Tessa Evans, an ordinary young girl, has an extraordinary characteristic—she was born without a nose, a medical condition known as aplasia.
This rare anomaly has been reported only 47 times in the entire United Kingdom, making it an exceptionally uncommon occurrence.
Tessa, now eight years old, was diagnosed with this condition, also referred to as congenital absence of the nose, which meant she would have a relatively flat facial profile, a detail the ultrasound had hinted at.
During her 11th week of life, Tessa underwent a surgery to address a cataract issue, which unfortunately resulted in blindness in one eye.
In addition to this visual impairment, she was diagnosed with heart problems, adding further complexity to her health challenges.
Tessa’s unique situation led to the necessity of a tracheostomy to facilitate breathing while eating, highlighting the intricate medical interventions required to address her specific needs.
Despite being born without a nose and facing multiple health issues, Tessa’s family remains dedicated to her well-being.
The absence of sinuses leaves her susceptible to colds and respiratory challenges. However, her parents, having chosen not to terminate the pregnancy, continue to provide love and support for Tessa.
Looking ahead, the family plans to pursue surgical procedures to reshape Tessa’s nose, aiming to enhance her overall health and quality of life. Throughout her journey, Tessa maintains a cheerful disposition, showcasing resilience and strength in the face of adversity.
