Deanna was diagnosed in 2015 with Temporal Lobe Epilepsy. This causes Deanna to have anywhere from 3-30 seizures per month. As a parent of a child with epilepsy, it is heartbreaking to watch helplessly as your child has a seizure. The Epilepsy Services Foundation has given our family so much such as support, educational materials, a laptop for Deanna to help her with school and several opportunities for Deanna to be a kid and be around other children with epilepsy at theme parks, parties, meet and greets and camp. Without ESF, I don't know how we would have been able to handle all of this. Please help families like ours fight this disease and continue receiving the assistance that we need so desperately. No one should fight alone!