PLEASE NOTE:

This website is not a substitute for professional advice, and the content here is not intended for use in diagnosing, curing, or preventing disease. The site does not employ and is not overseen by medical professionals. Articles and studies listed here are intended solely for personal use and reference.  Although you will find a great deal of information about HE/SREAT on this website, HESA cannot provide medical advice. If you have HE/SREAT, or think you may have it, consult a qualified neurologist,

preferably one with experience addressing immune-mediated illness. 

© 2019 Hashimoto's Encephalopathy SREAT Alliance

OUR COMMUNITY

Who is the HESA community? 

Patients and caregivers with 

Hashimoto's encephalopathy (or a type or AE) and experiencing it in one way or another.

We help each other on our Facebook support groups, or online in the U.S. and around the world.

In our community, we have met some of the 

most wonderful inspirational people and shared in their happiness and sadness in many areas of our lives.

Our community extends to other support networks as well and working together we have learned so much from one another.