Tessa Evans, a young girl from Maghera, Northern Ireland, was born with an incredibly rare condition called Bosma Arhinia Microphthalmia Syndrome (BAMS). This disorder affects fewer than 100 people worldwide and is characterized by the complete absence of a nose at birth.
Despite the rarity and challenges of her condition, Tessa has shown remarkable strength and positivity since day one. Her parents, especially her mother Grainne, have supported her with unwavering love and courage as she faced each new hurdle.
At just two years old, Tessa made medical history by becoming the first person in the world to receive a cosmetic nasal implant. This marked the beginning of a long-term process designed to help her build a realistic-looking nose as she grows.
The implant doesn’t serve any breathing function, but it was an important step in helping Tessa feel confident in her appearance. Surgeons planned to update the implant over time as her face matured, avoiding more invasive procedures during her teenage years.
In the meantime, Tessa has lived life like any other child. She’s playful, full of energy, and always smiling. Her parents describe her as having a “sparkling personality” and a “smile that lights up the room.” She loves animals, jumping on trampolines, and dancing to music.
At age 10, Tessa stunned social media followers by sharing a recent photo of herself. The transformation was striking, and people from all over the world praised her beauty, strength, and how much she had grown—both physically and emotionally.
Alongside the physical challenges, Tessa has also dealt with hurtful comments and online bullying. Still, she and her family have chosen to stay visible, using their story to educate others about diversity and the importance of embracing uniqueness.
In 2023, Tessa made a heartwarming appearance on Ireland’s popular “The Late Late Toy Show”, where she radiated joy and confidence. Her mother shared that Tessa had been “over the moon” to be part of the show and was excited for the world to see her shine.
Tessa’s journey has become a source of global inspiration. She’s living proof that inner strength and family love can overcome even the toughest obstacles. Her story shows that beauty isn’t found in perfection but in the courage to be different.
Tessa Evans is much more than a girl born without a nose. She is a symbol of hope, resilience, and self-acceptance. Her story reminds us all that in a world obsessed with appearances, it’s our heart, our spirit, and our authenticity that truly matter.