It is the mission of Hope for Gabe (H4G) to ensure a cure for the terminal disease Duchenne is found in time for this and all future generations of patients inflicted with this horrible disease, including Gabe. Our #1 goal is simple – to eradicate this disease! To see your son lose his ability to run, climb stairs, hug, chew, brush his teeth, breathe, and to pump his own heart is unimaginable. This is our reality and is happening to my son and will continue to happen until the end of this journey (usually mid 20s). But there is hope…as his muscle die, we are trying every thing in our power to see him and others like him beat the odds and with medical advancements, we grow closer every day! We decided that while we are embarking on this journey of life as a family, we are going to make the most of it. We wanted to create a legacy for our son no matter what happens down the road. That legacy will be the Hope for Gabe Foundation (Hope for Gabe Inc.). We are a 501(c)(3) non-profit organization (Federal tax ID# 27-1240341). We can’t wait to see what a difference Gabe and his foundation make in this role! With your help, our HOPE is to End Duchenne!