MOG Blog

MOG Squad Highlights

Katie’s Story of 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 strain from staring at a…
MOG Squad Highlights

The MOG Project

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. I had always been a…
Resources For The Blind

Breaking Through The Darkness

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…
MOG Squad Highlights

Early Signs of a Rare Disease

Now that I have been diagnosed with Myelin Oligodendrocyte Glycoprotein Antibody Disease, or MOG-AD, I have met others who are afflicted and have listened to their stories.  They all start…

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