Research studies performed using people as subjects that are aimed at evaluating a medical, surgical, or behavioral intervention to determine to what degree a new treatment (e.g., drugs or medical devices) is safe and effective for general populations.
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The MOG Project Awards 2025 Research Grants
The MOG Project’s Research for Rare program has awarded our 2025 MOGADOften referred to as MOGAD, Anti-MOG, MOG Ab+, MOG Antibody Disease, MOG Associated Antibody Disease, MOG positive disease global research grants: the Apollo Grant and the Accelerator Grant. These grants are
Eliza’s Story: Weaving Emotional Support into the Fabric of Rare Disease Advocacy
Hello everyone, My name is Eliza, and at the age of 34, I was diagnosed with MOGADOften referred to as MOGAD, Anti-MOG, MOG Ab+, MOG Antibody Disease, MOG Associated Antibody Disease, MOG positive disease – a disease I had never heard of
i have mogad , since 2007
Hello I was diagnosed with MOGAD, 7 days after burying my father in July 2021. I woke up completely blind thank God I have received much of my sight back. I currently receive my medication through a port located in my chest every two weeks, each treatment last about 6 hours each. I am still as lost with this Diagnosis as it appears that there is not much information on this illness. I am very interested in learning more information as well as doing clinical trials etc.
Thank you so much for these comments! We certainly feel for you and understand what you’re going through. Please consider joining one of our support groups either through our Facebook pages or through Zoom. The community has a lot to offer and it is a great place for information and comfort.