Born without a nose: This is what Tessa Evans looks like at 10 years old

Tessa Evans, who was born on February 14, 2013, was born without a nose, a rare condition that has sparked admiration and affection from her family and people around the world.

Tessa’s unique condition is known as Bosma Arhinia Microphthalmia Syndrome (BAMS) and there are fewer than 100 documented cases worldwide. Despite the rarity and complexity of her condition, her mother praises Tessa’s “charming” behavior and her “remarkable courage”.

Eight years into her journey, Tessa has become a symbol of resilience. She continues to do well and embrace life to the fullest, despite the challenges presented by her condition, which includes the inability to smell or breathe through her nose.

However, she can still cough, sneeze and catch colds. “It was pretty amusing the first time she sneezed”, recalls her father Nathan, “but we realized it was actually coming from her chest, which was a small but reassuring sign of normality”.

Tessa’s parents, Grainne and Nathan Evans, were stunned when their Valentine’s baby was born without a nose as the pregnancy was uneventful and there were no signs of problems.

A native of Maghera, Ireland, Tessa’s condition required immediate medical intervention. At less than two weeks old, she underwent surgery to insert a tracheostomy tube so she could eat and sleep comfortably.

At just two years old, Tessa achieved a medical milestone when she became the first person to receive a cosmetic nasal implant, marking a significant advance in the field and a remarkable solution to her rare condition.

World’s Hairiest Girl Embraces Change After Meeting Soulmate – See Her New Look

Supatra ‘Natty’ Susuphan, once known as ‘The World’s Hairiest Girl,’ has transformed her life. Natty, 17, from Bangkok, Thailand, battled Ambras Syndrome, causing excessive hair growth. Guinness World Records recognized her in 2010. She used laser treatments, but now shaves to maintain her look.

Natty found love and posted on social media: “You’re not just my first love, you’re the love of my life.” Ambras Syndrome was once misunderstood, leading to stigma. Natty faced teasing and cruel nicknames like ‘Wolf Girl’ and ‘Chewbacca’ in school. However, her family and friends supported her.

Natty’s perspective is inspiring. She said, “Being hairy makes me special.” Despite the teasing, she’s grown accustomed to her condition and hopes for a cure someday. Her journey highlights self-acceptance and the importance of a supportive network.

It’s a testament to resilience and redefining beauty on one’s terms.

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