Tuesday, March 31, 2009

Emily Update 3/31/09

Emily is doing great today. She had her first eye exam today, it went well. Her eyes are developing normally for her age. The reasoning for the eye exam was to check for Retinopathy of prematurity (ROP). This is a process of abnormal blood vessel growth in the retina of the eye. There is a strong association with ROP and prematurity as ROP is seen most frequently in infants born at less than 32 weeks gestational age. Besides prematurity, additional risk factors for ROP include respiratory problems, anemia (low blood count), heart problems, hemorrhage in the brain, and the need for supplemental oxygen necessity. Of course we are looking for the reasons of respriatory and oxygen use. She is up to 2 lbs 15 oz. So hopefully tomorrow she will break the 3 lb mark. She is active and fiesty. And is all about trying to help the nurses take care of her, usually by grabing the tubes they need or are trying to use and pulling on them.

Monday, March 30, 2009

Emily Update 3/30/09

Emily has had a great night and day. She put on 2 oz which now brings her to a whopping 2 lbs 14 oz. She is still really low on her oxygen intake. Which what we want. They ran her nutrition labs again today, and everything was nice and high. Her iron was really high, which also really good. And her bilirubin was nice low, which means she isn't jaundice. The 2 oz could also be partially water gain, since babies her size don't normally gain that much weight at a time. Thanks for following Emily's journey and keeping her in your prayers.

Sunday, March 29, 2009

Emily Update 3/29/09

Emily is still doing very well. They turned down her oxygen to 21%. Which basically means she is breathing the same air that we are, just it is a little more forceful to keep the air sacs in her lungs opened up. She is recieving 24 ccs of milk with 24 calories for every ounce in it. She is up to 2 lbs 12 oz now. She is geing so close to the 3 lb mark. We are hoping once she is up to that point she may not need all the help with her breathing. She can't get moved into an open crib until she is off the CPAP and is no longer in need of the ventilator. We finally found clothing that fits her, doll clothing. But I doubt that will last for very long at the rate she is growing. I just wanted to say thank you to everyone who is reading these blogs and keeping Emily in their prayers.

Wednesday, March 25, 2009

Emily Update 3/25/09

Emily is doing great. Her retick count was right where it needed to be. This means she is making her own red blood cells and at a good rate. She is tolerating the CPAP well. She did lose about 1/2 oz, due to the fact they skipped a feeding last night. They wanted to see how well she would tolerate being on CPAP and didn't want to overwhelm her. Her head ultrasound came back perfectly normal. Her brain is growing and function just as it should. I got to dress her for the first time today. It was to cute, even her preemie clothing is to big on her. But she will grow into it soon enough, at least I keep telling myself that.

Emily Update 3/25/09

Emily Maire is one month old today. She is doing great. They removed the ventilator yesterday, and is now back on CPAP by mouth. With a little (lot) of help from Miss Emily. She is keeping them very busy and on their toes. Emily seems to have many tricks up her little sleeve. She weighs 2 lbs 11 oz. They moved her feedings up again, she is now getting 24 cc of milk every three hours. They are doing a head ultrasound today, checking for white brain mass. The white brain mass is good. It shows the brain is developing like it should. They also are doing a rountine check. And doing what is called a retick count, this will see how fast she is making her own red blood cells. If she is making them at a fast enough rate, then they will leave her alone. But if not then they are talking about another transfusion. We are getting closer to getting her in an open crib. She has to have all leads and tubes taken off of her before that. So we have the CPAP and just the basic leads left. They are talking in about being able to dress her soon, so Mom and me have spent the last two nights getting clothes together for her. Thankfully we have plenty of preemie clothing. Thank you to all who gave them to us. I wanted to use these because by the time she gets home she be in newborn/0-3 monthes. And at 34 weeks they will attempt to feed her through a bottle. She has to be able to take it and keep most of it down for 48 hours before she comes home. Keeping our fingers crossed that she will be home before long.

Sunday, March 22, 2009

Emily Update 3/22/09

Emily Marie is doing beautiful today. She is up to full feedings now, which is 22 cc of milk every three hours. She is tolerating it very well and keeping it all down. She is still getting 24 calories added to every 30 ounces of milk. She now weighs 2 lbs 8 3/4 oz. She normally puts on about 20 grams a day. And once she reaches 34 weeks they will begin to bottle feed her. She got her ventilator settings turned down again today. She is now receiving 15 breathes per minute, and is pretty much driving it herself. Which means that it really only puts pressure on her when she falls below the set setting. She had a chest x-ray and it looked perfect. They are looking at taking her off the ventilator around Monday or Tuesday. Keep sending prayers and good thoughts our way.

Saturday, March 21, 2009

Update Emily 3/21/09

Emily is doing really good. She is up to 2 lb 8oz. They are weaning her off the ventilator. She has been stable for the last two days, and it is looking like a good night for her. She had another chest x-ray, which is clear. Her blood gas is excellent. All her levels are where they need to be. She is still getting 21 cc of milk every three hours and 24 calories added to every ounce of milk she takes. They won't increase her feedings until she stops gaining weight, then they will increase it again.

Wednesday, March 18, 2009

Emily Update 3/18/09

Today was a really good day for our little fighter. She is doing an awesome job. Emily is just getting enough help from the ventilator to be actually doing some help. She has been very stable while on the ventilator. She is eating 19 cc of milk every three hours. And has moved up to 24 calories per ounce of milk. Tomorrow she will be getting 21 cc of milk. Soon enough she will be eating from a bottle. Yippee!! She got to get her PICC line removed. Since there was no use for it, it was becoming a source of possible infection. Her lungs still are nice and clear. All her lab work and blood gases have been good. Starting today they are doing nutrition labs on her. This will check her iron, protein levels, and calcium intake. If these are lower then they would like them, they have to add more of the human milk fortifier to her milk. As of today she weighs 2 lbs and 5 1/2 oz. Just keep sending prayers and good thoughts our way.

Monday, March 16, 2009

Emily Update 3/16/09

Today Emily had to be out back on the ventilator at around 6:30 am. This wasn't a bad a thing, the doctors just want to give her a break, and allow her to build up some energy. She is getting very minimum support from the ventilator, she only gets 25 breathes per minute. Anything over that she takes on her own. Also while she is on a break they are hoping that she puts on some more weight. They have added human milk fortifier, which is giving an additional 22 calories to her milk. This is to help build up her iron and protein levels. Also it will help with calcium development. She now weighs 2 lbs and 4 3/4 oz. She also had to receive another blood transfusion at 10:30 am this morning. Again, this isn't a bad thing. She was getting to close to anemia and they wanted to stop it before she got to that point. With her being on the ventilator they stopped all caffeine doses, due to the fact that with the all the extra help she is getting the caffeine would result in negative results. In other words, make it look like she is doing a lot better then she really is. They have determined that the problem with her breathing episodes, aren't her lungs, but her airway. They are beginning to thing that it is to small and becomes restricted around her voice box and vocal cords. Her feedings are going to stay the same for today, just to make sure that she tolerates them well with everything else that is going on. She still hasn't been put back on phototherapy. Besides just being a little tired of working so hard on her own, Emily is doing fantastic. So just keep praying for her.

Saturday, March 14, 2009

Emily Update 3/14/09

As of today Emily is still on the NIPPV (similar to the CPAP) but is back and forth on the verge on being back on the ventilator. The only reason she may end back on the ventilator is just because she is tired, and may need some help. They took her off the photo therapy at least for the moment, but that isn't uncommon for her to be on and off it for a while. She is eating 14 cc of milk every three hours and will be moved up to 16 cc tomorrow. Last night her tummy was a little big and hard so they did an x-ray on it, but it was just air from the NIPPV, because the excess air has to go somewhere. So they are venting her feeding tube in between feedings. In a couple of days they are talking about removing her PICC line, since there is no reason they need it in. All in all everything is doing good. Keeping our fingers crossed.

Thursday, March 12, 2009

Emily's updates as of 3/12/09

AS of today Emily is off the ventilator and has a c-pap on getting 21% oxygen Labs are good and she is doing very good on her own without the ventilator eating 12cc of food every 3 hours.

Emily's Beginnings

Just thought we would let you know in case you haven’t heard as of yet. We have little miracle in our family. Sydney found out around the first part of November that she was pregnant and scared and not sure what to do next, keep it unannounced. Then Christmas time came around and she and I were out shopping after the holiday and she had a big problem. A trip to ER, and I find out about baby and she finds out about twins, so a big shock to the systems. But we get thru that and then on Dec. 29 back to the hospital and find out Baby A is coming out, so she has to deliver, it is a little boy. At this time he is only 18 weeks. Unfortunately he was too young to be on his own quite yet. Then this is where it gets very complicated. The placenta from Baby A decides to stay, and she closed up so Baby B, and the placenta is still there. After a week in hospital she comes home on bed rest weekly trips to the DR. Never knew getting blood drawn once every week and a sonogram the next would be so much fun, just getting out of the house. February 9th transferred to Saint Lukes down on the Plaza for two weeks and was starting her third week down there and then by now you guessed it, contractions started and when in to labor. Had to have an emergency C section and now Baby B turns out to be a baby girl, Emily Marie Hendrix, but only 26 weeks along so we have a long road ahead of us. She weighed in at 2lbs 3oz and 14.5 inches long. At the time of birth and to present doing very good for her age. She was ventilated early Monday morning 3/9/09. Dr’s have high hopes for her. She did have to have a blood transfusion on 3/5/09 and still doing very good on her on. She is in the NICU at St. Lukes. That is about all I have for now. Just keep us in your thoughts and prayers.