Our Mission & Vision
To improve public understanding of epilepsy
To make epilepsy research exciting
To educate the public regarding common mental health issues affecting those with epilepsy
To reduce the feelings of loneliness and shame felt by many affected by epilepsy
To reduce discrimination faced by many people regarding epilepsy
To reduce the communication gap between neurologists, scientists, researchers, employers, and those affected by epilepsy
What We Do
Share cool, educational blogs regarding epilepsy from patients, family members, medical professionals, and scientists from around the world
Provide up-to-date information and tips regarding epilepsy and mental health conditions
Encourage interaction between medical professionals and those affected by epilepsy
We feature guests from all over the world, with countries so far including the UK, Afghanistan, Australia, Canada, Colombia, France, India, Kenya, Poland, Qatar, Uganda and the US;
We work with organisations including Epilepsy Action (UK), Epilepsy Research UK, SUDEP Action (UK), Epilepsy Society (UK), Epilepsy Foundation (US), Cheeky Neurons (Australia), Epilepsy Connections Affiliated (Australia), Young Epilepsy, and more.
Active patronage goes a long way to making this all possible. These are monthly recurring contributions to my mission and what I’m trying to achieve. From as little as $1 you can be involved in helping me spread this positive message and continue to help the community. Just click the button above and name your price!
This is a one-off donation towards my creative projects. It’s ok if you can’t get involved regularly, and any amount does help. I appreciate anything you deem a valuable contribution to my creative mission!
Current Project: An Anthology of Experience
give voice to those
normalising for those dealing with and those around someone dealing with