Join us for an online support group meeting hosted by Megan, specifically for parents of people diagnosed with rare neuroimmune disorders! Anyone is welcome, no matter where you are located. If you are a parent of an individual diagnosed with ADEM, AFM, MOGAD, NMOSD, ON, or TM, we invite you to join us.
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.
SRNA 2025 education and support programs are supported by donations from our community and in part through grants from
* All educational content and programs are solely developed by the SRNA staff, members of the scientific board and approved by Board of Directors.
