2020RNDS
August 29 2020, Virtual Conference
Join us as we take the 2020 Virtual RNDS online for the very first time! The conference is free to attend.
During the COVID-19 pandemic, our SRNA community still needs you
At the Siegel Rare Neuroimmune Association (SRNA), we are devoted to keeping you connected – to education and support. In these most difficult times, if you can make a difference, we urge you to do so. Please help us to continue to provide vital resources and programming. Please support our mission to connect, care, and cure.
During the COVID-19 pandemic, our community still needs you
At the Siegel Rare Neuroimmune Association (SRNA), we are devoted to keeping you connected – to education and support. In these most difficult times, if you can make a difference, we urge you to do so. Please help us to continue to provide vital resources and programming. Please support our mission to connect, care, and cure.
During the COVID-19 pandemic, our community still needs you
At the Siegel Rare Neuroimmune Association (SRNA), we are devoted to keeping you connected – to education and support. In these most difficult times, if you can make a difference, we urge you to do so. Please help us to continue to provide vital resources and programming. Please support our mission to connect, care, and cure.
Coronavirus (COVID-19) and Rare Neuroimmune Disorders
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.
COVID-19 coronavirus and Rare Neuroimmune Disorders
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.
COVID-19 coronavirus and Rare Neuroimmune Disorders
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.
2020 Education Sponsor
All educational content and programs are solely developed by the SRNA staff, members of the scientific board and approved by Board of Directors.