Understanding Hashimoto's Encephalopathy 2016 Edition:
An Expanded and Updated Guide For Patients, Families, and Caregivers
– Now Available on Amazon
Follow us on Facebook, Twitter, LinkedIn, Pinterest, and Instagram!
#HEAwareness
"I believe you." 

Scientific Research

HESA has curated a catalog of scientific research articles about Hashimoto’s encephalopathy/SREAT. We regularly search for new and relevant research to share with those who have been diagnosed with Hashimoto’s encephalopathy/SREAT or wish to find out more. 

You can find these articles by year from 2010 to date. We will continue to add research as it becomes available. New studies will be added to our forthcoming 2nd edition of “Understanding Hashimoto’s Encephalopathy”. The book will be available on Amazon and will be available in print and for the Kindle e-reader. To find out more about the book, please check back on this site or follow HESA on social media sites +HesaOnlineOrgMedia and Twitter @hesaonlineorg

You can find additional links to scientific articles and case reports published between 2000 and 2013 by visiting HEnotebook.wordpress.com.

For those who want more in-depth information, we provide the a listing of online resources which will allow visitors to our website to delve as deeply into HE/SREAT as they wish.


Last edited by Web Team on March 18th, 2016

Find Our Page On The Mighty
More than half of Americans are facing serious health conditions or medical issues. They want more than information. They want to be inspired. The Mighty publishes real stories about real people facing real challenges.

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.