Katie’s Story: Walking Again
I’m not sure how long I’ve had MOG. After college, I battled headaches, nausea, and fatigue. I always attributed these symptoms to something else: eye…
I’m not sure how long I’ve had MOG. After college, I battled headaches, nausea, and fatigue. I always attributed these symptoms to something else: eye…
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…
In the Fall of 2013, my first year of college was finally beginning. I was loving life, embarking on new experiences, and finding my passions.…
The MOG Project is thrilled to announce our partnership with The Siegel Rare Neuroimmune Association (SRNA) to advance our shared mission in supporting the MOG-AD…
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.