The village with charity in its DNA
Nicola Swanborough explores how the village of Chalfont St Peter and Epilepsy Society are deeply connected.
Laura shares what it is like to work at Epilepsy Society
Our Donor Care and Direct Marketing Manager Laura Larrett, lives locally and has worked here for almost 20 years. She talks about the perks of working at Epilepsy Society.
Our CEO says "wow" to latest discoveries in epilepsy
In her New Year blog, our chief executive, Clare Pelham, shares her excitement at learning of the latest scientific discoveries in the field of epilepsy from researchers at Epilepsy Society.
Epilepsy - it's not what you think
My name is Hayley and I'm a 36 year old secondary school teacher from Essex. I was diagnosed with Juvenile Myclonic Epilepsy about 20 years ago. I've been able to live a pretty normal life since my diagnosis which has included having two children, completing a degree and teaching qualifications.
Amy Frost uses art as a coping mechanism for her epilepsy
Amy Frost, 25, has generalised epilepsy. She has been having seizures since she was 11 years old, but was diagnosed at 18. Here she explains how she started using art as a way to cope with her emotions associated with her epilepsy.
What one piece of advice would you give to someone who has just been diagnosed?
In September 2018, we asked our Facebook community what was the one piece of advice they would want to give to someone who had just been diagnosed with epilepsy. Our Marketing and Communications Executive, Paige Dawkins, talks more about the responses we received.