I almost hate to write this for fear of jinxing it, but Stephen is now 2 months seizure free. That is the longest he has gone since the big seizure in September 2009. He still has not gotten back to where he was, however I feel like part of that could be because we have gotten a bit lazy about pushing him to do very much. He isn't getting that stimulation he used to get. That, my friends, is about to change.

If any of you have stories or suggestions to share about "sensory diets" or sensory activities, I would love to hear them.

It will also be interesting to try some of these activities with Nathan (the baby). I am concerned about him because I was on bed rest for so long during his pregnancy. Not worried, just aware that there could eventually be issues.