We need your support now more than ever
Join our giving community and transform lives for families around the world. Make a difference in the lives of people affected by rare neuroimmune disorders today.
We need your support now more than ever
Join our giving community and transform lives for families around the world. Make a difference in the lives of people affected by rare neuroimmune disorders today.
We need your support now more than ever
Join our giving community and transform lives for families around the world. Make a difference in the lives of people affected by rare neuroimmune disorders today.
CDC Vital Signs Report Available
The latest CDC Vital Signs report focuses on acute flaccid myelitis (AFM) and the critical importance of timely diagnosis, treatment, and reporting of the condition by clinicians.
Please take a few moments to review the latest report and the detailed information to share with your clinicians, schools, health departments, family and communities.
Stay tuned as we continue to share more specific ways you may create awareness of this rare but often devastating neuroimmune disorder.
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 story. Elisa is one of SRNA’s Hope Ambassadors, a community of heroes for a common cause.