Each person living with epilepsy has a name.

Each one has hopes, dreams,

Her name is

"As someone who’s been living with epilepsy most of my life, I know how hard it is to accept it and deal with it. And I know how hard it was/is for my family to deal with it. I want to make a difference for people living with epilepsy and those who care for them as epilepsy doesn’t only affect us. The more people that know, the greater the impact.”

Remy, a mum and diagnosed with epilepsy.

Her name is

"My sweet daughter, Stella Rae, has a rare genetic mutation that presents with severe form of epilepsy. Our girl is bright, wild and a lot of fun, but despite 6 anti-epileptic medications and a specialised diet she still has countless seizures every day. We have been on our journey for seizure control for a little over 12 months now with ups and downs all along the way.”

Stella is just two years old. Her dad, Mitch, hopes there will be a cure one day.

Their names are

" A diagnosis very new to us, but extremely close to our hearts. Ben is hoping to be a role model for younger kids and students who may be navigating life with epilepsy. The aim is to empower others by taking a positive approach toward this life-long condition. To raise awareness for epilepsy and fight its taboo nature. ”

Ash with her partner Ben who has recently been diagnosed with epilepsy