Visit our new website hesaonline.info

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

Our Books

In December of 2013, the Hashimoto’s Encephalopathy SREAT Alliance published its first book, “Understanding Hashimoto’s Encephalopathy: A Guide for Patients, Families and Caregivers.” 

Following the publication of the original edition of “Understanding Hashimoto’s Encephalopathy,” HESA self-published a cookbook of recipes submitted by members of a diverse group of patients, with easy-to-follow instructions for delicious meals.

In January of 2014, HESA began work on the expanded, second edition of “Understanding Hashimoto’s Encephalopathy.” The goal in expanding on the first edition of the book was to update the scientific information in the book and address editing issues with the first edition, and to help those with HE/SREAT: (1) find the latest scientific information; (2) identify physicians with HE experience and learn how they approach the disease; and (3) locate additional resources and support systems.

In addition, the new edition is designed to help clinicians who encounter patients with suspected HE/SREAT and need to find current scientific information.

“Understanding Hashimoto’s Encephalopathy” is available for purchase from Amazon.com here:

It can also be ordered through your local bookseller.

HESA plans to publish additional books in the future for children and young people who need help understanding HE.

 

Last edited by Web Team on January 25, 2019

Giving Assistant

Donate to HESA via Giving Assistant when you shop online.

 

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.