The International Autoimmune Encephalitis Society is the only Family/Patient centered organization for people with a diagnosis of Autoimmune Encephalitis. The services we provide are all inclusive from getting a diagnosis to recovery and the many challenges experienced in that journey.
“Empowering victims of Autoimmune Encephalitis and their caregivers through Support and Education”.
Raising awareness of Autoimmune Encephalitis across the many specialties of medicine that come in contact with these disorders and raising awareness with the general public to ensure a timely and accurate diagnosis and aggressive treatment plan for best outcomes.
We recognized the need to help people understand the disease of Autoimmune encephalitis so they can partner with their treating physician in getting proper care. We believe that understanding through education is the most valuable tool an individual with this disease or caretaker can possess. Education is power and leads to strong self-advocacy which in turn leads to better care and outcomes.
Our Mission Statement
The International Autoimmune Encephalitis Society, (IAES), assists patients, family members and caregivers in all areas of their journey: locating expert physicians who have published in the field, and when necessary, assisting with appointments for fast and accurate diagnosis and treatment which leads to the best outcomes. We provide referrals for discounted ground and air travel and housing to make out-of-state travel to an expert possible.
Services provided include assisting with insurance issues or getting insurance coverage, assisting with over turning insurance denials for life saving treatment, (for members in the U.S.A.), crisis advocacy, directing patients to experts for confirmation of an accurate diagnosis. We connect families with free air travel and discounted stays near several major medical centers.
Additionally, IAES helps families and patients understand the disease and the treatments involved so they can become strong advocates/self-advocates and have more productive doctor appointments. Receiving an accurate diagnosis and appropriate treatment for best outcomes is the key component.
Board of Directors
Co-Founder and President
Co-Founder and Secretary
Co-Founder and Treasurer
Board Members with Medical Expertise
Dr. Alexander Rae-Grant
Cleveland Clinic, Ohio
Dr. Michael Geschwind
Behavioral Cognitive Neurologist
USCF AE Clinic
Dr. James Morrow
Retired Neurologist, UK
VGKC Limbic Encephalitis
patient in recovery
Dr. Michael E. Newmark
Medical Consultants with Expertise
Dr. Anna Moise
The medical information on the International Autoimmune Encephalitis Society, Inc. website is provided as informational and educational resources only and in no way should be taken to be the provision or practice of medical, nursing or professional health care advice or services. The information should not be considered complete or exhaustive and should not be used in place of a visit, call, consultation or advice of your physician or another healthcare provider. All content, including text, graphics, images, videos, podcasts, slideshows, any information, contained on or available through this website, is for general information purposes only. The information on this website is not to be used, implied, or relied upon as a substitute for professional medical advice, diagnosis or treatment for Autoimmune encephalitis or any medical disorder.
You are encouraged to confirm any information obtained from or through this web site with other sources, and review all information regarding any medical condition or treatment with your physician. NEVER DISREGARD PROFESSIONAL MEDICAL ADVICE OR DELAY SEEKING MEDICAL TREATMENT BECAUSE OF SOMETHING YOU HAVE READ ON OR ACCESSED THROUGH THIS WEB SITE.
Any referral to physicians is provided as a courtesy only