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We're currently not looking for any new EAIRs. However, we do have other ways you can volunteer.
Would you like to have a say about our advice and information materials? We are looking for people who would be willing to review our publications.
As a member-led organisation, Epilepsy Action believes it is important that people with epilepsy, or those who care for someone with epilepsy, have an opportunity to help us shape the future of our advice and information materials.
We want to recruit a number of people to become an Epilepsy Action Information Reviewer – an EAIR. As an EAIR, you will have the opportunity to give us feedback on our publications at different stages of their development.
What will I have to do as an EAIR?
We will ask you to complete a short, simple form, about a particular Epilepsy Action title. You can ask for a sample form to be emailed to you.
What is my commitment to Epilepsy Action?
You will agree to review at least one out of every five titles for review. You can review more if you want to. We will not ask you to review more than 12 titles during the course of a year.
What is Epilepsy Action’s commitment to you?
As an EAIR, we will listen to what you tell us and act on your suggestions where appropriate.
What experience or skills do I need to become an EAIR?
If you or a family member have epilepsy, or you care for someone with epilepsy, you have the experience we are looking for. You don’t need any special skills, but you do need to have an interest in epilepsy information. You also need access to the Internet and an email address where we can contact you.
How do I apply?
We're currently not looking for any new EAIRs. However, we do have other ways you can volunteer.
If you have any queries about becoming an EAIR, you can contact us at: eairs@epilepsy.org.uk.
What happens next?
We will consider your application and let you know if you have been accepted as an EAIR.
Where can I get more information?
Email us at eairs@epilepsy.org.uk.
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






