Helpline Appeal
Our helpline is busier than ever, with more and more people needing emotional support and vital information. This National Epilepsy Awareness Week, your donation, no matter the amount, can help us support the next caller.
We are Epilepsy Society. The UK’s only charity transforming the lives of people with epilepsy through world-leading research, advocacy and care.
What we do
Cutting edge research
Epilepsy Society is unique in bringing together experts from around the world to form a powerhouse multidisciplinary team who contribute to a wide ranging spectrum of research.
Advocacy
We are a voice for people with epilepsy, striving to push epilepsy up the political agenda and bring about change at government level.
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.
Epilepsy support
Our confidential epilepsy helpline and online information provide support to people who are affected by epilepsy.
Our research
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.
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.
Sodium valproate
Sodium valproate is an epilepsy medication prescribed for all seizure types including absence, myoclonus and tonic clonic seizures. New regulations have been introduced by the Medicines and Healthcare products Regulatory Agency (MHRA) around the way in which the drug, sodium valproate is prescribed. Find out about the changes and how they might affect you.
Latest news
Patients to receive appointment reminders, screening invitations and test results through the NHS app
As part of the reforms to the NHS, millions more patients will receive appointments, screening invitations and other important information directly via the NHS App as part of the digital-first upgrade.
Medications, epilepsy and climate change: the need for action
As we continue to experience increasingly hot summers, researchers warn that commonly prescribed anti-seizure medications could be affected by the heat. And they are calling for further studies to better understand what measures could be taken to prevent medications degrading.
Government announces new urgent and emergency care plan
Under the new Urgent and Emergency Care Plan for England announced today, the government has promised that patients will receive better, faster and more appropriate emergency care as it sets out reforms to shorten waiting times and tackle persistently failing trusts.
Rubgy balls and chocolate bars raise awareness of epilepsy in the corridors of power
Our exhibition in the House of Commons for National Epilepsy Week has really pushed epilepsy up the political agenda. We held a reception last Wednesday 21 May with guest speakers including the rugby player Tommy Freeman, Rosie Wrighting MP and an impromptu speech from Lord Heyward, who was so inspired by our work that he wanted to speak.
Daredevil daughter raising funds for Epilepsy Society
Sophie, 17, is going to be doing a skydive this July for Epilepsy Society but her inspiration is her mum, Nicola, who was diagnosed with epilepsy as a teenager. We caught up with them to learn more about the challenge and life with epilepsy.
Rugby player, Tommy Freeman and MP Rosie Wrighting putting epilepsy on political agenda
This week, 19-26 May, is National Epilepsy Week and we are in the Houses of Parliament with an exhibition to increase awareness of epilepsy among MPs and push the condition up the political agenda.
1,200 die every year in the UK from epilepsy related deaths
Personal stories
Simon's story
Inner Strength and Self-Belief – Confessions of a Marathon Runner with Epilepsy.
Becca's story
Sweet Success! How Becca and the amazing team at Gemini Chocolate raised an incredible £1,000 for the Epilepsy Society.
Eamonn's story
Eamonn is a restaurant and bar manager and he was diagnosed with epilepsy aged 18.
" They couldn't understand why going out into the sunlight would bring on seizures - until our genetic testing revealed the cause of Daniel's epilepsy. "
Genetic testing could mean a new world of personalised treatment that transforms lives. By understanding more about each person’s genes, we will understand more about their epilepsy and how to treat it.
