Help us provide hope and help to those living with ADEM, AFM, MOGAD, NMOSD, ON, and TM.
No matter how much you choose to give, 100% will directly fund SRNA’s education, research, and community support programs.
International supporters: Please donate using this form
We know you have many questions about the coronavirus (COVID-19) and rare neuroimmune disorders, which is why we’ve worked with our medical experts to bring you the latest information on treatments, care, and support.
We know you have many questions about COVID-19 coronavirus and rare neuroimmune disorders, which is why we’ve worked with our medical experts to bring you the latest information on treatments, care, and support.
We know you have many questions about COVID-19 coronavirus and rare neuroimmune disorders, which is why we’ve worked with our medical experts to bring you the latest information on treatments, care, and support.
Our Hope Ambassadors
“Time is of the essence when it comes to rare neuroimmune disorders and the time to get awareness out is now. I know this because my 2 ½ year old son has Acute Flaccid Myelitis (AFM) which is a subtype of Transverse Myelitis.”
Read more about Elisa’s and Noah’s story. Elisa and Noah are one of SRNA’s Hope Ambassadors, a community of heroes for a common cause.
2023 Education Sponsors
All educational content and programs are solely developed by the SRNA staff, members of the scientific board and approved by Board of Directors.
