This will encompass the last two days: Sunday, Mom and Dave spent the morning with Richard. He was confused and ornary. Memere and Wayne (grandparents) also met them there. He allowed them to take pictures of him again as long as he approved of them. A patient makes a noise like a goat so he thinks there is a goat in the building. All afternoon, we all went to Faith Ranch to the wonderful fundraiser that was put on. If you missed it, it was great! Mom visited Christie in the evening. She was asleep.
Now we are up to today. We spent the morning with Richard. He had speech therapy at 10 and physical therapy at 11. He did great with speech therapy. He remembered the days of the week, the first president, and his birthday. He also answered all the questions appropriately. They even asked him what does it mean when someone says dont judge a book by its cover. His answer was there might be more to that person than we know. They took out his trach!!!!! Now he cant pull it out. :) He walked (with assistance) to the bathroom. But that is exhausting so then he takes a nap. During physical therapy, they didnt help him push the wheelchair, he moved it by walking his feet. He is really thirsty and wants to drink so he is bribeing the nurses. He is saying, I'll do one more rep if you give me a drink first. He will have surgery tonight for a permanent feeding tube.
We visited Christie tonight. She looked good. Her right eye was completely opened and was looking around the room but not at us. She moved her right arm around several times and constantly moved her fingers. They changed her trach to a smaller more comfortable one. When we left, we put the TV on FOX so she can listen to her shows.
Monday, May 19, 2008
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3 comments:
Hey Angie I just wanted to say that I am so excited that he is doing so well but one thing that kinda made me wonder... What is a permantant feeding tube how does it work? Why does he need one? Thanks a million,
Amber
Amber,
The feeding tube they gave Richard originally is temporary and really skinny in diameter. So, its gets clogged easier. Also he has pulled it out twice. He failed his swallow test twice so they have chosen to give him a PEG tube. Its thicker in diameter so they can feed him thicker things and when he does begin to eat, if he cant eat enough food to give him adequate nutrition, they can supplement him through the tube until he can do it better. They can always take it out later, but its much better than what he has now. Also (Im pretty sure) they tube he has now goes straight into him small bowel so he doesnt digest anything. The PEG tube goes into his stomach so his body can get used to that again. He might get sick to his stomach at first because he hasnt had food there in a month so he'll have to deal with that also. Hope that answers you question!!
Angie
thanks it does.
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