Events

World Encephalitis Day Conference 2021 October 22, 2020

Mark your calendar! The World Encephalitis Day Alliance will be hosting the World Encephalitis Day Conference on Saturday February 20th, 2021. This will be a virtual conference, so anyone, anywhere can participate. We are literally taking you across the globe, with speakers from Australia, Europe, and the United States. Our Keynote Speakers are Prof. Tom […]

Florence Forth Virtual: A How To From The Experts! #2 February 1, 2022

Thank you Rachael for sharing your 2021 Florence Forth Virtual experience! We decided the best way for you to understand what it means to participate in the Florence Forth Virtual event is to ask the experts. What makes someone an expert? They’ve done it! Q1 What did you enjoy about the 2021 Virtual Florence Forth […]

Florence Forth Virtual: A How To From The Experts! #3 February 8, 2022

Thank you Lisa and Jackie for sharing your 2021 Florence Forth Virtual experiences on social media after the event and for providing expert tips for this year. What makes someone an expert? They’ve done it! The Florence Forth Virtual Event is an opportunity for you to get involved, celebrate your heroes, raise funds and awareness […]

Florence Forth Virtual: How Does A First-Timer Celebrate Heroes? February 15, 2022

Thank you Meg for sharing your plans for Florence Forth Virtual and In-Person! Are you still unsure how to create your Florence Forth Virtual Event? Our new Director of Patient Support, Programs and Administration focuses on the event everyday. We asked her a few questions and found out how she’s celebrating her heroes this year. […]

Celebrating Partnership: EUROIMMUN Neuroimmunology Summit May 5, 2022

Thank you EUROIMMUN for inviting the AE Alliance family to attend the EUROIMMUN Neuroimmunology Summit. All AE Alliance Clinicians and Support Network members are invited to attend this one-day virtual summit bringing together neurologic medical experts from across the United States. The topics to be discussed include: Updated guidelines for the diagnosis of neuroimmunology conditions […]

AEA Family Day 2022 October 14, 2022

We are excited to announce the Fall AEA Family Day (mini). Instead of a single, full-day, AEA Family Day, the AE Alliance and our program sponsor, EUROIMMUN offer several mini-days throughout the year. This gives us the opportunity to respond to topics that are important to you throughout the year. The Fall AEA Family Day […]

Develop an Attitude of Gratitude this December with the AE Alliance November 9, 2022

Whether you are living with AE, are a caregiver, family member, friend, physician, researcher, Board Member, MAB Member, program partner or sponsor or this is your first time ever to the Autoimmune Encephalitis website, we are excited you are here and ready to develop an attitude of gratitude! This program is inspired by a year […]

Join Us for an In-Person Autoimmune Encephalitis Day September 9, 2024

The AE Alliance is excited to partner with the University Hospitals Neurological Institute, Hashimoto’s Encephalopathy/SREAT & Seronegative Autoimmune Encephalitis Alliance (HESA) and Encephalitis411 to present and in-person AE Day: “Strides in Autoimmune Encephalitis.” This assembly is an all-day event focusing on pediatric and adult autoimmune encephalitis (AE) for clinicians, caregivers, and the survivors impacted. We […]

The World Encephalitis Day Alliance presents – WEDA 2025 Conference & Conversations December 20, 2024

WEDA 2025 Conference & Conversations Join us for 3 days of inspiring talks, networking, and thought-provoking discussions in person (cannot be attended virtually). CLICK HERE TO REGISTER FOR THE EVENT AND OPTIONAL DINNER VIA EVENTBRITE Come join us at the Kinne Auditorium, Mayo Building, Mayo Clinic Jacksonville FL for a three day event filled with insightful sessions, engaging […]

Happy 5th birthday to Autoimmune Encephalitis Alliance December 18, 2017

The AE Alliance turned five years old yesterday!  Five years ago on Dec. 17, two families that had kids with AE came together in hopes that they could start something to help others suffering from this little-understood disease.  The vision was to not only disseminate information to help patients but also to give support to […]