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Hope for Gabe Foundation was created in honor of a little red-headed boy named Gabe Griffin, who was diagnosed with Duchenne Muscular Dystrophy in June 2008 when he was just 3 years old. With funds from this foundation donated to research and clinical trials, and awareness brought to the public about this disease, it is a HOPE that Gabe and other precious boys like him will have a chance to live a full, happy life.
It is the mission of Hope for Gabe (H4G) to ensure a cure for Duchenne is found in time for this and all future generations of boys inflicted with this horrible disease, including Gabe. Their goal is simple – to eradicate this disease! They will do this by directing all fundraising dollars into the hands of lab researchers or other organizations that are determined to find a cure. Hope for Gabe will raise these research dollars by organizing and developing creative fundraising efforts among friends, family, and concerned volunteers, while at the same time, serving as an information database for the most current clinical trials and research programs taking place.
Hope for Gabe has decided that while they are embarking on this new journey of life as a family, they are going to make the most of it! They also want to create a legacy for their son no matter what happens down the road. That legacy will be the Hope for Gabe Foundation (Hope for Gabe Inc.). Hope for Gabe is a 501(c)(3) non-profit organization (Federal tax ID# 27-1240341).
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