The first ever MOG Antibody Disease phase 3 clinical trial is now taking place. A new drug called Rozanolixizumab will be trialed
Living with MOG Antibody Disease doesn't have to feel so Overwhelming
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Important Information Please be aware that this is an emerging area of research, and this could change in the future! I want
MOGAD support groups allow members to share experiences about their diagnosis, treatment, feelings, and other first-hand experiences. Healthcare providers treating patients with MOGAD
Myelin Oligodendrocyte Glycoprotein Antibody Associated Disease or MOG Antibody Disease (MOGAD) is a condition that causes inflammation to the optic nerve(s), brain,
MOG Antibody Disease (MOGAD) relapses are one of a patient's biggest challenges. In this blog post, you will learn what a relapse
In collaboration with The MOG Project, MyMyelitis created the Ignition Survey 2 to explore fatigue in MOG Antibody Disease (MOGAD) within the community. Below
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About Me
Hey, I'm Scott.
On the 6th of March 2020, I was diagnosed with a rare neurological disorder called Transverse Myelitis (TM). The results of a specialist blood test later changed my diagnosis to MOG Antibody Disease (MOGAD).
While recovering from my attack, I researched MOGAD to understand the disorder and what I could do to aid my recovery.
Through MyMyelitis, I want to share my recovery story and valuable information about MOG Antibody Disease to inspire you to discover ways to improve your condition and life.
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