The MOG Project Launches New Website

Welcome to The MOG Project! 

The MOG Project is thrilled to officially launch the new website and announce the incorporation of our organization. The MOG Project is on a mission to provide MOG-AD patients, doctors and caregivers access to accurate and current disease information, advocate for research, and bring together a compassionate community to share their stories and provide each other much needed support.. The goal is for this platform is to be a point of relief and comfort for the MOG-AD community.  To better understand where to get information and links, take a quick look at the site map: 

  • Resources provides access to five areas of educational materials:
    • Facts & Information Sheets provides links to information on MOG-AD from disease information to Fact Sheets for Educators.
    • MOGmentum provides access to the MOGmentum Series, which is a collaborative effort between The MOG Project and The Sumaira Foundation for NMO designed to help better understand this complicated disease.
    • Podcasts provides links to the Podcasts, with our partner, the Siegel Rare Neuroimmune Association (SRNA).
    • For the Blind provides educational materials and links to resources compiled by our Ambassador for the Blind, Andrea Mitchell.
    • Ignition Surveys¬†is a landing place for the results of our Ignition Surveys, which are non-scientific surveys from the ever-growing MOG-AD community designed to ignite areas of study for MOG-AD researchers and pharmaceutical companies.
  • News/Events¬†provides the latest new, announcements and events as well as results and pictures of past events.
  • MOG Blog¬†is a great place to find stories and articles designed to educate, inspire, read about other MOG-AD patient journeys and read about tips on living with MOG-AD.
  • MOG Gear page has all of the best MOG Awareness gear. New gear is added periodically to provide new ways to help advocate and raise awareness!
  • Community helps to¬†Connect to the MOG-AD community and¬†Contribute to the MOG Project mission. Please join the email list or consider becoming a volunteer.¬† There are many ways to help, so check it out

To learn more about The MOG Project and who we are, how we started, and what we want to accomplish, check out the About page!

For questions, wanting to get involved, or to contact The MOG Project, please reach out through Contact Us or email us at

Kristina Lefelar | Media Relations |

2 thoughts on “The MOG Project Launches New Website”

  1. Kirsi Kärkkäinen

    Hi !
    Last year at january i got new diagnostig…MOG positiv.
    I` ve beeb twise on hospital.
    In Finland there is not anykind knowing about that diagnostig…tree doctor said to me, that THEM don t know, How They should TaKe care about of me

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