I wrote two days ago the article on what people with chronic illnesses hate the most (besides the illness itself). See the article HERE.
The main purpose of the article was not to tell people that I have epilepsy or to take something off my soul. The idea was to explain to people what they do (around someone with chronic illnesses) and why they shouldn’t do anymore.
It`s funny: after people found out about my epilepsy, the first thing they did was to behave as they shouldn’t have done it. They sent me sympathy emails, Skype and Facebook messages in which they explained that they support me and that they are right behind me. As I said, it`s funny :). The real thing to read about