In a heartwarming tale of resilience and joy, we meet Tessa Evans, a young girl who radi ates happiness despite being born with a rare condition that left her without a nose.
Tessa’s story is one of strength and positivity, reminding us all that beauty can be found in the most unexpected places. In this article, we will explore Tessa’s journey and the challenges she faces with a smile on her face.
Tessa Evans, now a 17-month-old toddler, was born with a rare congenital condition known as complete congenital arhinia, which means she lacks a nose. This condition is incredibly rare, with only 47 recorded cases in Britain. Despite her lack of a nose, Tessa is just like any other child her age. She loves to dance, climb furniture, and blow kisses, proving that physical differences do not define one’s abilities or happiness.
Living without a nose poses certain challenges for Tessa. She has no sense of smell and lacks sinuses, but she can still cough, sneeze, and even catch a cold. Despite these obstacles, Tessa maintains an infectious smile that lights up the room. Her mother, Gráinne, shares that Tessa’s differences have become insignificant since bringing her home. Tessa’s remarkable ability to adapt and find joy in life is truly inspirational.
To enhance Tessa’s quality of life, she will undergo a prosthetic nose fitting later this year. While Tessa is perfect in her family’s eyes, they want to ensure that her life is as normal as possible. The prosthetic nose will not only help Tessa in her daily activities but also contribute to her self-confidence and sense of belonging.
