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.

 
 
 

the FACES of HE

IN OUR HESA SUPPORT COMMUNITY

FEATURING

Maddy Boehme

Diagnosed 2014

Since her sophomore year of high school, Maddy began to experience strange symptoms. An honor student and active with her friends these symptoms kept her from the typical enjoyments of her teenage years. At 19 and a freshman in college, she pushed on with difficulty. After getting her diagnosis, the HE had been taking everything out of her affecting every aspect of her life. Finally,  getting infusions, her health improved. Still fighting symptoms she began speaking about her experience at many different places advocating about  Hashimoto's Encephalopathy. Maddy has volunteers for HESA, she and her family work hard to support HESA in so many ways helping other HE survivors as well as in other AE and rare disease communities. 

See blog here

 
ae alliance support group ohio.png
 
 
  • Facebook
  • Twitter
  • YouTube
  • Pinterest
  • Instagram

Follow Us!

see what we are up to

CONTACT
 
IMG_2822

Medium Ground especially blended for HESA by Bellissimo Cofee Works

Go to link