EPILEPSY SPARKS

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.

I love Epilepsy Sparks and I look forward to seeing their posts. Great support and education! I recommend it to everyone with Epilepsy, have loved ones with Epilepsy or just interested in learning more about Epilepsy.

Very helpful and informative for all doctors and patients.

Deeply researched and reliable resource for all things educational about epilepsy. I’m not a sufferer and it’s been eye opening in a hilarious way to learn about what sufferers go through.

Great work! I really enjoy your positive posts. So true that many medics outside of neurology/neurophysiology are just as in the dark as the man on the street.

I love this page😍 I learned a lot and give me positive vibes!!! Cheers!!! It Sparks!!!

Thank you so much!! I love EVERYTHING you do! You keep me going every day! Thank you, thank you, thank you!

This is a great page that not only supports a lot of people who have epilepsy but offers the latest information and educates people too! Keep up the great work!

Thanks for sharing this very important information because many people don’t know how and what to do when affected or when giving care to the affected person since in most cases one often fails to explain to other people how they feel and what they go through but knowing about this page has helped me as a care giver.

As a Mum of a 1 year old with Epilepsy I have read a lot of your posts/Torie's posts and just wanted to say keep up all the good work that you do and feel free to share anything Epilepsy related in our Facebook Group - Tia's Treasures which is dedicated to Epilepsy Awareness 💜

A really friendly group with great advice...plenty of support in here...I'm learning so many things about myself and my daughter's epilepsy that I've never known before.

Patronage

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

everyone effected

normalising for those dealing with and those around someone dealing with

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