Thursday, March 19, 2009

Rough night and morning

I wish I had more detail, but all I know is that Katie Mei is not wanting to eat, was having some abdominal spasms last night and was curled in the fetal position because she didn't feel good, and her oxygen levels were in the low 80s without oxygen supplement.

Jay had them put the oxygen back on her and she went up to the higher 80s, but as of this morning she's on pain meds and still feeling bad.

A nurse reported to me this morning that she still has the fluid in her left lung which cannot be drained, but this is "not unusual" after the Fontan. I have come to hate the term "not unusual".

I am at such a low point and we all really need prayer for stamina and encouragement. This is so hard.

Love,
Petrie

Wednesday, March 18, 2009

Doing Better




As of this morning, Katie Mei has eaten a wonderful dinner and breakfast. Her potassium levels are fluctuating too high and too low, and she's on a diuretic to try to remove some of the fluid in her lungs. That's still not improved and is so critical for her oxygen levels. However, she pulled out her oxygen tube and her O2 sats stayed in the high 80s so the doctors said she could go without it.


Jay gave her a bath this morning and wheeled her to the play room where she got a little fun time playing with the dishes. I know she misses Merrilee and Jacob because they always make "kitchen time" fun for her. It's got to be lonely for her when she's been used to having lots of other children around her all her life.


She is otherwise continuing to improve in little steps. Please praise God for his wonderful works in her in the last 24 hours! I am so thankful that things are looking better today.


Blessings,
Petrie

Tuesday, March 17, 2009

Need prayers

Katie Mei is now with Daddy at the hospital and I am home. She is still not eating and drinking and that is seriously affecting her electrolytes. Jay tells me they are salting her food and I can only imagine that is going to make her want it even less.

She was moved from ICU to the step down unit yesterday afternoon after I left. She no longer has the constant 24-hour vigilance of a nurse, and I am concerned for her. The Momma in me doesn't trust the staff enough, though in my brain I know they are doing an excellent job. I had asked them to give her pain meds on schedule, but after I left the step-down unit put her on an as-needed program which I am not happy about. I asked Jay to change that today.

Please keep her in prayer for continued improvement. She was doing well with the right lung cavity drainage slowing down, but today I am told she has fluid on her left side now. That is bad because she does not have the chest tube on the left side so there is no external removal of fluid. I hope they do not have to take her back into surgery to put in another tube. The increased fluid levels mean lower lung funtion and thus, lower oxygen saturation.

I am feeling helpless and sad today, since I miss her deeply but cannot be in both places at the same time. Merrilee and Jacob need time with me, and they are both reacting to the upheaval in our family now. Please pray for them.

Love,
Petrie

Sunday, March 15, 2009

Huge Turnaround Late This Afternoon


I am so glad to report that prayers were answered at 3:45 pm today. After watching her be so sick all day yesterday, and being sad to see her so depressed and unresponsive today, I was thrilled when she "came back" at 3:45.


Her sodium level had gotten very low, to the point of the doctors worrying about her having seizures, so the nurse was preparing a sodium drip. Before the IV was even set up, Katie Mei turned to me and looked me in the eyes. She hadn't done that at all today. She started to babble a tiny bit, and even wanted to eat her cheerios and rasins. Her oxygen level started to climb and her chest drainage immediately slowed down. It was amazing. It was instant change. I can only attribute it to God's hand; He answers prayer! Even the nurse and staff was shocked at how it happened.


She is now resting comfortably. I need to go back and check on the results of her latest blood test, but I'm positive her sodium level is back up. She's been dosed up good.


Thank you all for praying, and please continue to hold the many other families in your prayers. Can you believe one local mom who's baby is in the CICU here actually went home today and cooked huge amounts of food for the rest of us tonight. I had a delicious home cooked meal, including salad and garlic toast. It was heavenly. She truly blessed us all even in her own time of need. I am so thankful for her graciousness to all of us. I have found a beautiful family in the other parents here, and am so enjoying their presence. I am uplifted many times a day, and have the opportunity to pray with others, for others, several times. It is a gift I never would have known if we hadn't brought Katie Mei home. Blessings abound!


Love,

Petrie

Difficult Weekend

Katie Mei has not been doing well this weekend. She spent most of yesterday (Saturday) vomiting. She has not eaten and kept down solid food since Wednesday. Her chest cavity is also still draining a lot of fluid and hasn't decreased since Friday, thus they cannot take out the drainage tube. Last night she was given an anti-emetic for the vomiting and today she took formula and a little yogurt, but still has no desire to eat. She just wants to lie there with her eyes closed. It's sad to see.

On a positive note, she returned to normal heart rhythm late Friday night and was taken off the pace maker, so she's been holding her own since then. She's had some minor arrhythmias, but nothing anyone here is concerned about. She also had the heart tube removed (that was for administering drugs directly to the heart if needed) and had no problems with that.

Our big prayer request now is that she get back to eating solids and that the drainage would decrease dramatically.

Thanks for holding us up,
Petrie

Friday, March 13, 2009

Pink Fingers!




Day two

Katie Mei is doing pretty well considering the trauma her body has just experienced. She's on a pace maker for the time being because her heart just won't keep it's own rhythm. She drank lots of pedialye and formula this morning, so she's satiated that way. I'm thankful she's able to keep the fluids down.

We're still seeing more chest drainage than we'd like, so her chest tube will probably stay in another day. Hopefully she'll do better by the end of the day and into tomorrow.

Thank you all for praying and thinking of us.

Love,
Petrie