Wednesday, November 30, 2011
A Bet With My Teacher
Every time I take a "big" math test, my teacher and I make a bet as to weither or not I will pass. I think the most highest amount was a couple of bucks and the lowest was a $.50 coke. I sure am glad that it is just a tiny bet because I don't think that I could afford anything else!!
Tuesday, November 29, 2011
Update on Mary Beth Miller
Update on Mary Beth, today has been a much better day. She is more alert today, she is following things with her eyes and started watching some movies on tv. Her doctors are saying today that they do not believe that she has post pump chorea, we will be meeting with them in the morning to discuss this further. We are very encouraged by what we are seeing today. She is trying so hard to talk, but it is very difficult for her. She appears to have control over the bottom of her body today, her arms are still shaking. We know that she can hear us, she was sitting up in the bed tonight with Dr Jefferey and he was showing her things on his phone and she was laughing with him, it was the sweetest sound I have heard in a very long time. I know that we will get our baby back, it is going to take time. It appears that Mary Beth may have had some type of stroke, just not sure at this time. We are hanging on what God can do, we have seen him work in the life of sweet Greer Underwood, another transplant patient that we have grown to love and we know that he can do the same thing for Mary Beth. Please continue to pray for us and for Mary Beth, I know that she does not understand all of this and we can tell that she wants so badly to get back to herself. Thank you, we love you all.
Monday, November 28, 2011
Update on Mary Beth Miller
I would like to give everyone an update on Mary Beth. Our daughter is not the little girl we had before she went into surgery. She can not respond to us, she can not hold things, her hands are very shakey, her legs are moving as if she are trying to ride a bike. We are told that the condition is called Choreoathetosis, or post pump chorea, we are told that this is very rare and that she could recover from this, it could take days, it could take months, or years if ever. We are being told that 25% to 30% of patients that get this do not recover, we have to pray that she is not in this range. We still need to have an MRI done to see if this is what is going on, but all of her semptums are leading to this, we can not have the MRI as long as she has the pacing wires in. I will try my best to update as I can, we are staying with her all day at this point and coming home to sleep. Please pray for our little angel and for Mark, Macon and I, this is very hard
Wednesday, November 23, 2011
It's late and I am on a mocha high!!
1: Your name is ..... (first names would be nice or just your initial)?
2. How you found my blog?
3. What is it that you would like for me to write about?
4. Where are you from?
I love Mocha but, I think that I drank to much of it. One time, I had 3 Mocha's before I found out that it had caffeine in it!!
Update on Will
Amy reports that Will made it through all of his chemo today with not side effects. This was the first day. Thanks again for the prayers.
Thomas will be flying in tomorrow from Alabama; Drew and Lia from North Carolina. Anna and I are looking forward to being with them.
Blessings to you all,Debbie