Transforming lives through advocacy, research and care
Earlier in 2021 we carried out a detailed survey to find out what concerns you most around epilepsy, and the changes that you would like to see. More than 1,000 of you responded and this gave us a unique insight into the landscape of epilepsy. Following this survey we have become clearer in describing our vision and setting out how we intend to make it happen.
We are Epilepsy Society. The UK's leading charity for epilepsy research and support.
Due to current circumstances in relation to the coronavirus some of our services have been reduced with our staff working from home. Despite this our top priority at Epilepsy Society is to support people living with epilepsy. You may notice a slight change in our communications. For the time being, we will focus our efforts on making sure you have all the information you need from us to help you as best we can in the current climate.
Leading care provider
Our range of care is tailored to the needs of each individual, and our professional staff are committed to maximising the life potential of everyone within our care homes.
Cutting edge research
Epilepsy Society's Chalfont Centre is unique in bringing together intellectual capital to form a powerhouse multidisciplinary team who contribute to a wide ranging spectrum of research.
Epilepsy Support
Our confidential epilepsy helpline and online information give help and support to people who are affected by epilepsy.
Advocacy
We are a voice for people with epilepsy, striving to push epilepsy up the political agenda and bring about change at government level.
Medical services
The Chalfont Centre and our Gowers unit lead the way in the most advanced techniques for the diagnosis and treatment of epilepsy.
Care services
We are the leading charity care provider, where people love to work and live. Our wide range of care is tailored to the needs of each individual, and our professional staff are committed to maximising the life potential of everyone within our care homes.
Campaigns
Our campaigns team lobby government and decision-makers on the issues that matter to people with epilepsy. From safer medicines for pregnant women to the dangers of online harm, and from medicines supply to public transport access, we raise awareness of the daily challenges facing people with epilepsy – putting your needs at the heart of what we do.
Latest news
Our researchers get on their bikes to support people with epilepsy
Twelve scientists from the Epilepsy Society and UCL are going the extra mile to raise money for a vital new piece of equipment that will help in the treatment of people with epilepsy.
Have your say on the Online Safety Bill
The Epilepsy Society is encouraging people affected by epilepsy to submit their views on online safety to an important parliamentary committee.
Epilepsy Society partners with Healthinote
Epilepsy Society is working in partnership with Healthinote - a digital platform for doctors, nurses and pharmacists to share personalised, trusted health information with patients.
Zach, 10, is short-listed for Unsung Hero Award
We are incredibly proud to announce that 10-year-old Zach Eagling – the figurehead of our Zach’s Law campaign – has been shortlisted as an Unsung Hero in the Third Sector Excellence Awards.
Law Commission recommends specific offence for malicious tweets sent to trigger seizures
We are thrilled to see that the Law Commission is calling on the government to introduce a specific offence to deal with flashing images posted on social media to trigger seizures in people with epilepsy.
Seizures in vaccine leaflet relate to rare blood clots in brain
Callers to our Helpline have expressed concerns that the latest version of the patient information leaflet for the Covid-19 Astra Zeneca vaccine, mentions seizures as a possible side effect.
Our research
Research
The ultimate goals of our current research are to spearhead personalised treatment and to incorporate genomic diagnosis into the NHS for people with epilepsy.
Therapeutic Drug Monitoring (TDM)
Therapeutic drug monitoring (TDM) is an area of clinical chemistry that specialises in measuring medication levels (concentrations) in patients, usually through blood samples but also through saliva samples.
Genomics
Read how we are working to understand the genetic architecture of each individual person's epilepsy through our world leading genomics research programme.
You can call our helpline on 01494 601 400.
Our Helpline is open five days a week, Monday to Friday 9am to 4pm, (Wednesday 9am to 7.30pm).
You can also reach us by email
helpline@epilepsysociety.org.uk.
Please support us.
In these challenging times, charities like Epilepsy Society rely on donations to ensure vital services for our beneficiaries can continue. If you can spare a donation or pledge a monthly gift, you will be helping to ensure we continue to support everyone affected by epilepsy. Thank you.