The Hashimoto’s Encephalopathy/SREAT Alliance was created in 2012 and 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 this illness. We provide links to research into this poorly understood and potentially under-diagnosed condition for the benefit of patients, their families, friends, and caregivers. In addition, we provide resources to help patients and the general public increase their knowledge of HE/SREAT and find help in the diagnosis and management of this condition through self-education.
HESA also administers several Facebook Groups dedicated to supporting families, friends, caregivers, and the inquires from the general public about HE/SREAT. The opinions or actions of individual members of these groups does not necessarily reflect the beliefs or opinions of HESA.
While we make very effort to share information and links to sites which contain quality information, the user is solely responsible for determining the relevancy, accuracy, and currency of the information linked to or provided for their personal use. We shall not be held responsible for the contents of links to studies, their errors, omissions, or any malicious software they may contain.