A girl from Australia who smiles all the time. How did her parents accept her

Remember Victor Hugo’s The Man Who Laughs. It was later made into a movie as well. But if in the book the poor guy suffered from bullying over his mouth, then in Australia in 2021 a girl was born with a very wide mouth by nature.

The birth of a new child is always a joyful event in the life of parents. Christina and Blaze, a young couple from Australia, were no exception. Their joy knew no bounds when they first saw the baby. But their joy was overshadowed when they learned that their baby girl was born with an unusual illness. This disease put the doctors and the girl’s parents to a standstill. But the young couple accepted the girl how she was and loved her unconditionally.

Christina got pregnant in 2021. They realized that their relationship was reaching a new level. now they are going to be parents. To celebrate, the future young mother shared this event on her social networks. The news of the pregnancy touched her chosen one. Blaise’s tears were watched by everyone who followed this story. At the end of December 2021, Isla Summer was born. It was the best Christmas present for them!

Ayla was born outwardly healthy. But the parents were shocked to find that their child’s mouth was unusual. It was very wide open. this was not visible on the ultrasound image. The child’s condition was so unusual that doctors had never seen anything like it before. It was later determined that the girl had a bilateral macrostomy. This is an extremely rare disease in which the borders of the mouth have not fused properly during formation in the womb.

The girl’s parents had never known about such a disease, and even more so they did not think that their child would be touched by such a fate. She is one of 14 newborns in the world who were diagnosed with this disease. Christina kept thinking about where and what she did wrong during the pregnancy. However, studies have shown that this is not her fault.

Parents’ initial concerns about a simple cosmetic anomaly quickly turned into concerns about Ayla’s ability to lead a normal, healthy lifestyle. Doctors say that babies with this condition may have difficulty fixating and feeding. Because of the impact this has on facial functionality, patients with this illness are often advised to have surgery to “fix” the problem at an early age. Christina assured that she and her husband studied the problem and this operation is a closure of the skin and will lead to minimal scarring in the baby. But the problems that could arise after the operation worried the young parents.

They would go to any lengths to provide their little one with the best possible life. After giving birth, Christina created an account and started posting videos of her baby and her unusual smile. She had no idea how much support she would receive. Almost everyone was touched by Ayla. Millions of people have praised this little one and her “permanent smile.” This gave Christina the courage to continue covering Isla’s life. As Christina assures, these videos were very motivating for young mothers who had “unusual” children.