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The 4 Jake’s Sake Charitable Foundation is a nonprofit organization founded by John and Sheryl Marrazzo in honor of their son, Jake, who has Duchenne Muscular Dystrophy (DMD), a severe genetic disorder that leads to progressive muscle degeneration. Established originally as a team for a walkathon in 2012, the foundation aims to raise awareness about DMD and support families facing the financial challenges associated with this condition. With a mission to enhance accessibility in the lives of those affected by DMD, 100% of donations go directly to helping families manage their needs. Through its efforts, the foundation not only provides practical support but also promotes a positive outlook, inspired by Jake’s resilience and achievements, including his success as a published author.

www.4jakessake.com

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4 Jake’s Sake: 7 Benefits to Working With a Charity

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Learn about Jake Marrazzo, a seventeen-year-old high school senior who is wildly creative, has a smile that lights up the room and has Duchenne Muscular Dystrophy. Jake was diagnosed when he was 8 and has been confined to a wheelchair since he was 12. Duchenne muscular dystrophy is the most aggressive form of muscular dystrophy, a genetic disorder characterized by progressive muscle degeneration and weakness due to the alterations of a protein called dystrophin that helps keep muscle cells intact. The prevalence of DMD is mostly in boys and affects approximately 6 people per 100,000. There is currently no cure for Duchenne but there are many promising developments.