He continues to fight the pneumonia – and is on antibiotics once again. He has a fever off and on – it is usually brought down with Tylenol. Shawn is off all other sedations and pain medication!! He continues to move a little more each day – his head, eyes (fluttering and opening), arms, legs, mouth (looks like he's yawning). He is beginning physiotherapy tomorrow. I also wanted to let everyone know – in case anyone is thinking of visiting him – that at this time, due to SARS, they are only allowing one person per day to visit him, and are limiting it to family. Hopefully these rules will change soon – and I will let you know when they do. Thank you for your continued positive thoughts and prayers for Shawn!!!! And keep hoping for more positive things to happen every day!!!!!