Dr Gareth Morris recently completed an ERUK Explore Pilot Study alongside Prof Stephanie Schorge, but the results were not as expected. In this blogpost Dr Morris discusses the values and learnings from research that has
In this Research Blog, Daniela discusses the impact this work could have for people living with uncontrolled seizures.
Rebecca joined our SHAPE NETWORK Steering Group to help develop the strategy for the network. Here, Rebecca explains why she wanted to be part of this network and why it’s so important for those affected
We look at how laboratory research is providing us with hope for new innovations. We also look at how people with epilepsy are shaping this vital work.
In this webinar, our fantastic blog contributors from the month, Dr Rhys Thomas, Dr Kate Baker’s and Professor Markus Reuber, discussed what clinical research is, how it makes a difference for people with epilepsy and
On the Research Blog today, we speak to Professor Markus Reuber who was awarded an Innovations in Healthcare Research Award. Professor Reuber discusses how his project will help improve the effectiveness of remote ‘teleconsultations’ between
We hear from our final Innovations in Healthcare awardee, Dr Rhys Thomas, who tells us how his project aims to increase awareness of SUDEP by rolling out an award-winning educational app and producing information videos
Clinical geneticist Dr Kate Baker shares the progress genetic testing has made in the last 10 years, including her own research into a specific genetic mutation, and explains why more research is still needed…
Epilepsy Research UK supporters, Amanda and John, discuss the challenges they faced before achieving a diagnosis for their son, Archer, and their hopes for future research into epilepsy.
This month, we’ll be looking at examples of clinical research and why it matters for people with epilepsy.
