I would like to say my son’s storyline how to live with Progressive Myoclonic Epilepsy. He was 10 years old on a vacation in Ecuador with his aunt. While he was sleeping, she heard the sound of his bed when she’s walking to his bedroom his body was shaking- his eyes rolling, and foam on his mouth. When he returns home to the US, he didn’t have seizures until a few months later and it was more frequently, stayed in different hospital for different treatments. Almost a year later he was diagnosed with PME. He’s 37 years old now and he is more stable. He had the VNS implant, and it was a miracle, but it relapsed again and it’s affected his speech his mobility and his daily living. He is a great person and resilient to accept his disability. Manuel continues surprising us, his family and friends, because he does not give up. Manny is strong and resilient.