Finding Hope with Young Epilepsy: Jamie’s Journey to CarFest Ambassador
Discover how Young Epilepsy supported Jamie through severe seizures to becoming seizure‑free and a CarFest ambassador, raising awareness for children with epilepsy.
This section covers epilepsy treatments, including anti-seizure medications, vagus nerve stimulation, neurosurgery, the ketogenic diet, and more.
It also includes FAQs for parents and carers on antiseizure medications for children.
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What treatment you have will vary from person-to-person. It also depends on the type of epilepsy you have. Your doctor will explain the main treatment options to you.
The main treatment for epilepsy is anti-seizure medications (meds). Other treatments include:
You may have to try a few treatments, or a combination of different treatments, until you find something that works well for you.
Most people can control and reduce their seizures with the right treatment and support. Anti-seizure meds work very well at controlling seizures. For some people they may help to stop seizures altogether.
Epilepsy cannot currently be cured. But, with the right anti-seizure meds seizures can be reduced, prevented and may stop altogether. If you have not had a seizure for two years, your doctor may suggest stopping or gradually reducing your treatment. Remember to always talk to your doctor before stopping any medication.
If you’ve had a seizure, or you think you may have had a seizure, it’s important to go to your General Practitioner (GP). They will talk to you about your health and any symptoms you’ve had.
If you’ve had a seizure, your GP should refer you to a specialist healthcare professional at the hospital. For example, a children’s doctor (paediatrician). You should have an appointment to see them within about two weeks. But it can sometimes take longer. They will talk to you in more detail about your health and may suggest doing some tests. This will help them decide if you have epilepsy.
If you are diagnosed with epilepsy, your specialist doctor will talk to you about the treatment options. They will work out a treatment plan with you. They will use the National Institute for Health and Care Excellence (NICE) guidelines to help work out which treatments to offer first. You will usually start with one treatment. Your doctor will suggest other options if the first treatment doesn’t work. Or if you have side effects that are difficult to manage.
The NICE guidelines are a set of trusted recommendations for how health and care should be delivered to people in England and Wales. NICE stands for National Institute for Health and Care Excellence.
Your healthcare team will use these guidelines to help them make decisions about your health, including what treatments you may have.
NICE create guidelines for all types of health problems, including epilepsy in adults, children and young people. To read the full guidelines for children and young people with epilepsy, visit the NICE website.
If you live in Scotland, your healthcare team may use SIGN guidelines. SIGN stands for Scottish Intercollegiate Guidelines Network. They are used in the same way as NICE guidelines. To read the full guidelines for children and young people with epilepsy, visit the SIGN website.
1. Epilepsy. nhs.uk. October 23, 2017. Accessed January 20, 2026. https://www.nhs.uk/conditions/epilepsy/
2. Epilepsy. Accessed January 20, 2026. https://www.who.int/news-room/fact-sheets/detail/epilepsy
3. Chen Y, Li W, Lu C, et al. Efficacy, tolerability and safety of add-on third-generation antiseizure medications in treating focal seizures worldwide: a network meta-analysis of randomised, placebo-controlled trials. eClinicalMedicine. 2024;70. doi:10.1016/j.eclinm.2024.102513
4. Epilepsy. nhs.uk. October 23, 2017. Accessed October 8, 2024. https://www.nhs.uk/conditions/epilepsy/
5. Heenan N, Coleman K, Tittensor P, Shepley S. Epilepsy in Children and Young People. Karger; 2024.
6. NICE. Epilepsies in children, young people and adults. Published online 2022.
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Last updated July 2026.
We're currently reviewing this information. The next update will be 2029. If you would like to find out more about how we produce our information, or the sources of evidence we use, please contact us at healthinfo@youngepilepsy.org.uk