MOGAD Awareness Month

March is MOGAD Awareness Month. To shine a light on MOG antibody disease (MOGAD) and the journeys of all those diagnosed with this rare disorder and their loved ones, we will be sharing stories, resources, facts, and helpful tips during the entire month of April.

Event Series MOGAD Together

MOGAD Together

Virtual Event Virtual Event

Learn more about MOG antibody disease, connect with others in the rare neuroimmune disorders community, and raise awareness for MOGAD! No matter where you are in the world, we invite you to join us.

International Support Group Meeting

Virtual Event Virtual Event

Join us for an online support group meeting hosted by Paul, our Ontario, Canada Support Group Leader! Come connect with others and discuss what it’s like living with a rare neuroimmune disorder. Ask questions, share your stories, or just listen – everyone is welcome.

Teen Support Group Meeting

Virtual Event Virtual Event

This group is peer-led by a teen with a rare neuroimmune disorder, and this meeting will not be led by medical professionals. Attendees can come and ask questions of one another and SRNA.

Online Support Group Meeting

Virtual Event Virtual Event

Please join us for an online support group meeting, hosted by Doug and Holly, our Utah Support Group Leaders! Come connect with others and discuss what it’s like living with a rare neuroimmune disorder. Ask questions, share your stories, or just listen – everyone is welcome.

International Support Group Meeting

Virtual Event Virtual Event

Join us for an online support group meeting hosted by Laura, our Australia Support Group Leader! Come connect with others and discuss what it’s like living with a rare neuroimmune disorder. Ask questions, share your stories, or just listen – everyone is welcome.

Event Series MOGAD Together

MOGAD Together

Virtual Event Virtual Event

Learn more about MOG antibody disease, connect with others in the rare neuroimmune disorders community, and raise awareness for MOGAD! No matter where you are in the world, we invite you to join us.

Online Support Group Meeting

Virtual Event Virtual Event

Join us for an online support group meeting, hosted by Megan, our Kansas City Support Group Leader! Come connect with others and discuss what it’s like living with a rare neuroimmune disorder. Ask questions, share your stories, or just listen – everyone is welcome.