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Understanding Hashimoto's Encephalopathy 2016 Edition:
An Expanded and Updated Guide For Patients, Families, and Caregivers
– Now Available on Amazon
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Hashimoto’s Encephalopathy SREAT Alliance (HESA) is the 501(c)(3) non-profit organization established to spread awareness and increase understanding of Hashimoto’s Encephalopathy/SREAT, while supporting those affected by the illness. HESA’s website provides information and links to a variety of resources for patients, physicians, caregivers, and others interested in this poorly understood disorder. HESA continues to operate as a direct result of your donations. We thank you for your support!

The 2016 edition of “Understanding Hashimoto’s Encephalopathy” has been greatly expanded, particularly in terms of providing the latest scientific research regarding HE/SREAT, interviews with experts in the field, and patient narratives that describe individual patient experiences with this perplexing and often debilitating disease.

HESA also raises funds to support scientific research, and is planning a documentary film project. Please consider visiting our “Store” page to purchase HE/SREAT awareness items for yourself, or for family and friends. The proceeds from sale of these items directly furthers our mission of educating the public and medical professionals about Hashimoto’s Encephalopathy/SREAT.

We appreciate your fully tax-deductible donations, and hope you will consider donating to HESA.


Last edited by Web Team on January 25, 2019

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