Remember Victor Hugo’s book “The Man Who Laughs. They even made a movie based on it. But while in the book the poor guy suffered from abuse of his mouth, in Australia in 2021 a girl was born with a very wide mouth by nature.
The birth of a new baby is always a joyous event in a parent’s life. Christina and Blaze, a young couple from Australia, were no exception. Their joy was boundless when they first saw their baby girl. But their happiness was dampened when they found out their baby girl was born with an unusual disease. The illness rattled both the doctors and the parents. But the young couple accepted the girl with her disease. They really wanted this child.
Christina Vercher and Blaze Mucha are a beautiful couple from Adelaide. They are young and madly in love. When Christina became pregnant in 2021. They realized that their relationship was reaching a new level. now they would also be parents. With joy, the young mother-to-be shared the event on her social networks. The news of the pregnancy touched her chosen one. Blaze’s tears were watched by everyone who followed the story.
A few months later, it became clear they were having a baby girl. And at the end of December 2021, Ayla Summer was born. It was the best New Year’s present ever for her parents. Ayla was born apparently healthy. But the parents were shocked to discover that their baby’s mouth was unusual. It was very wide open. This was not visible on the ultrasound scan. The baby’s condition was so unusual that doctors had never seen anything like it before. They later determined that the girl had bilateral macrostomia. This is an extremely rare condition in which the borders of the mouth do not properly articulate during formation in the womb.
As Christina admitted, it was very noticeable in tiny Ayla. She and Blaze had sounded the alarm, since they had never known of such a disease, much less thought that their child would suffer such a fate. Their baby was one of only 14 babies in the world to have the disease.
Kristina was very nervous about what had happened. She wondered where and what she had done wrong during her pregnancy. However, studies showed that it was not her fault. The parents’ initial fears about a simple cosmetic abnormality quickly turned into concerns about Eula’s ability to lead a normal, healthy life. Doctors say that babies with the condition may have difficulty fixing and feeding.
Because of the impact it has on facial functionality, patients with macrostomia are often recommended to have surgery to “fix” the problem at an early age. Christina assured that she and her spouse had studied the problem and this surgery was a skin closure and would result in minimal scarring for the baby girl. But the problems that could arise after the surgery worried the young parents.
Parents would go to any lengths to ensure their baby girl had the best possible life. After giving birth, Christina created an account on her social media accounts and began posting videos of her baby girl and her unusual smile. She had no idea how much support she would receive. Ayla was adored by just about everyone. Millions of people praised the little one and her “never-ending smile. This has given Christina the courage to continue covering Ayla’s life. As Christina assures us these videos motivated the young moms who had “unconventional” babies.