The Larry Family
Thursday, May 29, 2008
Wednesday, May 28, 2008
CPAP Update
Tuesday, May 27, 2008
The Boys Are Growing
The nasal cannula is a device used in the hospital, in a pre-hospital setting, or at home to deliver supplemental oxygen to a patient or person in need of extra oxygen. This device consists of a plastic tube which fits behind the ears, and a set of two prongs which are placed in the nose or nares. Oxygen flows from these prongs. The nasal cannula is connected to an oxygen tank, a portable oxygen generator, or a wall connection in a hospital via a flowmeter. The nasal cannula carries 1–6 litres of oxygen per minute. There are also infant or neonatal nasal cannulas which carry less than one litre per minute; these also have smaller prongs. The oxygen fraction provided to the patient ranges roughly from 24% to 35%.If the boys are able to get onto the nasal cannula that would be a huge step. Jordan really hates his CPAP and Jaxon begin to hate his as well. We will update you when we find out. Please continue to pray for our boys.
Friday, May 23, 2008
Birthday
Quick update on the boys:
* Jordan is 2 lbs 14 oz
*Jaxon is 3 lbs 8.5 oz
Both are still doing well and we are hoping that they will soon be able to wear clothes! Normally they want them to be at a certain weight (2000 grams) but the nurse tonight said she would talk to the doctors about it since they do so well being contained. That's pretty much all the has changed, please continue to pray for our boys.
Wednesday, May 21, 2008
Keep On Growing
The good thing about staying in the Medical Center is that we have the opportunity to see the boys all the time. During these last few weeks, Crichelle has come up with an observation about the boys' personalities. She believes that Jordan looks like me and acts like her and that Jaxon looks like her and acts like me.
Whenever nurses, or anyone else for that matter, are messing with Jordan he puts up a fit. He throws his arms and legs around all over the place. I was trying to hold his hands last night while Crichelle took his temperature and it was a tough job. He gripped my finger and starting moving my entire hand. He is also starting to let out a louder cry. Crichelle says that he has a temper and that she is responsible for that.
On the other hand, Jaxon is more mild mannered. When people mess with Jaxon you can see that he realizes it and that it bothers him, but he will sometimes just lay there as if he were saying, would you please hurry up so that I can get back to doing what I was doing. Crichelle says that is more indicative of me. Please continue to pray for both of the boys and again thanks to everyone for the thoughts, gifts and kind words. We have been very blessed during these times.
Sunday, May 18, 2008
Back on track
* Jaxon is 3 lbs 1 oz
* Jordan is 2 lbs 10.2 oz
* Jaxon is up to 26cc per feed
* Jordan is up to 22 cc per feed
We also moved out of apartment on Thursday and have actually been staying in our house ever since. We will be going to the Ronald McDonald House tomorrow and will be there for a while. A lot of people have been asking about the boy's head ultrasounds so here is the down and dirty:
* Jordan's bleed is almost completely gone!!!
* Jaxon's last ultrasound showed no change
So what does this all mean??? Well Jordan will not have another head ultrasound unless his head swells up. Jaxon's team of neurologists decided that their plan of action is to just monitor him!! He will continue to have his head measured everyday and will have weekly ultrasounds. We were so relieved to here this news. Please continue to keep the boys and the rest of my family in your prayers as we are still grieving for the loss of my uncle.
Thursday, May 15, 2008
Jordan Making Strides
Tuesday, May 13, 2008
Another Quick Update
By the way, for all of you Cub fans out there. I started singing "Go Cubs Go" to Jordan tonight and he woke up and starting smiling at me with his eyes. I know I have at least one Cub fan, now I just have one more to convince.
Please continue to keep Mrs. Vaughn's family in your prayers. Her brother passed away earlier today unexpectedly. Thank you.
Prayers
Sorry For the Delay
Saturday, May 10, 2008
Saturday Morning Updates
Thursday, May 8, 2008
Smart boys!
Just a few changes with the boys this week. Jordan is off IV fluids and at first his urine output decreased, but they started giving him a little sterile water through his NG tube after he eats and that has helped tons. Jaxon has his head ultrasound today so please continue to pray for improvement. Originally the neurologist wanted to treat his IVH with a reservoir (basically they go right under the skin and drain the fluid with a balloon type device) but after looking over him more thoroughly they decided it wasn't necessary yet. The good thing is that the IVH is resolving himself on one side so hopefully we will just have to give it time. As scary as this sounds these things are extremely common in preemies.
Tomorrow is a HUGE day for the boys.....1 month birthday! Jyusef and I can't believe it's been a month already. If you go back and look the pictures from the first few days and now you can see how they have gained weight. I will try to take some pictures today so you can really see the difference. I really want to thank everyone for all the support and visits but especially my best friends who just try to keep me from going insane. I got a visit from a friend that has been there for me more times than I can count. When I had surgery almost 4 years ago she drove from out of town to visit me for 2 hours and then went right back home. It took her longer to get here then she actually stayed. Last year after we lost Ashlyn she spent the night with me when Jyusef was out of town and I didn't want to stay by myself. I'm telling you all this because it's people like this that keep you in check. So thank you Ashley! I love you so much and I'm so blessed to have such a good friend like you(for over 12 years now)! We are blessed to have numerous friends like this and I don't mean to single one person out, I'm just trying to make a point. I can't wait for the boys to establish relationships with all these special people in our lives. Brandy, you better prepare Whitten and Titus, it won't be long until ALL of our boys will be playing together.
Well I guess I should stop rambling on and on, sorry about the big lapse between posts. Enjoy the picture!
Monday, May 5, 2008
HOORAY!
Now that we are at Children's things are done a little differently. The main thing is that we can hold the boys as much as we want. I held both of them today and nothing feels better than your children knowing right away that their momma has them. As I mentioned in an earlier post Jaxon is not as big of a snuggler as Jordan but, when I hold him it's a completely different story. I LOVE IT! This afternoon when I was holding him it was like he just melted in my arms. I held Jordan tonight and he was really fussy when the nurse was taking him out his isolette. As soon as the nurse handed him to me he opened his eyes and instantly relaxed. I thank God everyday for precious moments like these. It wasn't too long ago that I wondered if I'd ever be able to experience something like this. I have to admit that when I hold my boys I often think of my sweet angel Ashlyn. It's hard not to think about the what would have been when you lose a child. As much as I miss her I know that God has a plan. Every night before we leave we pray with our boys and always thank God for everything. When I rock them I remind them of how many people love them and how lucky they are to have so many people praying for them. I also remind them that they are lucky to have their own guardian angel watching over them that just happens to be their big sister. We will never forget our sweet Ashlyn and we couldn't ask for a better angel to watch over the boys.
Please continue to pray for the boys. We love you guys!
Sunday, May 4, 2008
Clarification and Update
- Jordan's IVH is now considered a Grade I
- Jaxon's IVH is considered a Grade II on one side and a Grade IV on the other
- Jaxon's head is growing normally so they are just going to continually monitor it
- Jaxon is now up to 20 cc's every 3 hours
- Jordan is up to 18.5 cc's every 3 hours
- Jaxon weighs 2 lbs. 6 ozs.
- Jordan weighs 1 lb. 14 ozs.
Saturday, May 3, 2008
Texas Children's Hospital
Yesterday was one full of emotions. Here are just a few of them:
- We learned of the move and thought the boys would be separated.
- We experienced a ton of joy when we found out they would be together.
- We saw them trying to get acclimated to a new environment.
- We had to get acclimated to a new environment.
- We met a lot of new caregivers that will be taking care of our boys.
Needless to say, Crichelle and I were very tired this morning. If we were tired, I am sure the boys were exhausted. Just an update on their weight, Jaxon is now 2 lbs. and 4 ozs. and Jordan is 1 lb. and 13 ozs. They have really been doing quite well. Jaxon had his permanent IV removed at about 2 PM today. He is now purely on his mom's milk and finished with the nutrients that were being fed through his IV. Jordan has a little more growing, but he should be getting close to finishing with his permanent IV as well.
All and all, Crichelle and I both believe that this is a good move for the boys. We like the hospital a lot, that's not to say that we had any problems at Texas Woman's Hospital. They are both fine institutions with great people working there. We are excited about the care our boys will receive while they are here.
Please check back later on today. I plan on updating the boys' photo albums so that you guys can see more pictures. Thanks again for all of your prayers. Please continue to remember the boys.
Friday, May 2, 2008
Update
Change in Scenery
As mentioned in previous post, Jaxon has a Grade III IVH. If you need to be caught up to date on what IVH is please read the "Bump In The Road" post on April 18th. I would just make a link, but I am at school and cannot get to the page through the firewall. They have been monitoring the situation over the past two weeks and have decided that it is best that he be moved to Texas Children's Hospital. They have a team of neurologist there who will be able to provide better care.
We are still awaiting the results of Jordan's head ultrasound. They should be back later today. I just finished speaking with the doctor at Texas Woman's to check and see if there was anyway that Jordan could be moved there as well so that the boys would not be separated. She said that it was possible, but that it wouldn't happen at the same time. Basically, they will put in a request for a transfer because his brother is there. Then, when there is room, they will move him to the same place. We are anxious for that day to come, because we believe that the boys really do sense one another pretty well. We know that they will be excited to be reunited as well.
While this is most definitely a change for all of us, and to be quite honest a little scary, we know that the Lord is the Great Physician. We know that he is able to do things that our human minds can't comprehend. We have faith that the Lord is taking care of Jordan and Jaxon and that this move is a positive one. We sing the boys a song occasionally that really describes this situation,
He's got the whole world,
In his hands,
He's got the whole wide world,
In his hands,
He's got the whole world,
In his hands,
He's got the whole world in his hands.
He's got Jordan and Jaxon,
In his hands,
He's got Jordan and Jaxon,
In his hands,
He's got Jordan and Jaxon,
In his hands,
He's got the whole world in his hands.
We truly believe that the Lord is in control of it all. We know that from the very first moment that the boys were born, and even before then, he has been looking out for them and holding them in his hands. While we sometimes fool ourselves into thinking that it is us who provide for people, we need not to forget that it is the Lord who is in control. He knows just what we need. He always has and he always will. Please pray that the Lord take care of Jordan and Jaxon and enable them to continue to progress during these difficult times.
