MOGAD support groups allow members to share experiences about their diagnosis, treatment, feelings, and other first-hand experiences. Healthcare providers treating patients with MOGAD
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The hunt for the first-ever approved treatment for MOG Antibody Disease continues with another phase 3 clinical trial involving satralizumab. satralizumab will
Myelin Oligodendrocyte Glycoprotein Antibody Associated Disease or MOG Antibody Disease (MOGAD) is a condition that causes inflammation to the optic nerve(s), brain,
A diagnosis of MOG Antibody Disease (MOGAD) can be overwhelming and trigger grief. Grief is a strong, often overwhelming emotion involving loss.
MOG Antibody Disease (MOGAD) relapses are one of a patient's biggest challenges. In this blog post, you will learn what a relapse
The first ever MOG Antibody Disease phase 3 clinical trial is now taking place. A new drug called Rozanolixizumab will be trialed
Last week we were featured in our first-ever MOG Antibody Disease research article! The results of the Ignition Survey #2 Fatigue in
In collaboration with The MOG Project, MyMyelitis created the Ignition Survey 2 to explore fatigue in MOG Antibody Disease (MOGAD) within the community. Below
Transverse Myelitis (TM) is a rare neurological condition involving the spinal cord's inflammation. The inflammation blocks nerve signals from the brain to
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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