Monday, December 7, 2009

Update #105 on Kevin

So, the staff at Meadowbrook has moved Kevin again. They did it because they are testing Kevin for tuberculosis. TB is a potentially serious infectious disease that primarily affects the lungs. They started testing Kevin for TB on Saturday with a skin test and samples. The odd part is that they didn’t move him until today. The room has negative pressure, which means it cycles the air out so that it can be filtered. If he does have TB how many people were infected? He doesn’t seem to have many of the symptoms of TB, except coughing and the occasional fever, although I appreciate them checking under every rock. The lung doctor just came in and said she doesn’t think he has TB, but I don’t think that was the final verdict. She said his chest X-Rays looked better, and that is pneumonia may be clearing up. She said it was most likely where he had aspirated (swallowed fluids into his lungs).


When you come to visit, you have to wear masks for the airborne possible TB, then gowns and gloves for the staff infection, which even though is colonized, still comes across as an isolation factor. One plus for moving into the negative pressure room isolation room is that it’s a private room again.

Kevin has both eyes closed right now and seems to be really resting. Usually, he doesn’t close the right eyelid on his own. Sometimes he does though and this is one of those times. Sitting here, I have seen his right arm move a little, his left arm twitch, his head rock back and forth a bit and just now his right foot moving. I remember the first few days just wishing to see anything move.

My mom is still in the hospital. They started treating her for cellulitis. Then for staff infection. Now they have her foot on a cold pack and can’t figure out what is causing the swelling. Angie and I finally got to see her yesterday afternoon. We took her a Sunday paper and went to tell the nurses they left the water out of mom’s ice/water chill pack. They have her on Vancomiacin for whatever it is that they don’t know yet. They have Kevin back on Vancomiacin for the pneumonia and possible TB.

Kevin is also on benedryl. If his physiology is anything like mine, it will make him drowsy, which he seems to be. Hopefully soon, we will know if Kevin has tuberculosis or not…that way we can get rid of these hot and humid masks.

Thanks for reading and praying,
Matt, Angie and family
_______________________________
http://www.prayforkevin.com/

3 comments:

  1. This comment has been removed by the author.

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  2. Hello,
    I'm from Ontario, Canada. I came across your blog through an online forum. After reading through the posts from the beginning I feel like I am a memeber of your family.
    I'm sitting here praying to God to help bring strength to your family in your time of need. I will continue to pray and read for updates.
    Just wanted to your family to know that they have many people supporting them that they don't even know.

    God Bless
    Keshia

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  3. Look into that Niessen fundoplication ASAP, he's never really gotten a good stretch without pneumonia of some kind, and his lungs will get less able to rebound with each bout. I admire you're family for muddling through, your strength astounds me.

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