Understanding Bosma Arhinia Microphthalmia Syndrome
Bosma arhinia microphthalmia syndrome (BAMS) is an extremely rare condition characterized by the absence of the nose (arhinia) and underdeveloped eyes (microphthalmia). This condition can also affect the development of the brain and other body parts. First documented in 1981, BAMS is so rare that only a few dozen cases have been reported worldwide. The condition is caused by mutations in certain genes, leading to developmental anomalies.

While BAMS is rare, it is important to note that with advances in genetics, medical practitioners have become better equipped to diagnose and manage the condition. The impact of BAMS on individuals can vary widely, but for many affected individuals, it results in lifelong challenges related to breathing, vision, and developmental delays.

Tessa Evans’ Journey with Bosma Arhinia Microphthalmia Syndrome
Tessa Evans’ condition has not only been a personal challenge but has also helped raise awareness of BAMS and its effects on individuals and their families. While much of Tessa’s medical history remains private, what is publicly known is that her parents, Grainne and Nathan Evans from Maghera, Northern Ireland, have been dedicated to seeking out the best possible care for their daughter.