Reagan has still been a little drowsy...sleeping a little more than usual during the day (but still sleeping well at night). I'm wondering is she's still adjusting to the medicine increase or if maybe she just has a little something she's trying to fight off. Her seizures have been a little better, although every time we think that we're seeing less...she starts having more. And she's still having stomach issues...I don't know what we're going to do with her. She's been very talkative tonight. We really have to get that on video, it's too cute!! Speaking of video...below is a video of Reagan's "twitches" at their worst. This was taken a few days before we had the EEG done (when we found out that they were non-epileptic), but I was concerned that her doctor may want to see exactly what she was doing so I taped them. They seem to have gotten better lately although they are still there and more pronounced in the morning when she first gets up. In the video they are happening every second or even more than one a second...you can see why I was so concerned about it. The best way I can describe them is it's like watching popcorn pop...almost constant...as soon as she would have one another one would pop up. Yuck. Hard to watch but I thought I should post it because it might be of use for others to see it. The doctor described it as non-epileptic myoclonus and we're still not sure what is causing them, but thankfully he does not think they are harmful to her and she seems no worse for wear. She does have one spasm during the video...it's obvious when she does it (the twisting movement and the dazed look in her eyes).