Understanding Hashimoto's Encephalopathy 2016 Edition:
An Expanded and Updated Guide For Patients, Families, and Caregivers
– Now Available on Amazon
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The Hashimoto's Encephalopathy SREAT Alliance welcomes your questions and comments! HESA is a volunteer-staffed organization and we are unable to address questions about HE/SREAT via email. We can only answer basic inquiries about our website or media. We cannot provide medical or treatment advice.

If you are experiencing an emergency, please contact your local emergency services. If your inquiry is of a medical nature, please contact your family physician or general practitioner for evaluation.


If you have questions about Hashimoto’s encephalopathy/SREAT, you can connect with others patients/families/or caregivers at our Facebook support page, Understanding Hashimoto’s Encephalopathy – A Support Forum.

 We can also be found on social media! You can find us on FacebookTwitter, Google+, Pinterest, YouTube, LinkedIn, and Instagram.

Disclaimer: Please note that our website, Facebook support page, and social media pages are not monitored by a physician and are not intended to provide a substitute for qualified medical advice. Last edited by Web Team on June 20th, 2016

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AE Alliance
"The Autoimmune Encephalitis Alliance promotes collaboration to improve care, find a cure and create community so that no one faces autoimmune encephalitis alone.

The Encephalitis Society
"The Encephalitis Society is an International organization providing information and support for all causes of Encephalitis."

Encephalitis Global
"Encephalitis Global is a U.S.A. 501(c)(3) non-profit organization formed in 2005 as an alliance connecting encephalitis survivors and caregivers around the world."

Scientific literature is growing at a rate of more than 2 new articles every single minute. It is impossible for scientists to consume and understand the rapidly expanding ocean of biomedical literature. You can help biomedical researchers find the information they need to discover cures faster.

"Connecting Rare Disease Patients Globally"

"Alone we are rare. Together we are strong.®"

Contact a Family
"For families with disabled children."

Madison's Foundation Provides information about rare diseases and connects parents whose children have the same rare disease.

NIH Health Hotline
Toll-free numbers from the National Library of Medicine's Health Hotlines Database.

HE Notebook - Wordpress Site
A great blog of an HE patient with a trove of information, personal stories, and links to medical studies.