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Charlotte Figi was three months old when she had her first epileptic seizure. The episode appeared to come out of nowhere, as Charlotte's early infancy, as well as her fraternal twin's first few months, had been easy crusing up till that time. As her parents, Matt and Paige, stood by, alarmed and involved, Charlotte underwent a battery of medical exams, including bloodwork, MRIs, spinal taps and more. All her results were normal. And but, every week later, Charlotte skilled her second, extra intense seizure. Fast ahead two years and toddler Charlotte's life had been taken over by every day seizures, stalled cognitive development, emotional modifications and fruitless medical tests. Just before her third birthday, the Figis lastly acquired some insight into what might be at the basis of Charlotte's problems: doctors at Children's Hospital in Colorado diagnosed her with a condition called Dravet syndrome (often known as myoclonic epilepsy). The incurable, extreme type of epilepsy is part of a bunch of diseases known as SCN1A-associated seizure disorders and while it typically develops in the primary year of life, it causes longer, extra intense seizures as time goes on.
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