SRNA’s Healthcare Professional Digest

2023 | Issue 1

Rare neuroimmune disorder info sheets now available in Spanish! Expandiendo nuestro alcance a la comunidad hispanohablante.

Monique Anderson, MD, PhD has been awarded a research grant funded through the Pauline H. Siegel Eclipse Fund.

Is your information up to date in SRNA's database? Check our Medical Professional Network page to make sure your info is current!

The 2022 RNDS was our first-ever hybrid symposium, where people could attend in person, online, or a combination of both.

You’re invited to become a guest speaker on a podcast! SRNA hosts three podcast series: Ask the Expert, ABCs of NMOSD, and ADEM Academy.

neurology live logo
SRNA is excited to expand our education and professional development efforts for clinicians through a partnership with NeurologyLive.

Illustration outline of two figures, one sitting in a chair on the left and one with a wheelchair on the right, outlined in blue. They have orange speech bubbles and the background is a light pink color.
SRNA launched our Peer Connect Program in 2021 to address the need for one-on-one connections between people diagnosed with rare neuroimmune disorders.

In 2017, SRNA created a patient registry to help advance research about rare neuroimmune disorders and identify participants for clinical trials.