SUPPORT GROUPS
Understanding Hashimoto's Encephalopathy
and
For Those Diagnosed With Hashimoto's Encephalopathy
*VIDEO CONFERENCE
MEET and GREET
with other support
members
*STAY TUNED
For our
next SYMPOSIUM in
spring 2021.
You can help
by DONATING or purchasing from the SHOPPE!
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.
VOLUNTEER
#SLOWtheSPREAD
HESA's
MADDY BOEHME & DR. ROBERT WEIR
Discuss Covid-19, how it affects those who are immune suppressed and the autoimmune encephalitis community.
World Encephalitis Day
2020 Conference Dallas,TX
Organization’s strategy:
We spread awareness through our website, social media, Facebook support groups, published books, and encephalitis conferences and symposiums. We join forces with other AE non-profits to give us more power to help people with autoimmune encephalopathy. If we cannot help someone, we try to find another group that can.
A TALK WITH MADDY
AUTOIMMUNE ENCEPHALITIS:
THE BRIDGE BETWEEN NEUROLOGY AND PSYCHIATRY
2019 Symposium NYC
Follow Us!
see what we are up to
If you have this disorder or know someone with it then you must have this book!
When my daughter was first diagnosed at age three with HE we were lost. I immediately bought this book and it was my survival guide to get through the beginning phases of this diagnosis. It gave me the power as a parent to go in to her doctors appointments knowing about this disorder which afforded me the opportunity to make more knowledgeable decisions for her care. I highly recommend it for patients, families and even our neurologist wanted a copy. It is a must read if you or a family member have this diagnosis.
