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

Who We Are

Hashimoto's Encephalopathy (SREAT) Alliance

A 501 3(c) not for profit organization for an autoimmune brain disease called Hashimoto's Encephalopathy (HE), a type of autoimmune encephalitis (AE).

What We Do

  • Provide support for patients/caregivers diagnosed with HE
      and those searching for a diagnosis on support groups.
  • Provide the latest available information and research
  • Tips & resources to help live with HE
  • Help raise awareness of this disease by writing books and
      participating in educational medical symposiums.
  • Donate money towards research.

All proceeds from the HESA store purchases go to projects such as symposium, raising awareness in the medical communities and the hopes for further research on Hashimoto's Encephalopathy and other forms of autoimmune encephalitis.

FEATURING

Claire Hill

Diagnosed 2019

the FACES of HE

IN OUR HESA SUPPORT COMMUNITY

 

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