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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

MOG Nation

Deby’s Story: Strength Through Shadows

Living with MOGADOften referred to as MOGAD, Anti-MOG, MOG Ab+, MOG Antibody Disease, MOG Associated Antibody Disease, MOG positive disease   as an adult has

MOG Nation

Pooja’s Story: I Am A Warrior

Hello, I am Pooja Bhagchandani, and this is my story I want to share with you. I was born onInflammation of the optic nerve that