More than Seizures

thingiverse

This is a 4-piece printable structure (I don't feel confident enough to call it a real sculpture) to raise a little awareness about epilepsy. I have been living with epilepsy since I was around 14. That meant I spent 13 years without having to worry about how many days seizures free I am. Not having to worry about medications and medication timings. Or to know about EEG's or have to do an MRI, or a sleep study; or worry that i have a 1 in 1,000 random chance of dying suddenly and for no reason currently understood by any medical professional. But now I do. The pixelized letters in this print are emblazoned with the number of things. From derogatory terms often used to describe people with epilepsy, to phrases like "I need a ride" that I have to repeat often. Or other things like the isolation you feel as you try and dodge your seizure triggers. This is a testament to living with epilepsy and how it is more than just seizures. If you feel at all inspired by my story here or any stories in the comments please do try and help the community. While I know many have fallen on hard times due to the pandemic there is a wonderful opportunity for free at learn.epilepsy.com to do a free training that only takes around 75 minutes for seizure first aid. 1 in 10 people will have a seizure in their lifetime. So please take this opportunity to do so