Partnerships
A group of talented local high school students from The Fine Arts Center will be holding “Play It FWD” …Kids with a Purpose on December 2nd to raise funds for The Autoimmune Encephalitis Alliance. “Play it FWD” will be an annual live music event with the purpose to support a nonprofit organization of the students’ choice […]
Dr. J. Nicholas Brenton (The Rector and Visitors of the University of Virginia, Charlottesville, VA, USA) was awarded a 2024 AEA Community Seed Grant for the investigation of Capacity, Endurance, and Physical Activity in Children with MOG+ Encephalitis. Learn more about his research and how it impacts those affected with autoimmune encephalitis. The start date for the […]
In the past few weeks we have had some amazing people raise awareness for Autoimmune Encephalitis and raise funds for the AE Alliance, so we can continue to invest in research and improve clinical care. Let’s start in New York City. A friend of one of NYU’s hockey players got diagnosed in the spring with […]
Dr. Julien Hebert (University of Toronto, Toronto, Ontario, Canada) was awarded a 2024 AEA Community Seed Grant for the investigation of Postacute Management of Anti-Seizure Medications in Autoimmune Encephalitis-Associated Epilepsy. Learn more about his research and how it impacts those affected with autoimmune encephalitis. The start date for the award is September 1, 2024. You have been […]
The Dewees Family is organizing a 5K run to raise awareness for Autoimmune Encephalitis. March 2019, just one day after turning 13, Luke Dewees was diagnosed with Autoimmune Encephalitis. The next month was a terrifying and trying time. Luke spent more than 3 weeks in the hospital battling this rare and evasive disease. With the […]
Dr. Juliette Brenner (Erasmus MC University Medical Center, Rotterdam, The Netherlands) was awarded a 2024 AEA Community Seed Grant for the investigation of Validation of a new (patient-reported) outcome measure for encephalitis. Learn more about her research and how it impacts those affected with autoimmune encephalitis. The start date for the award is September 1, 2024. You have […]
Department of Psychiatry and Behavioral Sciences and the Department of Pediatrics, January 24, 2013
When I was diagnosed with anti-NMDA receptor encephalitis in 2010, I didn’t understand what that meant – and not just because I had a brain disease. My symptoms, ranging from paranoia and mania to the inability to walk or use my hands, seizures, and no longer being able to read or follow conversations, varied so […]
Dr. Yuri Shisido (Emory University, Atlanta, Georgia, USA) was awarded a 2025 AEA Community Seed Grant for the investigation of Patient-Centered Assessment of Everyday Cognitive Function in Children with Pediatric Anti- NMDA Receptor Encephalitis with Novel MRI Biomarkers. Learn more about her research and how it will impact those affected with autoimmune encephalitis. The start date […]
World Encephalitis Day is February, 22, each year – just remember 222. This is a day for all of us affected by encephalitis, whether we are patients, family members, doctors, researchers, or caregivers, to come together and talk about our experiences with brain inflammation and the many forms it takes. While we at the Autoimmune […]