June 6, 2020/
I’m not sure how long I’ve had MOG. After college, I battled headaches, nausea, and fatigue. I always attributed these…
MOG Blog
- All Posts
- MOG Blog
- Back
- Medical Resource Blog
- MOG Nation
- Resources for the Blind
- MOG Project Champions
- MOG Squad Highlights
- Kids with MOG
- MOGCast Follow-Up
- MOG Project Trip Reports
- Research Article Rundown
June 6, 2020/
My name is Andrea Mitchell and this is my MOG Antibody Disease story. I am a patient ambassador for UCB…
June 3, 2020/
At 5 years old, my daughter Isabel was a beautiful, bubbly girl with no health problems. I took her to…
June 3, 2020/
In the Fall of 2013, my first year of college was finally beginning. I was loving life, embarking on new…
August 22, 2019/
My name is Andrea, and I was officially diagnosed with MOG antibody disease (MOGAD) in 2013. At that time, there…
August 15, 2019/
Now that I have been diagnosed with Myelin Oligodendrocyte Glycoprotein Antibody Disease, or MOG-AD, I have met others who are…
Load More
You're all caught up!
Search our blogs… Categories
- Announcements (8)
- Events (3)
- Kids with MOG (3)
- Medical Resource Blog (3)
- MOG Blog (33)
- MOG Nation (17)
- MOG Project Champions (2)
- MOG Project Trip Reports (2)
- MOG Squad Highlights (8)
- MOGCast Follow-Up (3)
- News (5)
- News/Events (16)
- Research Article Rundown (1)
- Resources for the Blind (2)