The MOG Project
Providing support and advocacy for those diagnosed with MOG-AD
THE MOG PROJECT
THE MOG PROJECT
Advocating for patients with Myelin Oligodendrocyte Glycoprotein Antibody Disease (MOG Antibody Disease or MOGAD) by education, bringing communities all over the world together, and fundraising to support medical research.
Register for the MOGAD Patient Summit 2026 | The MOG Project
Register for the MOGAD Patient Summit 2026 | The MOG Project
Join the MOGAD Patient Summit in Baltimore, MD. Connect with patients, caregivers, and experts for research updates, education, and community.
Donate or become a Charitable Ambassador to fight MOGAD | Save a Life | The MOG Project
Donate or become a Charitable Ambassador to fight MOGAD | Save a Life | The MOG Project
Our mission is to educate, support, and push for research to find a cure. Your donation will can help save a life! Please consider a donating to help us help you.
MOGAD Family Newsletter | The MOG Project
MOGAD Family Newsletter | The MOG Project
Join The MOG Project’s Family Newsletter for MOGAD families. Get resources, children’s events, support tools, and stories delivered throughout the year.
MOGAD Clinical Trials
Clinical Trials Overview | The MOG Project
Clinical Trials Overview | The MOG Project
Get the latest in MOGAD Clinical trials for Rozanolixizumab (cosMOG study) and Satralizumab (Meteoroid study). The purpose of clinical trials is to evaluate the effects of new treatments & tests for affected MOGAD patients.
cosMOG Clinical Trial | The MOG Project
cosMOG Clinical Trial | The MOG Project
Get the latest in MOGAD Clinical trials for Rozanolixizumab (cosMOG study) and Satralizumab (Meteoroid study). The purpose of clinical trials is to evaluate the effects of new treatments & tests for affected MOGAD patients.
Meteoroid Clinical Trial | The MOG Project
Meteoroid Clinical Trial | The MOG Project
Understand what is involved in the Satralizumab (Meteoroid study) and how to get into this as a MOGAD Patient.
cosMOG Town Hall Series (Recordings and Questions)
cosMOG Town Hall Series (Recordings and Questions)
The MOG Project Resources
The MOG Project Learning Center Resources
The MOG Project Learning Center Resources
We're working hard to empower the MOG-AD community and its caregivers with the latest Information while battling misinformation regarding the disease.
Questions to Ask Your Doctor About MOGAD | Checklist & Guide | The MOG Project
Questions to Ask Your Doctor About MOGAD | Checklist & Guide | The MOG Project
Prepare for appointments with questions to ask your doctor about MOGAD using our checklist and detailed discussion guide. Feel confident in your care.
Sign Up for our Monthly Music, Movement, and MOGAD
Sign Up for our Monthly Music, Movement, and MOGAD
My MOG Tracker | The MOG Project
My MOG Tracker | The MOG Project
The MOG Project YouTube Channel
The MOG Project YouTube Channel
Demystifying the Diagnosis of MOGAD: Take-Home Points for Patients from the 2023 International MOGAD Panel Proposed Diagnostic Criteria - The MOG Project
Demystifying the Diagnosis of MOGAD: Take-Home Points for Patients from the 2023 International MOGAD Panel Proposed Diagnostic Criteria - The MOG Project
FAQS | The MOG Project
FAQS | The MOG Project
Share Your MOGAD Story | The MOG Project
Share Your MOGAD Story | The MOG Project
Youth Champions | The MOG Project
Youth Champions | The MOG Project
Children's Ambassadors | The MOG Project
Children's Ambassadors | The MOG Project
Trip Report for the American Academy of Neurology Summer Conference (AANSC) - The MOG Project
Trip Report for the American Academy of Neurology Summer Conference (AANSC) - The MOG Project
Fact Sheet For Educators
Fact Sheet For Educators
Patient Brochure in Polish
Patient Brochure in Polish
MOGAD Support Groups
Join the MOG Support Groups | The MOG Project
Join the MOG Support Groups | The MOG Project
We've have a variety of support groups that enable the MOG-Ad community to share similar experiences with one another. Join our support groups today!
Register for the AUSNZ Support Group 2026 Sessions
Register for the AUSNZ Support Group 2026 Sessions
A monthly zoom-based support group for those afflicted with MOGAD and living in Australia and New Zealand. Hosted by Kathy Ferella.
Register for Canadian Support Group 2026 Sessions
Register for Canadian Support Group 2026 Sessions
Join this Support Group headed by Sandra Jessop specifically for Canadian MOGAD patients who want to discuss managing their disease and supporting each other in Canada.
Register for Lifting the MOG Fog Support Group 2026 Sessions
Register for Lifting the MOG Fog Support Group 2026 Sessions
Register for the MOG Sloggers Support Group 2026 Sessions
Register for the MOG Sloggers Support Group 2026 Sessions
Register for our Spanish-Language Support Group 2026 Session
Register for our Spanish-Language Support Group 2026 Session
MOGAD New Zealand Support Group on Facebook
MOGAD New Zealand Support Group on Facebook
MOG Antibody / Anti MOG Support and Info Private Facebook Group: must log into Facebook
MOG Antibody / Anti MOG Support and Info Private Facebook Group: must log into Facebook
Latest MOG Blogs
Eight Years Old and Running for Her Brother | The MOG Project
Eight Years Old and Running for Her Brother | The MOG Project
Aria, age 8 and one of The MOG Project's Children's Ambassadors, ran the Great Manchester Run to raise funds and awareness for MOGAD in honor of her twin brother Isaac.
The MOG Project Kicks Off Inaugural MOGAD Patient Summit at Mayo Clinic - The MOG Project
The MOG Project Kicks Off Inaugural MOGAD Patient Summit at Mayo Clinic - The MOG Project
OLNEY, MD (September 2025) – The MOG Project, a nonprofit organization committed to supporting the research and treatment of Myelin Oligodendrocyte Glycoprotein Antibody Disease (MOGAD), officially kicked off its Children’s Ambassador and Children’s Champions programs at the US MOGAD Patient Summit at the Mayo Clinic this past August.
Eliza's Story: Weaving Emotional Support into the Fabric of Rare Disease Advocacy
Eliza's Story: Weaving Emotional Support into the Fabric of Rare Disease Advocacy
In Poland, very few people live with this condition, and there is still little awareness or understanding of it. That’s why I often look for knowledge and support abroad. I would love to connect with others around the world who also live with MOGAD — to exchange experiences, learn from one another, and remind ourselves that none of us are truly alone in this.
Eliza's Story: Our Health is the Goal
Eliza's Story: Our Health is the Goal
Deby's Story: Strength Through Shadows
Deby's Story: Strength Through Shadows
MOGAD News, Updates, and Research
Jonathan D. Santoro, MD, Appointed Chief of Neurology and Co-Director of the Neurological Institute at Children's Hospital Los Angeles | Children's Hospital Los Angeles
Jonathan D. Santoro, MD, Appointed Chief of Neurology and Co-Director of the Neurological Institute at Children's Hospital Los Angeles | Children's Hospital Los Angeles
Nationally recognized pediatric neurologist to guide department-wide programs in patient care, research, and education.
The MOG Project Featured by Johns Hopkins Medicine - The MOG Project
The MOG Project Featured by Johns Hopkins Medicine - The MOG Project
Press release: The Nobel Prize in Physiology or Medicine 2025 - NobelPrize.org
Press release: The Nobel Prize in Physiology or Medicine 2025 - NobelPrize.org
The Nobel Prize in Physiology or Medicine 2025 was awarded jointly to Mary E. Brunkow, Frederick J. Ramsdell and Shimon Sakaguchi "for their discoveries concerning peripheral immune tolerance"
Dad has headache that "would not go away"—diagnosis shocks young family
Dad has headache that "would not go away"—diagnosis shocks young family
The MOG Project, Pediatric Neurologist Secure CDC Approval to Adopt ICD-10 Code for Rare Disease MOGAD
The MOG Project, Pediatric Neurologist Secure CDC Approval to Adopt ICD-10 Code for Rare Disease MOGAD
Survey: Residuals from Transverse Myelitis in MOGAD
Survey: Residuals from Transverse Myelitis in MOGAD
MOGAD Patient & Caregiver Survey | MOGAD Patient & Caregiver Survey
MOGAD Patient & Caregiver Survey | MOGAD Patient & Caregiver Survey
Quality of life is impaired in myelin oligodendrocyte glycoprotein antibody associated disease - Yana Said, Dimitrios C Ladakis, Julia M Lefelar, Jenny M Khazen, Jennifer Gould, Kathryn C Fitzgerald, Elias S Sotirchos, 2024
Quality of life is impaired in myelin oligodendrocyte glycoprotein antibody associated disease - Yana Said, Dimitrios C Ladakis, Julia M Lefelar, Jenny M Khazen, Jennifer Gould, Kathryn C Fitzgerald, Elias S Sotirchos, 2024
The MOG Project Instagram
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The MOG Project Email
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