Epilepsy Society's information - tell us what you think

Epilepsy Society's epilepsy information. This survey should only take a few minutes to complete.

Please fill in all the questions with a red star next to them as well as any other questions you would like to answer.
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1. Which of our leaflets, factsheets or other information resources have you used? Please tick all you have used.
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2. Where do you normally get our information from?
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3. If you asked for information by phone or email, which department or email address did you contact?

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4. Who was the information for?
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5. Did you find our information useful?
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6. Please explain how the information was useful to you.

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7. Was the information easy to understand?
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8. Is there anything that would make it easier to understand?

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9. Looking at the amount of information, do you think:
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10. If the information you read had a contents page, did you find this useful?
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11. If the information you read had a glossary of terms, did you find this useful?

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12. Had you heard of Epilepsy Society (formerly the National Society for Epilepsy) before reading our information?
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13. Did you know that the information on the website is also often available as printed copies?
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14. If you read the information on our website, what do you like to do with it?
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15. Were you aware that Epilepsy Society has a confidential helpline that can provide information as well as emotional support?
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16. Is there anything else you would like to say about any of our leaflets, factsheets or information?

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17.
Is there anything you would like to tell us about this information topic, for example, about your own personal experiences?

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18. We may like to include your answer to the previous question (question 17) as a quote within our leaflets. If you are happy for us to use your response as a quote please say so here.