I just wanted to take a minute to add a special post here so no one missed out on the conversation.
Check out the questions
I’ve posed several questions. The they are:
What does “stigma from epilepsy” mean to you?
All you have to do is ask
I was pleasantly surprised to find out how many people were willing to talk about stigma from epilepsy when they were asked. Sometimes its just a matter of not being afraid to talk about the elephant in the room.
Common experience draws us together
I encourage you to take a look at the responses. You may be surprised at how familiar the answers are. The common themes are: isolation, inability to do the things you love to do, fear and anxiety.
Check it out at Facebook.com/livingwellwithepilepsy. Add to the conversation. Lend your voice.