My name is Andrea Mitchell and this is my MOG Antibody Disease story. I am a patient ambassador for UCB and the Director of Blind
At 5 years old, my daughter Isabel was a beautiful, bubbly girl with no health problems. I took her to the Father-Daughter Dance and she
My name is Andrea, and I was officially diagnosed with MOG antibody disease (MOGAD) in 2013. At that time, there was not much known about the disease. The first two years after the diagnosis were especially hard as I lost most of my sight in both eyes. I am writing my story to help others and provide a resource for the newly blind.