
The International Autoimmune Encephalitis Society was started by families and patients affected by autoimmune encephalitis. Founded September 1, 2016, the International Autoimmune Encephalitis Society (IAES), is a 501(c)(3) non-profit organization based in the state of Delaware that strives to educate the public about this emerging sub specialty in neurology, Autoimmune Encephalitis.
Our Motto:
"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:
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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. One on one support services offered are: Financial assistance advice that prevents a family’s bankruptcy or becoming financially destitute from out of pocket expenses due to a medical crisis. Education about medical insurance options that lead to the highest benefits including charity care, guidance on how to keep medical records and ensure best outcomes when faced with emergency health crisis including being placed on Psychiatric holds or commitment. We assist and educate members in the appeals process of life-saving treatments their insurance company has denied with a very high success rate of overturned denials. Volunteers experienced in the understanding of autoimmune encephalitis assist in crisis management as patient advocates when their help is called upon and is appropriate. Click pictures to learn more.
Board of Directors
Anji Fesler
Co-Founder and President
Houston, Texas
Tabitha Orth
Co-Founder and Secretary
Beaverton, Oregon
Gene Desotell
Co-Founder and Treasurer
Fredricksburg, Virginia
Board Members with Medical Expertise
Medical Consultants with Expertise
Dr. Anna Moise
Neurology, Psychiatry
Asheville, NC
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.
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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
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