Thursday, March 31, 2011
Tomorrow! tomorrow!
Tuesday, March 29, 2011
Eating Update
Sunday, March 27, 2011
Kara - better and better!
Friday, March 25, 2011
Milk... Mmm, good!
*Yesterday and today she's had high blood potassium levels. This is pretty rare. She had 3 blood draws to "double check" that this was real. A lot of times, the draw itself creates a false reading of high potassium levels. The 3rd verified that for sure, it was real. In the meanwhile they were able to get those levels down (diuretic with a saline IV to compensate... bummer, thought we were past the I.V.s!) It is just above the high side of normal right now. Hopefully today we can figure out why her potassium levels are high. Apparently high potassium messes with the electrical circuits in the heart (hers is currently doing fine, known thanks to the EKG).
*Kara was not very pacified with sugar-water when she was being poked (at least 3 tried... =( for her I.V. Milk in my finger, however? "YUM! Thanks, Mom!"
*Today PT and I started her on a bottle. She took 25 mL in 5 minutes (not bad with a tiny premie niple and for her first try). We are going to try again, with PT, again today to get some guidance for the weekend. Just this past Tuesday she was having a hard time swallowing even drops. Thank you, God, for her amazing progress!
*She is getting more milk to try to up her calories (her weight was down the past 2 days in a row). Her doctors were originally going to just add more calories (i.e. powdered formula) but agreed to do more volume and see how she does. What a blessing to be part of the decision-making process.
*Jeremy & I have had the pleasure of being interviewed, with Kara to be highlighted in a video to help raise money for NICU expansion. It was a blessing to be able to share our experiences and recommendations (like maybe a nearby potty for postpartum women!!) for the NICU.
Looking forward to the weekend!
Thursday, March 24, 2011
Kara - looking forward
*Kara is OFF morphine =)
*Kara had her PICC (long term IV) line removed so she now has a "bare" right hand =)
*OT/PT thinks it may take Kara weeks (as opposed to days or a week) to get to a bottle, so we discussed our discharge/transfer options yesterday. Looks like we may stay another week and then discharge with "home hospital" support and feeding support from an Issaquah entity.
*Our nurse yesterday said we had the BEST surgeons (she thinks 3 are the best and 2 are taking care of Kara). She wants her Mom to be operated on by these surgeons instead of adult surgeons. Thanks, God! Again, we have gotten the BEST healthcare this whole process.
*I have finally figured the traffic out. Leave at 6:45 or 8:30 (but not in between!)
*Yesterday at noon, Kara did an excellent job on her "binkie trainer". So to get her sucking/swallowing, we are doing 2 things
1) finger/pacifier in mouth, dropping drops on top and letting them roll into her mouth so she has to swallow tiny amounts at a time and gets used to sucking with swallowing
2) binkie trainer which is a pacifier with a tiny tube going through the hole, connected with a syringe filled with milk. If she sucks well, she will get small amounts of milk each suck. I can "hold back" the syringe if it's too much for her to swallow, or advance a little milk from the syringe to get her started. Yesterday she powered through 2, 5mL syringes without choking or coughing and wanted more (but we are starting slowly). Hooray! Good job, Kara.
We are thankful for the support of our family and friends. Connor & Katie continue to do well (said 'goodbye' to both of us this morning with smiles). God has been giving them lots of grace, no wonder when we know how many of you are praying for us. Thank you.
Sorry no pictures, apparently I can't use the USB ports at the Chidlren's computer and our internet has been down at home.
Monday, March 21, 2011
Kara Update - Monday
Hello all,
Mom & I went in to see Kara today (Monday). She is now off of morphine. Well, she's off the drip. She did need a bolus at 1 p.m., but no more as of 5 p.m. and hopefully will not need any tomorrow.
I got to talk to the chief surgeon and a few things were clarified. It sounds like he is in NO rush to send us home (not even discussed) and certainly does not want to send us to another hospital. The increased the amount of calories they are adding (they call it fortification, I chuckle and call it "additives") to my milk to compensate for Kara's high respiratory rate. This will most likely be needed for a long while. (It's adding powdered formula to the milk, but we're still at a 5:1 milk to formula ratio, so that's good).
I also got to watch Kara get an "echo" (ECG) and her pulmonary hypertension looks like it's resolved.
The Occupational Therapist (OT) came to work with us on watching Kara suck and start to give her little drops of milk to help her learn to swallow. We are seeing that we need to be at the hospital more to work with Kara during her awake times. With this, we would appreciate prayer for wisdom in how to balance time with C&K, work, and time at the hospital. We know we can't do it all and that's where we need wisdom in choosing what is "best" vs. what is "good" (for all of us).
We're thrilled Jeremy's Mom is coming into town on Wednesday for a week. Yay for Grandma Dot!