The MOG Project is a non-profit, patient-led organization devoted to raising awareness for Myelin Oligodendrocyte Glycoprotein Antibody Disease (MOGAD). Our organization provides education for patients, caregivers, and medical professionals. In addition, we provide support to those struggling with this disease and have built a global network to bridge the gap between patients and researchers. These activities ultimately lead to improved quality of life for those afflicted with this life-changing disease. We have laid the groundwork for our community outreach with our website, social media presence and virtual support groups. We have also built a large Medical Advisory Board of the top clinicians and researchers in MOGAD around the world.