The Encephalitis Society is a UK based charity set up by people affected by encephalitis
in 1994.
• We are the only resource of our kind in the world providing a dedicated service
to people affected by encephalitis and their loved ones
• We provide a telephone information line: Monday to Friday 9am to 5pm. Answerphone
outside these hours
• We have a range of information materials including books, DVD, leaflets and factsheets
• We have a dedicated direct support service offered via telephone, letter, e-mail
and, on occasion, outreach visiting
• We provide a range of opportunities to get together including an Annual meeting,
Retreat weekend, Children and Family breaks
• We send out a regular Newsletter with news and information on developments in
the consequences of, and treatment of Encephalitis
• An expert Professional Panel contributes to the strategy of the Society, particularly
with regard to the production of evidence based information and research
• Our web site, www.encephalitis.info offers access to a wide range of up to date
information on the condition, its consequences, treatment and rehabilitation
• The Society is managed by a Board of Directors, the majority of whom have been
personally affected, or have a direct professional interest in encephalitis
• We contribute to ongoing research in the field either by the funding of, the support
of, or conducting research to further understand the causes and consequences of
encephalitis.
• We have developed a Regional Representative Volunteer Service in several areas
within UK, facilitating a more effective way of obtaining local information and
support.
Last modified: January 2012