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Epilepsy Action provides freephone and email helplines and a wide range of information booklets, web pages and e-learning courses. It has around 100 local support groups across England , Wales and Northern Ireland and a network of volunteers working in the community.
Epilepsy Outlook is a charity based in Hartlepool which provides free and confidential practical support, advice and information for people with epilepsy and their carers. [4] Their support services include supported volunteer placements, a drop-in centre, epilepsy awareness training, an art therapy group and welfare benefits advice.
Epilepsy Society is a leading epilepsy medical charity supporting all people affected by epilepsy. The services provided by the charity include: Residential care for over 100 adults within care homes at the Chalfont Centre and also in supported living accommodation.
Epilepsy Research Institute, formerly Epilepsy Research UK, is a British medical research charity dedicated to funding and supporting research into epilepsy. [ 1 ] In March 2007, the Epilepsy Research Foundation merged with the Fund for Epilepsy to become Epilepsy Research UK (ERUK).
Epilepsy can force a child to be left out of activities common for children to be involved in, such as sports. [6] Epilepsy can affect a child's education. The child may be forced to miss a lot of school due to seizures. The seizures can impair a child's ability to memorize learning materials.
Purple is the international color for epilepsy and is also a color that symbolizes solitude. [citation needed] The goal of Purple Day is to increase general public awareness, to reduce the social stigma endured by many individuals with the condition, and to empower individuals living with epilepsy to take action in their communities. [10]
David Lewis (also known as the 'David Lewis National Epilepsy Centre', David Lewis School and 'The David Lewis Centre' is a health foundation based in Little Warford, Cheshire. It provides residential accommodation, education and health services to people with epilepsy , autism learning and physical disabilities.
The Epilepsy Foundation received anecdotal reports of patients experiencing seizures and side effects after switching drugs, and tried to convince the U.S. Food and Drug Administration (FDA) in 1999 that there was a problem, but the FDA decided there was no evidence. In 2006, foundation leaders convened a committee of medical experts, and its ...
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