Epilepsy Action’s education work 2008-2010
Our work in the field of education is guided by a plan, or strategy. Our new strategy for 2008-2010 outlines the main aims we will work towards over the next three years. It has been drawn up by our Education Committee and staff, and approved by Epilepsy Action’s Council of Management.
Summary of the education strategy
The education strategy is built on two key principles:
- involving the people who use Epilepsy Action’s education services and making sure their opinions are taken into account, and
- measuring how successful we are and evaluating the difference our work is making.
Our aims:
- To develop and communicate policies on epilepsy and education.
For example, by writing policies and statements that are practical and relevant;- making sure that Epilepsy Action’s policies are current, by keeping up to date with national trends;
- making sure that Epilepsy Action’s education policies represent the views of people who use our services; and
- communicating our policies clearly.
- To raise awareness and influence decision makers, by delivering education campaigns.
For example, by- planning and carrying out campaigns, and
- recognising and publicising good practice in education services for people with epilepsy.
- To raise the awareness of epilepsy, and the needs of learners with epilepsy, among policy makers (such as the government).
For example, by- seeking to raise the awareness of policy makers about the education needs of people with epilepsy, and
- maximising opportunities to influence policy makers by working together with our colleagues.
- To increase the awareness and understanding of epilepsy and its impact on education among people with the condition, and their carers and friends.
For example, by- providing good advice and information about education for people with epilepsy and their families;
- providing information and resources for children and young adults, parents and carers through our website; and
- raising awareness of our education services through publicity and campaigns.
- To increase the awareness and understanding of epilepsy, and its impact on education, among people working in the education sector and other relevant professions.
For example, by- providing good advice and information for people who work in education;
- providing training and awareness sessions for professionals; and
- raising awareness of education issues through publicity, writing articles and participating in events.
- To promote research on how epilepsy affects learning, skills, and other aspects of education.
For example, by- seeking to commission research into education, working with Epilepsy Action’s Research Committee, and
- seeking to influence external research bodies to carry out research into epilepsy and education.
Download the full education strategy
We can provide references and information on the source material we use to write our epilepsy advice and information pages. Please contact our Epilepsy Helpline by email at helpline@epilepsy.org.uk.
- Information for...
- Information on...
- Fundraise
- Donate
- Membership
- Campaigns
- Take epilepsy action campaign
- Automatic substitution of anti-epileptic drugs
- National commissioning of paediatric epilepsy surgery
- National Epilepsy Week
- Save our Sapphires, protecting all epilepsy specialist nurse posts
- Women's campaigns
- Epilepsy in England: time for change
- 'Epilepsy Aware' scheme for GP practices and pharmacies
- Campaign Supporters' Group
- Surveys
- News
- Research
- Our services
- Forum
- About us
Epilepsy advice and information
- What is epilepsy?
- Caring for a baby or young child when you have epilepsy: a detailed guide
- Children
- Depression and epilepsy
- Developing epilepsy in later life
- Driving and epilepsy
- Education
- Entitlements and benefits for people with epilepsy
- Epilepsy and learning disabilities
- Epilepsy and Travel abroad
- Epilepsy information for prisons
- Epilepsy, osteoporosis and osteomalacia
- Epilepsy: diagnosis, treatment and healthcare in the UK
- Epileptic seizures explained
- Flu and epilepsy
- Identity jewellery
- Inheritance
- Me and my dad
- Memory
- Mobile phones and epilepsy
- Photosensitive epilepsy
- Safety advice for people with epilepsy
- Sports and leisure
- Stress and epilepsy
- Sudden unexpected death in epilepsy (SUDEP)
- Syndromes
- The Disability Discrimination Act
- The Equality Act and epilepsy
- Vagus nerve stimulation therapy in epilepsy
- Work and epilepsy
- Women and epilepsy
- Young people and epilepsy
- Epilepsy Action and the Information Standard
- The Epilepsies: You, Epilepsy and the NICE Guideline
- Epilepsy Action Information Reviewers (EAIRs)
- Technical editing/writing and copyright
Epilepsy Helpline
- UK freephone 0808 800 5050
- International +44 113 210 8850
- Email: helpline@epilepsy.org.uk
- Twitter: epilepsyadvice
- Txt msg: 0753 741 0044 info






