Last updated 13 Jun 2011, review date due 13 Jun 2013
Introduction
The aim of these web pages is to tell you how epilepsy is diagnosed and how it can be treated. They also give information about healthcare services and what you can do if you live in the UK and are not happy with your treatment.
If you have any further questions about anything to do with epilepsy, contact an adviser on the Epilepsy Helpline. You can also contact your family doctor, epilepsy specialist, or epilepsy specialist nurse.
In this section
- Introduction
- What to do if you think you’ve had a seizure
- Diagnosing epilepsy
- Anti-epileptic drug treatment
- List of AEDs available in the UK
- Getting the same version of your anti-epileptic drugs every time
- Other ways of treating epilepsy
- Effects of other things on epilepsy treatment
- Sudden unexpected death in epilepsy
- Getting healthcare
- Getting help if you are unhappy with your care or treatment
- NICE guideline for epilepsy treatment UK
- Keeping a seizure dairy
- Visiting your doctor
This information was written by Epilepsy Action’s advice and information team with guidance and input from people living with epilepsy and medical experts.
Our thanks
Epilepsy Action wishes to thank Dr John Paul Leach, consultant neurologist, Southern General Hospital, Glasgow, UK for reviewing this information.
What to do if you think you’ve had a seizure
This information is relevant for people who live in UK
- Visiting your GP (family doctor)
- Epilepsy clinics
Visiting your GP (family doctor)
If you think that you’ve had a seizure, the first person to see is your GP. If your GP thinks you might have epilepsy, they will usually arrange for you to see an epilepsy specialist at the hospital. This is to make sure you get the right diagnosis and have the best treatment for your epilepsy. The epilepsy specialist is usually a neurologist (for adults) or a paediatrician (for children).
Epilepsy clinics
If there is an epilepsy clinic in your area, your GP will usually refer you there. Epilepsy clinics provide things like ‘fast-track’ appointments for people who have had their first seizure, and the latest scanning equipment.
- Diagnosing epilepsy
- Anti-epileptic drug treatment
- Other ways of treating epilepsy
- Effects of other things on epilepsy treatment
- Sudden unexpected death in epilepsy
- Getting healthcare in the UK
- Getting help if you are unhappy with your care or treatment in the UK
- Complementary Treatment
- Epilepsy and Surgery
- Ketogenic Diet
- Visiting your doctor
- Epilepsy medicines available in the United Kingdom
- Getting the same version of your anti-epileptic drugs every time
- St John's Wort
- The Mozart Effect
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.
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- Women's campaigns
- Epilepsy in England: time for change
- 'Epilepsy Aware' scheme for GP practices and pharmacies
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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
- Diagnosing epilepsy
- Anti-epileptic drug treatment
- Other ways of treating epilepsy
- Effects of other things on epilepsy treatment
- Sudden unexpected death in epilepsy
- Getting healthcare in the UK
- Getting help if you are unhappy with your care or treatment in the UK
- Complementary Treatment
- Epilepsy and Surgery
- Ketogenic Diet
- Visiting your doctor
- Epilepsy medicines available in the United Kingdom
- Getting the same version of your anti-epileptic drugs every time
- St John's Wort
- The Mozart Effect
- 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








