Online Support Group Meeting

Virtual Event Virtual Event

Join us for an online support group meeting hosted by Jamie, our newest Support Group Leader for New Jersey! 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.

Young Adults Group

Virtual Event Virtual Event

Please join us on Tuesday, Jan. 28, for an online support group meeting hosted by Andrew, our Young Adults Support Group Leader! This group is for those in their 20's and 30's with ADEM, AFM, MOGAD, NMOSD, ON, or TM.

Oklahoma Support Group Meeting

Join us for an online support group meeting hosted by Leah, our Oklahoma Support Group Leader! This meeting is for those located in Oklahoma.

Online Support Group Meeting

Virtual Event Virtual Event

Join us for an online support group meeting hosted by Doug and Holly, our Utah Support Group Leaders, in collaboration with the Guthy-Jackson Charitable Foundation! 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.

Online Support Group Meeting

Virtual Event Virtual Event

Join us for an online support group meeting hosted by Darlene, our Michigan 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.

Young Adults Group

Virtual Event Virtual Event

Join us for an online social hour hosted by Andrew, for those in their 20's and 30's with ADEM, AFM, MOGAD, NMOSD, ON, or TM! This month, we'll be joined by Dr. Sonia Singh from the Medical University of South Carolina. Dr. Singh will be discussing family planning and pregnancy with a rare neuroimmune disorder.

Online Support Group Meeting

Virtual Event Virtual Event

Join us for an online support group meeting hosted by Doug and Holly, our Utah Support Group Leaders, in collaboration with the Guthy-Jackson Charitable Foundation!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.