Our vision
To live in a society where everyone understands epilepsy and where attitudes towards the condition are based on fact not fiction.
Our mission
To take action to meet the identified needs and aspirations of all people with epilepsy and those with an interest in the condition.
Our aims
- Raise and maintain awareness about epilepsy and about Epilepsy Action’s work.
- Educate people about the facts about epilepsy and improve their understanding of the condition.
- Bring about permanent change for the social and medical benefit of people with epilepsy.
- Provide advice and information about epilepsy that is relevant to peoples’ needs and that is accessible in terms of location, availability and cost.
- Promote all types of research into epilepsy and undertake non-laboratory social and medical research into epilepsy.
- Maximise Epilepsy Action’s resources by developing its fundraising activities and income consistent with its immediate and long term financial needs and using its resources effectively and efficiently.
- Engage with the Education, Healthcare and Social Care sectors to ensure that epilepsy is fully understood and the needs of people with epilepsy are supported.
Our values and beliefs
- Epilepsy Action will be representative and inclusive of and accessible to all people with an interest in epilepsy.
- Epilepsy Action will encourage and enable the active involvement of its members and other stakeholders.
- Epilepsy Action believes that people with epilepsy must have equality of opportunity in their lives to allow them to achieve their full potential.
- Vision, Mission and Strategic Aims 2007-2011
(approved and adopted by the Council of Management on 12 December 2006)
About Epilepsy Action
- Annual Review 2006
- Council of Management
- Epilepsy Action Award
- Epilepsy Action Departments
- Epilepsy Action Position Statements
- Headquarters
- History of Epilepsy Action
- Impact Report
- John Jarrett (1926-2007)
- Lord Hastings (1912-2007)
- National Conference and Annual General Meeting
- Vacancies
- Vision, mission, aims, values and beliefs of Epilepsy Action
- What we do
Epilepsy Helpline
- UK freephone 0808 800 5050
- International +44 113 210 8850
- Online Tuesdays 1900-2100
- Email: helpline@epilepsy.org.uk
- Txt msg: 07797 805 390 info
Latest News
Less than half of patients with active epilepsy in the United States are informed by their doctors about treatment options, according to a survey by the American Epilepsy Society and the Epilepsy Foundation.
Asking people who have partial seizures how often they have seizures does not appear to provide an accurate count, according to a report in the journal Archives of Neurology.
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