Born on Valentine’s Day in 2013, Tessa Evans is a remarkable 10-year-old girl from Maghera, Ireland, who has captured the hearts of many with her extraordinary story. Tessa was born without a nose due to a rare condition known as Bosma arhinia microphthalmia syndrome (BAMS), which affects less than 100 people worldwide.
Despite the challenges she faces, Tessa is a beacon of hope and inspiration. Her parents, Grainne and Nathan Evans, were shocked when they discovered their daughter’s condition during pregnancy. However, they have been a pillar of strength and support for Tessa, helping her navigate the difficulties that come with BAMS.
Tessa’s condition means she cannot smell or breathe through her nose, but she can still cough, sneeze, and get a cold. In her early years, she underwent several surgeries, including a tracheostomy tube insertion to facilitate eating and sleeping. At just two years old, Tessa became the first person to receive a cosmetic nasal implant to create a nose-like structure.
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The road to recovery has not been easy, with one implant having to be removed due to complications. Nevertheless, Tessa remains strong and happy, with her parents by her side. Her mother, Grainne, praises her “charming” attitude and “infallible courage,” saying, “Every day she inspires me with her zest for life and infallible courage.”
Tessa’s story has touched many hearts, with people gushing over her Facebook page, “Tessa; Born Extraordinary.” One supporter writes, “Her face may not be ordinary, but I find it exceptionally beautiful. Intelligence, character as well. Shine on, young one.” Another adds, “Tessa has grown and is beautiful and looks happy.”
As Tessa continues on her journey, she serves as a reminder that being different doesn’t dim your shine; it makes you extraordinary. Her story is a testament to the power of resilience, courage, and the human spirit ¹ ².