Epilepsy: The Shameful Misunderstanding | Documentary Idea
by Eric
(Portland, Oregon)
I was diagnosed with epilepsy when I was 8 years old. Over the years, I was shunned and fell victim to stereotyping by many people in the close knit community that I still live in with my family, though many now have quietly accepted the fact that I have epilepsy. I am very open about being an epileptic and talk about it to whoever asks me about it.
The idea for this documentary came from a seizure that I had in March of 2012 during a church service. The parish priest still believes I faked the seizure just to get attention for myself, which of course I was not. He even threatened to force my head into a baptismal font if I said anything more about “having convulsions.” {He has not forced my head into a baptismal font, which I am glad has not happened.}
This documentary would address the following to try and set the record straight on epilepsy:
1.} What epilepsy actually is and how more people can be diagnosed.
2.} Why people believe in epilepsy-related stereotypes and why people need to stop believing in such stereotypes.
3.} How to increase more awareness of Epilepsy with a message that people with Epilepsy can live fulfilling lives without discrimination.
Another inspiration for this documentary came from a documentary called Bully, which was released last year. Growing up with epilepsy, I never realized that a lot of people never thought of epilepsy very much, which would explain why I fell victim to stereotyping.
The title comes from many people who believe that epilepsy is a disease, which of course it is not, and that such people should be ashamed for believing in such a misconception. This documentary could be the first part of a series of documentaries if received well.