Jennie Update!!-- a beautiful day in Boston

I started my day out with the sun in my face and wind in my hair, and waking up thinking about my Caleb. It is a beautiful day in Boston today, with the sun shining and not a cloud in the sky. Caleb is on a new medication that Sharyn and I are researching because it is altering his mood and alterness. These nurses at Spaulding Rehab are so caring and they want us to understand everything that is going on with Caleb. They print out information about his medications and give them to us, so that we understand what the effects will be and important information we need to know about the meds.
I just wanted to remind everone of a couple things when Caleb comes home. Yes, Our Caleb is coming home on Saturday and will probably be home around noon-time. We will give a better update on this later in the week and as you all know, we are all meeting on the town hall lawn to greet Caleb. Sharyn will be calling me and Sky when they are leaving Boston, so that we know exactly what time they will be arriving. If you are in a time crunch, or have to work, you can call me that morning, and I can tell you exactly when they will be in Fleet. I know that you are all going to want to go to Sharyn's house to see Caleb, but for the first week, as Sharyn said before, no one is allowed to just "stop by". I know we are all used to going over her house whenever we want, but now we can not do that. Caleb is still going to be having therapies many times a day so that we can ensure progress, and he will have a very scheduled day. Sharyn and I are going to make a schedule for visitors and there will be certain days and times for certain people to come see him. People will have certain times and days that come, it won't just be a free-for-all. I know this may seem harsh, but for Caleb's sake we need to ease into people seeing him, and do not get me wrong, having his friends visit is definitly making him get better and it sparks his personality, but we just have to do it slowly.
Other than Caleb being alittle foggy this morning, which iswe expect to happen with his medications and not sleeping well sometimes, ( as we all get grouchy with no sleep), Caleb is still making progress. He is walking on his own and his balance is getting better and better. His speech is coming and going, because sometimes he just speaks when he wants. He is eating really well and going great.. That is all for today, because caleb just started typing on my computer. he just typed all this by himself. he is off for his 4th therapy of the day and its on 11am. he is a busy man, and working sooo hard. love you all

Caleb just typed this--->" hi lads and girls I love you all very much yeah yeah!!!!!!!!"