Blogs
Here you will find tips, opinions, and info on different topics
Discover Bethany's inspiring story overcoming stigma at school and finding community with Young Epilepsy.
Rachel tells the story of how her son Charlie was diagnosed with Lennox-Gastaut Syndrome, and how her family is looking forward.
Discover Amelia’s story of overcoming epilepsy at school with support and understanding from teachers and friends.
Stigma and seizures pushed Jess to a frighteningly dark place. Discover how speaking out, finding community, and embracing the stage helped her find the light.
Charlotte's epilepsy diagnosis at 18 compromised her A-levels, but perseverance and openness to support led her from rejection on results day to her dream job.
Discover how Tee pursues her dreams, breaking barriers and inspiring others to thrive with epilepsy.
Discover Zaid’s story and tips for young people seeking support and pursuing a future in social work.
Zac’s story is a powerful reminder that epilepsy doesn’t have to hold you back. From wild swims to mountain runs, he tackled every challenge of his school’s Adventure Race with courage, teamwork, and a whole lot of heart.
OPM-MEG is a wearable brain imaging technology that makes epilepsy diagnosis easier and more accurate for children. By allowing movement and creating a welcoming environment, it can provide better data than traditional EEGs. Sam’s story shows why funding is needed to make this technology available, helping children get faster, more effective diagnoses and care.
Follow Dylan McHale's inspiring journey as he runs the Paris Marathon to support Young Epilepsy. Learn about his motivations and how you can help.