Links to more information
Encephalitis Global’s Support Community at Inspire.com
Encephalitis411.org 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