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!!Keep it up, *TT*!! And prayers added for a good CF non-report tomorrow!!
Well, Logan had an uneventful day...... and that's good! He slept most of the day. At first I was concerned, but considering that he has had NO rest for so many days..... I guess his little body just said enough! He even slept thru his breathing treatment and the "poundings" on his back they do to loosen the stuff in his lungs. He did wake up and eat a little lunch, but he's fallen so far behind on eating that I'm sure his little tummy has shrunk. And that's not good because he's definitely not a good eater.
The plans are......... to have him take the Cystic Fibrosis sweat test at 8 in the morning. Then back on the monitor to see how he's doing with his oxygen. The Pulmo doc said she "may" release him tomorrow evening IF Beth will stay home with him for 2 days and then I will take care of him when she goes back to work. He is going to be sent home with oxygen and a monitor. But there's so many "bugs" going around the hospital, they just don't want him exposed to anymore any longer than necessary. He will not be released to go back to day school for 2 weeks at least. Here we go again!! LOL
Considering how very, very sick he was, the only explanation of his rapid road to recovery is good care and LOTS of prayers and well wishes! While he was sleeping, his little ears had color once more and he didn't have those dark, dark circles under his eyes. Now we just have to keep him well!!
One note......the doctor said that they now believe that RSV is a "contact" virus. Meaning that anything you touch has the virus on it. And that it "sheds" for 10 days. So everything he touched at home, toys, furniture, doors..... the whole tamale... has to be sprayed with Clorox spray. Thank Heaven he never puts stuff in his mouth! We have to wash our clothes and our bodies after we leave him so as not to take a chance of infecting others. Nasty stuff!
That's it for this evening. I will let you know as soon as we are sure he's going home. And please, offer a special prayer for a negative test result tomorrow.
My love and thanks to all.......
Nana ~~~~~~~~~
Thank you Lord for the progess, and please, Lord, PLEASE let that test be negative tomorrow....please continue to heal this child.
In Your Holy Name, AMEN!!
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Sure thing,BG.
Prayers up for tonight...and will give him a double dose int he morning for the test. Please God, do not let him have CF...he has enough to handle already.
Stay strong Logan...we are with you buddy.
sleuth
Good news, hang in the Logan, you're doing great!
Fervent prayers continuing for all. Please, Dear Lord, we pray for Logan and his family. God bless them all.
You know us... right there with ya.
Matt 18:20
Hang in there Logan. You are loved by many.
Can't wait to hear that he's home, and his normal self.
Hugs and kisses for Logan, and hug for you, Nana, to sustain you during all this.
WOW .... bless his little pea-pickin', Texas king-size heart.
Keep fighting, sweet Logan ... God, keep Your angels and TC nearby. I've not heard of this virus ..sounds deadly. And it's easily spread, sounds like. Thanks, Nana .. give him hugs from his FReeping aunties and uncles ... and MORE HUGS.
h!!Keep it up, *TT*!! And prayers added for a good CF non-report tomorrow!!
So glad to hear he's making progress. Now we just have to get through that test in the morning and hope for the best.RSV is treacherous. Noelle has been sick for 12 weeks now (with a day in the hospital) and no real diagnosis. She coughed for 8 weeks!They thought it was pneumonia, then RSV, then allergy-related...who knows?
Anyway, we're all sending our love to the little Termite and with all that love, he's surely protected.
Thank you for the updates.
Prayers continuing.
BTTT
Please let the test for cystic fibrosis be negative.
I've been gone for Thanksgiving, but am now back in my chair so prayers are going to be DOUBLED for lil Logan that he will PASS his test today and that he'll heal and return home SOON!