The road to recovery is filled with lots of twists and turns, highs and lows. Today Lisa was moved to the Hurstbourne Care Center (on Stonybrook, off Taylorsville Rd.) I am not sure how to classify today. It was a twist that we haven't experienced before, Lisa not being completely independent. While it was a high for us that she was well enough to be discharged from the hospital, it was a low for Lisa that she didn't get to go home.
She has a roomate, Joan. Her side of the room is completely fixed up - she has 'nested,' complete with flat screen tv, mini fridge, etc. Mom is going to watch Graylen tomorrow while Jen and I give her side of the room some personality and home-like touches. We don't want to give her the sense that it is her new home, just some things that will make it easier to be there.
We will know more tomorrow about how long she might need to be there. Please pray that she will not be discouraged, her therapy tomorrow will give her hope of getting stronger and healthier.
Thanks again for praying for her!
Tuesday, April 29, 2008
Sunday, April 27, 2008
Hospital Decor
Well, today Lisa was feeling well enough for she, Jen and I to talk decorating ideas. I think that someone should hire the sisters three for upgrading their hospitals to a more cheery environment. Jen says that yellow rooms would make the patients feel more happy. Lisa said that the gray tones just make her feel blah and like she wants to take a nap. Hey, wait a minute. Do you think that hospital employees lobbied for a color that would make their day 'nurse button' free? Hmmm, something to think about.
I could offer some feedback on what other family members say at the vending machines ... one day I sat camped out by the coke/snack machines. First, they need a change machine somewhere - people sometimes only have 5 or 10 dollar bills. Well, I guess they don't really want $5 in quarters, but.. well - they complained about it. Luckily, I was packing change and helped a few folks out. $1 for peanuts or a twix seemed to be an outrage many. I was happy that they offered both bottles and can options in the coke machine. I generally hate drinking from a bottle - cans are the way to go!
Lisa looked really good today. She ate half of a 4 cheese souffle from Panera - that is one of her favs, although I think it doesn't look too tasty. She didn't feel nauseous after she ate, that's progress. Maybe her stomach stuff is working itself out. We still need to figure out what they are going to do about her thyroid. They are having to give her blood thinner medicine for her blood clot - so I bet they can't take the tumor out until after her clot is resolved.
Maybe she will be on her way to a rehab facility this week even. I would love for her to get stronger and feel more like her old self. I think part of her depression lately is because she has felt so weak that she doesn't want to get off the couch. She is a great cook and for the longest time has not felt like even fixing anything - so I am praying that she will have good physical therapists that will encourage, challenge and inspire her to focus on what she "can'' do.
I am also praying she will be open to some kind of counseling. I don't even know how that would work, but I think that after 10 years of chronic health problems and the loss of Pam it is a lot for her to work through on her own. Will you pray about that?
Thanks for checking our blog - and thanks for praying for our family!
Saturday, April 26, 2008
Movin' Up
Lisa moved up last night to the 5th floor...no more ICU! YEA!
She seems to be feeling better, although really weak and tired. She was on dialysis this morning so there was very little room for visitors - so we will go up this afternoon. She has a roommate and said that she snored ALL night! :-(
It looks like when she is finally released that she will go to a rehab facility before getting home. She is so weak that someone would have to be with her all the time - she is way to independent for that! I was glad that she seemed to 'want' to do that.
Dr. Saad will be back on Monday so we will get a better feel for where she is medically when he sees her. The two big things are her stomach and thyroid. The list has dramatically dwindled - hooray!
Thanks for your prayers!
Wednesday, April 23, 2008
Wednesday
We are becoming so familiar with Baptist East that we can give directions, make recommendations at the little cafe, show people how to 'buzz in' to ICU and know the routines of the doctors and nurses. We have watched families happy transitions to regular rooms and the sadness of saying goodbye. I wonder how doctors and nurses deal with people in such dire situations - not to mention their families, which you see the best and worst sides of, day in and day out.
Ilka, Lisa's day nurse is great. She got Lisa into a chair today and she even ate a bit more. There is something going on with her breathing and she had chills and sweats at different points in the day. They said she may get moved to a regular room in the next day or two - her blood pressure is stable and her vital signs are also stable; but to us, she still looks like she needs more personalized care. Physical therapy came today and tried to get her to walk a little bit and she just couldn't. That was really discouraging to her.
Dr. Saad is at Suburban this week and won't be back until Monday. His group is good, so she is getting good care - but we have such a comfort level with him, that we really wished he were the one checking her this week. He will be back on Monday and we are really looking forward to that .. I hope he has enjoyed the break! :-)
We are praying that as the doctors see her in the morning, they can assess her correctly, that we will be able describe how we see her and ask good questions and that Lisa will have the ability to sit up longer and eat more. It is scary to see how thin she has gotten.
Thanks for your prayers!
Tuesday
It is past the 2 week mark that Lisa has been in the hospital. 2 hospitals and 2 weeks later, she is still in ICU. She was pretty weak yesterday and her blood pressure still refuses to cooperate. She did well through dialysis, but afterwards was having some breathing issues. They did an x-ray of her chest and it all looked ok, so they thought it was maybe anxiety.
She is still not able to eat much, so she looks more and more thin. Will you pray that she will have an appetite and can keep what she is allowed to eat, down.
Thanks!
She is still not able to eat much, so she looks more and more thin. Will you pray that she will have an appetite and can keep what she is allowed to eat, down.
Thanks!
Tuesday, April 22, 2008
Monday
Yesterday morning Lisa was more like herself than she has been in 2 weeks. She is on a clear liquid diet, her NG tube is out and she was only running a very low temperature. Her blood pressure is still up and down a little, so they are having to supplement with iv medicine to get it down from time to time, but she is mostly on oral medications now.
She was complaining that her legs hurt, sometimes after dialysis they bother her, but the nurse had them checked for blood clots and sure enough...she had one! They are giving her medicine for that and also upped her pain medicine a bit.
Long hospital stays are not new to Lisa, but it never gets easy.
Thanks for your prayers!
She was complaining that her legs hurt, sometimes after dialysis they bother her, but the nurse had them checked for blood clots and sure enough...she had one! They are giving her medicine for that and also upped her pain medicine a bit.
Long hospital stays are not new to Lisa, but it never gets easy.
Thanks for your prayers!
Sunday, April 20, 2008
Weekend Update
Lisa was pretty sleepy Saturday. Billy and Brenda went to see her and I don't think she woke up the whole time they were there. Her central line had to be changed to a new site and before the doctor got there to change it, she woke up in a very agitated state. When we got back there she was yelling and trying to pull her nose tube out - it was crazy. My guess is that the pain medicine she is on at home is a higher amount than what she is on in the hospital, so maybe it was some withdrawal or something making her act crazy. We waited in the hall while they tried to get her settled down. By the time we got back in there, she was restrained and in dream world. They had to give her some ativan (sp?) to get her to stop pulling at her tubes. YIKES. I would not want to be a nurse!
This morning she was better, you could tell she was tired, and an understandable degree of grouchiness. She is so tired of being sick. She can only have ice chips and popsicles until they get her stomach problem figured out, but she seemed ok with that - it is certainly better than nothing. They did another scan of her stomach yesterday and I think we might hear something about that tomorrow.
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