Ayla Summer Mucha, born in December 2021, astonished her parents with a bright smile on her small face. Even though her parents were initially perplexed by the fact that she had an unusual illness that caused her smile to be permanent, they quickly fell for her. Now, Ayla is well-known on social media, and people all around the world appreciate her sweet smile.Cristina Vercher and her husband Blaize Mucha were thrilled to meet their newborn girl on December 30, 2021, after nine months of anticipation. However, during the C-section birth, doctors delivered some startling news.
Ayla Summer Mucha was born with bilateral macrostomia, which means her mouth did not develop normally.The malformation, known as a facial cleft, occurs when the corners of the mouth do not come together properly when the baby is growing inside the mother. It is so uncommon that only 14 cases like it have been documented in medical books.Ayla’s parents were unaware of this until she was born because ultrasounds revealed no issues. When they noticed her mouth open wider than usual, they became really concerned.
Ayla’s mother, who is now 23, and father, who is 22, were astonished and concerned because the problem was clear even though Ayla was so small.”Blaize and I didn’t know about this condition, and I had never met anyone born with a macrostomia,” Vercher, the Adelaide native, said. “So, it was a big surprise.”The parents weren’t the only ones who were surprised. Even the doctors were unprepared to handle a baby with bilateral macrostomia.”What made it much more alarming was that it took hours for a doctor to respond.
“And the hospital knew very little about this rare condition,” she explained. “As a mother, all I could think about was where I went wrong.”However, physicians informed the frightened parents that there was nothing they could have done differently. Cristina was scared that she had made a mistake during her pregnancy or had caused her daughter’s ailment.”I couldn’t stop thinking about where I might have gone wrong as a mother,” she told me.
However, after days of genetic testing and imaging, they were persuaded that they had no influence over the situation and were not to blame.The Mucha family focused on assisting Ayla in living peacefully with her disability, which impairs her ability to eat and drink. Sometimes babies with this disease require surgery to help them.To learn more, Ayla’s parents posted her tale on social media.
Ayla’s adorable smile was loved by almost 6.5 million people on TikTok. The Muchas were startled by the outpouring of support.One individual said, “I just researched it up, and there are only 14 cases like hers that are known. She’s very unique. “You should be proud, Mom.”Another individual online commented on Ayla’s smile, “She is beautiful and just perfect the way she is.” “Seeing her smile made me smile, too.”However, some people online have expressed negative things about Ayla. However, Ayla’s supporters instantly backed her.”Your daughter is just stunning. Don’t listen to those negative folks. “She’s like an angel,” one person commented.
Another commented, “Oh my gosh! You are really cute!! Don’t pay attention to those negative comments. “You are just too adorable.”Another reader commented, “You are a strong mother, and your daughter is gorgeous. I’m sorry you had to witness those negative comments.”In reaction to the negative comments regarding her baby, Vercher stated, “I think it’s important to be kind and accept everyone, no matter what.”She hoped that people would treat her and her kid with the same dignity if they were in a similar circumstance.
Vercher stated that situations like these may happen to anyone. She also stated that social media may be a difficult environment since you cannot control what others say.Despite the hostility, Vercher emphasised the positive feedback and support. She continued: “We won’t stop sharing our experiences and favourite memories because we’re really proud.”
