As the world changed in 2020, we strived to adapt our programs to offer our community the same support, education, and scientific advancements that we always have in the past. It is with great pride we present our 2020 Annual Report.
In 2020, the Rare Neuroimmune Disorders Symposium transitioned to an all-virtual format, which allowed over 400 participants to register from 22 countries and laid the foundation for future virtual RNDS elements. The annual Quality of Life Family Camp was held virtually as well, and families were able to connect with medical experts in rare neuroimmune disorders. We created a COVID-19 resource center on our website to keep our community informed about the impact of this pandemic on people living with ADEM, AFM, MOGAD, NMOSD, ON, and TM. We launched a new podcast series, ABCs of NMOSD, and hosted nine Ask the Expert podcasts that covered a variety of topics. Because of your enthusiastic participation, our continuing research efforts with the SRNA Registry were significantly expanded, and we introduced a study on how the COVID-19 pandemic was impacting our community. You can read about these programs, accomplishments, and so much more in our 2020 Annual Report!
Read about our year in our 2020 Annual Report.