I don’t have a lots of followers for this blog or a huge number of view – about 150-200 views/day. And most of these go to a post about humanity that I wrote in 2013.
However, how I wrote in my previous post, I get questions from time to time. Some stupid, some not. Some from lazy people (as someone commented to my post), some from people who just stumbled upon my blog and don’t care about epilepsy.
At the beginning of each year, I take some time to go back through the questions I got. With 2020 being a hard year on all of us, some of the “good” questions were a bit weird.
Here you go my top three favorites:
- What is epilepsy and why should I care about it? My (honest) response: you shouldn’t care if you don’t know anyone who has epilepsy: friend, family, colleague. Epilepsy is a disorder, not a disease so the only thing you could do is be there and be a friend that person.
- Why are people afraid of people with epilepsy? My (abridged) response: I’m not sure what you mean. I only met people afraid of someone having a (grand mal) seizure while they are with them. But that’s it. Unfortunately, I see that people actually consider those with epilepsy as inferior because we can’t do some things aka drive (for some of us), drink (I wouldn’t drink if I didn’t have epilepsy) etc.
- Is epilepsy dangerous? My response: yes, it is for some of us. For epileptics, imagine having a seizure in the middle of the street. It doesn’t matter if it’s grand mal or absence seizure. You could get hit by a car. For non-epileptics, it’s mostly the scare: imagine you are in a car with someone having a seizure (grand mal). If s/he sits next to you, you might lose focus/attention and get into an accident. But 95% of the time there is no problem.