The Muscle Movement Foundation (MMF) is an IRS-registered 501(c)(3) organization founded by way of Rob DeMasi in 2012. After four years of misdiagnoses, hospital visits, and tests, Rob was finally properly diagnosed with an autoimmune form of muscle disease called myasthenia gravis (MG). After enduring the worst of the physical, financial, and emotional trauma attributable to the disease, he founded the Muscle Movement Foundation to ensure an active resource would be available to families affected by ALS, muscular dystrophy, and additional forms of neuromuscular diseases.
MMF's mission is to provide life-changing accommodations to individuals living with muscle disease to enhance their strength, autonomy, and quality of life. Our vision is to unite communities across the United States in advocacy, volunteerism, and involvement to address alarming issues and fulfill the unmet needs of children and adults affected by neuromuscular disease. We envision the state of Delaware free from the physical, financial, and emotional restraints attributable to neuromuscular disease.
By making a secure donation, you can help families affected by muscle disease live life stronger. For the ability to walk, talk, swallow, hug their loved ones, and breathe...
ID #: 46-0554462