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Empowering victims of Autoimmune Encephalitis and caregivers through support and education

The International Autoimmune Encephalitis Society is a Family/Patient centered organization that assists members from getting a diagnosis to recovery and the many challenges experienced throughout that journey.
Shay

Shay

Kara

Kara

Heather Smith

Heather Smith

Kamren

Kamren

Jordan

Jordan

Barbara Layt Vujaklija

Barbara Layt Vujaklija

Kelly McCabe

Kelly McCabe

Sharon

Sharon

Michelle & John

Michelle & John

Trish Desotell

Trish Desotell

Kylie

Kylie

Samantha

Samantha

Patrick

Patrick

Jessica

Jessica

Mark

Mark

Noah

Noah

Shaylee

Shaylee

Julia

Julia

Tara

Tara

Whitney

Whitney

Neli

Neli

Colban

Colban

Gene

Gene

Seri

Seri

Anji

Anji

Amy

Amy

Tabitha & Melody

Tabitha & Melody

#antiNMDAr
#Autoimmune      #Encephalitis
#AutoimmuneEncephalitis
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Love your Brain by becoming an IAES card carrying member. Keep up-to-date on the latest research and events. (Click picture to join)

autoimmune encephalitis survivor warrior

Doctor's Information:
The latest research at
your fingertips

Diagnostic Testing:
Current testing
criteria for AE

Living with AE:
Support and tips
for daily living

The above Facebook educational support group is for individuals and their loved ones who have a dx of Antibody-mediated Autoimmune Encephalitis, Paraneoplastic Autoimmune Encephalitis, Antibody negative Autoimmune Encephalitis and ADEM and have received a diagnosis by a neurologist.

TESTIMONIALS

These posters may be printed and distributed (ie. hospitals, doctor's office, clinics, etc.) to raise awareness of AE and provide access to our sites. 

Example of poster is to the left

Click "Amazon logo" above to support IAES with every Amazon purchase. Smilematic is a free Firefox extension that will automatically turn your everyday Amazon purchases into AmazonSmile donations.

amazon-smile-530x325.png
donate.png

The movie Brain on Fire is now available on Netflix.   The movie is based on the 2012 autobiography Brain on Fire My Month of Madness by Susannah Cahalan.  A young reported for the New York Post who came down with anti-NMDA receptor encephalitis.  Susannah's book has raised awareness about Autoimmune Encephalitis world-wide and lead to many patients receiving and accurate diagnosis.   


Our website is not a substitute for independent professional medical advice. Nothing contained on our website is intended to be used as medical advice. No content is intended to be used to diagnose, treat, cure or prevent any disease, nor should it be used for therapeutic purposes or as a substitute for your own health professional's advice. Although THE INTERNATIONAL AUTOIMMUNE ENCEPHALITIS SOCIETY  provides a great deal of information about AUTOIMMUNE ENCEPHALITIS, all content is provided for informational purposes only. The International Autoimmune Encephalitis Society  cannot provide medical advice.

IAE Society is a Delaware Charitable Nonprofit and a registered 501(c)(3) organization.

© 2019 International Autoimmune Encephalitis Society- All Rights Reserved.

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