe through her nose. However, despite this challenge, Tessa’s spirit remains unbroken. Her parents, Grainne and Nathan Evans, praise her courage and zest for life, inspiring everyone around her.
Tessa’s journey has not been easy. She spent five weeks in intensive care after birth and underwent surgery to insert a tracheostomy tube, enabling her to eat and sleep normally. At just two years old, Tessa became the first person to receive a cosmetic nasal implant, paving the way for future procedures.
Grainne and Nathan made the difficult decision to undergo the implant surgery to normalize Tessa’s appearance and avoid more invasive procedures in the future. The process has been long and arduous, with setbacks and adjustments along the way.
Despite the challenges, Tessa remains a beacon of hope and inspiration. Her Facebook page, “Tessa; Born Extraordinary,” has garnered widespread attention and admiration, with many praising her beauty, intelligence, and character.
As Tessa continues on her journey, she remains optimistic and enthusiastic. “My BAMs syndrome will not stop me from doing anything,” she said. Her story serves as a powerful reminder of resilience, courage, and the importance of embracing our unique qualities.
Tessa’s family and supporters celebrate her strength and beauty, both inside and out. As she grows and thrives, Tessa Evans inspires us all to reevaluate our perceptions of beauty and to appreciate the extraordinary qualities that make each person special.
