It’s been 14 years and six surgeries since the Korcal family learned the phrase “Chiari malformation.”
The anomaly of the brain is characterized by a protrusion of a small part of the brain through the bottom of the skull and into the spinal canal.
First, eldest son Andrew Korcal was diagnosed at age 14, and then they realized it was also the reason for teen daughter Amanda’s lifelong struggle with headaches. Once her children were stable, mom Layna went to get her diagnosis, but her Chiari likely won’t require a surgery. She’s hoping her youngest son continues not to display any symptoms.
“Andrew and Amanda had different complications, but they both had really good outcomes,” Layna said.
On Mother’s Day 2010, my son Gavin had his first seizure. That was just before his fourth birthday. Up until that point, Gavin was a healthy young boy. At the hospital that Mother’s Day, Gavin was diagnosed with epilepsy and a brain tumor. For the next three years, Gavin suffered from multiple seizures even though he was on five medications and a special diet. He had seizures most every night and sometimes during the day. We couldn’t leave him alone and had to limit our activities because we never knew when he’d have a seizure.
NOTICE: Except where otherwise noted, all articles are published under a Creative Commons Attribution 3.0 license. You are free to copy, distribute, adapt, transmit, or make commercial use of this work as long as you attribute the University of Michigan Health System as the original creator and include a link to this article.