Join us for an online support group meeting hosted by Megan specifically for parents and caregivers of those diagnosed with ADEM, AFM, MOGAD, NMOSD, ON, or TM! Anyone is welcome, no matter where you are located. Come connect with others and discuss what it’s like caring for a child with a rare neuroimmune disorder. Ask questions, share your stories, or just listen – everyone is welcome.
SRNA 2025 education and support programs are supported by donations from our community and in part through grants from
