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I don’t like feeling like I’m a burden, or less than other people. It’s something that I have to accept. I’m just finding it very hard to come to terms with my disease and the toll it puts on my loved ones. Being in a state that doesn’t see

It’s very discouraging when I put myself in old situation. For example a seizure at work when going to a grocery store, it doesn’t make anything easier. I get anxious and it makes everything worse. I already don’t even like getting twitchy (myoclonic

Epilepsy I wish I had someone who also had frontal lobe epilepsy to talk to. I just want to ask for advice and know how to keep myself safe. I want to know how they feel and what we endure. I want to know how it effects out behavior and what I do.

It’s scaryI picked up the new laundry detergent.My grip was firm and steady I was totally aware of where I’m moving it to. The next second, as if I didn’t miss a beat, it’s on the floor. With a crack I snap back. The cap busts and it flows

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