Epilepsy Action Information Reviewers (EAIRs)
Last checked 12/09/2008
Become an Epilepsy Action Information Reviewer (EAIR)
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. See a sample form here.
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 want to recruit a wide cross-section of people, so we need you to tell us a little about yourself. Please complete the online application form. 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.
Epilepsy advice and information
- What is epilepsy?
- Children
- Depression
- Disability Discrimination Act (UK)
- Driving
- Education
- Employment
- Epilepsy in later life
- Getting a diagnosis
- Health care and welfare benefits
- Inheritance
- Learning disabilities
- Me and my dad
- Memory
- Men and Epilepsy
- Mobile phones and epilepsy
- Osteoporosis, osteomalacia and epilepsy
- Photosensitive epilepsy
- Relationships and epilepsy
- Safety
- Seizures
- Sports and leisure
- Stress and epilepsy
- Sudden Unexpected Death in Epilepsy (SUDEP)
- Syndromes
- Travel abroad
- Treatment
- Women and epilepsy
- Young people and epilepsy
- 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
- Txt msg: 07797 805 390 info





