Carry on ... LolPrayers sent. I will be thinking of you guys.
Let us know when it is okay to crack jokes about you finally following thru with some of your threats.
Glad to hear it.Carry on ... Lol
Ok fellas!! Y'all have no idea how much I appreciate the thoughts, prayers and offers to help out. I am good. Scott's brother and his wife showed up today.
Surprised the **** out of me. It's not like they live down the street -- more like the East Coast. I spoke to them on the phone last night and I guess they caught the first flight out that they could find but didn't tell me they were coming. I came back from running to the house to let the kids in so they could mow for me (and I could pay them) and came back and there they were!! I am SO happy they are here! He has been quite a bit more responsive since he heard his brother's voice.
I am beyond happy because now Scott won't be alone up here ever. One of us will be here with him 24/7 for at least the next week. The nurses have been so helpful. They found me a recliner that is actually quite comfy so I can stay overnight and his brother can cover for me for a couple of hours morning and evening so I can take care of the critters, shower and handle anything else that pops up.
He is resting so much better now. But then again propofol will do that to you. His pneumonia is still getting worse so they are doing a biopsy this afternoon. May wind up changing his antibiotics. Already took the x-rays but I didn't get a look at them and I don't have yesterday's to compare them to.
His blood sugar is still high. He has blood in his urine again. His heart and lungs are full of fluid. Electrolytes are ****ed (potassium, sodium, magnesium, that sort of thing). Not exactly unexpected. Basically this whole adventure is an extremely difficult balancing act. We get one thing straightened out and another thing or three goes haywire.
The doc says the next 48 hours will tell us a lot about how the rest of his stay will go.
Again I cannot tell you guys what a comfort your kindness has been to me. I am so grateful for the friendship each and every one of you have extended to Scott and me. Thank you all.
Yea the first time they released me from the hospital I went straight home. That did not work out so well and a week later I was back in the hospital. Next time I went to rehab and did not go home until I was strong enough to take care of myself.
I should have known better that wifey was not strong enough to take care of me, if just from the number of times I fell at the hospital trying to do things myself. I thought I was ready but I was not.
I hope so. I just have to be really careful the diseases I get and the antibiotics I can and can't take. I've been on the infusions over a year now so I know what Grumpy is going through. I think he waited too long to get to the ER. That is why he's had such a hard time. I was diagnosed because my eyelids were slamming shut. They got that fixed and warned me my breathing might be affected. Two days later I was almost gasping for breath just sitting down in my chair. Walking to the bathroom I was winded. I went to the ER and told them my diagnosis, my doctor's name and my symptoms. Boom, I was in a room in intensive care.Just asked my wife who is an RN about the condition Scott has. She was familiar with it after having a few patients with it.
It’s an autoimmune disease that with treatment will allow people to live to full life expectancy.
Continued prayers.
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