Charlotte Misko is a unique individual. One in 2,000 to 2,500 people have a condition called craniosynostosis, which the 1-year-old child of Zeb and Bethany Misko has.
Crâniosynostosis: What is it? It occurs when a newborn’s skull bones fuse quicker than anticipated, and it might give birth to a kid with a head that is shaped like a cone.
Although her head shape was known to Zeb and Bethany, they were first informed that it was typical and would disappear on its own. These circumstances do often improve.
but, not when craniosynostosis is included. Zeb had had it as a youngster, so they were aware that it was a possibility.
AThey were informed that Charlotte’s skull would appear unusual before she was even born, as Zeb revealed to People magazine.
He stated, “Charlotte was first born breech and the doctor thought her head abnormalities will go away after a few weeks.
“In the end, it lasted for a month or a month and a half and persisted. We sought the advice of neurology because I had the same diagnosis when I was 5 12 months old.”
It was formally identified in Zeb 27 years ago. His skull was able to expand properly as a result of surgery.
Some kids could require several operations before their disease is adequately treated.
Parents are often terrified when they find that their kid may require surgery.
But fortunately, Zeb’s experience gave the Misko fam some peace of mind.
We felt super comfy with the experts at the Cancer Center doing the same identical operation, just 27 years later since “I had the same complete cranial bolt operation 27 years ago.”
And “I’m convinced that the medical advances and surgical processes have only advanced in those 27 years,” he added.
Watch the Inside Edition video to find out more information about her and her uncommon disease.
