Mark and Ben, two local children, both suffer from a mutation on the SCN2a gene which causes a spectrum of ailments from developmental delays to severe intractable epilepsy. Most of the children with this diagnosis are unable to walk, talk, eat, and suffer from daily seizures, pain, and Autism. Their families have formed a foundation, the FamilieSCN2a Foundation to promote and fund research to find a cure for our children.

YOUR CHANCE TO BE A HERO, 100% of proceeds to go directly toward researching a cure for all children impacted by the SCN2a gene mutation.