We are Epilepsy Society. The UK’s only charity transforming the lives of people with epilepsy through world-leading research, advocacy and care.
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 trolling, and from medicines supply to public transport access, we raise awareness of the daily challenges facing people with epilepsy.
Medical services
The Chalfont Centre and our Gowers unit lead the way in the most advanced techniques for the diagnosis and treatment of epilepsy.
Latest news
It’s never right to use epilepsy to “go compare”
We are always quick to call out any publications or broadcasters who use epilepsy-related terms in an inappropriate and offensive manner, even when it is sloppy journalism and presenting and there is no deliberate intent to cause harm and upset.
One-stop clinic offers cardiology alongside neurology
A unique one-stop clinic for people with Dravet syndrome has been launched at the Epilepsy Society’s Chalfont Centre.
Epilepsy Society response to government online platform Change.NHS.uk
We welcome the Government’s ambition of realising three big shifts in healthcare as part of its 10 Year Health Plan – hospital to community, analogue to digital and sickness to prevention.
Public Health Scotland issues report on the use of anti-seizure medicines during pregnancy
Epilepsy Society has been campaigning for many years to raise awareness of the risks many epilepsy drugs pose to babies during pregnancy. Public Health Scotland (PHS) has released a new report focusing on the use of anti-seizure medicines (ASMs) among women of reproductive age in Scotland, including those who were pregnant.
Red Tape Challenge should be matched by medicines supply chain review
As Health Secretary Wes Streeting launched his Red Tape Challenge to free up more GP time for patients, the Epilepsy Society issued a sharp reminder that resolving medication shortages would also reduce the burden on GP surgeries.
Write to your MP about medication shortages
Join our campaign to end medication shortages by asking your MP to write to Health Minister Karin Smyth. Our templated letter is easy to use and will also find your constituency MP according to your postcode. Image ©House of Commons
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.
Genomics
Read how we are working to understand the genetic architecture of each individual person's epilepsy through our world leading genomics research programme.
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.
You can call our helpline on 01494 601 400.
We're open:
Monday and Wednesday - 9am to 7.30pm
Tuesday, Thursday, and Friday - 9am to 4pm
Saturday - 9am to 12.30pm
You can also reach us by email
helpline@epilepsysociety.org.uk.