Links to more information

Encephalitis Global’s Support Community  at 

Encephalitis Global on YouTube 

Encephalitis Global on Twitter

Encephalitis Global on Facebook is a 501(c)(3) organization which aims to advocate for those impacted by encephalitis, resulting in early diagnosis and best possible treatment outcomes. 

The Hashimoto’s Encephalopathy SREAT Alliance (“HESA”) is a 501(c)(3) nonprofit organization formed in 2012.  HESA’s purpose is collect, archive, and share information regarding Hashimoto’s Encephalopathy (“HE”), also known as Steroid Responsive Encephalopathy Associated with Thyroiditis (“SREAT”), or simply autoimmune encephalopathy (“AE”), with the public and medical professionals.

The Anti-NMDA Receptor Encephalitis Foundation exists for all patients and caregivers, at all stages of illness and recovery.   

I’m Not the Me I Remember: Fighting Encephalitis A special 32-page report from Inspire and Encephalitis Global in recognition of Rare Disease Day 2012 

Fighting Encephalitis  Encephalitis Global’s entry in the American Academy of Neurology’s 2012 Neuro Film Festival (5 minutes long) 

In-Depth Report on the West Nile Virus and Encephalitis  ( from the New York Times, August 2012)  

The Encephalitis Society in the United Kingdom

Encephalitis  at The Mayo Clinic website 

The Encephalitis Center at Johns Hopkins Hospital in Baltimore, Maryland 

The CDC: Centers for Disease Control and Prevention



Ruth at FACES 2004 Enfield, CT

Ruth at FACES 2004 Enfield, CT

Ruth Fell, encephalitis survivor, touched the heart of everyone she met, including members of the Encephalitis Community. This is a brief story of Ruth, with love, from Encephaltiis Global.