Izaiah Ruiz, of Conroe, Tex., was diagnosed with Dravet syndrome, a rare form of pediatric epilepsy, when he was 7 months old. The Dravet Syndrome Foundation estimates that anywhere from 1 in 20 to 1 in 40,000 children have the condition. Causing hundreds of seizures a day, it is commonly misdiagnosed.(Photo courtesy Lori Fountain) Six-year-old Izaiah Ruiz has countless seizures a day due to a rare form of pediatric epilepsy. Now, a marijuana-derived drug may help him and his family avoid the debilitating attacks. Izaiah had his first seizure when he was just 2 months old and was diagnosed with Dravet syndrome, a condition that begins in infancy, five months later. The disease, also called Severe Myoclonic Epilepsy of Infancy (SMEI), is intractable, meaning it does not respond to any currently available treatment. While 60 percent of epilepsy cases do respond, 40 percent, including those linked to Dravet syndrome, do not. When Izaiah has a tonic clonic seizure the type with muscles spasms that most people think of when they hear the word seizure his grandmother, Lori Fountain, follows a military-like procedure to calm and monitor him. Immediately, its getting on the floor and laying him down on his side, … Continue reading
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