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What is MOG Antibody Disease?

Myelin Oligodendrocyte Glycoprotein Antibody Disease (MOG Antibody Disease or MOGAD) is a neuroimmune disorder that causes inflammation primarily in the optic nerve but can also affect the spinal cord and brain. MOG is a protein located on the surface of myelin sheaths in the central nervous system. MOGAD is diagnosed through a test that looks for the level of MOG antibodies in the blood. The test should be given to any patient who has an inflammatory attack of the central nervous system. Because of the rare nature of the disorder, it is often misdiagnosed or not diagnosed at all.

Our Mission

The MOG Project is devoted to raising awareness, educating doctors, patients and caregivers, advancing research through expert collaboration and fundraising, and providing support and advocacy for our community in hopes of finding a cure.

Who we are

We are the preeminent 501(c)3 organization solely devoted to globally advocating for patients of Myelin Oligodendrocyte Glycoprotein Antibody Disease (MOGAD). We strive to bring a community of MOGAD patients, caregivers, clinicians, researchers, community partners and industry partners together, creating a patient-led network that puts patients first.

The Story Behind the Hummingbird & The Power of the Flock

In 2017, a scientific breakthrough transformed the lives of people living with MOGAD, providing a clearer pathway to diagnosis and the foundation for the growth of a global community. The development of the live cell-based assay for the MOG antibody enabled physicians to more accurately diagnose Myelin Oligodendrocyte Glycoprotein Antibody Disease (MOGAD), a rare autoimmune neurological condition affecting the central nervous system. This scientific advancement served as the catalyst for the creation of the first digital community, what is now The MOG Project’s Facebook Support Group, MOG Antibody / Anti MOG Support and Info. Created by a MOGAD patient in the UK, the Facebook Support Group became the first global gathering place for people affected by MOGAD. As members connected across countries and continents, sharing experiences and navigating this disease, a collective identity emerged. From that sense of unity, the community chose a symbol to reflect its spirit: the hummingbird.

The hummingbird embodies the tenacity required to live with MOGAD, while its vibrant teal and ruby hues carry layered clinical and historical meaning. Optic neuritis (ON), one of the most common manifestations of MOGAD, can temporarily impair color perception, particularly red and blue. The ruby and blue tones within the hummingbird’s plumage therefore hold particular resonance while teal, a blend of blue and green, highlights the condition’s shared history with NMOSD, a related neuroimmune disorder with overlapping clinical features. Green has long been associated with the NMOSD community, particularly those connected to the Patient Health Alliance.

But more than its colors, it was the spirit of the hummingbird that captured the heart of the MOGAD community. Though small in size, hummingbirds are fierce, resilient, and relentless. They embody strength, stamina, courage, tenacity, and warrior spirit in the face of adversity. Hummingbirds are intelligent, beautiful, and widely recognized around the world as symbols of hope, devotion, love, and even good luck. Perhaps most significantly, the hummingbird is an international symbol of hope. From the very beginning, this community saw itself in this small but mighty bird.

This symbol belongs to the MOGAD community as a whole, before The MOG Project adopted it as part of our logo. We use it because we represent the global “flock” or “charm” that first came together in that support group. The hummingbird is not just a logo, but rather, a reflection of who we are.

Today, The MOG Project serves the international MOGAD community through patient support education, advocacy, and research awareness. The MOGAD community stands as one flock. small but mighty. Rooted in hope. United with purpose. Together, we raise awareness of MOGAD, support individuals and families navigating diagnosis and treatment, and work to improve outcomes for everyone affected by this rare neuroimmune disease.

Watch the video below from MOGAD Awareness Month, April 2024, to understand The Power of the Flock!

Our Financial Contributions to Furthering MOGAD Research

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MOGAD Research Grants
Research for Rare Program

Our Research for Rare Grants Program is designed to hit the hottest topics in MOGAD. With a grant selection process backed by members of our Scientific Council and other unbiased  members of the neuroimmunology community who have expertise in MOGAD, we are able to use our funds in the most impactful way possible.

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MOGAD Professional Education & Researcher Collaboration Grants

Through grants from The MOG Project, we are proud to have been a major contributor to collaborative meetings where researchers and clinicians gather to discuss their latest research on MOGAD.  The importance of these gatherings like the 2023 MOGAD Summit hosted by Dr. Michael Levy has made a huge impact by getting the world’s experts in MOGAD on the same page concerning diagnosis and disease management.

Strength ♦ Resilience ♦ Courage ♦ Hope

Support our Fight against MOGAD

Determination ♦ Flexibility ♦ Adaptability

Our sponsors and partners share our mission, finding power in numbers to create a larger voice of shared experience so that we all can achieve better care for MOGAD and all other rare neuroimmune conditions.

Sponsor or partner with us and let’s work toward a cure for MOGAD together!

Our Corporate Sponsors

QuestionPro’s survey software plays a major role in helping us keep in touch with our MOGAD Community, volunteers, donors and other affiliates. Surveying them has helped strengthen our relationship.

Our Collaborative Partners

Related Resources

For Help with IVIG or SCIG Insurance contact mvogel@ivsolutionsrx.com

Partners for Patient Education