Intro

This blog is dedicated to updates and info on the life of Jackson Nathanael Adam. Jackson was critically ill when born and had to go on ECMO (heart and lung bypass). He made a miraculous recovery, and this is his story! Our intention with this blog was to update friends and family on Jackson's progress and specific prayer requests we had during his extensive stay in the NICU. We will probably move to a family website at some point. :) Thank you for loving him!

Wednesday, July 2, 2008

Midnight Post =)


Quick little post tonight. Highlights:
Praise: Jack is taking full feedings, doing well tolerating digestion of the breastmilk. They are stopping the lipids so we managed to eliminate one tube! :)

Prayer Request: Jackson is having trouble learning to swallow and cough. We are working with O.T. (as mentioned before) on techniques to help teach him some of these things. Please pray that he will continue to improve and get the "suck, breathe, swallow" technique down. We had a little "freak out" moment tonight when he spit up during his feeding...which normally isn't a huge issue, but we freaked out a bit b/c he doesn't have the normal "coughing" response and it is so easy for him to get things down in his lungs again and cause serious damage quickly. Everything was okay I think, and the nurse suctioned him immediately and no aspiration or anything, but please please pray for little Jack to start picking those things up.

Prayer Request: Jackson is having difficulty keeping his right lung fully inflated so has begun breathing treatments daily to help with that. This consists of giving him extra breaths with a compression bag several times a day to try to reinflate parts of his lungs that have collapsed. Jackson is not a big fan of the process. :) They will be taking x-rays in the morning to see if there has been any progress made throughout the day today.

Prayer Request: Jackson continues to be extremely congested and swollen. He breathes very raspy and gargly, it is really difficult to listen to, poor little thing. He still doesn't have a voice yet as being intubated requires separation of the vocal cords, so that is not uncommon, but we are anxious to hear him make some noise as that would indicate healing of his vocal cords. :)

Praise: He is doing well on his weaning off of the sedatives and drugs. He has some minimal withdrawal symptoms, but nothing extremely serious, so we are thankful. It does make me sad to see his little chin quiver (one of his withdrawal symptoms, poor little thing), but compared to a lot of babies, that isn't bad. Continue to pray for that to continue as he comes down lower off his morphine and sedative.

Prayer Request: Jack's oxygen saturation levels still aren't extremely high, probably due to lung congestion. He is now on 40% assistance, and initially was around 25% following being on ECMO, so we have gone backwards a bit. They don't seem extremely concerned, but we do know if it gets to a serious point, there would probably be talk of reintubation, so we are praying that he starts doing better or at least doesn't decline more. Please pray for that- as reintubation would be a major step backwards.
Here's a pic of Jack's pod and me holding him with all the wires/tubes/ivs...we have to scoot really close to the bed to usually hold him. We actually don't have that many anymore, but they are still a challenge. :)

Now we are off to get some more things done around the house and prepare for another day a the hospital tomorrow... so I had best be going. Sorry to post in such a "list" fashion, just thought it the easiest way of listing highlights from today and the highs and lows. :) Thanks again for all of your comments, prayers, and support in so many ways- we are so thankful. Know that even though we cannot get you all written or called back, we are so appreciative of all of the support and pray that God will bless you all so much for blessing us! =)

I've posted some pics from today/tonight of our cute little man!

Love to all!

Joe, Miss, and Jack


These are pictures of me getting ready to eat. Mommy is working with me and my pacifier to help get me to learn to "suck" while I am being fed. I think she's trying to brainwash me. =)
This is a picture of my daddy trying to make me laugh. I like to watch him make funny faces. He is a funny fellow. =)

8 comments:

Anonymous said...

It is so great you are able to hold your big boy and have that contact with him even when he isn't responding back to you as much as you wish. All three of you are in our prayers. It was neat that you said in another letter how you sang to him that is really good too. Letting him see the movements of your lips etc.
God Bless you with another great day with more blessings in store for you.
Love
Aunt Sarah & Family

Shadley said...

I can't help but laugh when Joe makes funny faces at me :) He IS a funny fellow!!

Anonymous said...

I am thankful for how the Lord is carrying you. So fun to see you be a family. Maybe you can snatch a nurse to take a 3-some pix. I need it on the "family" wall.
Praying for continued healing. God is good all the time. We trust His heart and ask in complete faith - nothing wavering.
Much love,
Grandma Min and Grandpa Dick

abrahamjerichomccoy said...

Hitting up all your prayer requests. We think of you all daily and are so thankful to hear all of Jack's progress. Remember that God is BIGGER than steps backwards in Jackson's progress as well. Thinking and praying for your family...

The Monsons

Anonymous said...

Joe, Melissa and Jackson,
We are so happy that things are progressing at this rate. Our prayers certainly continue to be with all of you and we are looking forward to having little Jackson home in the neighborhood!

Chris and Rita Hamilton

Sodacoaster said...

love these pics!!

Anonymous said...

The life of a NICU parent is so hard. We're believing with you for healing of the lungs so that Jackson can soon go home with you.
We love you guys!
Brent & Amy

Buck and Jess! said...

Hi guys--just a funny note from my 2 yr old. We were catching up on your blog and saw the cute picture on this post of the baby looking at the camera. My little guy said, "Mom, who is that?" I said, "That's Jackson." "Oh," he replied thoughtfully, "Jackson has a moustache?" :o) I think he was wondering why his little brother didn't have one and was a little concerned we were missing out on something :) I told him it is a special tube that helps the baby breath, and he thought that was pretty cool too. We'll keep praying his "moustache" helps and Jackson's lungs work the way their supposed to.