Angeline’s Story: Navigating Life’s Unexpected Turns
This is what my MOGAD Pain Feels like Amid a thriving career and relentless pursuit of success, life threw me a curveball. My legs started…
MOG Blog
MOG Project Blogs
Demystifying the Diagnosis of MOGAD: Take-Home Points for Patients from the 2023 International MOGAD Panel Proposed Diagnostic Criteria
Background and importance: While several prior publications have suggested diagnostic criteria for MOGAD, formal guidelines for diagnosis had not been proposed until March 2023 in…
MOGAD: Follow-up Questions From the September 29th 2022 Q&A Roundtable at the Harvard Faculty Club, Cambridge, MA.
Bio Pictures with Circle crop (1) SudarshiniRamanathanCircle Dr. John J. Chen, MD, PhD Dr. Tanuja Chitnis, MD Dr. Elias Sotirchos, MD Dr. Brenda Banwell, MD…
Triumph Through Hardship
April is MOGAD Awareness Month. This month was created “To shine a light on MOG antibody disease (MOGAD) and the journeys of all those diagnosed…
Gaia’s Story: Transformation Through Self-Expression
The following story is reproduced with permission from the author. Source material is accessible here. Okay so my hands are shaking a little, it’s probably…
Dana’s Story: Painting a Brighter Future, Together.
My weird case started in September 2020 when I had a high fever of 102 with no other symptoms. The fever continued for 30 days,…