Understanding Hashimoto's Encephalopathy 2016 Edition:
An Expanded and Updated Guide For Patients, Families, and Caregivers
– Now Available on Amazon
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Finding Out More

A comprehensive list of recent scientific publications regarding HE/SREAT is available under Scientific Research. Research is divided by topic and in some cases, by year published.

As our mission states, we collect and catalog information and educational materials on HE/SREAT as well as autoimmune encephalitis/encephalopathy. You can find a wealth of information located on our YouTube channel and our Google+ collections. In addition, we regularly post useful information on our Facebook fan page, HESA – Hashimoto’s Encephalopathy SREAT Alliance.

In addition to this website, our book, “Understanding Hashimoto’s Encephalopathy“, may be a starting point for individuals, families, and caregivers to learning more about the condition. The book can be purchased from Amazon.com

For those interested in educating themselves and/or those treating them, about the complexity of HE/SREAT and other forms of autoimmune encephalitis, the Autoimmune Encephalitis Alliance has a series of videos that can be viewed at their Youtube page, Autoimmune Encephalitis Alliance.


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."


Mark2Cure
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.


RareConnect.org
"Connecting Rare Disease Patients Globally"


RareDisesases.org
"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.