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Please read before continuing:

We would ask that prior to proceeding further in your search for information about Encephalitis you take a few moments to read and consider the comments below.

In some instances where people are affected by Encephalitis the long-term prognosis can be very good, with many people coming through the illness with little or no difficulties. However because there are occasions where more severe problems can occur, we have had to make our information as broad and far-reaching as possible. Therefore the details provided in the forthcoming web pages are fairly extensive. Taking this into account we would ask that anyone seeking information consider the following factors.

The difficulties stated in the information are not reflective of every situation where Encephalitis is involved and that some of the information stated may not be relevant to your situation.

Taking into account the emotional strain that a diagnosis of Encephalitis may bring coupled with the amount of information available through our website consideration may be required into gauging how much information is accessed at any one time.

Should any of the information raise issues or give you reason for concern we would ask that you contact the national office via our information line 01653 699599 or alternatively we can be contacted by email on support@Encephalitis.info

Thank you


The information provided on www.Encephalitis.info is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician. Any information collected by our website, such as email address, will never be passed on to any third party, unless required by law



About the Encephalitis Society

The Encephalitis Society is a UK based charity set up for 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 have a dedicated direct support service offered via telephone (Monday to Friday 9am to 5pm), letter, e-mail and, on occasion, outreach visiting.
  • We have a range of information materials including books, DVD, leaflets and factsheets, available in hard copy or electronically.
  • We provide a range of opportunities to get together including an Annual meeting, Retreat weekend, Children and Family breaks, regional meetings and VIP Member Events.
  • 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 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 information and support in your local communities.